On the Anniversary of His Death, Another Thank You to My Mentor, Frank Ginn, Ph.D.

You left so suddenly, dead before you hit the ground, we were all stunned.  I was on vacation, I got the call and my then spouse and I went out to the beach and I sang songs to you.  Did you hear them?  Were you already gone too far from this earthly plane to hear? I thought I felt you at dinner that night very briefly when I looked out at an amazing sunset over the ocean.  Was that you or was that wishful human thinking?  You taught me so much that I still use in my daily life.  You taught me tolerance and acceptance and shared your wisdom and even Patsy Cline (well I bought a CD but must admit she’s not my favorite Frank :) ).  You are my near priest, the one who should have been except than I and all the others who learned from you would never have met you.   But you would have been an excellent priest in a Church that needed folks like you with integrity and compassion and wisdom and always faith. 

I respect you, I learned from you, you were kind and you “got” me, I still miss you 17 years after your death at 55.  I know you are at peace Frank and I know you are with our Father, how I know I can’t say, but I know.  I hope I will see you again some day.  I wish you were here to read this and I wish I had told you how much you meant to me while you were still with us so I’m telling you now.  Don’t rest in peace, delight in the joy of being with the Father Frank.  :) .

Here Are Some of My Flashbacks: For Doctors and Delegates and Professors to Dream About Like I Do

I just thought about the resident who not only pulled out my PIC line so hard it left a fistula that caused severe pain that was ignored by UVA dialysis for months years later because he didn’t want to be the doctor to a “mental case” who also told my mother I must be sneaking lithium on the side because of course everyone wants to throw up all day every day and be tied to a PIC line for hydration on their 40th birthday….. Same resident, taught by UVA medical faculty, theorized I had late developed bulimia despite 7+ weeks in the hospital and acute kidney failure I now know.  Or it was lithium toxicity, who knows, UVA doesn’t keep medical records very well.  And they certainly don’t dialysize wastes of space like me who have diagnoses no matter how sick we are….

I remember the attending who complained over my bedside about the cost of the Zofranthat was helping my intense nausea a little to the fellow. As if I wasn’t worth anything. Mysteriously my Zofran was stopped one night and I was wretchedly ill all night until another doctor intervened and gave me back the Zofran.

I remember the nurse who wouldn’t talk to me but would gossip about me to my room mate and other nurses and who contradicted the doctors and also told me I must want to vomit. 

I remember being treated like a piece of meat and dragged from one room to another to be catheterized (now that I have heard the real story from UVAnurses I remember it correctly) because my room bed wasn’t set up for such procedures and I know I ended up with symptoms from this rough treatment for a month.  I remember nobody comforting me or warning me it might hurt as is usual medical procedure but instead scaring me by saying my bladder was 80% full and could burst and it must have been the resident since UVAswears both nurses present say they didn’t say it but mysteriously no one can identify or will identify the resident present.  Her name was on the wall, not so hard to find..

I remember being told my kidneys would be fine or they didn’t know what would happen and not being referred to a nephrologist as I should have been.  I remember leaving UVA in early ‘97 thinking I was the lowest of the low having never been a medical patient before and being in so long treated as the lowest patient of the low, all due to prejudice.  The few polite doctors and nurses stand out they were so rare.

I remember being afraid of doctors for years after this, finally overcoming it and now regaining my fear after 2 unnecessary weeks in UVA 5 East for a steroid reaction an arrogant attending was determined to diagnose as bipolar disorder and even more determined to be absolutely adored and obeyed. 

Most of all I will never forget losing my half-sister because I was drugged up on drugs I should never have been on, withdrawing, forgetting, not myself and having her one visit spend with her refusing to even speak to me.  I will never forget the pain of that nor what UVA doctors did lying to my mother and terrifying her and lying to my brother and scaring him and sending false information about me to all of my doctors without my permission and the threat of being sent to Western if I let my lawyer ask for my medical records or if I exercised my legal right to do so.  Now that I have read them, I know why.  So tomorrow I am not waiting for the “internal and probably endless possible investigation” into falsifying medical records, I’m calling the Charlottesville Commonwealth’s Attorney Office and reporting a crime.  Because who knows how many others have had their records completely falsified to suit some psychiatrist’s power agenda or just need to lie and who knows what damage could be done to another fine UVA program if this complete fabrication got out in court or elsewhere and I care about that unlike UVA 5 East psychiatry. 

Oh, and thanks for the fear of sleeping in my own bed and the need to sleep on my couch with a light on.  PTSD from UVA, the gift that keeps on giving and giving.  A special thanks to my delegate who knew that lowering the standard for commitment was not necessary and pushed it anyway for political reasons.  This is the woman who sat in your office and told you what the commitment rate was and you said it was like hitting a flea with a hammer.  Well I’m one of the fleas who got hit, living in your district, afraid to sleep in my own bed. Thank you Delegate David Toscano, former friend to people with disabilities. You might think about starting an investigation or study into the number of folks involuntarily hospitalized unnecessarily under the laws you passed and the rates of PTSD, unemployment, eviction, divorce, family alienation, even suicide since the rate goes up on release. Don’t worry about me, I’m too busy taking my transplant drugs on time, something 5 East couldn’t manage and too busy fighting back for all the other folks affected to give up, much to some’s chagrin..

Someone Alert Region Ten that the APA Does Not Support Their Service Approach

http://pn.psychiatryonline.org/cgi/content/full/44/13/8?etoc

Psychiatrists Lament Decline of Key Treatment Modality

Evidence of the efficacy of psychotherapy has increased dramatically in recent years even as the place of psychotherapy in the identity, practice, and training of psychiatrists is diminishing—a fact that was widely recognized and just as widely deplored during a workshop at APA’s 2009 annual meeting in San Francisco in May.

Stop the Shame, Stop the Blame, Stop the Threats and Use of Force and Then You Can Talk About “Recovery”

I am exceedingly tired of hearing about recovery by mental health administrators and public providers and even some with lived experience.  It has 1) become another way to make people with emotional issues feel inadequate if they don’t meet societal norms that most without emotional issues don’t meet these days (most American households are single adults, the ranks of the unemployed and underemployed are high, those who don’t comply with health recommendations are legion etc.)  and 2) is not possible in an atmosphere of continued shaming and blaming and high expressed emotion with low willingness to listen by mental health providers, especially in psychiatric units and hospitals and in an atmosphere of coercion with the ultimate threat of violence in a take down and restraint and isolation still available in every psychiatric hospital except perhaps those for the rich and even there those who can not fit in risk transfer to the coercive regular psychiatric hospital.  There can be no recovery in an atmosphere of coercion, blaming and shaming.  Mental health providers, especially psychiatrists, have to stop having it both ways by both insisting people with emotional differences have a real illness and emphasizing to the public and to their patients that they are bad and not good enough for society and need to be fixed to have a reasonable life.   Medical doctors of people with life threatening diseases whose patients may well die on them often do not imply nor tell their patients that they are to blame for their illness and need to take responsibility in order to fit into society.  They offer their advice and voluntary treatment and the best and even the mediocre try to provide hope and encouragement and support for the hard work of medical treatment.  Medical doctors and nurses warn their patients when a procedure will hurt.  Mental health workers and psychiatrists pretend that huting and humiliating their patients by taking them down leaving bruises, injecting them, tying them up and isolating them and mocking them is good treatment and never tell their patients it will hurt them and leave scars that will give them shame and nightmares and fear and low self esteem for the rest of their lives. 

Let us stop pretending we are ready to talk about recovery in a system that still uses power as its main “treatment” modality.  It is not possible, it is harmful and it has already stolen too many lives and souls.  I am taking my soul back but I have lost too many years of my life to the scars of psychiatric mistreatment, not just my kidneys, that is almost the least of it, but the self-blame and the fear and the shame have made me afraid of interaction with others, made me feel less than, enabled a bully in my circle to bully me for 26 years until this weekend when she continued to bully but I broke the cycle by standing up to her, perpetuated my problems and now, after years away from psychiatric power misuse and coercion changed my life yet again, made me question my life, made me fragmented for a time, made me unable to do what I used to be able to do effortlessly.  I will survive and thrive this time because I faced down every implanted fear and shame and lie this time, but how many years were lost, how much potential and how many will not survive and will and are having their lives wasted by the abuse of power and shaming and blaming?  It is time to stop, way past time.  If psychiatry and public mental health systems will not control their own acting out it is time for society to act and take away their power over the lives of others once and for all until they can prove they have anything to offer that is more  helpful than harmful.

DMHMRSAS is DBHDS as of Today. I Like It :).

No longer will the Department as I always call them anyway be able to claim they care about anything but behavior.  Emotions and feeling? Symptoms to be eliminated with drugs and CBT or DBT.  Flashbacks–they’re in your head, not behaviors, get over yourself with your flashbacks and nightmares, also in your head.  Now if you sleepwalk maybe UVA can help you gain more flashbacks or maybe even UVA will stop doing that and learn how to deal appropriately with sleepwalkers, but feelings? Memories? Sadness? Anger? Family dysfunction? You’re kidding me right? How could any of that be treated except with expensive trained, compassionate and accepting non-judgmental professionals who are hard to find and cost real money?  So much easier and convenient to eliminate behaviors while eliminating brain cells and volume and teaching people who feel too much that their feelings are bad and they by extension are bad.  That’s the American way.  Lost too many buddies in the war?  Get over it.  Take some pills.  Don’t cry, don’t bother anyone with your nightmares and flashbacks, not at a DBHDS facility or licensed facility anyway.  Better pay some of that high salary they gave you to go to Iraq and see if you can find a well trained private therapist and good luck with that too because they are a dying breed, modern programs teach behaviorism and blame, not unconditional positive regard crapola.  What are you thinking? Just because you served your country and got hurt people should have compassion for you? Get over it.  DBHDS will have none of that girly nonsense. 

I love truth in advertising so I like the new name.  I do wish to mention that I do know hidden employees of DBHDS who have compassion, caring, integrity and concern for emotions, I keep them in witness protection and hope their covers are never blown……  :) .

Thank You UVA 5 East for Fabricating My Medical Record

Gee, does anyone who knows me think I have a New York City accent, because UVA’s psychiatric record writes that I am from New York and was hospitalized there.  Interesting since I have not visited NYC in 25 years and NEVER lived there.  Also very interesting is that they found it “significant” that I had recently dropped off on my mental health advocacy after being President of the Governor’s Commission on Mental Health.  Well A. There is no such Commission in Virginia, B. I would sure like to have been President of such a Commission if it existed but that was never going to happen in the real world I live in as opposed to UVA psychiatry and C) in what way have I dropped off my mental health advocacy? I am still past-President of the Virginia Mental Health Planning Council and although the powers that be helped by someone I thought was my friend have kept me off every committee of importance other than that since then and even revamped the Supreme Court Commission’s website in such a way that the Commitment Taskforce on which I served and spent much hard work and its non-consensus report is almost impossible to find, I am still here, still advocating, still making noise about human rights and still afflicting the comfortable and comforting the afflicted.  And I still have advocate friends in high places who let me know what is going on and strive to get me included despite the dangers of doing so since I am persona non grata to many people who are not used to any kind of disagreement or criticism from “the likes of me”, a person with lived experience, with years of work experience in the MH system and with a degree, intelligence and a computer to write on……….

There are worse fabrications on my medical record, all from psychiatry and none from nephrology but those must wait for another day when they have been confronted as they involve other people and could terribly hurt a program that helps so many in our region if ever found by a federal agency.  But apparently being right and bullying patients is more important to Dr. B. than the very lives of children and adults in our area.  Not being Dr. B., I won’t endanger their lives because I have something she appears not to have, a conscience and a caring heart and a sense of obligation and gratitude to those who actually save lives instead of destroying them in the name of medicine.  Can we go back to calling hospital psychiatrists alienists now? Pretty please?  The rest of medicine would thank us I am sure.

How Many Dogs and Cats Die or Suffer Each Year Because Virginia’s TDO Screening Does Not Ask About Pets in the Home?

When people are involuntarily detained in an ER in Virginia an unlicensed Community Services Board employee comes in and goes through a screening form which besides not asking about domestic violence, leading to a preventable murder trial in Fairfax in the last few years, also does not ask about pets in the home.  Picture a pet owner strapped to a gurney with a non-licensed clinician going through an inadequate form, trying to answer questions usually after being shot up with Haldol and barely able to speak and ask yourself if the question if not asked, how many barely conscious adults will remember to tell this person with the power of freedom or hell over them that they have a dog or cat at home that needs feeding and walking and tending?  Not too many is my guess.  Do hospitals ask about pets in the home? No, they do not.  So unless the person being locked up against their will for being different or annoying or unable to care for themselves supposedly or suicidal sometimes has friends or family who still act like they care and who have keys to their homes and will take on the care of a dog or a cat, a dog or cat or more than one dog or cat may starve to death or suffer with no water or end up dead for the person locked up “for their own good” to find on their return from the hell that are all our psychiatric hospitals in this great state.  Good job Virginia!

Psychiatric Trauma and Other Traumas, the Gift that Keeps On Giving

Yes I woke up from a nightmare, no this does not mean I am ignoring my “sleep hygiene” nor that I am manic, I wish I was, I would feel better.  No it’s just the usual but I know better now than to call SAARA nor SHE in Stepford/C’ville because people like me don’t have real trauma, we have the fake kind that just requires years of therapy to give the appearance of Stepford normality in public….  Funny how so many years ago, 25 I believe or more, Philadelphia’s Women Organized Against Rape had a special self-defense course for women with trauma histories, guess they were just stupid instead of one of the first Rape hotlines and organizations against rape led by women in the nation.  Stepford knows better.  Stepford knows only certain women count when it comes to trauma of any kind.  Stepford knows that a homeless women 3 weeks away from her abuser is past it already and too late for SHE’s help.  Stepford knows people with psychiatric traumas even if they have other traumas too can only be helped by “Professionals” and shouldn’t bother SAARA.  Or they can go to a regular group where they will feel right at home talking about being assaulted in a psychiatric unit in this oh so enlightened town about psychiatric survivors….  Or they could just be quiet or go away.  Oops, that sounds like the patriarchy talking a bit doesn’t it?  Oh well.  You can’t buy books on feminism in used book stores here, can’t even find Sonia Sanchez in new book stores, Adrienne Rich isn’t in Barnes and Noble, we have overcome, we don’t need to read feminist writers any more.  Audre Lorde is dead of cancer, who would want to read her cancer chronicles, women aren’t getting cancer anymore, especially not lesbians nor women of color…  We have the women’s Four Miler, we are going to cure cancer by running and walking and too bad if sick women can’t run nor even walk 4 miles, and too bad if more women are dying of lung cancer because lung cancer is just, well, icky, how could Christopher Reeves’ widow die of such an icky disease? Let’s not talk about it, that will help.  Let’s teach our children to yell at adults who smoke because yelling at addicts in public is a proven method of rehab.,not.  Let’s sit in front of an ashtray outside with our expensive earbuds and not hear the person asking us if we mind if they smoke until we glare at them and then do the fake smile when they walk away from the smoking area to bow to your superior non-addiction and superior electronic gadgetry….. 

Let’s tell everyone they can be healthy too even if they have kidney failure or cancer or heart failure or liver disease if they just keep a perfect blood pressure and get a massage, that’s the ticket, than we can save money on icky expensive medical treatment and all live forever in fantasy land, a land called Charlottesville that looks like Stepford except for the hopeful signs of all these icky newcomers moving in who don’t know how to act in Stepford and break the rules by being themselves and don’t care who you know or who your parents were…..

Oops, got off on a rant, nightmares will do that to you as will the prospect of getting up in a few hours for blood work with too little sleep.  Maybe I’ll cancel and put off till Tuesday, would that be okay with the compliance police? Because these nightmares and flashbacks are really kicking my butt despite my long swim today and yesterday and walking several times each day and giving to a soup kitchen, how could that be, bad things only happen to bad people, right?

The “Abuse Excuse”, Not What You Think It Is

I’m sure you have heard the term the “abuse excuse” used to say that people who commit crimes or even people who don’t fit in are using the “abuse excuse” if they mention a history of trauma.  Well my observations in this town and others is that the REAL “abuse excuse” is the excuse for abusive behavior towards people labelled with psychiatric problems used by not just professionals but many family members as well.  I heard a young man blame himself for his mother shaking the car and putting him out on the side of the road because, get this, he kept talking when she asked him to stop.  This was her excuse for her abusive behavior towards her adult and conveniently psychiatrically labelled adult son.  He blames himself and does not even see this as abuse.  Do you think he is getting any help obtaining insight into the ways his mother continues to damage him emotionally into adulthood at Region Ten? Think again.  There is no family therapy available at Region Ten.  There is virtually no therapy available at Region Ten.  There are drugs and a clubhouse to perform simple tasks for free and for some services in the home and “case management” to refer to services that are increasingly not available but no chance to process what happened to someone that put them into the position of identified patient in their family.  Why? I could say I blame the patriarchy and I do.  Psychiatry has been misogynistic since its founding and men are hurt by this too because a man who breaks under abuse is still seen as feminine in our town and our culture and thus is a victim of misogyny just as much as a woman.  And because there has NEVER been a woman Commissioner of Mental Health etc. in Virginia, remarkable even for a Southern state and because there has NEVER been a woman director of Region Ten, remarkable even for Virginia.  But that is only one layer, the utter dominance of men in the administrative positions of power at the state and local level in mental health.  Not to mention the completely white board of Region Ten and the completely white top administrative structure of our Department of Mental Health soon to change its name to something more descriptive of what it’s about, the Department of “Behavioral Health” since emotions have no place in our system of care for those who ask for or are forced into our mental health system in Virginia in the main.  Some areas still have therapy available, some may even have family therapy, but neither are “evidence based practices” and neither are reimbursed at a rate to pay their way nor encouraged by the state. 

Our mental health system in this country began to maintain the social order by locking up women and men who couldn’t or wouldn’t fit in, were poor, were “bad” wives, were going through menopause, were unable to get over a romantic loss in the proper amount of time, were a financial burden on their families or communities and back in the beginning the heads of the state institutions were called keepers not doctors nor directors and the caretakers were called “alienists” not M.D.’s and certainly not psychiatrists because psychiatry had not been invented yet. 

How much have things changed since then? Well common mythology is that things have improved oh so much since the bad old days.  I’m here to say that’s not true, things just look different than they used to and the worst oppressions have gone underground where most can’t see them.  No longer can the public go gawk at people in state hospitals but then again, neither can the public see what actually goes on in state hospitals and the people who get out aren’t listened to and only talk amongst themselves.  We have a psychiatric unit at UVA and at Martha Jefferson run by UVA.  We have an ECT machine at Martha Jefferson, the only one in miles around, people come from West Virginia to be “treated” with it.  How many readers from the Charlottesville area even knew that? How many know that involuntary ECT is still legal in Virginia? How many knew that more commonly an “authorized representative” chosen by an institution head or doctor is allowed to “volunteer” an unwilling patient for ECT with no hearing and no oversight by anyone?

How many know that drugs are coerced on many, many people in our community in their own homes as a condition of having housing or services or sometimes even staying out of jail? How many knew that commitment hearings in this region are a joke with a 99.5 per cent commitment rate?  How many knew that 2 doctors with no training in competency examinations can simply declare any psychiatric patient incapacitated and appoint a family member to make all decisions for them or if they think that won’t work simply get a “Judicial Authorization of Treatment” without any history of non-compliance with treatment nor proof of its need at all?  With this they can force a person to take any and all drugs against their will with the threat of restraints and a needle to back them up.  And if those threats don’t work there is always the threat of sending someone from UVA to Western State for up to 6 months. 

How many knew that all possessions are routinely taken from patients admitted to UVA 5 East including human rights booklets with a phone number to call if ones rights are violated.  Booklets being so dangerous of course.  That cell phones are taken and left on for the battery to die and patients not allowed to make a phone call to a friend or lawyer before they lose all their contact numbers?  How many knew there is no right to a phone call for someone detained under a temporary detention order? How many knew that someone with connections will get out if they have memorized the right phone numbers and someone without or who hasn’t memorized their numbers will not? 

Back to the “Abuse Excuse”. People who are labelled mentally ill have one of the highest rates of child and adult abuse and trauma experiences in the population.  Is this even a question on the routine screening for detention? No it is not.  Are there services for trauma survivors that they want? No, not at Region Ten which hands out booklets and uses CBT otherwise known as clean up your behavior and don’t think about your past among the abused who have experienced it. 

I have met too, too many abuse survivors in our community looking for or supposedly receiving services from Region Ten and UVA. What I see is re-enactment of their abuse and denial of their real experiences and covering up of their feelings and possible insight and recovery with heavy duty and medically and brain shrinking drugs that make money for big pharma.  What I see is a lack of basic respect for people who have survived trauma with a Region Ten website that still says “Our Consumers” and “For Our Staff” and doesn’t even get how disrespectful and accurate as to their attitude this is.  What I see is an Albemarle County Board of Supervisors who listens to the director of Region Ten who doesn’t want any out and outspoken people with lived experience on his board, a director who is patronizing and rude to outspoken people with lived experience.  What I see is co-optation of anyone who shows signs of becoming a leader who isn’t too stubborn to be bought or praised into toeing the Region Ten line.

What I see makes me very sad and angry for my people and not hopeful about the future.

Thank You to 2 Catholic Hospitals for Telling Me Being a Lesbian Was Mental Illness

Misercordia, I don’t remember the psychiatrist’s name, but he was so confident that I was delusional that I was a lesbian.  Sacred Heart Hospital, who violated my rights in so many ways and wanted me to quit graduate school to go on welfare and live in a group home with no sex, I remember your telling me so many times that my lesbian therapist had corrupted and misled me and that you refused to let her visit me.  You kept me so many days longer than others until I gave in and said I wasn’t a lesbian, I was crazy.  Just like 5 East tried to convert me to bipolarism instead of the reality of a common steroid reaction  to for 6 + months, 2 Catholic hospitals tried to convert me to the idea that lesbianism was a delusion and a mental illness.  The only difference is neither of the Catholic hospitals threatened to send me to a state hospital even though that was so much more common all those years ago and 5 East decided I belonged in Western the first day I got there.  For my hereticism I guess.  If psychiatry isn’t a religion, a false one, than I guess it is more like the Spanish Inquisition, but not the funny kind.  Thanks for all you have done to mess up my life with your false prophecy and arrogance and moralism in the guise of medicine and most of all, your bigotry.  Your welcome is that I am still here and I am free to be whoever I want to be and you can not force toxic drugs on me and you can not hinder my free speech outside your snake pits.  Nor can you threaten me with physical assault without being arrested.  So sad.  For you.

Thank You UVA 5 East for the Bruises that Lasted 25 Days, I Finally Went Swimming Today

How could I forget to mention the bright red bruises on both arms that I left UVA5 East with on May 30th? I noticed they were fading to yellow this week and by today they were completely gone, so let’s round it off at 25 days of being marked and reminded of psychiatric assault and being re-traumatized every day even after I left your snake pit.  Huh, you have video cameras in the halls but don’t as is standard practice elsewhere for 20 plus years take a record of marks on your patients as they arrive and leave?  Wonder why.  Well no I don’t wonder why, you have your reasons I’m sure.  Assault is assault is assault.  Oh and how could I forget to mention that the 600+ dollars would have been much more money if I had not requested a change from the dis solvable, newest and most expensive version of Zyprexa that money conscious  UVA  prescribed to me in the hospital while changing my beta blocker to one I wasn’t supposed to have to save money.  Huh, what’s up with that? How much money was my decent insurance charged for an unnecessarily expensive drug proven to “work” no better than generic drugs in many independent studies? Guess that lack of submission of information on drug company ties I blogged on some time ago might mean something after all? Or is it all a big coincidence that the most expensive drug was prescribed to someone with insurance that would pay for any drug inpatient and not to someone whose insurance would not? 

And thanks for suggesting that the nurse who disliked me the most and tried to limit my water supply once which is dangerous to my kidney be one of the people for our informal meeting next week.  Too bad I remembered who she was–see previous nursie post.  Do you really think there is anything any nurse can say that will intimidate or embarrass me? I was given toxic drugs, drugs that made me crazy at dangerous doses, I was not taken off the drug that clearly caused my problem in the first place and now you think I feel responsible for anything I did or didn’t do while I was in your snake pit? That would be a big no or put it this way–I feel as responsible for my behavior as a woman who was given a mickey or GBH by a date.  That of course is a crime in our state, unfortunately what you did to me is still legal for now and unfortunately the chief perpetrator is conveniently out of the country and the hospital’s lawyer, usually so resourceful, just can’t seem to figure out who the 3rd member of the team was, a fellow who will be out of UVA before our meeting.  How convenient this sudden lack of research skills in a long experienced general counsel.  How stupid do you think I am? Keep thinking that way,  I like it, it helps me every time you over estimate yourselves and underestimate me, so keep it up and make me happy.  Except for the bruises and the renewed phobias and the lost time and the money I can’t afford and the worry to my friends, except for all that you arrogant poor excuses for professionals.

Small Town/City Gossip Blues

I hail from Philadelphia where you can find a dead body on the corner and be given a hard time by dispatch as to which exact corner as if there were likely to be a dead body on all 4 corners.  (True story from my youth).  In Philadelphia if you aren’t hitting someones car or robbing them they really don’t care much what you are or what you do.  So imagine my culture shock in moving to Stepford/oops/C’ville in 1996/7 and watching an older man and a young man politely discuss an accident on the side of the road and then discovering that everyone knew everything about everyone it seemed.  I heard stories about people who weren’t even alive anymore and how they died, people I had never and clearly would never meet.  Finally it happened, I started hearing stories about myself.  I was shocked at what an exciting life I was leading all unbeknownst to me.  I was startled to learn about diagnoses no doctor had ever given me were being applied to me and spread around.  I was rather stunned to hear I was HIV positive given the low chances of such for me. 

So I have decided to fight back in my own way and create my own rumors or gossip about myself.  Only I and friends who won’t tell you know which if any of these rumors is true, so have fun guessing and be my guest in spreading them if that is what you like to do with your time….

I was engaged to an English South African.

I was best man at a wedding.

I grew up in the ghetto.

I grew up on the Main Line of Philadelphia.

I am independently wealthy.

I receive alimony.

I am poor.

I am anti-Green in all ways.

I am a vegan.

I summer on Fire Island.

I summer at home.

I have many connections across the globe and commonwealth.

I am a loner.

I am a party animal.

I am never invited to parties because I don’t fit into the proper categories in Stepford.

I drink.

I can’t drink without falling asleep after half a glass.

I am a heroic kidney failure survivor.

I am a lucky kidney failure survivor.

I made up the whole kidney failure thing and fooled several nephrologists despite their blood tests and vast training.

I hate men.

I hate women.

I love men and women but hate children.

I eat chocolate for every meal unless I eat Sugar Smacks.

I never walk if I can drive.

I walk several times a day starting first thing in the morning.

I have scars from a knife fight in my youth.

I have scars from several dialysis accesses.

Feel free to add your own rumors below but don’t ask if any are true because I’m not telling and neither are my real friends.  :)

Hospital in my Hometown that Psychiatric Solutions Took Over for Profit Now in Trouble

I was so sad when I found out that Psychiatric Solutions had taken over one of the oldest psychiatric hospitals in Philadelphia, a non-profit before Psychiatric Solutions, the Charter of this decade, took over.  Now it seems that yet again where Psychiatric Solutions goes into a hospital patient safety issues follow, issues I never heard of in years of working as a mental health counselor in this hospitals region.  Here is the short blurb in a business blog, strange the mainstream press doesn’t seem to be covering this sad tale of patients endangered for profit,  some of whom are there against their will by the order of a lawyer called a master in a kangaroo court hearing.  Here is the sad blurb:

Psych Solutions replaces Philly hospital CEO

By Geert De Lombaerde Posted on June 23, 2009 at 3:31 pm

After more bad PR over alleged patient safety issues, Franklin-based Psychiatric Solutions has shown the door to the CEO of its Northeast Philadelphia hospital. A national search is underway.

Thanks for the 600 plus dollars out of my pocket UVA 5 East for Zyprexa I Shouldn’t Have Been Prescribed and Didn’t Agree for you to Fill at YOUR Pharmacy

Warning: PTSD patient anger displayed below, watch out, anger by people like me in words on a blog has been known to cause hurricanes and linked to global warming………

That’s right, over 600 dollars towards my reaching the doughnut hole on my Medicare D for a drug I only took for 3 weeks and that you didn’t ask if I agreed to have filled at your pharmacy instead of shopping around or maybe just not taking it as was my perfect right since you had no order to force me to take it once I left your “care”.   The nurse who thought I couldn’t drive just handed them to me and expected gratitude, I thought maybe they were free the way she expected gratitude for  a pharmacist not herself filling them without my request nor permission.  Well I’m not grateful and I don’t have a spare 600 dollars.  So thanks again for not respecting me as a citizen and “consumer” in this instance with choices and legal rights.  I don’t suppose you will be offering to pay me back Nurse you must be stupid because you are a patient here.  Guess what Nursie, I have a Masters and almost a Ph.D. What you got besides an inability to control your eating habits?  I got off of dialysis by controlling mine, so guess I am up in the self-control competition too.  But you like yourself so well and think you are so superior to your patients there is no need for me to like you.

Transplant Steroids and Psychiatric Side Effects–Please Take Seriously

So from recent posts it’s clear to the discerning reader I had the lovely experience of being a guest of University of Virginia’s 5 East, their psychiatric unit.  But I failed to say why.  Here’s why: I was put on steroids per protocol after transplant in October of ‘08.   I was taken off of them a month or so later due to side effects.  I was put back on when my doctor was changed and he wanted to protect my kidney to the utmost, a laudable goal but one with disastrous effects for my sanity.  Turns out I am one of the many people who can not tolerate steroids.  I endured them from January and still have a little over 2 weeks until I am completely off of them.  In between I lost my mind despite my best efforts to use all my knowledge and skills from being a mental health counselor, being a compliant PTSD client and patient, reminding myself each day to take care of myself, minding sleep hygeine, everything I could think of.  Finally when I couldn’t sleep for 23 hours and was clearly not well I voluntarily went for help.  I did not get help, I got hell, but that’s a different story I have already told. 

Turns out the trade off for going offf of steroids is only a 10% increased risk of having to go into the transplant unit of the hospital for treatment of an acute rejection episode, not losing my new kidney as I was repeatedly told and believed.  I’ll take a 10% risk of hospitalization in the nice transplant unit over the hell that is 5 East any day.  Fully informed consent and patient choice anyone in all fields of medicine?  And less prejudice against those of us who have psychiatric side effects to drugs, nah, that would be too much to ask in this community.

Withdrawal from Neuroleptics Does Not Have to be Hard Nor Painful–Hope, Truth.

I was forced onto Zyprexa by doctors at 5 East despite no history of non-compliance and strong medical and historical reasons not to put me on this class of drugs–medical that drying out drugs in lay people’s terms are not good for kidneys and historical in  my past bad response to this class of drugs and even in the present my observable bad reaction by worsening as the dose was raised again and again against my will.   I was lucky to have good sense, knowledge and a lack of fear of phantoms along with a good psychiatrist to get off of the 25 mg. of Zyprexa on May 31st to 0 mg. of Zyprexa as of tonight, June 21st.  I had some tiredness, a few extra naps, some disturbed sleep a few nights, a little pain in my body but nothing I couldn’t ignore and nothing that needed even a Tylenol.   If you were not counting, I went from 25 mg. of Zyprexa to 0, none, in 21 days.  I am not bed-bound, far from it, I went out to our local drop in center twice today, once to drop off a Father’s Day cake and hang out for a while and once later on to drop off some clothes for donation and have a chat with two members sitting outside.  I did laundry.  I did Facebook, walked my dog, ate, talked with people on the phone, am writing this from my desk chair since I only have a desk top albeit one with a great big screen for my old eyes.  I suppose I could turn into a bed bound invalid in need of home care tomorrow, but I’m not guessing that’s going to happen.  In fact if I can avoid the temptation of after 9 coffee, one of my worst vices, I expect I will be asleep by midnight and up by 8 and walking my dog tomorrow as per usual. 

So next time you read a story of years of pain and suffering and extreme measures, remember the story of the woman with a kidney transplant less than a year old, still titrating off of steroids,  and wonder if you really have to suffer so much if you titrate off under a doctor’s supervision after a decision that this is best for you as an individual between you and your doctor.  This woman’s body is glad I had the choice and the help of my doctor instead of the many who are unfortunate enough to fall under outpatient commitment laws, strangely enough most of whom are in the public (read poor folks or folks whose parents won’t pay for private care) system of “mental health” in our state and others.  This woman is very grateful tonight and this woman says that’s a good thing.  :)

Happy Father’s Day to all the Fathers in my Life

To those waiting to be fathers for the firs time, and you know who you are if you read this in C’ville, to all the fathers so old we must remind them of the good times and their good deeds, to all the fathers raising young ones, especially young ones with a disability and the courage they must show every day so their child doesn’t know how hard it is to see your young one in pain,  to all the fathers with empty nests who worry and hope and wish they could change something, to all the fathers whose young ones never left home, to all the fathers who had to search for their lost sheep scared out of their minds but determined and successful, to all the fathers who never had children so fathered the children of others, the priest and the near priests, the ordinary men who know that not every father can be everything to their children and offer themselves to fill in the gaps, to all the teachers who share their wisdom like a father, to all the fathers, biological and adopted, here and gone in my life: Happy Father’s Day!

Thank You for Setting Me Back at Least 6 Months in my Recovery 5 East at UVA

Thank you for listening to my mother who was diagnosed bipolar when I was a teenager and never accepted the diagnosis and most likely has PTSD also and is now losing her short term memory as if she were anyone you should listen to about her daughter.  Thank you for calling someone in my family who didn’t even know my diagnosis had changed because we only started talking again recently after I got out of your charming facility with its crazy-making ways. 

Thank you for listening to everyone but me and your preconceived, one size fits all notions, not science nor medicine nor even art about what  my diagnosis must be even as I got worse and worse under your so called care.

Thank you for pretending or actually not knowing what dissociation and sleep walking are even though they are listed in the DSM, the same place your flavor of the day, bipolar, which is not properly treated with atypicals someone has had previous bad reactions to nor with Lamictal which raises creatinine and is bad for kidneys and may cause Parkinsons’ or Tardive Dyskensia in susceptible, such as me, individuals according to an M.D. who is researching this now unlike you whose responsibility it was and most of all, thank you for violating my human rights and the standard of care over and over and over and forcing your resident to sign her name to your so called treatment plans to evade responsibility or because you were too lazy.

Thank you for telling me my bladder would burst if you didn’t do an “in and out” catheterization which you wanted to do in my bedroom until I objected and for not calling in experienced medical nurses to do it leaving me with pain and trouble urinating for several weeks not to mention the nightmares and fear of sleeping in my own bed.

Thank you for assuming me I could not drive at 52 as I was on my way out the door.  Insults are always a great way to say good-byel.

Thank you for confiscating my human rights booklet in my purse which could harm no one but could have helped me a lot.

Thank you leaving me blowing in the wind for services when I left by listing non-available to me services in my discharge plan, the one I never got a copy of but my providers did.

Thank you for discharging me on what your eldest psychiatrist called a dangerous dose of Zyprexa on the pretext that you could not lower it and scaring  me yet again.

Thank you for putting me on 3 drugs that were either listed as ones I could not take or were dangerous to my kidney and over all health, those being Inderal, Zyprexa and Lamictal.

Thank you for the shakes I have from Lamicatal which my nephrologist is resesarching as I write-well hopefully he is sleeping, but he is reseraching it because he said there are bad side effects.

Thank you for ignoring my licensed clinical psychologist and my psychiatrist.

Thank you for my fear of sleeping in my own bed due to putting a male sitter in my bedroom at your fine establishment despite my trauma history, oh right, you don’t believe in trauma, G-d help our veterans when put under your care.

Thank you for threatening me with Western State Hospital for a one time psychiatric side effect from a medication I had been begging to go off for 6 months and still not taking me off of it but choosing to blame and shame me instead and not consult nephrology who could have told you what the problem was.  Oh and a special thanks for being disrespectful to my very well respected and elder nephrologist when he went above and beyond to help me out.

Thank you for not listening.

Thank you for being rude to my lawyer, incredibly rude.

Thank you for scaring me each and every day.

Thank you for not informing me of my rights under Medicare in a way I could understand at the time so I could have avoided the fear of being transferred to Western.

Thank you for making me sleeping for 3 nights through noise and fear the criterion for my release.

Thank you for never offering me comfort nor a therapist to talk to about my fears and trauma in your  unit.

Thank you for allowing a man to touch himself in front of me and a very young woman and not listening to the young woman and letting this man go around looking for who complained about him.  I hope this young woman is okay.

Thank you for being disrespectful, hostile, arrogant and bullying every single treatement “team” meeting.

Thank you for the non-existent referral to available and helpful resources in our town.

Thank you for telling me I did not deserve anything better than traumatic treatment plans.

Thank you for telling me I was not dissociating when I opened the wrong doors when I was and calling me a bad person yet again.

Thank you for your blindness to my actual problem, which was you and steroids and dissociation to escape the trauma of being told my bladder might burst with no gentleness and certainly no debriefing let along ordinary human kindness.

Thank you for letting me know once again what I had suppressed: that I am not a person with rights once in a psychiatric ward.

Thank you for being you, may your treatment team which has bullied and railroaded so many be disbanded by the adults very soon.

Thank you for the flashbacks and the nightmares.

And thank you for every previously overcome phobia which have returned in full force and most of all, thank you for locking me inside for 2 weeks of my favorite time of year: 2 weeks I will never get back and months of recovery from your re-traumatization.

Hopeful New Drug in the Pipeline for People Like Me with Chronic Anxiety or PTSD

http://www.reuters.com/article/healthNews/idUSTRE55H57N20090618?feedType=RSS&feedName=healthNews

I take klonopin and take the side effects with it.  It’s been a fair trade off for me given klonopin is the only psychotropic I can safely take and given its ability to enable me to function; to drive, to attend social events, be in crowds, go grocery shopping, and on and on.  But an anti-anxiety drug that worked without the side effects of klonopin which include clumsiness and forgetfulness and for me possibly the weakness in my hands would be a G-d send, truly a G-d send.   I can’t imagine how anyone could be fear mongering about an anti-anxiety medicaiton that could free millions from side effects and might even be safe in older people.  But they are if you look at Beyond Meds today.  By the way, all comments are moderated and comments claiming I am hurting or otherwise defaming the author of Beyond Meds simply by strongly disagreeing with her will lead to permanent listing in my blocked  filter that WordPress so kindly provides.

“LONDON (Reuters) – German scientists believe they may have found a better anxiety drug that can counteract panic attacks without the side effects caused by existing treatments like Valium.

Anxiety drugs such as Valium work well but produce side-effects that include drowsiness, forgetfulness and clumsiness and, when taken over time, can induce dependency.

The new compound, XBD173, appears to avoid these problems by targeting a different biological “don’t panic” button, making it a good potential candidate for use as a safe and fast-acting anxiety pill….”

Am I Not a Member of This “Community”?

I was psychiatrically assaulted more than once.   The last time was a month or so ago.  I call the SAARA hot line and am told there is no place for people like me, as I knew there would not be, people, women and men, like me, people who were assaulted in a system everyone in group think thinks is benign, do not need or do not belong in groups for survivors, we should talk to our specialists who of course we already talk to as often as we can after another unearned and violent assault as sexual and pornographic as any rape, tying a woman or man down and injecting them in front of or by men, what is that if not an assault? A sexual assault?  It is not medical treatment, that is a perversion of the term medical treatment.  Yet once again I am told the only resource for people like me is psychiatric and psychological professionals.  This is not unique to Charlottesville, the UVA company town, it happens in every town and every city.  Men and women like me are patronized or avoided or treated like lepers or told to keep quiet if we want to keep our jobs and reputations or chance at friendship and the community support we never get except from each other and a few others who get it sort of.  

I went to church on Sunday.  It had been a long time for me. I exchanged the peace with many in that church including someone who doesn’t agree with me on most things but 2 people who have known me the longest and knew I had been in a psychiatric uni against reason and justice would not exchange the peace with me, pretended not to see me.  This is what we live with as psychiatric survivors.  I will not return to that church.  I will keep looking for a Christian church that takes me as I am or perhaps where no one knows me but why should I have to be ostracized by the fact my assaults came in the medical establishment (and not all did)?  Why is there no group?  Why am I told the only option for people like me is the professionals I already rely on heavily?  Why can I not be a full member of this community with full support or even a little support? Am I not your sister, your daughter, your mother, your aunt? Am I not a person?

What Part of 12 Hours Apart Exactly Doesn’t 5 East Understand Inre Transplant Drugs?

Ever since my transplant in October of 2008 I have taken my anti-rejection drugs 12 hours apart.  It’s not that hard, well not after I learned to use my cell phone alarms, but apparently it is too hard for medical doctors on 5 East to understand and execute.  During my stay they consistently were either late or early with my anti-rejection drugs and when I mentioned 12 hours for all drugs was easier a nurse agreed but doctors did nothing to ensure I got my oh so importantly timed anti-rejection drugs 12 hours apart.   In fact they got me out of the habit of writing down my intake because I was too busy despite all the trauma and chaos trying to remember and memorize when they gave me my medications including the calcitrol which is every other day so I had it written down by week in the nice book transplant gives out at UVA.  These were the people who were protecting me from what?  I never heard and never knew and it’s taking forever even to find out.   Obstruction all they way.  I asked for my papers repeatedly but was always given the wrong ones.  Oh and just to be clear, you can’t discharge someone to home care if they are homebound Ms. Social Worker nor can you discharge someone to a case manager they don’t have, you haven’t made an appointment with and they are not qualified to use under CSB guidelines.  Why? Because I don’t have a serious mental illness, I have PTSD and that’s not serious.  Anyway, a drug reaction with psychiatric side effects is never a serious mental illness.  But hey docs, let’s spend all my precious time converting me to the one true religion of “you have bipolar” despite what everyone who is a professional and known me for years tells you.  Let’s keep trying until you can find someone out of the loop with no reason to know to agree with you.  Nice work 5 East.  Home and well despite you.  Not to spite you, despite you.  Your drugs made me sicker than I have been in years, luckily I have a smart psychiatrist who is rapidly titrating me off of them and a transplant doctor who has seen many cases of steroid induced psychiatric problems.  And a psychologist from heaven who you tried to argue with who would not argue but who has stood by me as has my psychiatrist.   But hey, you must be right, you are UVA (not even in the top 50 or maybe not in the top 100 in psychiatry) Health Systems’ doctors so you must be omniscient, right.  Hubris, not a pretty thing in action.  Oh and your reputation? Not so great among the other patients.  But keep on keeping loving yourself, you do it so well that I don’t have to.

Hey 5 East, You Might Want to Check This Out, It’s in Your Bible. Or Are You Non-Believers or Atheists?

http://allpsych.com/disorders/sleep/sleepwalking.html

Psychiatric Disorders


 

Sleepwalking Disorder (COMING SOON)

 

Category


Sleep Disorders

Subtle Cues You Might Be a Good Mental Health Professional

These are subtle, so you would have to spend the time to look for them and I know that’s hard given today’s economic and reimbursement climate but I list them nonetheless to encourage those who are often embattled and even maybe embittered by the lack of respect and dignity given to their profession, something I know about as a former mental health counselor myself years ago.

First subtle hint:  Your patient or client thanks you after each visit. 

Second subtle hint:  Your patient or client smiles when they see you.

Third subtle hint:  Your patient or client returns to see you voluntarily.

Fourth subtle hint:  Your patient or client feels free enough to speak “French” in front of you. 

Fifth subtle hint:   Your patient or client does not run out of the room screaming nor slam the door when they leave.

Sixth subtle hint:  Your patient or client changes in a positive direction.

Seventh subtle hint: Your patient or client does not change for the worse under your care.

Eighth subtle hint: You have never been sued for malpractice and never been afraid that you might be.

Ninth subtle hint:  Your name is not splashed across Court TV.

Tenth subtle hint:   You believe change is possible and that every human being has the potential for growth.

Nevada to Shut Troubled Psych Hospital by Christina Jewett , ProPublica – June 10, 2009

Also see Pro Publica’s “Steal Our Stories” link and explanation and rules here:  http://www.propublica.org/about/steal-our-stories/

http://www.propublica.org/feature/nevada-to-shut-troubled-psych-hospital-610

Nevada to Shut Troubled Psych Hospital by Christina Jewett , ProPublica – June 10, 2009 12:11 pm EDT West Hills Hospital (Photo from PSI) The Reno Gazette-Journal reported [1] yesterday that authorities in Nevada plan to shut down a local psychiatric hospital [2] after a patient overdosed on pills she brought into the facility. West Hills Hospital is part of a Tennessee-based chain, Psychiatric Solutions, that we’ve covered quite a bit. In November, we co-published an article [3] with the Los Angeles Times documenting the chain’s rapid growth [4] and star status on Wall Street, even as patient care lagged [5] behind similar hospitals. We co-published two articles with the Chicago Tribune in February about a troubled Psychiatric Solutions hospital in the Chicago area that, even while under federal investigation, continued to experience patient care problems [6] with illicit sexual encounters between young and vulnerable patients. The other article [7] documented details of a patient death at Riveredge Hospital that officials said should have been reported by the facility a year sooner. Since then, the Philadelphia Inquirer reported that [8] city officials decided to stop sending psychiatric patients to another PSI facility, Friends Hospital. Authorities decided to cease referring about 6,500 patients per year after a 21 year-old committed suicide while he should have been monitored via a camera system that, regulators found, was broken; In Reno, health officials notified West Hills Hospital that it plans to close the 95-bed facility within 30 days and immediately pull its operating license. A PSI spokesman responded, saying the facility plans to appeal the decision. “The community needs the mental health services we provide, and we are cooperating fully with state officials to provide all the information that is needed so that our ability to receive patients will be restored,” corporate spokesman John Van Mol told the Post-Gazette. The news report documents other problems there. In December, two young female patients attempted suicide [9] by putting nooses around their necks while they were not being adequately monitored. A state report says one girl was found unconscious and red-faced after the attempt. Earlier this year, teenage patients locked staff members out of a unit. A month later, teenage patient hit another teen. During our investigation of the chain, we ran across an older incident in which the hospital was cited for failing to “provide services for the care of its patients.” A state report dated Oct. 4, 2006 (PDF [10]), documents a patient who was on suicide watch barricading himself in a room. Then the man ran down a hall, locked doors behind him and escaped. Outside, a police officer responding to the incident shot and killed the man. State regulators cited the hospital for insufficient staffing after they learned that a nurse who had difficulty walking was the only staff member assigned to perform routine checks on 19 patients. We posted the rest of the state investigation reports (PDF [10]) that we received from the state of Nevada late in 2008. Take a look.

My Quote of the Day by Me, Myself and I. :)

Do the right thing, rise above pettiness and grudge holding and grudge holders, ignore people who vilify you or your friends, rise above, take the high road, not just because it is the right thing, but because it will annoy your enemies more than any reaction ever could.   Is this doing the right thing for the wrong reason?  I don’t know, I am not a philosopher of any stripe, but I know it works for me.  And when I forget to do this, I don’t feel good about myself and I don’t accomplish my own goals, I get caught up in petty B.S. and people who aren’t worth my time.

Someone Alert the True Believers in Psychiatry–Die Gedanken Sind Frei

Happy Birthday Dad! Or Dell Hymes, My Father, Turns 82 Today :)

Thank you for the wisdom, thank you for the love, thank you for the values and principles, thank you for your prayers, thank you for your hard work, thank you for your courage as a man to cry when it was time to cry, thank you even for retelling our jokes and laughing louder than when we told them, thank you for the silliness and thank you for the coyote stories and thank you most of all for the books and the love of learning and the belief that the revolution (not that kind :) ) is always coming.  I love you Dad.

Sunday Link Fest

http://www.boston.com/news/local/massachusetts/articles/2009/05/22/advocate_for_others_fights_to_die_at_home/

Judi Chamberlin, an advocaate for the rights of people with psychiatric disabilities for 43 years, is now fighting for her own right to die at home after UnitedHealthcare informed her that her hospice benefit has run out.  Her hospice services have not been cut off as of yet but she is afraid that her daughter will be left with large bills for her care after her death.  

http://psychrights.org/index.htm

“Alaska Supreme Court Grants Mental Patients Constitutional Rights

In an important decision issued today, William S. Bigley v. Alaska Psychiatric Institute, the Alaska Supreme Court significantly advanced psychiatric patients’ constitutional due process rights when the state seeks to force them to take psychiatric drugs against their will.  “One of the things they held,” said Jim Gottstein, President and CEO of the Law Project for Psychiatric Rights (PsychRights) and the attorney who handled the case, “is that if the State is holding someone in a psychiatric facility, they must provide a feasible alternative to the forced drugging if the alternative satisfies the State’s asserted justification.  The State’s only other option is to let the person go.” The Court also held that in order to allow the person a realistic opportunity to prepare a defense, when filing a forced drugging petition, the State must provide a written statement of the facts underlying the petition, including the reasons for the forced drugging, information about the patient’s symptoms and diagnosis; the medication to be used; the method of administration; the likely dosage; possible side effects, risks and expected benefits; and the risks and benefits of alternative treatments and nontreatment.  “This is very important,” Mr. Gottstein said, “because up until now, they just checked a box that said the person was incompetent to decline and the facility wants to drug the person.  Then the State comes in with a witness who testifies untruthfully and there is no way to have been prepared to rebut it.” 

http://www.theopalproject.org/vigil.html

Esmin Green Did Not Survive. Survivors of Psychiatry & Allies Demand Report from NYC Dept of Investigations

WE THE PEOPLE to Hold a Demonstration and Vigil in Her Memory, June 19, 2009 at Kings County Hospital Center Psychiatric Emergency Room, Building R. from 5-10 Pm. Justice for Esmin Green. Justice for All

ROCKVILLE CENTRE, NY (05/29/2009; 1149)(readMedia)– W E THE PEOPLE is reaching out to friends and family of Esmin Green who was murdered-by-neglect at the Kings County Hospital Center Psychiatric Emergency Room June 19, 2008. They are also looking for survivors of psychiatry, anyone affected by mental health or psychiatric systems, and allies who want to see change and make their voices heard.

Facility staff looked at Esmin face down on the floor – did nothing – and then tried to cover it up. The blatant negligence that was exhibited by facility staff should not be allowed to be brushed under the carpet – or excused for lack of team spirit, which Mr. Aviles, the President of Health and Hospitals Corporation which oversees Kings County Hospital Center, has tried to do. WE THE PEOPLE is demanding criminal charges in this murder-by-neglect and attempted cover-up. This ultimate violation of human rights can not be accepted by our society.

WE THE PEOPLE is demanding that the New York City Department of Investigations release the report of the investigation into the death of Esmin Green and asks why the city is holding back such information?

On June 19, beginning at 5 PM, WE THE PEOPLE will be holding a demonstration calling for human rights in psychiatric systems. A candle light vigil to remember Esmin Green, a woman who should still be alive, will begin at 8 PM.

Sanford Rubenstein, the attorney for the family is a confirmed speaker at the demonstration. He states,
“It is really important for people to make their voices heard so that what happened to Esmin Green never happens again”.

WE THE PEOPLE invite you to stand with them in front of Kings County Hospital Center on June 19, 2009 from 5-10 PM to demand human rights in the psychiatric and mental health systems. Justice for Esmin Green. Justice for all.

Contact: Lauren Tenney (516) 319-4295 Daniel Hazen (301) 395-5378 website: www.TheOpalProject.org/Vigil.html
###

What:
A Call to All People:Stop Human Rights Violations In memory of Esmin Green, murdered-by-neglect, one year later.

Date:
June 19, 2009

Time:
5-10 PM

Location:
Kings County Hospital Center Psychiatric Emergency Room Building R. (Clarkson Avenue at New York Avenue and Winthrop Street) Brooklyn, NY 11203

Weekend You Tube

First Swine Flu Death in Virginia in a State Training Center, What is the Plan to Prevent More Deaths?

People in congregate settings are particularly vulnerable to catching viruses.  It is not surprising at all to me that Virginia’s first death from H1N1 influenza virus was a woman living in  a state training center.   What I want to know and hope others want to know is what is being done to prevent more deaths of people who have been institutionalized by the state of Virginia through no fault of their own.   What exactly is the plan to keep residents of state hospitals and state training centers safe from this and future viruses?  The public but most especially the residents of these state run facilities and their families and friends deserve a real and detailed answer and they/we deserve it now. 

 

Statement OF Governor Kaine

~ On first Virginia death associated with H1N1 influenza virus ~

 

RICHMOND – Governor Timothy M. Kaine released the following statement today regarding the Commonwealth’s first confirmed death associated with the H1N1 influenza virus commonly known as “swine flu”:

 

“The news today that the Commonwealth has witnessed its first death associated with the H1N1 influenza virus is a sad and sharp reminder that Virginians must remain vigilant against the spread of this potentially fatal illness. My heart goes out to the family and friends of the young woman who passed away this afternoon in Chesapeake.

 

“Although this particular individual—a resident at the Southeastern Virginia Training Center—had serious underlying health conditions that likely exacerbated the impact of the H1N1 virus, it is important that all Virginians take the necessary steps to protect ourselves and our loved ones against spreading germs during the normal course of the flu season. Individuals with symptoms should be particularly cautious and take proactive measures to prevent infection and spread of the disease.

 

“I know all Virginians join me in offering our sympathies to the family for their deep personal loss.”

New York Times Prints a “Disability Debate” Without Any People On Disability Included, hmm.

http://roomfordebate.blogs.nytimes.com/2009/05/07/the-disability-mess/?8ty&emc=ty

What a great idea! Let’s have a young professor who doesn’t know the history of the Reagan era apparently from her part of the debate, Jennifer L. Erkulwater, an associate professor of political science at the University of Richmond, is the author of “Disability Rights and the American Social Safety Net.”  who blames bipartisan policy changes made 2 decades ago but fails to mention this was after the late President Reagan’s administration threw people off off Social Security Disability willy nilly, resulting in many suicides, especially among the group that she mentions: people with mental illness.  Um, yes, Congress responded to the outrage over the tragic consequences of Reagan’s policies by Fixing them.  I bet any disability rights activist could have told the New York Times that, but of course they just did not think to ask someone who actually is on disability.  And yes, it is just like Clinton’s horrible so called Welfare “Reform” which has left millions now in this new Depression/Recession with no safety net and only now finding out what horrible barriers and what demeaning procedures including requirements to work for no money, usually called by other names in  other circumstances, they voted for the poor to suffer from.  It was not going to be them, so why not continue the war on the poor that started under Reagan?

Then we have Richard V. Burkhauser is the Sarah Gibson Blanding professor of public policy in the department of policy analysis at Cornell ,  a person with tenure for life in his job unless he goes to jail and if he becomes disabled, most likely has a very nice long term disability plan through his university, comparing people with no jobs and no prospects for jobs in this or past economies with a 90% unemployment rate among all adults with disabilities and the ongoing employment discrimination in hiring against people with disabilities that is impossible for individuals to prove in court as long as the employer does not “say” it’s because the applicant has a disability.  He wants to subject people on disability, people with chronic and incurable medical conditions, people with psychiatric disabilities who are likely to have co-morbid medical conditions from the drugs prescribed to them and die 25 years younger than the rest of the population, let alone parents who are poor (and you have to be poor to qualify for SSI for your under 18 child), to the horrors that are and were the “Reform of Welfare”.   Well must be nice when you have employment for life to decide that people with disabilities just need “incentives” to “get a job you loafer”, not that he said that, but you know, that is exactly how it sounds to my ears and I bet what a lot of people with invisible disabilities and visible disabilities have been told by all kinds of not so nice folks.

At least  Gary Burtless, a former Labor Department economist, is a senior fellowat the Brookings Institution,  who must remember his history, says: “There will be collateral damage, however. The reviews will impose real hardship on some disabled workers whose cases are reviewed.” I do not like the sound of “tough-minded reviews” on people on disability as if up until now everyone has found these reviews a cake walk, not something that people actually turn to professionals to help them through in many cases and as if what everyone on disability needs is just a little more “toughness” in their lives, but still, he remembers his history and suggests focusing on people who might actually be able to return to work rather than the scatter shot that was the Reagan debacle in the 1980’s. 

Then we have at the very bottom of the article someone who actually gets it, that SSI is the only real social safety net we have left for people who are unemployable and poor:  

It’s the System, Not the Individual

Morley White is an administrative law judge in Cleveland for the Social Security Administration. The views here are his own and in no way are they expressions of the Social Security Administration, who has empathy, something some Republican propagandists now make fun of in their alternate reality and says in part: “I generally believe in the sincerity of what they say. They are poor and the benefits they receive are now only $674 a month for an eligible individual. What are these people supposed to do in this economy with the limitations they say they have?”

So the war on the poor, the sick and people with disabilities  continues.  People who are not “overcomers” or simply aren’t lucky or heck, simply can not work due to say, a disability?  A severe and chronic condition expected to last at least a year, including people who have incurable cancer, people who can not even get out of a hospital or nursing home because they have no home health care, people who no one will hire because of prejudice, people who do not have foundations named after them, people who can not get a job no matter what”incentive” the non-disabled have in mind “for” them and “about” “them” but definitely not “with them” and not even deigning to include such a person in the discussion as if people with disabilities have no voice.  Well look at my blogroll, go to Google and go to “blogs” and type in “disability” and see how many voices people with disabilities have.  But not, of course, at one of the “Papers of Record”.  Couldn’t have those kind of people included in a debate about them, now could we?

An Old Essay of Mine for World Mental Health Day for our Local MHA-Learning to Cope With the Medical System

Learning to cope with the medical system

February 24, 2007 by hymes

How to reconcile oneself to a medical system that almost killed one and in the end most likely will be the cause of one’s death? I think you don’t, but that instead you make compromises and deals with yourself to do what you need to do to survive and keep the anger intact so that when one wants to despair one can instead say, “I’m not going to let “them” kill me!” in jest, under one’s breath.  And of course one develops a really warped sense of humor or maybe you already had one and that is why you survived in the first place.  Or perhaps a friend is right who says that G-d has a really odd sense of humor.  And seeing a whooping crane, well you have to agree with that.

But day to day the anger can’t keep you going and you have to reach for grace and transcendence.  Friends past and present, living and dead, provide models of how to do this and you think to yourself you will never be as agile as them in handling everything thrown your way but trying makes you quicker on your feet.

You learn to let go of the small stuff and how much stuff is small, you learn to forgive others and yourself for most things and when you can’t you learn to move on.  You learn to smile and laugh at each little piece of beauty that comes your way, whether it is a friend who is there for you or a river beach you didn’t expect or your dogs playing a very silly game they are far too old to be playing.

You begin to accept that these doctors and nurses are neither evil nor saintly but human like yourself no matter whether they agree with that assessment or not and that helps a lot when they disappoint you or hurt you or discount you.  And you learn to treasure the ones who care the way you used to think they all should care, for their worth is beyond measure.

Keeping Yourself Safe: Articles on Possible Dangers of Re-Evaluation Counseling

http://home.comcast.net/~reevaluation-counseling/articles.html

Included in one article is a recommendation that people seeking psychological counseling go elsewhere and not to this group and other issues of concern.

Psychophobia 201

Last time I posted for Blogging for Disablism Day I wrote Psychophobia 101 which actually to my surprise is now an external link on Wikipedia and thank you to whoever inserted that link.  This year I want to talk about more subtle forms of psychophobia, also known as mentalism or ablism or simply institutionalized or individual prejudice and discrimination against people with or who are perceived by others, correctly or not, to have a psychiatric history or diagnosis.  As people who study prejudice and discrimination know, institutionalized prejudice is much harder to both identify and to combat than individual prejudice.  With an individual, there is always the chance to engage, educate, change hearts and minds.  When people are faced with institutionalized prejudice that opportunity is rarely available and the risks entailed in even attempting to educate can be so dangerous to the individual that most of us can not even afford to try.

In the United States, we have psychiatry and a mental health system and advocacy groups such as NAMI repeating over and over that mental illness is real, the same as any other illness, all the while in NAMI”s case they also argue that people with mental illness should be granted less freedom and less civil rights and less choices than people with any other illness.  We also have the folks at the unfortunately named Treatment Advocacy Center who continually harp on the danger, danger, danger Will Robinson of anyone with a perceived or actual psychiatric history who is not ingesting medication under a psychiatrist’s supervision, well they don’t actually care if it is a psychiatrist, could be anybody, as long as the medication is ingested and the person “lacks insight” into the fact that they are not doing what their families or others want them to do as adults in the United States who are supposed to have equal citizenship with all those who do not take their high blood pressure medication or who do not take care of their diabetes through lack of funds or other reasons.

But these are the “usual suspects” in the fear-mongering, prejudice spreading business.  They are not hard to spot, not hard to speak up about.  More insidious and damaging in the day to day lives of people with or perceived to have psychiatric histories are everyday people and agencies and programs that continue to assume that they know best, that they are the best advocates for a group they Do Not Even Belong To.  Can you imagine if instead of wearing “Straight but not narrow” buttons people wore “Knows best for people with mental illness because I am not one of them” buttons?  No, I suspect you can not.  It is never that obvious, never that open, never that honestly stated and often not even in the person or agency’s conscious mind at all.   In fact the unconscious nature of this kind of psychophobia is what makes it the hardest to engage and change.  It is not hard to point out as I and many others have done that naming a doughnut shop “Psycho Donuts” is offensive and hurtful.  It is a heck of a lot harder to point out to someone you know and like and respect that they are appropriating the issues and concerns of a group they do not belong to, no matter how much they care, and speaking and acting as if theirs is the only voice that needs to be heard, that people with psychiatric histories can not or should not or may not speak for themselves and that they NEVER know best what is right for them and members of their group.  Unless of course, they have been chosen by the powers that be in the mental health system to be the representative that the powers that be want in their corner.  And we all know that as soon as someone in that position starts to feel uncomfortable with that role, starts to speak out, starts to actually represent all voices in their community, they will be silenced or fired or retaliated against or otherwise made miserable or invisible or both.

The system has created a lovely double bind for people who want to advocate and work with the system.  (So sad no one seems to read Gregory Bateson in mental health as an aside.)  Go along to get along or speak up and they will make sure you regret it.  Even people without psychiatric histories who ally themselves with people with who are outspoken about their rights fear being marginalized and found “guilty by association” and this fear is  quite reality based in my opinion.

So we who have spoken out and the many who have not for many good reasons are left with institutions and agencies that treat people with known psychiatric diagnoses or histories differently and less well day after day after day.  If a person with a mental illness label pays their own money for a service from a professional they can not assume that they will be treated with the same respect or even civility or even lack of open disparagement as someone without.  They can seek help with legal matters and be told that they do not know what they know, for instance that in Virginia no one who has worked long enough to get Disability retirement is ever going to be eligible for Medicaid and therefore it is hurtful and not helpful to advise them to stay as poor as possible.  They can have their honest statements about their real personal situations discounted and trivialized as “your issues”.

In medical care, people with any psychiatric diagnosis on their medical records face a huge barrier to getting equal medical treatment and even basic respect and civility.  Medical professionals will yell and threaten and humiliate people with psychiatric labels secure in the assumption that the person in front of them has no recourse because they know full well from experience that any expression of discomfort at their treatment will be further “proof” to the medical establishment of their otherness even when right next door a person without such a label may be raising the roof about waiting or poor care or lack of respect.  Different rules for “different” folks, and is that not the very essence of all conscious or unconscious prejudice and discrimination? That is Psychophobia 201.

ADAPT Action Report Including Video of ADAPTERs Getting Up Capitol Steps at link Below

http://www.adapt.org/freeourpeople/cca09/video.htm

The Community Choice Act is for all of us and all of our families.  It must not be left out of health care reform for all our sakes.

Class Action Lawsuit on Drug Prices: Information You or Someone You Know May Be Able to Use

http://www.katu.com/news/medicalalert/43754227.html

“Court settlement lowers some Rx drug prices | KATU.com – Portland, Oregon | Health Source: www.katu.com SEATTLE – The prices of more than a thousand brand name drugs are about to get a little cheaper, thanks to a huge settlement with a major drug distributor.The settlement is for more than $350 million and …”

Many, many drugs are in this list, including the $1,000+ Valcyte I paid for twice after transplant, :) , but really, it’s an amazing list of drugs that you may qualify for a refund for overpayment if you meet certain classes. Check it out especially if you have a chronic medical condition and have paid a lot out of pocket or paid cash when your insurance didn’t cover you until January 23, 2009  or paid co-payments and have records from 2001-2005, and please, let’s make this go viral and tell people you know who are not on the Internet and won’t see this. If you call the number as I did they say a 15 minute wait, so if you can check it out on-line for yourself or someone else, probably easiest but you will have to send an actual postal letter to file your claim.  They also say people may be sent payments automatically even without filing a claim but advise people to file a claim to be sure.  People also have the right to “opt out” of the settlement for the cash payor class but not the co-pay from 2001-2005 class.

List of drugs covered by the class action here:  http://www.mckessonawpsettlement.com/PDFs/SubjectDrugList.pdf

Consumer Cash Payor page here: (this includes if you paid cash because you were underinsured) http://www.mckessonawpsettlement.com/ConsumerCashClass.htm

Consumer Co-Pay Home Page here:  http://www.mckessonawpsettlement.com/ConsumerCoPayClass.htm

Welcome to the McKesson Proposed Settlement Website page here:  http://www.mckessonawpsettlement.com/index.htm

Florida Allows Their Baker Act to add to Company’s Profit Margin, Is This What We Really Want?

http://www.ocala.com/article/20090425/ARTICLES/904251017/1402/NEWS?Title=Vines-Hospital-now-a-Baker-Act-facility

A Psychiatric Solutions owned facility in Florida has won approval to accept “Baker acted” people over 14 (people who have been committed by the state for inability to care for themselves or danger to themselves and rarely danger to others) as of this past Monday.  The hospital was bought by Psychiatric Solutions, the country’s largest owner or leaser of free standing psychiatric facilities just one year ago.  Pro Publica’s sweeping investigation of Psychiatric Solutions, here: http://www.propublica.org/feature/psychatric-cares-peril-and-profits-psychiatric-solutions-inc , showed that when Psychiatric Solutions buys a facility, trouble for patients often follows but more to the point in this story is the fact that the state of Florida has decided (and this may not be unusual at all), to allow a for profit company to make money out of the state’s detention of individuals who it has deemed vulnerable due to their disability or perceived disability or even just individuals who have disagreed with a psychiatrist’s treatment plan for them as so often happens in commitments in this country. 

Many activists are decrying the privatization of prisons and detention facilities for undocumented immigrants, but we continue to allow the privatization of forced detention of people with psychiatric diagnoses.  So what’s that about? Why no outcry from progressives about this?  Are they just not aware or do they just not care?  No way to know but it is a reasonable question I believe.

Resource for Family Members and Advocates and PWD in Institutions Trying to Find Each Other

https://www.thearclink.org/findfamily/

hat tip to Patricia Bauer of Disability News.  One of the family members featured searching in the People Magazine article, (not on the web) is from Virginia.

Alas, Comments Again

I expect some spam to get through the excellent spam filter Word Press provides for free and do not mind taking care of it. However, lately there has been an increase in what I would politely call “hostile” comments on my blog. So just so you know, all comments to this blog are moderated and have been for some time since the last influx of nastygrams/comments some time ago. I do not approve hate speech, I do not approve personal attacks on myself  or others, I do not approve screeds and off-topic rants, I do not approve comments that don’t make sense. In fact this is a case of my blog, my rules. Luckily for anyone who wants to spend their time writing hate filled screeds, there are many free blogging platforms and unless somebody reports you for hate speech, you can go at it to your audience of one to your heart’s delight. But not on my blog.

Charlottesville Clinic on Fair Housing for People With Disabilities, Tues., April 21st

Fair Housing for People with Disabilities

When: Tuesday, April 21st, 2009, 12:00 to 2:00 PM
Where: Independence Resource Center, 815 Cherry Avenue, Charlottesville
This clinic is designed to give people with disabilities and their advocates detailed information and one-on-one assistance on their fair housing rights.
Highlights:
Learn How the Fair Housing Act Protects People with Physical and Mental Disabilities from Housing Discrimination.
Review the Rights of People with Disabilities to Reasonable Accommodations (changes in rules and policies) and Modifications (structural changes for accessibility) in Housing.
Discuss Examples of Local Housing Discrimination and Successful Advocacy Efforts in Support of Fair Housing Rights.
Get One-on-One Assistance with Your Fair Housing Concern.
Receive Take-Home Materials and Local Resource Information.

Sponsored by: Piedmont Housing Alliance (PHA) & Independence Resource Center (IRC)
This event is free and open to the public, but please register by April 20th. Lunch will be available for all registered attendees.
For more information and to reserve your seat, contact: Tryshan Ravenell at Piedmont Housing Alliance at 817-2436 ext. 113.

C’ville Weekly Journalist Calls Local Children and Teens with Psych. Disabilities “head cases”.

I am reposting this because the article remains in the C’ville Weekly archive with no retraction and no apology for the demeaning and prejudiced and inaccurate language used about children and adolescents treated in the Commonwealth Center for Children and Adolescents. Children (and their parents) with psychiatric disabilities are members of our community, for a popular weekly to publish this kind of prejudiced language without apology is saying that they are not “really” members of our community in my view. I had hoped that mental health providers and agencies and advocates in our community would speak up about this degradation of members of our community by now, but only one person wrote a letter to the editor and as far as I know she is not associated with any mental health provider nor mental health advocacy group in our community.

http://c-ville.com/index.php?cat=121304062461064&ShowArticle_ID=11802302094565042

He also speculates with no evidence that most of the children (as young as 3 and 4 at  Commonwealth) are violent and dangerous.  But go read the whole thing if you can stand it.  This is a complex issue, reasonable people can disagree on what is best but nothing is gained and much is lost by perpetuating prejudice and ignorance about children with emotional disabilities and focusing on violence when every expert knows that kids and teens and adults with all disabilities but especially psychiatric are much more likely to be victims of crime than the average person and more likely to be victims than perpetrators by far. 

This is unacceptable hate speech about children.  Speak up, speak out, object to this sensationalized simplistic article that fails to address any of the complexities of the issue but chooses instead to make it even less likely that children with emotional problems will be accepted and integrated into our schools, neighborhoods, Little League, churches, homes of friends in our home town because it is our children he is writing about. 

This must not go unchallenged.  It is prejudice.  It is about children.  It is not okay.

Excellent Blog Post at Bad Cripple Got Me Thinking About Psychophobia Again

http://badcripple.blogspot.com/2009/04/cumulative-impact-of-disability-based.html

Please read his post about the cumulative impact of disability based prejudice on all people with disabilities, especially the part about how Governor Patterson said the Saturday Night Live sketch that made fun of his disability actually affected his behavior and feelings for some time afterwards despite thinking he was beyond all that at this point in his life and the analysis of the deliberate attempt to humiliate Governor Patterson for his disability.

Please read it and substitute psychiatric disability and see if you can even get yourself to do so.  I suspect many will not be able to.  I suspect many will say that Governor Patterson has a “real” disability and that it should not be mocked but that somehow, for some reason, people who have been diagnosed with a psychiatric disability or have a psychiatric history or have come home from Iraq and Afghanistan with Post Traumatic Stress Disorder or survived a childhood or adult trauma but emerged with Post Traumatic Stress Disorder or any other psychiatric diagnosis do not.   I suspect that the analogy will not work for most.  And I keep wondering why that is?  Part of it clearly is the continual demonization and fear-mongering of all people with psychiatric diagnoses and histories in the press, in the blogosphere and in every day life.  Part of it is the attempt by some to say that psychiatric disability does not exist and that people just need to buck up or become “mindful” or take a pill, that will fix it.  Or the oh so helpful suggestion that what people really need is a better social network.  Um. Well, yes.  But how exactly is that going to happen if the people who would be in that social network exclude people who they suspect or know to have a history of psychiatric disability, even if they are in recovery, even if they are doing well, let alone if they are having a bad day or two?  How exactly is that going to happen outside of the ghettoization of people with psychiatric diagnoses into their own groups, their own special housing, their own day programs, their “own kind” if psychophobia persists?

I also wonder if people think that someone with a psychiatric history will necessarily ask more of them than someone without.  That is certainly not my personal experience, in fact I know many folks with psychiatric histories who are more reluctant to ask for help from their friends or family than people who do not have diagnoses, out of long reinforced ideas that they are too “needy” even if they are in real need, in a situation where anyone would ask for support such as the death of a loved one or a medical problem or a move or a new job or the loss of a a job or any of the situations that we all face in our lives.  I also wonder about the responses those who do reach out to friends and family get that lead them to stop asking for ordinary every day human support.  I have seen people with common, everyday stresses in their lives told that they are symptomatic when in fact they are not.  I have seen unasked for advice given that trivializes the real issue a person is facing, whether it be a loss, a  major life stresser, an illness, a death, a scare.  I have seen people try to “fix” real life problems with magic solutions rather than listen and really hear what is going on in a person’s life when if it were a person without a label or diagnosis this would not be the usual reaction. 

Life is not easy for anyone.  We all have real life problems and stressors.  We all need each other at times.  What people with psychiatric histories or labels do not need is to get less support for real life stressors and problems than people without do.  What people with psychiatric diagnoses do not need is to to have ordinary reactions pathologized or trivialized as not real or valid.  People do not need or want to be told how to feel, how to think, what to think about, what to do when every day problems and stressors arise in their lives as they do for everyone.  Nor do they want to be offered whatever someone else thinks will be “healing” when the only thing that will heal many losses and stresses is time and support and freedom to feel what needs to be felt.    I do not mean that all advice and suggestions are unhelpful, but if your first response to someone who is grieving or stressed for good reason and who also happens to have a psychiatric label is to stop listening and start “fixing”, how is that not prejudice, conscious or not, at work?

Psychiatric Solutions Asking To Add More Long Term But Not Acute Patient Beds in Virginia

http://hamptonroads.com/2009/04/2-facilities-propose-add-more-beds-psych-patients

In fact they report that they have had to send patients out of state in the last year due to a lack of acute beds but they are asking to add more long term beds.  I would find this strange if I did not think that any for profit psychiatric provider probably makes more profit on long term stays than they do on short term (acute) stays in their facilities.  Think about it.  For a short term, acute stay, which returns a child or adolescent to their family and community as soon as possible, thus preventing the risk of institutionalization effects on the child or teen, a facility has to do the same full evaluation and treatment planning that they do for a long term stay but for less reimbursement.  Acute beds are also for children and adolescents who are in the most distress and thus require more trained staff and more attention from staff. 

There will be a hearing on this proposal.  I hope that people will speak up and talk about what they really need for their children and teens and that the long history of problems in Psychiatric Solutions facilities for children in this state and other states as reported by Pro Publica will be taken into account in considering this request.

I also hope that more successful and more proven programs such as wrap-around services for children in their own homes will be considered for more funding as cheaper and better alternatives to long term psychiatric institutionalization for children and adolescents and for children and teens without families that more therapeutic foster homes will be created and funded.  Do we really want more children and teenagers to be put at risk of abuse, trauma and dependency on institutions in our state?  The effect of institutionalization on children and teenagers is profound, it leaves scars, it is something to be avoided by the provision of alternatives that work.

Florida Considering Turning a State Hospital Over to a For-Profit Prison and Psychiatric Inpatient Company

http://www.jacksonville.com/news/metro/2009-04-04/story/hospital_fight_divides_gop_in_legislature

Florida legislators are fighting over whether to privatize Northeast Florida State Hospital and give the contract to run it to the Geo Group–see below to see what else they do:

“Welcome to The GEO Group, Inc. You might already know that GEO is a world leader in privatized correctional and detention management. But did you also know that we offer a wide range of other diversified services – from home detention to the development of residential treatment and mental health facilities?”

According to an article here,”care for each residential patient costs $233 a day, the lowest cost for inpatient psychiatric care in the country” and 4 million dollars would have to be spent to buy out existing employment contracts with current state employees if the hospital was sold to this private prison and psychiatric inpatient company.  It is hard to imagine how such a company could make a profit unless they cut staff, cut training of staff, cut expenses for food and treatment of patients and generally made this psychiatric hospital for people with psychiatric diagnoses committed to the facility by the state of Florida less safe and less patient-centered.

I think it is important to keep an eye on this in every state as states cut budgets, that in the name of budget cutting for-profit companies do not take over and make a profit at the expense of  the least protected groups in our society, both state hospital residents and prisoners both, but especially psychiatric patients who have been most often committed for inability to care for themselves.

More On Psychiatric Solutions from Pro Publica Including Link to Report by University of Illinois Department of Psychiatry

http://s3.amazonaws.com/propublica/assets/docs/DCFS-UICRiveredgeReport040309.pdf   Long report on Illinois Psychiatric Solutions Hospital but includes analysis of company wide issues with accountability.  Prepared by an actual University Department of Psychiatry for the State of Illinois.  Hmm, which University Psychiatry Department in Virginia would be 1)asked to do this by the state of Virginia and 2) do it. 

http://www.propublica.org/article/illinois-report-blasts-care-as-psychiatric-hospitals-0304

State of Illinois puts admissions on hold for troubled Psychiatric Solutions Facility, when will Virginia do the same?

Illinois is actually outraged that children have been hurt, state officials are outraged.  Where is the outrage in Virginia’s state Department of BHDS/DMHMRSAS/DMAS/Governor’s Office/Children’s Advocacy Groups in Virginia? 

Will Virginia be the last state to close this company’s  facilities down as they go under if they do like Charter Hospitals  did?  If so, why?

Before You Check the Box Allowing Research When You Are Incapacitated on Virginia’s New Advanced Directive Read This

http://www.propublica.org/article/reports-show-weaknesses-in-oversight-of-clinical-trials-0402

Virginia’s newly amended Health Care Decisions Act allows people to agree to research when they are incapacitated both with the prospect of benefit for themselves AND for research NOT with any prospect of benefit for them.  Thankfully the House Amendment separated these 2 options so that people filling out the new Advanced Directives are more likely to notice the “not for patient’s benefit research” section although I am still amazed that we have such a bill in Virginia at all. 

But here’s the rub folks, Institutional Review Boards are not always careful about what they approve and sometimes in fact do not check carefully enough for conflicts of interest in their own members according to Pro Publica.  So think very carefully before you agree to research when you are incapacitated and if you don’t think you want to trust your life, your physical comfort and your health to Institutional Review Boards that may or may not be acting in patients’ best interest at all times, cross that section out of your advanced directive.  (this is not legal advice, I am not a lawyer and have not yet seen the new form except in the amendment passed and signed by Governor Kaine, so talk to your lawyer when making your directive about how to best protect yourself in the way you want to be protected.)

Nostalgic Look Back at When the U.S. Investigated Charter Psychiatric Hospitals

http://www.nytimes.com/1999/12/30/business/us-is-investigating-charter-hospitals.html

U.S. Is Investigating Charter Hospitals
Published: Thursday, December 30, 1999
 
Magellan Health Services Inc. said today that the Justice Department is conducting a nationwide Medicare fraud investigation of Charter psychiatric hospitals, in which Magellan holds a 10 percent stake.
Magellan, which is based in Columbia, Md., manages psychiatric health plans, and Charter Behavioral Health Systems L.L.C. also face a Justice Department investigation into whether the psychiatric hospitals failed to provide medically necessary treatment, Magellan said in its annual report filed Monday with the Securities and Exchange Commission.
Magellan disclosed the Justice Department investigation a year ago, and the new filing says for the first time that the investigation is nationwide.

Read the rest at the link on top.

This was right before Bush came into office.  Since then Psychiatric Solutions has grown and shown the same kind of problems as the Charter Hospitals did nationwide, see Pro Publica Investigation in the Links of Interest, but we finally are rid of Bush and I am trying to hope that a new Justice Department and a new CMS will pay heed to the painstaking investigation done by Pro Publica of continuing deaths, assaults, suicides and failure to provide adequate medical treatment in so many psychiatric hospitals and residential treatment centers owned by Psychiatric Solutions and that maybe there are even TV investigative journalist left willing to take this on.  Maybe. 

For those who don’t know, Charter Hospitals closed down nationwide.

26 Hate Groups in Virginia, You Can Take a Stand Against Hate Using the SPLC Map Below

FAIL–”Psycho Donuts” Owners Think Strait Jackets and Traumatic Brain Injury Are Hilarious

http://www.mercurynews.com/ci_11926613?IADID=Search-www.mercurynews.com-www.mercurynews.com

Hat tip to Justice For All’s blog-  http://jfactivist.typepad.com/jfactivist/2009/03/psycho-donuts-to-open-with-a-fun-mental-institution-theme.html for finding this and writing about it. You can see there a comment from one of the owners that they had no intention of offending.
Um, well maybe, but how could they think in this day and age that “massive brain injury” was something funny? Do they think our soldiers’ injuries are hilarious? Do they think letting Children play with strait jackets will make them more sensitive to the rights and feelings of citizens with psychiatric disabilities or hospitalization experience when they are grown? What are the parents of these kids thinking taking their children to such a place?

Maybe the problem is just total lack of thought and therefore thoughtfulness at all. FAIL as the younger folks say. Just FAIL.

Saturday Link Fest

Two from the amazing and tireless advocate for people living in nursing homes and other institutions who could live at home if supports were available, Steve Gold:

   1.  “Do Non-Institutional Long-Term Care Services Reduce Medicaid
Spending?” written by H.S Kaye, M. LaPlante, and C. Harrington.  It is in
the journal Health Affairs, vol 28, no 1 (Jan/Feb 2009). 
http://content.healthaffairs.org/index.dtl

    2.  “Taking the Long View: Investing in Medicaid Home and
Community-Based Services Is Cost-Effective” written by R. Mollica, E.
Kasser, L. Walker, and A. Houser. It is in the publication entitled
INSIGHT on the Issues, vol I26 (March 2009), a publication of the AARP
Public Policy Institute.  www.aarp.org/ppi

From Stephen Drake of Not Dead Yet (yes it’s on

 Fox, yes I know you can deal if you have to, I did ;) ).

http://notdeadyetnewscommentary.blogspot.com/2009/03/georgia-ndydisability-activist-on-fox5.html

How will people struggling with substance use disorders and trying to get treatment with inevitable lapses along the way get that help if this kind of thing goes forward?  See below:

http://dissentingjustice.blogspot.com/2009/03/targeting-poor-some-states-propose-drug.html

Poverty, Race and Diabetes

I don’t have diabetes and I hope the steroids I have to take for my transplant don’t ever cause it but I know lots of folks who do.  Some folks have Type I from childhood but I’m going to talk here about Type 2, the one acquired in older age and now sadly even in childhood on occasion.  So what does poverty have to do with it I hear you ask?  It has to do with access to healthy food and money to pay for it.  Foods filled with sugar or worse high fructose corn syrup are cheap.  Vegetables, fresh food, meat, fish, poultry to make home cooked meals are expensive.  Poor neighborhoods often lack a full scale supermarket and have only convenience stores and mom and pop stores with few choices and expensive choices at that.  So if someone is choosing between paying their rent or their child’s health care bill or clothes or diapers for their baby, they will not only have trouble finding healthy food in their neighborhood, they probably can not afford to make the choice to buy it if it is available. 

Another issue often overlooked with diabetes is the impact of race.  African-Americans and Native Americans are much more likely to develop diabetes regardless of diet.  There have been many articles written about this and many theories as to why it is the case, but it has been known for years to be the case.

So the next time you see someone blame someones lifestyle or you find yourself blaming someones lifestyle choices for their diabetes, think again.  You may be making assumptions that are not true, you may be blaming the victim so to speak.  No one chooses to have any illness, the best thing we can do is to support people when they do to have the best access to medical care and the best access to healthy food for people, especially children, who do not have access otherwise due to poverty.  And it wouldn’t hurt if we did not congratulate ourselves for not having an illness many people have to live with for the rest of their lives due to drugs they have been prescribed, poverty or genetic propensity.  In fact it might even make us look as if we care about all people and all people’s health, no matter who they are or what their circumstances are.  Everybody matters as the great old slogan says. :)

Patients Win Settlement against Psychiatric Hospital in Canada for Everyday Practices in the United States

http://www.cbc.ca/canada/montreal/story/2009/03/19/pinel-settlement.html

1 million Canadian dollars to 200 former patients for being shackled and strip searched and as mainstream media in Canada describe it “treated like criminals” and “mistreated”.  And supportive comments for the patients by citizens below the story!  Can we bottle whatever they have going in Canada and ship it over the border?

Alexis Glover Update: Neighbors and Caregivers Reported Abuse to Police for 2 Years before her Death.

Alexis Glover, Child with disability and illness, police did not respond to 2 years of reports of abuse

Alexis Glover, Child with disability and illness, police did not respond to 2 years of reports of abuse

Thank you to Linda Edwards at F.R.I.D.A.   http://fridanow.blogspot.com

Even sadder news about Alexis Glover whose foster mother is now charged with killing her.   It has been reported that bus drivers, neighbors and others contacted the police in the last 2 years of Alexis’s life to report injuries and neglect by her mother as well as an actual statement that she had been abused by Alexis herself to a neighbor and yet Alexis was still in her foster mother’s custody all that time.  This was a preventable tragedy.  Police need to respond to reports of a child being hurt.  It is hard to imagine why they did not.  It is hard not to wonder if race and disability had a role in their failure to respond.  We are still hearing about temporarily able-bodied white young girls who were killed long after their deaths, years later in some cases.  And in those cases police definitely responded.  What happened here must not happen again.  Let’s hope there is some training for the police in her region in disability issues and maybe  a little consciousness raising thrown in for good measure.  If children can not count on the police for protection, who can?

We Must Demand Medical Screening of All Involuntarily Treated People in Our MH System

http://www.nytimes.com/2009/03/15/magazine/15wwln-diagnosis-t.html?emc=tnt&tntemail1=y

This woman could have died, now she is medication free.  But if she lived in Virginia or one of the many other states where forced outpatient and inpatient drugging occurs without adequate medical screening, what do you think her chances of survival would have been?  What are the chances anyone would have explored the possibility that she had a tumor and not a mental illness before sentencing/oops I mean “compassionate forced treatment for her own good” her to take drugs that almost killed her against her will? How many others HAVE died in Virginia because their medical condition was never discovered? 

Yes, medical screenings take time and money.  Cost.  Saving lives? Priceless.

Sign and Share the Petition for Optimal Dialysis in the U.S.: Save Lives

 
Every Other Day Dialysis

 

  

View Current Signatures   –   Sign the Petition  

The Petition Lives! Make it viral!


 

To:  Congressional Kidney CaucusWe, the undersigned, ask the Congressional Kidney Caucus to advocate for the Centers for Medicare and Medicaid Services (CMS) to increase the number of routinely reimbursed hemodialysis treatments from three per week (156/year) to every other day (183/year).

We are people on dialysis, care partners, health professionals, family, and friends. Dialysis is not the end of life, but can and should be a new beginning. We believe that so-called “adequate dialysis” (three short treatments per week) merely allows people who need dialysis to hang onto life unproductively–in essence, many are prevented from living the life they were meant to live. This need not be the case! Research has proven that more treatments mean healthier lives, fewer hospitalizations, longer survival, increased productivity, and less overall cost to the healthcare system for people on dialysis.

The U.S has the worst dialysis outcomes of any industrialized nation. Supporting every other day treatments will allow those managing their illness with conventional hemodialysis to avoid the ‘long weekend’ with no treatment—which many studies have shown triples the risk of sudden death from a heart attack. Even this won’t allow the U.S. to catch up; that won’t happen until longer and more frequent treatments are made more widely available. But it’s a start! Please give this vital change your support!

Sincerely,

The Undersigned

 

 

View Current Signatures
 


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tags:   CMS   Dialysis   Hemodialysis   kidney   Medicare   Renal  

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Anna Nicole Smith: Finally Charges Brought Against Her Psychiatrist

It seemed as if Anna Nicole Smith’s psychiatrist was never going to face any consequences for prescribing drugs to aliases, prescribing drugs in outrageous quantities, prescribing addictive drugs to someone who struggled with addiction, but after all this time she is finally being charged with several counts and has been arrested. This may seem like a small thing or a trivial topic, but it isn’t, because Anna Nicole Smith was a person in trouble, a person who wanted or needed help after the death of her son and instead of grief counseling or support, all she got was drugs and far too many of them.  Unfortunately this is also the case for far too many folks who do not have Anna Nicole Smith’s money or celebrity status.  When folks suffered a death in the family when I was younger, we offered counseling and support in our mental health centers to deal with a normal reaction to a great loss.  Now counseling is very hard to come by in our public and it seems even sometimes in in our private mental health system and a person who is grieving who does not know about or have access to grief counseling is likely to be prescribed a pill rather than given the chance to talk their pain through with a supportive, trained person or group.  So I am glad to see charges brought against a psychiatrist who failed to look at the needs of her patient (allegedly) and just gave her more and more drugs until the drugs finally killed her patient.

Until the Killing of People With Disabilities Is As Important as the Killing of Temporarily Able-Bodied, We Who Believe in Freedom Can Not Rest

People with disabilities are being murdered by family members and caretakers and staff in institutions and allegedly by the Final Exit Network all over this country and this world. (For factual information on how far the Final Exit Networks wants to go including killing people with Alzheimer’s, children with severe disabilities  and any adult who someone considers a burden please read Stephen Drake’s latest post at:  http://notdeadyetnewscommentary.blogspot.com/2009/03/final-exit-advisory-board-members.html )  Until the killing of people with disabilities is as important to our society as the killing of temporarily able-bodied people in this country,  we do not have freedom nor equality and we can not rest until we get it. 

When major media insist on calling alleged forcing of folks to continue with suicide “assisted suicide” instead of murder, when they continue to ignore the non-terminal status and the admission of FEN that they do not restrict their death work to people who are at the end of their natural life, we know how far we have to go before we reach equality, freedom and simple respect for our person-hood. 

Speak up when you hear someone using demeaning terminology about anyone with a disability of any kind.  Don’t be polite about it, don’t let someone else do it, don’t not speak up because you think it isn’t important enough to speak up and educate about, your silence in the presence of demeaning language is taken as agreement, it reinforces the prejudice and it tells people with disabilities that you do not see them as equals no matter how much of a good person you may be.  It takes practice, it takes courage, it takes time and patience and I don’t expect that everyone will be able to do it every time, but if people don’t start practicing, start at least noticing when this demeaning language is being used and thinking of a response later, don’t think about what they could do to be a real ally to people with disabilities when people with disabilities are not there, we will not get there, we will not be free, we will not be equals.  As Romanovsky and Phillips wrote: 

Be Political, Not Polite
When you speak you often use
Some racist word or sexist phrase
That makes me stop you in your tracks
To note the error of your ways
And I know you find it boring
But it seems to me the only way
To correct you, to object to
The hurtful things you say

chorus:
Right the wrongs of human rights
The risk you take could save a life
Silence keeps us all in darkness
We can’t change it overnight
But we can shed a little light
Be political, not polite

I cannot be satisfied
Knowing just how much you care
I want an ally with a voice
Defending me when I’m not there
‘Cause being actively supportive
Is the greatest gift that you could give
By demanding understanding
We can change the world in which we live

(chorus)

Words can hurt, words can heal
Make us think, make us feel
And they’re every bit as deadly
As a bullet tearing through the land
For if our words create the climate
Then the blood is on our hands

Every time we hear a joke
That takes a shot at someone else
If we speak up for their rights
We are speaking for ourselves
‘Cause we will never have true freedom
‘Til everyone one of us is free
From the silence, and the violence
That’s become our history

Saturday Morning Link Fest

http://icad.wordpress.com/2009/03/04/autistic-grandson-murdered/  (19 year old with autism murdered by his grandmother in murder/suicide in Virginia from the International Coalition on Abuse and Disability)

http://alexschadenberg.blogspot.com/  (Euthanasis Prevention Coaliton outside the U.S.)

http://ableism.wordpress.com/  Ableism and Ability Ethics and Governance

http://www.ualberta.ca/~initativ/Home.html  (Ethics and Disability, The Disability Ethics Initiative based in Canada)

Treatment Advocacy Center, So Many False Assumptions, So Little Time to Correct Them :)

I know the Treatment Advocacy Center folks are trying very hard to improve their image, I see their efforts to be more compassionate and less fear-mongering about people with psychiatric disabilities/diagnoses/histories, but it seems they just can’t stop themselves from making huge assumptions about the relationship between mental illness and homelessness. 
I wonder if the good folks at the Treatment Advocacy Center are aware of how many people diagnosed with mental illness are put out on the street by their families of origin?  Or how many are not allowed to come home if they leave home and then realize they need support and help only a family could give?  Or how many parents have bought into or been fooled into believing “tough love” is appropriate for their children in emotional distress?  I am aware of it.  I know too many people who as young adults, in some cases very young adults, were disowned by their families because they were given a serious mental illness diagnosis.  It is not the majority of folks of course, but it is a real and not uncommon phenomenon. How exactly will more forced outpatient treatment laws, which is what the good folks at the Treatment Advocacy Center want, help any of these people who have been disowned by their families and forced onto the streets or left on the streets?  If a person, any person, is homeless, what they need first is a home.
And how does the Treatment Advocacy Center make the leap from homelessness to jail? Sure some people end up in jail for status crimes who also happen to be homeless but to write that the choice is homelessness or jails is a big reach.  The choice is giving people who are homeless a place to live and lay their head or not making that commitment as a society and as individuals.  Unfortunately in most places in this country we have not made the commitment to provide a safe place to lay their head for every citizen who through hard times or hard situations or disownment due to emotional crisis has become homeless.  I would opine we have made a bad choice in that regard and that no amount of expensive outpatient commitment programs will help if we do not make the decision as a society to support people through hard times with at least a  bed and food. 
Yes, homelessness will get worse with these bad economic times and yes living on the streets will cause some folks to go into an emotional crisis and all to be unhappy and distressed, how could it not?  But no drug will fix their distress when it is caused by no place to call their own or even a pillow inside to lay their head on.  If a person, any person, is homeless, what they need first is a home.
Okay, that’s all I have time for tonight, tune in for more updates on the good but assumption-prone folks at the Treatment Advocacy Center as I have time. :)
From the Treatment Advocacy Center’s new and improved blog that still allows no comments and has no RSS feed (silly rabbits, no RSS feed is for kids :) ).
“Too many people with mental illness end up homeless. People with untreated psychiatric illnesses constitute one-third, or between 150,000 and 200,000 people, of the estimated 744,000 homeless population. The quality of life for these individuals is abysmal. Many are regularly victimized.

For some of those homeless, it is often part of a cycle between life on the streets and jail.  A choice no one, especially someone with a serious illness, should face.
When someone with a mental illness lives on the streets, they face a number of threats from the environment and weather, the lack of sanitation, theft, and violence.  At any given time, there are approximately twice as many people with untreated severe psychiatric illnesses living on America’s streets than are receiving care in hospital.

Given the current state of the economy, many fear the problem will grow worse. 
“With the nation and state in recession, the problem is likely to grow before it improves, but how a society treats those citizens who most need the help of other people or institutions says a great deal about it,” wrote a recent editorial in the Tennessee Knox News Sentinel.  Like in other states, the jail there has become the state’s largest mental hospital. 

Living on the streets-and all that it entails-is a difficult circumstance for someone without a severe mental illness to adapt.  For someone with schizophrenia or bipolar disorder it can be a living hell. 
There need to be better alternatives.  The choice between life on the streets and jail is not choice at all.  As the Tennessee paper wrote, “Jail is not the proper place for any society to house homeless people with mental health issues.”"

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Mainstream Media Not Covering What the Final Exit Network Does–It “Helps” and May Murder People Who Are NOT Dying but Disabled or Old or Depressed.

Please read Not Dead Yet’s blog for full coverage on the problem with how the media is covering the arrests of Final Exit Network members here:  http://notdeadyetnewscommentary.blogspot.com/

This is NOT about people who would be eligible for a prescription from a doctor in Oregon and Washington who must be within 6 months of natural death.  This is about encouraging people who are not dying but may have  a chronic illness, disability or are just old and isolated perhaps.  Their guides have been accused of promising to HOLD DOWN THE HANDS of the undercover agent who infiltrated them in Georgia.  What is that but murder?  A person changes their mind and wants to live but these guides may actually prevent them from choosing to live. 

Final Exit Network is being investigated for the death of a woman with depression and nowhere near a natural death.  Final Exit Network openly admitted that they think appearance is a good enough reason for them to help someone kill themselves who is not dying.   They target people who are not dying just as Kevorkian did.  

Folks, this is not about people who are about to die a natural death, this is about enabling suicide of people who the Nazis murdered without fancy web sites and without pretense of dignity or compassion.  This is about targeting folks who the Nazis called “useless eaters”.  This is about folks who are in our own country have been the target of a campaign for eugenics and euthanasia before the news came out after World War 2 and all  those folks went underground.   Well they’re back.  Don’t expect the full story from the mainstream media on this story any more than you did or should have before the War in Irag began.  Read http://notdeadyetnewscommentary.blogspot.com/

In Western State Hospital in Virginia, There is a Men’s Only Forensic Ward but No Women’s Only Civil Ward–???

Um, let me try and understand this fact.  Forensic, i.e. Not Guilty by Reason of Insanity or people deemed incapable of assisting in their own defense in a criminal trial and committed to Western for restoration of capacity to stand trial, male, patients have a single gender unit/ward at the hospital.  I do not know if female forensic patients also have a single gender unit.  I do know that patients  civilly (i.e. committed  for lack of ability to care for self, danger to self, very occasionally (the lowest percentage of all commitments) for danger to others do not have any option for a single gender unit or ward, female or male.  How in the world does this make sense?  The state of Virginia uses its power to lock up women and men for being ill or diagnosed as ill by a marriage and family therapist come July 1 or a nurse specialist as of July 1 of last year or other licensed mental health professional for their own protection and than fails to protect them from the risk, a known risk, of sexual assault, of re-traumatization, of being harassed, of being intimidated, of having their religious beliefs violated if they belong to certain religions, of having their very sense of themselves as safe and of the mental health system as safe destroyed or damaged? 

If someone can explain why NO ONE in DMHMRSAS, soon to be DBHDS or anyone else in this state will address this issue at the time a New Western State Hospital is being built, I would appreciate it.  But I don’t think there is an explanation beyond “we just do not get it and we just do not care enough to spend any money to keep women and men safe from trauma at Western State Hospital.”  Why do I think this? Well for one because Virginia’s so called plan to implement trauma informed care on SAMSHA’s website lists someone who is retired as the head of their program to implement trauma-informed care and because outside of one center of excellence there is no plan to implement trauma informed care and no working groups on the issue in Virginia’s public mental health system. 

But don’t let this keep you up at night or worry you or anything, these patients are “other”, they wouldn’t be there if they were not “head cases” or losers or poor or traumatized………oops.

C’ville Weekly Reader Speaks Out, Speaks Up in Print about Fear-Mongering and Prejudice

http://www.c-ville.com/index.php?cat=141404064423910&ShowArticle_ID=11800203092814347

Don’t blame the victim

I am writing in response to the cover story, “Under Threat” [February 24].  I appreciate your attention to the important issue of ensuring adequate mental health treatment resources for Virginia’s children and adolescents. To meet these needs, a spectrum of treatment options should be available, including community-based treatment and acute inpatient hospitalization. However, I was profoundly disturbed by the irresponsible and inflammatory language used to portray the children and adolescents in need of such treatment. The author’s descriptions of people with mental illness as “the off-kilter minds of Virginia’s most disturbed children” and “kids who are so messed up in the head”  and “deranged kids,” only serve to reinforce existing pervasive negative stereotypes. In addition, the article’s repeated focus on violent themes is misleading and unbalanced. The general public continues to link mental illness to violence, with little understanding of the true picture. The vast majority of people with mental illness are not violent, and the vast majority of violent acts are perpetrated by people without mental illness. In fact, people with mental illness are more likely to be victims of violent crime than to be perpetrators. This fear mongering is irresponsible. Inaccurate stereotyping of people with mental illness strengthens stigma and fear. Societal discrimination against the mentally ill is actually largely responsible for the chronic underfunding of the U.S. mental health system, leading to woefully inadequate treatment resources. It is vital that the media work to create an accurate portrayal of mental illness and its treatment in order to correct public misperceptions and build the support needed to appropriately care for these children and their communities.
 
Lillian Mezey
Albemarle County

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Look to the Young to Lead Medicine out of Corruption/HOPE! :)

http://www.nytimes.com/2009/03/03/business/03medschool.html?ref=business

March 3, 2009
Harvard Medical School in Ethics Quandary
By DUFF WILSON

BOSTON – In a first-year pharmacology class at Harvard Medical School, Matt
Zerden grew wary as the professor promoted the benefits of cholesterol drugs
and seemed to belittle a student who asked about side effects.

Mr. Zerden later discovered something by searching online that he began
sharing with his classmates. The professor was not only a full-time member
of the Harvard Medical faculty, but a paid consultant to 10 drug companies,
including five makers of cholesterol treatments.

“I felt really violated,” Mr. Zerden, now a fourth-year student, recently
recalled. “Here we have 160 open minds trying to learn the basics in a
protected space, and the information he was giving wasn’t as pure as I think
it should be.”

Mr. Zerden’s minor stir four years ago has lately grown into a full-blown
movement by more than 200 Harvard Medical School students and sympathetic
faculty, intent on exposing and curtailing the industry influence in their
classrooms and laboratories, as well as in Harvard’s 17 affiliated teaching
hospitals and institutes.

They say they are concerned that the same money that helped build the
school’s world-class status may in fact be hurting its reputation and
affecting its teaching.

The students argue, for example, that Harvard should be embarrassed by the F
grade it recently received from the American Medical Student Association, a
national group that rates how well medical schools monitor and control drug
industry money.

Harvard Medical School’s peers received much higher grades, ranging from the
A for the University of Pennsylvania, to B’s received by Stanford, Columbia
and New York University, to the C for Yale.

Harvard has fallen behind, some faculty and administrators say, because its
teaching hospitals are not owned by the university, complicating reform;
because the dean is fairly new and his predecessor was such an industry
booster that he served on a pharmaceutical company board; and because a
crackdown, simply put, could cost it money or faculty.

Further, the potential embarrassments – a Senate investigation of several
medical professors, the F grade, a new state law effective July 1 requiring
Massachusetts doctors to disclose corporate gifts over $50 – are only now
adding to pressure for change.

The dean, Dr. Jeffrey S. Flier, who says he wants Harvard to catch up with
the best practices at other leading medical schools, recently announced a
19-member committee to re-examine his school’s conflict-of-interest
policies. The group, which includes three students, is to meet in private on
Thursday.

Advising the group will be Dr. David Korn, a former dean of the Stanford
Medical School who started work at Harvard about four months ago as vice
provost for research. Last year he helped the Association of American
Medical Colleges draft a model conflict-of-interest policy for medical
schools.

The Harvard students have already secured a requirement that all professors
and lecturers disclose their industry ties in class – a blanket policy that
has been adopted by no other leading medical school. (One Harvard
professor’s disclosure in class listed 47 company affiliations.)

“Harvard needs to live up to its name,” said Kirsten Austad, 24, a
first-year Harvard Medical student who is one of the movement’s leaders. “We
are really being indoctrinated into a field of medicine that is becoming
more and more commercialized.”

David Tian, 24, a first-year Harvard Medical student, said: “Before coming
here, I had no idea how much influence companies had on medical education.
And it’s something that’s purposely meant to be under the table, providing
information under the guise of education when that information is also
presented for marketing purposes.”

The students say they worry that pharmaceutical industry scandals in recent
years – including some criminal convictions, billions of dollars in fines,
proof of bias in research and publishing and false marketing claims – have
cast a bad light on the medical profession. And they criticize Harvard as
being less vigilant than other leading medical schools in monitoring
potential financial conflicts by faculty members.

Dr. Flier says that the Harvard Medical faculty may lead the nation in
receiving money from industry, as well as government and charities, and he
does not want to tighten the spigot. “One entirely appropriate source, if
done properly, is industrial funds,” Dr. Flier said in an interview.

And school officials see corporate support for their faculty as all the more
crucial, as the university endowment has lost 22 percent of its value since
last July and the recession has caused philanthropic contributors to
retrench. The school said it was unable to provide annual measures of the
money flow to its faculty, beyond the $8.6 million that pharmaceutical
companies contributed last year for basic science research and the $3
million for continuing education classes on campus. Most of the money goes
to professors at the Harvard-affiliated teaching hospitals, and the dean’s
office does not keep track of the total.

But no one disputes that many individual Harvard Medical faculty members
receive tens or even hundreds of thousands of dollars a year through
industry consulting and speaking fees. Under the school’s disclosure rules,
about 1,600 of 8,900 professors and lecturers have reported to the dean that
they or a family member had a financial interest in a business related to
their teaching, research or clinical care. The reports show 149 with
financial ties to Pfizer and 130 with Merck.

The rules, though, do not require them to report specific amounts received
for speaking or consulting, other than broad indications like “more than
$30,000.” Some faculty who conduct research have limits of $30,000 in stock
and $20,000 a year in fees. But there are no limits on companies’ making
outright gifts to faculty – free meals, tickets, trips or the like.

Other blandishments include industry-endowed chairs like the three Harvard
created with $8 million from sleep research companies; faculty prizes like
the $50,000 award named after Bristol-Myers Squibb, and sponsorships like
Pfizer’s $1 million annual subsidy for 20 new M.D.’s in a two-year program
to learn clinical investigation and pursue Harvard Master of Medical Science
degrees, including classes taught by Pfizer scientists.

Dr. Flier, who became dean 17 months ago, previously received a $500,000
research grant from Bristol-Myers Squibb. He also consulted for three
Cambridge biotechnology companies, but says that those relationships have
ended and that he has accepted no new industry affiliations.

That is in contrast to his predecessor as dean, Dr. Joseph B. Martin.
Harvard’s rules allowed Dr. Martin to sit on the board of the medical
products company Baxter International for 5 of the 10 years he led the
medical school, supplementing his university salary with up to $197,000 a
year from Baxter, according to company filings.

Dr. Martin is still on the medical faculty and is founder and co-chairman of
the Harvard NeuroDiscovery Center, which researches degenerative diseases,
and actively solicits industry money to do so. Dr. Martin declined any
comment.

A smaller rival faction among Harvard’s 750 medical students has circulated
a petition signed by about 100 people that calls for “continued interaction
between medicine and industry at Harvard Medical School.”

A leader of the group, Vijay Yanamadala, 22, said, “To say that because
these industry sources are inherently biased, physicians should never listen
to them, is wrong.”

Encouraging them is Dr. Thomas P. Stossel, a Harvard Medical professor who
has served on advisory boards for Merck, Biogen Idec and Dyax, and has
written widely on academic-industry ties. “I think if you look at it with
intellectual honesty, you see industry interaction has produced far more
good than harm,” Dr. Stossel said. “Harvard absolutely could get more from
industry but I think they’re very skittish. There’s a huge opportunity we
ought to mine.”

Brian Fuchs, 26, a second-year student from Queens, credited drug companies
with great medical discoveries. “It’s not a problem,” he said, pointing out
a classroom window to a 12-story building nearby. “In fact, Merck is right
there.”

Merck built a corporate research center in 2004 across the street from
Harvard’s own big new medical research and class building. And Merck
underwrites plenty of work on the Harvard campus, including the immunology
lab run by Dr. Laurie H. Glimcher – a professor who also sits on the board
of the drug maker Bristol-Myers Squibb, which paid her nearly $270,000 in
2007.

Dr. Glimcher says industry money is not only appropriate but necessary.
“Without the support of the private sector, we would not have been able to
develop what I call our ‘bone team’ in our lab,” she said at a recent
student and faculty forum to discuss industry relationships. Merck is
counting on her team to help come up with a successor to Fosamax, the
formerly $3 billion-a-year bone drug that went generic last year. But Dr.
Marcia Angell, a faculty member and former editor in chief of The New
England Journal of Medicine, is among the professors who argue that industry
profit motives do not correspond to the scientific aims of academic medicine
and that much of the financing needs to be not only disclosed, but banned.
Too many medical schools, she says, have struck a “Faustian bargain” with
pharmaceutical companies.

“If a school like Harvard can’t behave itself,” Dr. Angell said, “who can?”

Copyright 2009 The New York Times Company

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Ring That Allegedly Helped Kill People with Disabilities and Older Folks Going Down

Final Exit, and no don’t google and go to their site or any site connected with them please, is going down.  Read Not Dead Yet’s last 3 posts about it at:  http://notdeadyetnewscommentary.blogspot.com/  Stephen Drake who writes the blog and works for Not Dead Yet is going to be on TV tomorrow, Sunday at 11:45 on Fox News–if you have never watched Fox news you have time to figure out which channel it is between now and 11:45 a.m. :) .

Final Exit talks about “assisting” and people who are “terminal” but in reality an investigation by Georgia’s Bureau of Investigation using an undercover agent found that if the person accepts their “help” they tell them they will hold down their hands if they change their minds after starting to use the suicide  method they use.  Um, how is that not murder?  They are being investigated for the death of a man who had recovered from cancer and was cancer-free at the time of his death.  People who knew him said he drank too much and was upset about his post-surgery appearance but in no way was this man expected to die by his doctor. 

They are also under investigation for the death of a depressed woman who had family near by but wanted to commit suicide so despite their claims that they thoroughly screen their “clients” if they are guilty in that case it is clear they did not screen at all because if they had they would have found out that this woman had family who loved her and were ready, willing and able to love and be there for her if Final Exit had contacted them instead of telling her it was fine for her to kill herself.  And of course now we know it is possible that if this depressed woman changed her mind her Final Exit helpers might have exercised a Ulysses clause and killed her by holding down her hands. 

I have to say it’ s been a good few days.  Legislators stood up for their principles today, police are arresting really bad folks who are suspected in up to 200 deaths and President Obama and Congress is giving  a one time payment of $250 to everyone on SSDI and SSI: (SSDI is disability social security for people under 65 who payed FICA taxes for a long enough time to qualify and can no longer work due to illness or disability, SSI is for children, older folks and people between 18 and 65 who did not earn enough FICA credits to receive SSDI or minimum Social Security Retirement benefits.  Children will not be getting the payments.)  This time instead of making folks fill out a form and trying to let everyone know they are eligible, payments will simply and efficiently be deposited into the bank accounts Social Security now requires folks on SS to have to prevent theft of checks that used to be rampant. 

Yup, a good few days. :)

Children Left in Old Vermin-Infested Barracks by North Carolina Mental Health System

Makes Virginia look good anyway….What is wrong with people is all I can really say about this one.  Children as young as 5, not that different than Virginia where children as young as 3 and 4 have been admitted to our children’s state hospital, but in North Carolina  left behind in unhealthy conditions including poor heating in winter and poor air conditioning in summer because they built a new state hospital but didn’t make enough room for children.  Well kids should never be with adults anyway, but what was the plan here?  Throw away the kids?  They are just kids with psychiatric labels so who cares?  They may be foster kids so who cares?  Some will be orphans so who cares?  I’m a little old for the history of the meme “failed” but I think this just might be the place to use it: North Carolina Mental Health System for children for Failed, just Failed. 
RALEIGH, N.C., Feb. 24 (UPI) — Mentally ill children at a state hospital in North Carolina remain in an old Army barracks while older patients have been transferred to a new building. 

Conditions in the John Umstead Hospital are so bad that a job posting for a social worker last year warned potential candidates, The (Raleigh) News & Observer reported.

“Because of the age of the building, there is a constant battle against ants and roaches,” the posting said. “The heating and air conditioning units are unpredictably hot/cold regardless of outside temperatures (i.e. 80-plus degree in summer and/or 50 … in winter).”

The new Central Regional Hospital about a mile from Umstead proved to be too small to take all the patients, so the children , some of them as young as 5, were left behind. About 40 are being treated there. 

In addition to the problems with heat and vermin, the gym was closed down last month to be tested for mold contamination.

Vicki Smith, executive director of Disability Rights North Carolina, said the children should be moved immediately.

“We’ve never been really happy with the kids in the larger facility,” Smith said. “We are less happy with the kids in the old, outdated facility that, quite frankly, they determined was unsuitable for the adults to be in.”

© 2009 United Press International, Inc. All Rights Reserved.

There Is No Hierarchy of Cause of Death and No Hierarchy of Disability nor Illness.

Post Traumatic Stress Disorder is  what I have lived with for many years.  I am fortunate, very fortunate, to have found someone to work with who really gets it and to be in recovery, to have learned how to manage my post-traumatic stress disorder by many every day and common sense (once you learn them, not before) self-care activities and methods.   I can manage triggers much better, can figure out when I need to take a break or distract myself or talk it out or think or write it out for myself or just take a rest or a walk or reach out to help someone else, often the most useful way of taking care of myself but not always. 

Keeping things in perspective is important and very helpful to me personally.  Reality testing–is this as scary as I feel it is? Can I do it even if I am scared? Can I get support or do I need support? Asking myself what I need and what will help me get through keeps me steady.  It doesn’t mean I don’t have times when things get rough internally.  But I am so used to that and have learned so much that I can handle much more than I ever thought I could on my own.

I have also learned how ordinary and expected many of my reactions are to situations.  What I used to see as a symptom is often a common response to a difficult and scary situation, in fact my reactions to many situations are the same as many people’s reactions, I have learned to try not to “patholigize” every feeling and every fear and every sadness.  For instance, very few people are not afraid of surgery or would not be scared if they had reason to believe they were having a heart attack. (I wasn’t, I’m fine, it was a rare complication of anti-rejection drugs).  Most people are going to be very upset if they lose a dog to death or  face the need to choose between two dogs they love becaue those two dogs can not get along no matter what you try and one has to be re-homed. 

I have noticed that many people assume because my kidney failure was due to the use of lithium for 14 years (strangely enough I said 12 years for years and only recently corrected my arithmetic and realized it was 14 years)  that I must have bipolar disorder.  I do not.  I had PTSD when I was mis-diagnosed with bipolar disorder but because I was not very questioning and because I believed the experts, it took a very long time for me to realize and accept that this did not apply to me, even though many experts questioned my diagnosis along the way.  I was determined not to be “one of those bipolars who go off their meds” as I heard and my family heard all too often, that horrible and damaging stereotype, as soon as I was mis-diagnosed.  I was going to be the exception. I would never listen to a doctor who questioned whether I was correctly diagnosed as I had heard warnings from other people of the dire consequences to them of doing just that.  I was stubborn and determined and scared all at once.  Scared of being seen as “one of them”.  Stubborn about not fitting that horrible and prejudiced stereotype.  Determined to be a model patient and success story.  I was wrong.  I failed to listen to my own instincts.  I accepted the labels and boxes of others and not my own experience and my own feelings. 

I am very grateful not to still be in that box.  I am grateful to experts who were gentle with me as they led me to understand and accept that what I had been told was not true about me. I am grateful to a doctor who stuck with me as I resisted ceasing my last mood stabilizer years ago even though it had warnings out about it that I should take seriously. 

I am not grateful for having kidney failure due to a wrong diagnosis.  I am not grateful for in the past and occasionally in the present being treated differently and with less respect in medical settings which I have no choice but to be in anymore.  I am not grateful for attitudes from anyone that say “get over it” or on the other hand “you are other, you are less, you are not one of us”.  I am not grateful when people feel okay about asking me very personal questions they have no reason to know the answer to when I (rarely) disclose that I have PTSD.  I understand the instinct to ask what happened, I do not attribute bad intentions to those who ask what caused this in you or who ask what were you doing that caused you to be misdiagnosed.  People want to know and understand and that is not coming from a bad place in anyone.  But my personal history  is mine and shared only with those I trust very much and those to whom I am very close and not even to all who fit in those categories.  I think I share a lot actually, but some things I will not share and that is my choice to make.  I am resigned by now to the fact that there will always be those who will ask or those who will assume I am at fault for my wrong diagnosis, that I must have been “doing” something or it wouldn’t have happened. 

Strangely enough I am equally bothered when people assume I am “good” or “better than others” or virtuous or something along those lines when I share my great luck at being able to get off of dialysis about 9 months after I got on it and stay off of it for over a year and a half. I know where this comes from in me though, it is not strange to me.  I was much younger when AIDS hit my home town of Philadelphia and hit the United States in general and people were dying before the cocktail and I listened to all the folks making distinctions between people who had AIDS based on how they got it, even asking people how they got it as if it were their business.  Even before any of us had heard of AIDS, I was disturbed by a story from a former therapist of mine about her father’s death–and yes I now know she should never have shared it with me–how determined she was to get the doctor at the time of her elderly father’s death to tell her and her mother that it was smoking cigarettes that killed him and how angry she was that the doctor would not do that.  From memory, he was old, he had many medical problems, his cause of death was complicated and not clear cut as is so often the case both in death and in life.  But she wanted to blame him.  She was grieving, I get that, when people are grieving they are not themselves.  I do not blame her now.  But it made an impact on me.  It made me think early on about how we talk about people and their illnesses and disabilities and their deaths.  I came to the maybe simplistic conclusion/statement that no one deserves the death penalty for “fill in the blank” with smoking cigarettes, drinking alcohol, using recreational/illegal drugs, not eating a healthy diet and on and on.  We all will die.  We may hasten our deaths by our actions or we may not.  We may be lucky or we may be unlucky.  I knew and admired a man who lived to 96 who smoked into his 50’s and drank decades beyond that.  My great-aunt smoke until she died from complications from an earlier car accident at 83.  And little children die of dysentery in places without clean water, people are dying of AIDS all over the world due to lack of medicine and lack of protection, people who  never smoked get lung cancer, people who never drank lose their livers, death is not fair, death is never deserved, death is death and comes to us all even if we do everything “right” all the time every day of our lives, short or long. 

There is no hierarchy of cause of death.  There is no hierarchy of disability.  We all will die and if we live long enough we all will face disability and illness.

Do You Think You Are In a Home When You Are in a Large Hotel? If Not, Why Would You Think People With Disabilities Do?

http://www.nytimes.com/2009/02/20/nyregion/20adult.html?_r=1&emc=tnt&tntemail1=y

After at least 20 years of ongoing coverage of scandals, exploitation, deaths, horrible conditions for people with psychiatric disabilities unfortunate enough to be placed in Adult “Homes” in New York City, a lawsuit to change the practice of forcing thousands of New Yorkers to live in these institutions is going to trial.  Every state has these places, they go under different names in different states.  In Virginia they are called ALF’s of Assisted Living Facilities but not the kind run by Marriot that folks buy into when they get older.  In Pennsylvania they are called boarding homes (or were last I was familiar with them.)  What they all have in common is none of them are “homes”.  If you put over 15 unrelated adults in a building and give them room mates and tell them when they may leave and what they may eat (often sub-standard nutritionally and even in number of calories per day) and what they may do, you are not putting people in a “home”, you are putting them in an institution. 

Nursing homes for folks who could function at home with adequate personal care and nursing assistance are also not “homes”.  We have too many folks in nursing homes as Steve Gold has worked so hard to show over the years that do not need to be there and do not want to be there if we offered them adequate care in their own homes, younger people with disabilities and older people with disabilities and medical conditions that require assistance in daily living.  That is what Aging in Place is about and what activists such as Steve Gold have worked so hard to change. 

Training centers, “Schools” and other names for institutional living for people with intellectual disabilities are not homes either.  And yet they continue to exist in many states, particularly my own state of Virginia and still politicians listen more often to people who are not the people with intellectual disabilities who want a real home nor their allies and advocates but to communities that worry about job loss, to employees who (understandably) worry about job loss or lower pay, to a minority of parents who are very afraid for their own children and may not think about the consequences for other people’s children who could live in the community of insisting on keeping these institutions just as they are.  Fear is understandable of course.  Love of ones child.  Fear of the future.  But it is the responsibility of legislators and others in positions to make these decisions to look at the whole picture and be both brave and careful (and dare I add empathetic?) to the needs and wishes of the majority of folks in these institutions.  For folks who can not live in a home of their own there are other options and these should be carefully and wisely considered and planned for each individual. 

So why the hotel analogy?  Because most people who do not have a disability or who do not love someone with a disability the closest you will come to an institution  being called a “home” as in “home away from home” is to stay in a large hotel.  And you will choose to go to that hotel, you will be free to leave at any time, you will choose your own food and your own bed time, you will do as you like within the ordinary limits of courtesy and legality.  But do you ever think it is a home when you are in a hotel? So why do we persist in calling these large segregating settings for people with disabilities of whatever kind “Homes”?

Charlottesville Blog Recommendation: The Carpenter Chronicles

http://thecarpentersx4chronicles.blogspot.com/

Parents of a now one year old born with Downs Syndrome write lovingly about their child.

What I Would Write if Virginia Wasn’t an Authoritarian Commonwealth

McDonnell Announces $1 Million Challenge Grant for Statewide Mental Health Care

COMMONWEALTH of VIRGINIA

Office of the Attorney General

Richmond 23219

Robert F. McDonnell 900 East Main Street

Attorney General Richmond, Virginia 23219

For Release: February 18, 2009 Contact: J. Tucker Martin or David Clementson

Website: www.vaag.com
McDonnell Announces $1 Million Challenge Grant for Statewide Mental Health Care

Grant Provided to Virginia Health Care Foundation

-Foundation to Double Grant Amount; Funds Result of Two Settlements-

Richmond- Attorney General Bob McDonnell today formally announced a $1 million challenge grant for the Virginia Health Care Foundation (VHCF) to provide mental health care in the Commonwealth. The grant is the result of two successful multi-state settlements secured by the Office of Attorney General Bob McDonnell, and Attorneys General from other states, with two national pharmacy benefits management companies. The settlements occurred in 2008.

McDonnell was joined at this morning’s press conference by Debbie Oswalt, Executive Director of the VHCF; Mary Ann Bergeron, Executive Director of the Virginia Association of Community Services Boards; Lou Markwith, Executive Director of the Virginia Association of Free Clinics; Neil Graham, Chief Executive Officer of the Virginia Community Healthcare Association; Gil Minor, Chairman of Owens and Minor, and Chairman of the VHCF Fund Development Committee; Chief Deputy Attorney General Bill Mims, and other statewide leaders in the public health arena.

Speaking about today’s announcement Attorney General McDonnell noted, “Our office has worked with the Governor, leaders in the General Assembly, mental health advocates and other stakeholders to make mental health reform a top priority. Mental illness is treatable, and we must do all we can to help those who suffer from it. This grant will assist in that effort. The Virginia Health Care Foundation will use these initial funds to raise an additional $1 million, and then use all those funds to augment community mental health care resources. Today’s announcement means treatment for uninsured Virginians in need of mental health care. This doesn’t just benefit these individuals, it benefits our entire Commonwealth.”

Debbie Oswalt, executive director of the VHCF remarked, “The Attorney General’s innovative approach of using the settlement funds as a challenge grant will double the amount of funding available to treat uninsured Virginians with basic medical or mental health needs. This creative leveraging has produced a financial incentive for collaboration among local community services boards and health safety net organizations, which should result in substantial long term dividends for uninsured Virginians with mental illness.”

The VHCF will use the $1 million grant for a special Mental Health Leadership Initiative. The full $2 million (the initial $1 million plus the $1 million match to be raised by the VHCF) will be distributed by the VHCF through a competitive grant process to Virginia’s health safety net providers. Approximately 8-10 three-year grants could be made to Virginia communities that want to offer primary health care to the seriously mentally ill or expand basic mental health services. All grants will ensure access to needed prescription medications. For example, those entities interested in providing basic mental health services could use the funds to hire mental health professionals to treat uninsured patients suffering from depression, anxiety, and similar illnesses. Those entities interested in providing basic medical care to seriously mentally ill clients from local Community Services Boards could use the funds to hire necessary medical staff, and underwrite related costs, including prescription medications. The VHCF will be working in collaboration with the Virginia Association of Community Services Boards, Inc., the Virginia Association of Free Clinics, and the Virginia Community Healthcare Association.

Today’s grant is the result of two multi-state settlements entered into with Caremark Rx, L.L.C. and Express Scripts, Inc in February and May of 2008. Both settlements involved claims that these pharmacy benefits management (”PBM”) companies engaged in deceptive business practices by encouraging doctors to switch patients to different brand name prescription drugs and representing that the patients and/or health plans would save money. It was alleged that doctors were not adequately informed of the effect certain drug switches would have on costs to patients and health plans. It also was alleged that these PBMs did not clearly disclose to their clients that rebates accrued from the drug switching process would be retained by the PBM and not passed directly to the client plan. From these two settlements Virginia received $1,030,116.94 to be used to benefit low income, disabled, or elderly consumers of prescription medications, to promote lower drug costs for state residents, to educate consumers concerning the cost differences among medications, or for similar purposes.
###
J. Tucker Martin
Director of Communications
Virginia Attorney General Bob McDonnell

www.vaag.com

 

Humor: What Can We Expect to be Named a Mental Disorder Next?

The New York Times ran an article a few weeks back on “Scrupulosity” as a possible mental disorder according to one psychiatrist.  I didn’t write about it at the time and therefore have lost the link, but it got me thinking about what else might end up being diagnosed as a mental disorder next? Here are some of my predictions, feel free to add your own in comments :) .

1.  Compulsive Obedience to the Law

This disorder is characterized by

 1) no parking nor speeding tickets over a patient’s entire lifetime despite possession of a driver’s license.

2) No criminal record, not even any misdemeanours in youth, youth being defined as under 50 years old…

3) Insistence that others not break the law in front of them nor ask them to break the law in any fashion.

4) Annoying others by asking them to follow their own rules and regulations.

2.  Celibacy-

This disorder is characterized by an unhealthy adherence to religious or personal  beliefs and can lead to:

1)  lack of children

2) lack of unsafe sexual practices

3) lack of morning after regrets/remorse/what was I thinking due to lack of one night stands.

Community Organizing

This disorder is characterized by an unhealthy interest in the welfare of others and can lead to:

1) actively encouraging people without power to speak up for themselves

2) getting people in dis-empowered groups together and helping them to become an organized group with a voice

3) and worst of all:  Becoming President of the United States of America :)

Cliches I Would Like to See Eliminated: Add Your Own in Comments if You Like :)

1. Often seen on plaques: “You won’t be given more to carry than you can bear”.  (Comment–what a crock)

2.  “This too shall pass.”  (Comment-yeah, but then something else is going to come along and bite you you know where, sometimes on the very same day.)

3.  “You are as young as you feel” (Comment-no, you are as old as it says on your birth certificate and so are all your organs, so if you are over 50 get your prostate checked, if you are at risk for skin cancer and older get your skin checked by a dermatologist, if you are over 50 get that darn colonoscopy, if you are a woman get mammograms as recommended for your risk group, if you are over 90, get your driving skills evaluated, if you are over 40 and are having trouble reading this, get your eyes checked for far-sightedness and on an on.)

4.  If you just do everything right you won’t get: Alzheimers, cancer, AIDS, old and fragile, heck you won’t even die at all! Comment: Put it on the ground, spread it all around, dig it with a hoe, it will help your garden grow :) .

5.  Adversity makes you stronger.  (Comment–or it kills you, or it makes you so strong you intimidate people without trying, or you crawl into a hole and never come out, or you take it out on someone else, or and or and or….)

6.  “fill in your group” are the last group on the planet it’s acceptable to discriminate against.  (Comment:  Get in line behind the people of Darfur and the Sudan and unwealthy citizens of New Orleans and on and on please.)

7.  All good things come to those who wait.  (Comment, no, you really have to get up and speak up and do something and even then bad things may happen, not good.)

8.  Bi-partisanship.  (Comment: why doesn’t anyone ever point out that the very word is an oxymoron?)

9. Politically Correct.  (Comment: This term arose in the far, far left many years ago and has nothing to do with what you think it does so just stop using it if you don’t know what it means.)

10.  The enemy of my enemy is my friend.  (Comment: probably not, given how prone to eneminess you both are :) )

Virginia Residents Only: Link to Easily Contact Your Senator and Delegate About SB1142 and HB2396

http://salsa.democracyinaction.org/o/1838/t/8648/campaign.jsp?campaign_KEY=26595

Please note this easy to use online tool is only available to Virginia residents.  If you are not from Virginia it will not click you through to any Virginia legislator.  Please use this tool to let your Senator and Delegate know what you think.

What Could Go Wrong If You Don’t Require a Lawyer for Juveniles in Commitment Hearings? This.

Thank you to the Senate Courts of Justice Committee for passing by indefinitely SB 1303 which would have allowed commitment hearings for juveniles to be held without a lawyer and without a Guardian ad litem.  It would have left this up to the judge’s discretion instead of current law which requires the presence of both.  Since juveniles as well as adults can be committed to for-profit psychiatric hospitals, although the story below is beyond rare, in Virginia there was a problem with abuse of process with adults in commitment hearings for gain more than a decade ago.  So by killing this bill, the Senate Courts of Justice Committee has ensured that the below could not happen to teenagers in the psychiatric commitment setting as it did shockingly for years in Pennsylvania in the Juvenile criminal court. 

Pa. judges accused of jailing kids for cash

WILKES-BARRE, Pa. – For years, the juvenile court system in Wilkes-Barre operated like a conveyor belt: Youngsters were brought before judges without a lawyer, given hearings that lasted only a minute or two, and then sent off to juvenile prison for months for minor offenses.

The explanation, prosecutors say, was corruption on the bench.

In one of the most shocking cases of courtroom graft on record, two Pennsylvania judges have been charged with taking millions of dollars in kickbacks to send teenagers to two privately run youth detention centers.

“I’ve never encountered, and I don’t think that we will in our lifetimes, a case where literally thousands of kids’ lives were just tossed aside in order for a couple of judges to make some money,” said Marsha Levick, an attorney with the Philadelphia-based Juvenile Law Center, which is representing hundreds of youths sentenced in Wilkes-Barre.

Prosecutors say Luzerne County Judges Mark Ciavarella and Michael Conahan took $2.6 million in payoffs to put juvenile offenders in lockups run by PA Child Care LLC and a sister company, Western PA Child Care LLC. The judges were charged on Jan. 26 and removed from the bench by the Pennsylvania Supreme Court shortly afterward.

No company officials have been charged, but the investigation is still going on.

The high court, meanwhile, is looking into whether hundreds or even thousands of sentences should be overturned and the juveniles’ records expunged.

Among the offenders were teenagers who were locked up for months for stealing loose change from cars, writing a prank note and possessing drug paraphernalia. Many had never been in trouble before. Some were imprisoned even after probation officers recommended against it.

Many appeared without lawyers, despite the U.S. Supreme Court’s landmark 1967 ruling that children have a constitutional right to counsel.

The judges are scheduled to plead guilty to fraud Thursday in federal court. Their plea agreements call for sentences of more than seven years behind bars.

Ciavarella, 58, who presided over Luzerne County’s juvenile court for 12 years, acknowledged last week in a letter to his former colleagues, “I have disgraced my judgeship. My actions have destroyed everything I worked to accomplish and I have only myself to blame.” Ciavarella, though, has denied he got kickbacks for sending youths to prison.

Conahan, 56, has remained silent about the case.

Many Pennsylvania counties contract with privately run juvenile detention centers, paying them either a fixed overall fee or a certain amount per youth, per day.

In Luzerne County, prosecutors say, Conahan shut down the county-run juvenile prison in 2002 and helped the two companies secure rich contracts worth tens of millions of dollars, at least some of that dependent on how many juveniles were locked up.

One of the contracts — a 20-year agreement with PA Child Care worth an estimated $58 million — was later canceled by the county as exorbitant.

The judges are accused of taking payoffs between 2003 and 2006.

Robert J. Powell co-owned PA Child Care and Western PA Child Care until June. His attorney, Mark Sheppard, said his client was the victim of an extortion scheme.

“Bob Powell never solicited a nickel from these judges and really was a victim of their demands,” he said. “These judges made it very plain to Mr. Powell that he was going to be required to pay certain monies.”

For years, youth advocacy groups complained that Ciavarella was ridiculously harsh and ran roughshod over youngsters’ constitutional rights. Ciavarella sent a quarter of his juvenile defendants to detention centers from 2002 to 2006, compared with a statewide rate of one in 10.

The criminal charges confirmed the advocacy groups’ worst suspicions and have called into question all the sentences he pronounced.

Hillary Transue did not have an attorney, nor was she told of her right to one, when she appeared in Ciavarella’s courtroom in 2007 for building a MySpace page that lampooned her assistant principal.

Her mother, Laurene Transue, worked for 16 years in the child services department of another county and said she was certain Hillary would get a slap on the wrist. Instead, Ciavarella sentenced her to three months; she got out after a month, with help from a lawyer.

“I felt so disgraced for a while, like, what do people think of me now?” said Hillary, now 17 and a high school senior who plans to become an English teacher.

Laurene Transue said Ciavarella “was playing God. And not only was he doing that, he was getting money for it. He was betraying the trust put in him to do what is best for children.”

Kurt Kruger, now 22, had never been in trouble with the law until the day police accused him of acting as a lookout while his friend shoplifted less than $200 worth of DVDs from Wal-Mart. He said he didn’t know his friend was going to steal anything.

Kruger pleaded guilty before Ciavarella and spent three days in a company-run juvenile detention center, plus four months at a youth wilderness camp run by a different operator.

“Never in a million years did I think that I would actually get sent away. I was completely destroyed,” said Kruger, who later dropped out of school. He said he wants to get his record expunged, earn his high school equivalency diploma and go to college.

“I got a raw deal, and yeah, it’s not fair,” he said, “but now it’s 100 times bigger than me.”

Copyright © 2009 The Associated Press.

SB 1142 Senate Substitute Elimates Civil Rights in Health Care for Every Virginia Citizen

http://leg1.state.va.us/cgi-bin/legp504.exe?091+ful+SB1142S1

B. If there is no individual eligible to make health care decisions in subsection A, the patient’s attending physician shall be authorized to provide, continue, withhold, or withdraw health care without obtaining a court order if such health care decision has been affirmed and documented as being ethically acceptable by the health care facility’s ethics committee, if one exists, or by two physicians who are not currently involved in the treatment of the patient and who did not make the determination that the patient was incapable of making an informed decision.

If you live long enough or even if you are young, you have every chance of being considered incapacitated at some point through accident or illness.  The Senate version of SB 1142, the bill that allows research not for their benefit on incapacitated and dying patients, now has a section added that says that if you have no advanced directive and no willing or available family member to act on your behalf, two doctors or an ethics committee (who are appointed by hospitals and one of which approved the Ashley X treatment out West) to decide to give you care you may not want or to withhold care you would want if you could communicate your wishes.  This bill essentially leaves no Virginia citizen safe from unwanted medical interventions or unwanted withdrawal of medical interventions.  

In addition, this bill is clearly aimed at people with psychiatric diagnoses, not people with dementia or Alzheimer’s as some have claimed as no where is dementia mentioned, but “severe and persistent mental illness” is specifically mentioned as a grounds for guardianship and a right for a guardian to admit a person without due process to a psychiatric facility for 10 days with no hearing, no lawyer, no protections against abuse of the law by bad actors at ALL. 

You thought last year was bad? This year the Virginia General Assembly is trying to take away all rights to make our own health care decisions if we even end up delirious from a temporary condition and G-d forbid have a disability or illness that some doctors consider our life a “life not worth living” or alternatively some doctor wants to give your family member a drug that could kill them such as an anti-psychotic to an elderly person with dementia instead of Alzheimer’s specific drugs which do not have the high risk of heart attack and stroke that commonly prescribed  psychiatric drugs do to the point where numerous articles clearly not read by the General Assembly have come out this year warning of the dangers to the elderly of psychiatric drugs in common use. 

Your only protection against this bill is to never have a serious car accident resulting in temporary incapacity, not have a label of “serious mental illness” pinned on you at any point in your life and that can be interpreted to include severe depression, to never have an illness that results in temporary unconsciousness, in short, to never get old and never get sick or injured. 

We are back to doctors as G-ds and incredible and dangerous intrusion by the state of Virginia into our most private and personal values and decisions including our right to live. 

This bill is crossing over.  If you don’t care if your civil rights are being further eroded, don’t do anything.  If you do, write your Senator and Delegate and tell them you will not stand for this incredible intrusion into your civil rights and liberty interest in your medical care and in your right to decide how and whether you die.  Or move to another state (except Texas) that still believes in individual rights to puruse life, liberty and the pursuit of happiness.  Thomas Jefferson would hang his head in shame and so should the General Assembly of Virginia if they pass this bill as written.

New Blogs on my Blog Roll

Bad Cripple–  http://badcripple.blogspot.com/  a cultural anthropologist writes about disability rights from all kinds of perspectives including his own as someone who was paralyzed 30 years ago at 18 and whose parents fought for his right to rehab. and a real life which he achieved.

http://judi-lifeasahospicepatient.blogspot.com/ Judy Chamberlain, author of On Our Own and so much more as an activist and speaker and leader’s blog on her personal experience as a hospice patient. 

Different Thoughts, Once You Label Me You Negate Me. -Kierkegaard

http://activegreymatter.org/  employment for people with disabilities and much, much more

http://lawprofessors.typepad.com/poverty/    Poverty Law Blog

Changing, Evolving, Getting Back to my Roots on this Blog

This blog was intended to be a strategic blog, a political blog, a blog to influence.  And in that choice to make it that kind of blog I lost some of who I want to be, who I used to be when I was quite young actually, who I want to be again.  I read about prison reform when I was 11 from a great present from my parents for children with packets and booklets etc.  I aspired to work on that when I grew up.  It never worked out, for one because my one tour of a prison as an adult freaked me out and I thought I could never do this, and because I went in different directions as an adult.  But in trying to fight for the rights of people labelled with mental illness and to fight the criminalization of psychiatric services and psychiatric hospitals and public perception fueled by propagandists such as the mainstream media and the Treatment (forced treatment only) Advocacy Center, I became a propagandist myself oftentimes and I tried to separate out my principles that prisoners and convicted criminals are people who should be treated as people and given good medical care, rehabilitation if wanted and needed, chances to learn skills, take courses, be prepared for life outside prison and most especially to be safe in prison from assaults and rapes by guards or other prisoners from my principles that people with mental illness labels should not be treated as if they were criminals.  Well no one should be treated as we treat criminals in this country.  No one.  So no longer will I separate out the issues of human rights in the mental health system and human rights in our prisons and jails and justice system.  It is harder to be nuanced, more work, but less emotional toil, more true to myself and less damage to my spirit.

I also believe that it is too early in our civil rights movement as people who have been in the psychiatric system to be thinking we have any real place at the table of decision makers that is not decided and “granted” by the powers that be and that as soon as any of us strays too far from the dominant paradigm of those powers that be we will be excluded from those tables.  And others will be willing to take our place and then learn that they too will be excluded if they stray and have to make their own decisions about how much good they can do versus how much independence they are willing to sacrifice.  Some will do great good despite not being able to state their minds, have and will find ways to do good without losing their place at the table and I think that is great.  But I think we are really at the place where we need to try to capture media attention in non-rigged circumstances to educate the general public on our issues. 

For instance, how many Americans do you think know that forced ECT continues in this country and in this state of Virginia? I suspect  very few folks know that.  How many Americans know the medical and brain damage caused by many of the drugs forced on people in hospitals and now outpatient forced treatment programs?  Not many but maybe a few more as drug companies come under scrutiny more in general.  Still Zyprexa stays on the market having caused more deaths than Vioxx and Vioxx is off the market.  What does that say about where we are in our history as a movement?  I say we are on a hundred year plan.  I say we are where Susan B. Anthony and her colleagues were.  And that we need to act on all fronts but we need to be realistic about where we stand and that to me means we need to find the will and the way and the courage to have protests, old fashioned protests of human rights violations in the mental health system and that we need to think about what will work more than we have. 

But for me it means that this blog will no longer be polemic as it has been at times.  I do not like the way it makes me feel nor act and I am changing it for my own sake.   I am under no illusion that I will not still be considered too “radical” (what a joke!) for the powers that be to be included in their taskforces and hidden committees and committees that mysteriously do not meet or whose meeting times mysteriously don’t reach me even if I am officially on them.  I do not feel bad about being disliked by the powers that be, as the old song says, you ain’t done nothing if you ain’t been called a red, which translates to me as I should be proud of how much animosity there is to me among the powers that be in our Department of MH/BH/MR/SA/DS whatever they are while we await the offensive name change the Department wanted all along and from folks who want me to “just be quiet” in many circles I will not mention. 

I also will not judge those who are in a different place than I.  They are where they are, they do what they do, they are not my concern.

Large Study Shows Mental Illness Without Drug Abuse Is Not Correlated With Violence

International Herald Tribune
Mental illness alone is no trigger for violence
Monday, February 2, 2009

CHICAGO: A new large U.S. study challenges the idea that mental illness alone is a leading cause of violence.

Researchers instead blame a combination of factors, specifically substance abuse and a history of violent acts, that drives up the danger when combined with mental illness in what they call an “intricate link.”

People with serious mental illness, without other big risk factors, are no more violent than most people, according to the study of more than 34,000 U.S. adults. The research was released Monday in Archives of General Psychiatry.

“Mental illness can provide the knee-jerk explanation for the Virginia Tech shootings,” but it’s not a strong predictor of violence by itself, said lead author Eric Elbogen of the University of North Carolina at Chapel Hill School of Medicine.

Elbogen compiled a “top 10″ list of things that predict violent behavior, based on the analysis.

Younger age topped the list. History of violence came next, followed by male gender, history of juvenile detention, divorce or separation in the past year, history of physical abuse, parental criminal history and unemployment in the past year. Rounding out the list were severe mental illness with substance abuse and being a crime victim in the past year.

After the 2007 Virginia Tech killings by a student ordered to get psychiatric treatment, some states considered laws adding mental health questions to background checks for gun buyers or denying weapons to people who’ve been involuntarily committed for mental health treatment.

The new research, which bolsters other similar findings, raises questions about such laws, experts said. Such legislation may be both ineffective and discourage people who need help from getting treatment.

“We are being misled by our own fears,” said Columbia University psychiatry professor Dr. Paul Appelbaum, who wasn’t involved in the new study. “We ought to be concerned about providing good treatment and helping people lead fulfilling lives, not obsessed with protecting ourselves from phantom threats that appear to be unrelated to mental illness.”

U.S. systems to treat mental illness and substance abuse are separate, uncoordinated and could do a better job treating people with both problems, Appelbaum said.

For the new study, the researchers analyzed data from the National Epidemiologic Survey on Alcohol and Related Conditions. The original survey in 2001-2002 involved more than 43,000 face-to-face interviews with a representative sample of American adults. Three years later, many of the same people, more than 34,000, were interviewed again.

Questions about violence in both interviews included:

_”Ever use a weapon like a stick, knife or gun in a fight?”

_”Ever hit someone so hard that you injured them or they had to see a doctor?”

_”Ever start a fire on purpose to destroy someone’s property or just to see it burn?”

_”Ever force someone to have sex with you against their will?”

From the responses, the researchers determined what elements raised the risk of violent behavior.

There were 3,089 people deemed to have severe mental illness — schizophrenia, bipolar disorder and major depression — but no history of either violence or substance abuse. They reported very few violent acts, about 50, between interviews.

But when mental illness was combined with a history of violence and a history of substance abuse, as in about 1,600 people, the risk of future violence increased by a factor of 10.

The relationship between mental illness and violence is there, “but it’s not as strong as people think,” Elbogen said.

Predicting who will act violently is complex, said John Monahan, a psychologist at University of Virginia’s law school, who has done similar research but was not involved in the new study.

“It is true that our crystal balls are very murky,” Monahan said. “The vast majority of violence that occurs in American society has absolutely nothing to do with mental illness.”

The large national survey, conducted by the National Institute on Alcohol Abuse and Alcoholism, included people living in shelters, hotels and group homes, as well as houses and apartments, but it didn’t include people living in hospitals, jails or prisons.

Rosanna Esposito of the nonprofit Treatment Advocacy Center in Arlington, Virginia, applauded the study but pointed out the researchers weren’t able to analyze whether the subjects were in psychiatric treatment or not. Medication for serious mental illness can reduce the risk of violence, she said.

___

On the Net:

Archives of General Psychiatry: http://www.archgenpsychiatry.com

SB1142 Proposes to Violate the Nuremberg Code In One of its Provisions

The hearing for this bill has been moved to this Thursday, February 5th at 9 a.m. in Senate Room B in the Education and Health Committee.

http://www.richmondsunlight.com/bill/2009/sb1142/fulltext/

SB1142: Advance medical directives; revises Health Care Decisions Act regarding.

An advance directive may authorize an agent to approve participation by the declarant in any health care study approved by an institutional review board pursuant to applicable federal regulations, or by a research review committee pursuant to Chapter 5.1 ( 32.1-123 et seq.) of Title 32.1 that (i) snipped OR

(ii) aims to increase scientific understanding of any condition that the declarant may have or otherwise to promote human well-being, even though it offers no prospect of direct benefit to the patient.

 Regulations and Ethical Guidelines

Back to Regulations and Ethical Guidelines Menu

Directives for Human Experimentation

NUREMBERG CODE

  1. The voluntary consent of the human subject is absolutely essential. This means that the person involved should have legal capacity to give consent; should be so situated as to be able to exercise free power of choice, without the intervention of any element of force, fraud, deceit, duress, over-reaching, or other ulterior form of constraint or coercion; and should have sufficient knowledge and comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision. This latter element requires that before the acceptance of an affirmative decision by the experimental subject there should be made known to him the nature, duration, and purpose of the experiment; the method and means by which it is to be conducted; all inconveniences and hazards reasonable to be expected; and the effects upon his health or person which may possibly come from his participation in the experiment.The duty and responsibility for ascertaining the quality of the consent rests upon each individual who initiates, directs or engages in the experiment. It is a personal duty and responsibility which may not be delegated to another with impunity.
  2. The experiment should be such as to yield fruitful results for the good of society, unprocurable by other methods or means of study, and not random and unnecessary in nature.
  3. The experiment should be so designed and based on the results of animal experimentation and a knowledge of the natural history of the disease or other problem under study that the anticipated results will justify the performance of the experiment.
  4. The experiment should be so conducted as to avoid all unnecessary physical and mental suffering and injury.
  5. No experiment should be conducted where there is an a priori reason to believe that death or disabling injury will occur; except, perhaps, in those experiments where the experimental physicians also serve as subjects.
  6. The degree of risk to be taken should never exceed that determined by the humanitarian importance of the problem to be solved by the experiment.
  7. Proper preparations should be made and adequate facilities provided to protect the experimental subject against even remote possibilities of injury, disability, or death.
  8. The experiment should be conducted only by scientifically qualified persons. The highest degree of skill and care should be required through all stages of the experiment of those who conduct or engage in the experiment.
  9. During the course of the experiment the human subject should be at liberty to bring the experiment to an end if he has reached the physical or mental state where continuation of the experiment seems to him to be impossible.
  10. During the course of the experiment the scientist in charge must be prepared to terminate the experiment at any stage, if he has probable cause to believe, in the exercise of the good faith, superior skill and careful judgment required of him that a continuation of the experiment is likely to result in injury, disability, or death to the experimental subject.

Reprinted from Trials of War Criminals before the Nuremberg Military Tribunals under Control Council Law No. 10, Vol. 2, pp. 181-182.. Washington, D.C.: U.S. Government Printing Office, 1949.

Why Did Republicans Vote to Violate the Nuremberg Code Today? Are They Anti-Life?

What is going on in Virginia’s General Assembly and who is pushing an anti-life agenda through under cover of a mental health bill  and clarifying the Health Care Decisions Act? Yes, anti-life.  Allowing guardians and powers of attorney and oral consent from the dying to experiments that have no expectation of health benefit to them as patients is anti-life and anti-people with disabilities and evil. 

Me, I am going to tear up my living will/durable medical power of attorney when/if this bill/bills pass.  And wait until I move to a less anti-life state than Virginia to write another one.  I never thought I would be writing these words.  Never.  Right and wrong do exist and manipulation and deceit in the service of an anti-life,, anti-disability rights agenda are unethical no matter who you are nor how well you think of yourself and your intellect.  Very intelligent people supported eugenics in Virginia and the rest of the United States.  Very intelligent people supported killing psychiatric patients in hospitals in the ’40’s until the revelations of the Nazi regime made such a stance untenable (or politically incorrect).  Very intelligent people are equally capable of evil acts as anyone else.  And equally likely to be completely lacking in insight into the consequences of their actions on others or perhaps not to care about the effects of their actions on others.

Good News for Children with Disabilities and Their Parents in Virginia

I have to wonder why no Democratic legislators appear to be involved in this effort to protect the rights of children with disabilities and their parents.  Certainly we have Democratic legislators who are familiar with disability issues, so why are they not leading the charge on this extremely important issue of rights to an appropriate and free public education for all Virginia students with disabilities?  Maybe they were left out of the story?

Va. lawmakers: Preserve year for special-ed appeals
Times Dispatch / Olympia Meola
Published: January 28, 2009
State lawmakers don’t want to take a chance that special education students in Virginia will lose their one-year window to appeal a due-process hearing decision, so they are trying to write it into law.
The move circumvents the Virginia Board of Education, which is considering broad changes to the state’s special education regulations, in many instances bringing them in line with federal practices.
Due-process hearings are held to resolve disputes between parents and a school system over special-education services.
Virginia gives parents one year to appeal due-process hearing decisions; federal regulations allow 90 days.
Rather than risk the Board of Education deciding to shorten the time frame extended to Virginia families, House Republican Leader Del. Morgan Griffith, R-Salem, wants to codify the practice into law.
The proposed changes to special education regulations have been contentious and drawn thousands of comments from parents, special education advocates, educators and politicians—including high-ranking Republicans in the House of Delegates.
Last fall Speaker of the House William J. Howell, R-Stafford, fired off letters to Board of Education President Mark Emblidge and Secretary of Education Thomas Morris, alerting them to his objections and informing them that lawmakers were prepared to take legislative action if necessary.
Today, House Bill 2304 breezed through the House Education Committee over the objection of the Virginia School Boards Association, which wants to leave the decision to the Board of Education. The board could vote on the regulations in the coming months.
Griffith said parents of special education students in many cases need one year to find an attorney to take their case to court, and then, when they find out how much it will cost, need time to raise the cash. Griffith estimated about 80 percent of parents do not hire an attorney for the due-process hearing.
D. Patrick Lacy Jr., for the Virginia School Boards Association, said disputes should be resolved in a reasonable amount of time. Parents are told where to find help if they choose to appeal the due-process decision, and, he assured the committee, special education lawyers are not hard to come by. “They come out of the woodwork,“ he said.
Not really, countered Darrel Mason, a special education lawyer and former Board of Education member. She said the legal resources parents are given include entities such as the state bar association, and not specific names. Cases are expensive and take hundreds of hours of preparation, she said.
The committee sent the bill out and, Mason, with the Center for Special Education Advocacy, walked away gratified.
“For some time there have been end runs to the legislature by the School Boards, especially in discipline areas,“ she said. “It’s refreshing to see an end run for parents.“
Contact Olympia Meola at (804) 649-6812 or omeola@timesdispatch.com .

Stand Up For What You Know Is Right Even if You Are the Only Voice

Virginia Senate Passes Name Change to Behavioral Health and Developmental Services with 5 Nays

After a push poll with 3 out of 4 suggestions including the name “Behavioral Health” on the former Department of Mental Health etc.’s website, after one Senator spoke very eloquently about how wrong and inappropriate it was to call mental health and mental retardation “behaviors”, after one woman senator said that the former DMHMRSAS said they only had 28 votes in opposition to Behavioral Health, a disappointing behavior on the part of the Department, Virginia’s Senate changed the name of the Department of Mental Health, Mental Retardation and Substance Abuse to a  name no one in any of those groups served wanted and a name that makes Virginia look backwards (Developmental) and corporate and sheep-like (Behavioral Health) and offended every citizen and their families who are forced to use the Department’s services due to lack of money or insurance or lack of alternatives where they live.

After last year I thought maybe the General Assembly was finished with insulting and degrading and ignoring the voice of people with disabilities, but I was far too optimistic to think that.    I do wish to thank the gentleman who spoke so eloquently againsgt the name change despite knowing he would lose and will try to find his name and update this post to reflect that.

Yup, “Behavioral” Is a GREAT Name for DMHMRSAS: This is what Behavioral Looks Like in Practice

 

Our Lady of Peace psychiatric hospital under state investigation

Head-banging incident sparks inquiry at Our Lady of Peace

By Patrick Howington
phowington@courier-journal.com

Locked alone in a room at Our Lady of Peace psychiatric hospital, a 17-year-old girl was allowed to beat her unprotected head on a hard floor more than 120 times last spring while as many as three employees watched.

Those employees — including a behavioral analyst — were trying to determine the cause of the teen’s self-injuring behavior. But now, the Kentucky attorney general’s office is investigating the May 13 session as a possible crime.

The investigation follows an August report from state Cabinet for Health and Family Services inspectors that concluded that the hospital “failed to … assure the safety of the patient.”

Though the girl — whose diagnoses include autism, cerebral palsy and mental retardation — “appeared dazed” afterward, a doctor wasn’t told about the incident until almost 21 hours later. The call was made after hospital staff helping the teen shower noticed a bald spot that was “pretty swollen with popped blood vessels,” one worker told inspectors.

The inspectors’ report, based partly on a video of the procedure, didn’t detail the girl’s eventual medical care or the extent of her injury. She was discharged in August.

Hospital officials declined to give her name or discuss her treatment, citing confidentiality rules. The Courier-Journal obtained the state inspector’s report through a state open-records request.

The state conducted the inspection on behalf of the federal Centers for Medicare and Medicaid Services — which requires hospitals to meet safety conditions and other requirements to receive federal funding.

The findings prompted the agency to threaten to cut off reimbursements to the Louisville psychiatric hospital and its parent company, Jewish Hospital & St. Mary’s HealthCare.

But the cutoff was averted after Our Lady of Peace changed its procedures, including adding a requirement that doctors be involved in such assessments.

Based on those changes, the Medicare program told hospital officials Sept. 12 that the facility was back in compliance with federal regulations.

“We’re trying to put in every single protection and process and policy in place to prevent any injury to any patient,” said Thomas Gessel, the hospital’s interim chief executive. “We want to make sure that we have a safe environment.”

Allison Martin, spokeswoman for Attorney General Jack Conway, confirmed Friday that the office’s Medicaid Fraud and Abuse unit is investigating the incident.

The case was referred to the office by the health services cabinet’s Child Protective Services section in July, she said.

Martin said that she could not release details of the investigation. No charges have been filed.

When asked why the six-month-old investigation has not been concluded, she said: “It’s a complex issue (and) we are looking at many different factors … and it is our goal to be thorough.”

She said Conway wasn’t available for an interview Friday because he was traveling out of state.

JoAnne Maamry, chief executive officer of Our Lady of Peace at the time of the incident, resigned in August. She is not working now.

Reached by e-mail, Maamry declined to comment on the case or her resignation.

Gessel, the interim chief, would not say if Maamry’s resignation was related to the incident,