November
16, 2006
SPITZER-PATERSON
ANNOUNCE CREATION OF POLICY ADVISORY
COMMITTEES TO PARTICIPATE AS PART OF TRANSITION TEAM:
MHANYS
Note: We are exceptionally excited to see one of our very own, Michael
Friedman (Director of The Center for Policy and Advocacy for the
MHAs of NYC and Westchester) and our very good friend and colleague,
Karen Schimke (President and CEO of the Schuyler Center for Analysis
and Advocacy (SCAA)), named to the Spitzer-Paterson Transition Team’s
Policy Advisory Committees.
Following
below are some of the appointments made to the Spitzer-Paterson
Transition Team Policy Advisory Committees. For the entire list
of appointments in other areas besides those listed below, go to
http://www.transitionny.org/main.cfm?actionID=globalShowStaticContent&screen
Key=cmpLearnTeam&s=transitionny.
Following
below are the individuals who have been named to the Health
Policy Advisory Committee:
•
CO-CHAIR James Tallon, President, United Hospital Fund
• Alan Aviles, President of the Health and Hospital Corporation
• Jo Ivey Boufford, Professor of Public Service, Health Policy
and Management, Wagner Graduate School at NYU
• Michael Burgess, Executive Director, New York State Alliance
for Retired Americans
• Janice L. Charles, Executive Director, North Country Children's
Clinic, Inc
• Jon Cohen, M.D., Senior Vice President, North Shore Long
Island Jewish Health System, Inc.
• Kelli Conlin, Executive Director, NARAL Pro Choice New York
• Jo Ann A. Constantino, CEO, The EDDY; Executive Vice President,
Northeast Health
• Mike Dowling, CEO, North Shore Long Island Jewish Health
System, Inc.
• Michael Friedman, Director, The Center for Policy and Advocacy
of The Mental Health Associations of NYC and Westchester
• Kristine M. Gebbie DrPH, RN, Elizabeth Standish Gill Associate
Professor of Nursing
• Jay Laudato, Executive Director, Callen-Lorde Community
Health Center
• Stan Lundine, Executive Director, Chautauqua County Health
Network
• Brian McLane, Executive Director, Burton Blatt Institute
• Gail B. Nayowith, Executive Director, Citizens' Committee
for Children of New York, Inc.
• Carol Raphael, President and CEO, Visiting Nurse Service
of New York
• John Rugge, M.D., CEO, Hudson Headwaters Health Network
• Paul Samuels, Director and President, Legal Action Center
• Michael Stocker, Former President and CEO, Empire Blue Cross
Blue Shield
• William Streck, President and CEO, Bassett Healthcare
• Monica Sweeney, M.D., Vice President of Medical Affairs,
Bedford-Stuyvesant Family Health Center
• Greg Tarpinian, Executive Director, Change to Win Federation
• Robert Thompson, CEO, Monroe Plan for Medical Care
• Karen Carpenter-Palumbo, Vice President, American Cancer
Society
• Dennis Rivera, President, 1199 SEIU
• Kenneth Rasky, Greater New York Hospital Association
Following
below are the individuals who have been named to the Human
Services Policy Advisory Committee:
•
CO-CHAIR Geoffrey Canada, President and CEO, Harlem Children’s
Zone
• CO-CHAIR Karen Schimke, President and CEO, Schuyler Center
for Analysis and Advocacy
• Gordon Berlin, President, MDRC
• Rev. Dr. Calvin Butts, Pastor, Abyssinian Baptist Church
• Gladys Carrion, Senior VP for Community Investment, United
Way of New York City
• Andrew Celli, Jr., Partner, Emery, Celli, Brinckerhoff &
Abady, LLP
• Darwin M. Davis, President and CEO, New York Urban League
• Olivia A. Golden, Senior Fellow, The Urban Institute
• Dr. Marjorie Hill, Executive Director, Gay Men’s Health
Crisis
• Joel Kaplan, Executive Director, United Jewish Council of
the East Side
• Virgina Kee, Founding Member, Chinese-American Planning
Council
• Sarah S. Kovner, Former Special Assistant to US Secretary
of Health and Human Services, Donna Shalala
• David Mandel, Chief Executive Officer, Ohel Children's Home
and Family Services
• Jim Peluso, Vocational Rehabilitation Specialist, US Department
of Veterans Affairs
• William E. Rapfogel, Chief Executive Officer and Executive
Director, Metropolitan Council on Jewish Poverty
• Trudi Renwick, Senior Economist, Fiscal Policy Institute
• Joseph L. Rich, Executive Director, Disabled Person's Action
Organization of Jefferson County
• Rev. Dr. Marcos Rivera, Senior Pastor, Primitive Christian
Church
• Ellen Schall, Dean, Robert F. Wagner Graduate School of
Public Service
• Anne N. Shkuda, Associate Director, United Neighborhood
Houses of NY
• Msg. Kevin Sullivan, Chief Executive Officer and Executive
Director, The Catholic Charities of the Archdiocese of New York
• Alan Van Capelle, Executive Director, Empire State Pride
Agenda
• Fred Wulczyn, Research Fellow, Chapin Hall Center for Children,
University of Chicago
• Betsy Seidman, Executive Director of Development, York College,
CUNY
• Stanley Grayson, President and CEO, M.R. Beal & Company
• Bryna Sanger, Professor of Urban Policy and Management,
The New School
SAMARITANS SUICIDE PREVENTION CENTER’S JANUARY 2007
VOLUNTEER TRAINING CLASS IS NOW FORMING: Each day in the
Capital Region there are individuals who are feeling lonely, depressed,
or suicidal that reach out to the Samaritans Suicide Prevention
Center Helpline, to talk to trained community volunteers who provide
unconditional and non-judgmental support. A caller may feel overwhelmed
with circumstances they feel unable to face alone or he/she may
be considering suicide and is looking for support during a difficult
time. Whatever the caller's challenge or struggle, one can find
a caring, patient, empathetic ear, ready to listen and seek to understand
his/her feelings. Are you interested in becoming one of our trained
volunteers, who makes a difference?
Skills
Needed:
• An interest in making a difference.
• Compassion, empathy, and patience.
• Commitment.
• A desire to meet other great volunteers
If you would like to be part of the January 2007 Volunteer Class,
please send us an email at
sams@fcscapitalregion.org or call us at 518-689-0080 ext. 125/126.
IN THE NEWS:
A
Casualty Far From the Battlefield - For veterans, coming home from
war can be harder than being deployed. By Kate Gurnett
Albany Times Union, November 13, 2006
(MHANYS
Note – MHANYS’ own Helena Davis and her work toward
helping returning veterans is featured prominently in this article)
Clifton
Park-- Last month, Jeanne "Linda" Michel came home from
Iraq. Back in the suburbs, she tried to feel normal.
She'd
been homesick for months. She couldn't wait to see her kids, ages
11, 5 and 4. Between her husband's deployment and her own, the children
had been with just one parent for nearly three years.
She
was 33, with a bright smile and stubborn determination. Reuniting
should be easy. In another month, she'd be discharged from the Navy
after five years of service.
"She
had come through a lot and she had always risen to challenges,"
her husband, Frantz Michel, said last week.
What
her family didn't see, and what she herself may not have realized,
was the enormity of what she faced.
Like
thousands of others returning from Iraq, her mental state was fractured.
And it went untreated. Within two weeks, Linda Michel would become
a private casualty of war.
Re-entry
into the world of peace can be harder than deployment, experts say.
Picking up where you left off doesn't just happen.
Husbands
and wives report feeling like strangers to each other at first,
according to Military OneSource, a support Web site for military
families.
"Family
roles, rituals, dynamics have changed," said Helena Davis,
deputy director of the Mental Health Association in New York State.
"And the vet has changed. Bonds have been fractured and need
to be re-established."
Linda
Michel was no exception. A self-sufficient medic known to help others,
she was uncomfortable asking for that help for herself.
But
treatment and self-care are critical for returnees, Davis said.
Without it, "the anxiety keeps them spiraling down." Some
turn to alcohol, drugs or domestic violence. Or, Davis said, "they
hurt themselves." August, three veterans in New York's Adirondack
region committed suicide within three weeks, Davis told a recent
gathering of mental health professionals.
And
the third American female to die in Iraq, Army interpreter Spc.
Alyssa Peterson, 27, of Flagstaff, Ariz., shot herself with her
service weapon. A devout Mormon and Arabic interpreter, Peterson
had objected to U.S. techniques after just two days of participating
in interrogations.
Women
experience stronger forms of post-traumatic stress disorder and
have higher PTSD rates, experts say. In response, the Veterans Affairs
Department launched a $6 million study of female veterans.
Seeking
treatment -- seen by some as a weakness -- may be even tougher for
women, who still feel the need to prove themselves to men in military
service.
In
Iraq, female troops experience attacks, mortar fire and critical
injuries such as amputation. And, women soldiers also are more at
risk for sexual assaults, up 40 percent in combat zones from last
year, Davis said.
Camp
Bucca, the U.S.-run military prison where Michel was stationed,
was investigated after a female mud-wrestling match was staged there.
Two
weeks after she got home to Clifton Park, Linda Michel shot herself
to death, stunning her colleagues and family.
Like
many women who are assigned to Iraq, Linda Michel wanted to serve.
She
grew up in Montreal, with her parents and five sisters. In the states,
she married Frantz Michel, a native of Haiti who grew up in Rockland
County and became a State Police investigator. They had three children,
two boys and a girl, and lived in a quiet Clifton Park development
dotted with kids' bicycles and basketball hoops.
By
2004, Frantz, a lieutenant colonel in the U.S. Army National Guard,
was serving in Iraq with the 42nd Infantry Division.
Linda
had joined the Navy in 2001.
"It was the best fit for her," Frantz said. It meant they
likely wouldn't be deployed together. And her chances of being assigned
to a combat zone were slim.
When
Linda was called up in 2005, she didn't want a deferment.
"She
felt she needed to do it," Frantz said. "So I couldn't
stop her."
What
she hadn't expected was a shortage of Army personnel that forced
Navy and Air Force members into land-based and combat areas.
Linda
went to Camp Bucca in southern Iraq, the largest U.S. military prison
there and the site of a 2005 riot that saw four prisoners killed
by guards.
Inevitably
dubbed "Doc" by her patients, she worked hard "doing
her part to accomplish a mission many people said the Navy could
not do," Rob Hallmark of Virginia Beach, Va., wrote in her
on-line memorial guest book. "She was always a bright shining
light in such a dark, dark place."
"She
was more than 'Just in the Navy' or just a 'Corpsman' or 'Sailor,'
she was there for us," added Linda's Camp Bucca roommate, Tammy
Cartwright, of Anchorage, Alaska. "She was the one that helped
me get out of bed every morning when all I wanted to do was give
up and go home."
But
in private, Michel faced demons. She saw a Navy doctor and was diagnosed
with depression. The doctor prescribed Paxil.
Frantz
Michel knew his wife's days were long and grueling. But he didn't
know about the Paxil.
Studies
have linked Paxil to adverse effects, including suicide, sparking
an FDA warning in May.
When
Linda came home, the Navy discontinued her medication. Again, Frantz
Michel wasn't told.
"I
just wish the Navy would have done some more follow-up, instead
of just letting her come home," said Frantz, who is on the
division staff of the Army National Guard. "If somebody needs
Paxil in a combat zone, then that's not the place for them to be.
You either send them to a hospital or you send them home and then
make sure that the family members know and that they get follow-up
care."
Talking
his way up the Navy's chain of command, Frantz sought answers. "Why
wasn't she sent to a facility to resolve the issues? Not keep her
in Iraq and give her some antidepressant medication and then just
send her home. So those are the answers that I don't have. Which
makes me a little angry because I know what is supposed to occur."
Duty
Officer Chris Pratt of the Navy Operational Support Center in Albany
could not be reached for comment Friday, a holiday.
Linda
Michel's suicide drew pages of on-line condolences, from California
to Iraq.
Her
death came amid rising demands for counseling from veterans returning
from Iraq and Afghanistan. A 2005 Government Accountability Office
study called services inadequate.
Lots
of resources for vets aren't utilized, Davis said. Often, veterans
don't retain what they hear during two-day stateside demobilization
sessions. "They don't have the focus. All they want to do is
get home."
Health
care visits every four to six weeks aren't enough, she said.
Frantz
Michel wishes the Navy hadn't cleared his wife for re-entry, or
left her alone to withdraw from Paxil.
"You
look (back) at things," he said last week. "I just wish
that I had more information."
Linda
Michel was given a full military funeral Oct. 23 and buried in the
Gerald B.H. Solomon Saratoga National Cemetery. Friends donated
to a fund for the Michels' three children.
Shortly
before she died, Linda attended a Navy weekend drill. Fellow reservist
Robert Stanziano saw her there, and waved, but never got a chance
to talk.
When
she was mobilized "we were extremely proud ... and sent them
care packages from time to time," he wrote in her memorial
guest book. "We couldn't wait for them to return. Now she is
gone and I'll never get the chance to ask her how it was over there.
"She
was a great sailor, soldier, hospital corpsman, mom and a great
woman of war for our country," he wrote in her memorial guest
book. "Shipmate, I never had a chance to say this to you. Well
done! Goodbye and farewell shipmate, you will be dearly missed."
PICKING
UP THE PIECES
Expert
advice for returning vets:
* Go easy on yourself and loved ones who are traumatized.
* Take things one day at a time.
* Remember: Everyone has bad days.
* Make yourself connect with people you care about.
* Keep your life as simple as possible. Rest when you can.
* Stay away from alcohol and caffeine to manage moods.
* Try to eat balanced meals.
* Take time to play with your children.
* Anniversaries, birthdays and holidays will be more difficult than
other days. Plan ahead for how you can make them easier. Expect
your children to act out. Give them extra support. This will pass.
* If you need support, ask for it. Family members and neighbors
can help. You can coach them in what you need.
* We may not share your experience, but we do care.
Sources:
Courtesy of Helena Davis, Mental Health Association in New York
State
What
combat vets want families and friends to know about living with
PTSD:
* Give me space when I need to be alone -- don't overwhelm me with
questions. I'll come and talk to you when I'm ready.
* Get away from me if I am out of control, threatening or violent.
* Be patient with me, especially when I'm irritable.
* Don't personalize my behavior when I explode or get quiet.
* Learn and rehearse a time-out process.
* Don't patronize me or tell me what to do. Treat me with respect
and include me in conversations and decision making.
* Don't pity me.
* Don't say "I understand" when there are some things
that you cannot understand.
* Realize that I have unpredictable highs and lows, good and bad
days.
* Anticipate my anniversary dates -- recognize that these could
be tough times.
* I'd like to share my traumatic experiences with you, but I fear
overwhelming you and losing you.
* I want to be close to you and share my feelings, but I'm afraid
to -- and sometimes I don't know how to express my emotions.
* I also fear your judgment.
* Know that I still love and care about you, even if I act like
a jerk sometimes.
* Don't ask me to go to crowded or noisy places because I'm uncomfortable
in those settings.
Sources:
Courtesy of Vietnam combat vets and the Oklahoma City VA Medical
Center
There is hopeResources for veterans and their families.
BOOKS
"Courage
After Fire: Coping Strategies for Returning Soldiers and Their Families,"
by Keith Armstrong, Suzanne Best and Paula Domenici (2006).
"Surviving
Deployment: A Guide for Military Families," by Karen M. Pavlicin
(2003).
"Helping
Children Cope with the Challenges of War and Terrorism," by
Annette M. LaGreca. Available for download at http://www.7-dippity.com/other/UWA_war_book.pdf
WEB
SITES
National
Center for PTSD at http://www.ncptsd.va.gov
S.A.F.E.
Program. Support and Family Education: Mental Health Facts for Families.
An 18-session curriculum on PTSD at http://w3.ouhsc.edu/Safeprogram
"When
the Letdown Doesn't Let Up" and "How to Get Back to 'Normal'
" by the National Mental Health Association at http://www.nmha.org/reunions/infoBacktoNormal.cfm
FOR
KIDS
Deployment
Kids at http://www.deploymentkids.com
Operation Purple. Free summer camps for military kids, through
National Military Family Association at http://www.
operationpurple.com
"Talk,
Listen, Connect: Helping Families During Military Deployment."
Sesame Street DVD, free to active duty personnel through Military
OneSource -- (800) 342-9647 -- or at http://www.sesameworkshop.org/tlc
Time Again to Choose or Switch Drug Plans. By Robert
Pear
The New York Times, November 15, 2006
WASHINGTON,
Nov. 14 — Starting Wednesday, Medicare beneficiaries can sign
up for prescription drug coverage or switch plans, and many may
want to do so because prices have changed, with some of the most
popular plans charging much higher premiums for 2007.
In
every state but Alaska and Hawaii, more than 50 drug plans are available.
Beneficiaries have until Dec. 31 to sign up or change plans, but
federal officials said they should act by Dec. 8 to avoid the problems
that caused turmoil at pharmacies in January, when many people were
unable to get their drugs.
Several
recent surveys, including one by J. D. Power & Associates, the
market research company, suggest that three-fourths of the people
with Medicare drug coverage are satisfied. Michael O. Leavitt, the
secretary of health and human services, said: “The program
is working. People are happy. ”
The
Bush administration says that premiums for Medicare drug coverage
will average $24 a month in 2007, about the same as in 2006. But
for many beneficiaries, the reality may be substantially different.
Melvin
London, an 83-year-old retired filmmaker in New York City, said
Tuesday that the new Medicare benefit had saved $245 for him and
$685 for his wife. He was annoyed at the prospect of a sharp increase
in premiums in 2007. For Mr. London’s plan, known as Humana
Enhanced, the monthly premium will be $29.60, up from $9.42.
“I
call that bait and switch, when the company charges $9 to get you
in and then goes to $29,” Mr. London said. “It took
me three months to find a plan that was suitable. Am I now supposed
to go through the same process every year to determine which plan
is best for me? That’s an unfair burden for beneficiaries.”
Thomas
T. Noland Jr., a senior vice president of Humana, said: “We
still offer excellent value. We will have the lowest premium in
38 states, the second-lowest in 10 states and the third-lowest in
the remaining two states.”
About
4.5 million Medicare beneficiaries receive drug coverage from Humana
plans. Humana has been wooing people with free showings of the Humphrey
Bogart movie “Casablanca.” Medicare beneficiaries eat
popcorn and sip sodas while watching the film, along with a short
extolling Humana’s Medicare plans.
The
$24 premium emphasized by the Bush administration is for basic coverage,
the minimum required by law, and many plans provide additional benefits
for an extra premium. Moreover, the average includes premiums for
drug coverage offered by managed care plans and by free-standing
drug plans, which serve people in the traditional Medicare program.
Both
types of plans charged about $24 a month, on average, for drug coverage
this year. In 2007, the average premium will increase about 10 percent
for free-standing drug plans, but will decrease about 35 percent
for drug coverage offered by managed care plans.
Most
drug plans have a gap in coverage. “Beneficiaries tell us
this was a helpful benefit for six or eight months, until they fell
into the coverage gap,” said Deane R. Beebe, a spokeswoman
for the Medicare Rights Center, a consumer group that counsels people
with Medicare.
Some
insurers provide coverage for generic drugs in the coverage gap,
and a few also provide coverage for brand-name drugs in the gap.
But Ms. Beebe said, “In 11 states, we cannot find any free-standing
drug plan that provides coverage for brand-name drugs in the gap.”
The
Medicare handbook, sent to all beneficiaries, says that a plan offered
by Coventry Health Care will pay for generic and brand-name drugs
in the coverage gap. But Francis S. Soistman Jr., executive vice
president of Coventry, said Tuesday that only five brand-name drugs,
out of the many available, were covered in the gap.
Jeff
Nelligan, a Medicare spokesman, said, “We corrected the online
version of the information.”
Sixteen
Democratic senators, led by Byron L. Dorgan of North Dakota, said
this week that some insurers were misleading consumers by marketing
drug plans under names that included the word “complete.”
“How
can a plan be called ‘complete’ when it contains a gap
in drug coverage?” they asked in a letter to Mr. Leavitt.
John
C. Rother, policy director of AARP, the lobby for older Americans,
said the new program had helped many people. His “biggest
disappointment,” Mr. Rother said, was that several million
low-income people had not applied for the extra help available to
them.
Pass Mental Health Parity Legislation. Letter to
the Editor
Watertown Daily Times, November 06, 2006
Since
I wrote about Timothy's Law, there have been some serious negotiations
between the Timothy's Law Coalition and state Assembly and Senate
leaders regarding the mental health parity law that is named in
honor of Timothy O'Clair.
As
a result of those negotiations, the Senate finally passed the bill
unanimously. Now due to changes in Timothy's Law, we wait for the
Assembly to reconvene and once again pass the mental health parity
bill that will free those people with mental health issues from
the discriminatory shackles that certain employer health insurance
companies have them chained to by not giving them access to the
full health care that they need.
After
the Assembly has passed Timothy's Law, it will go to Gov. George
Pataki to be signed and he has said that he might not sign it. Timothy's
Law has to be signed by the governor by Jan. 1. If he does not sign
it, we will have to start all over from scratch.
Though
most of the original law is still intact, the part about alcohol
and substance abuse had to be eliminated. Let's hope it can be added
in the future. Right now, it is imperative to get Gov. Pataki to
sign Timothy's Law this year thereby putting an end to the discriminatory
practices of the health insurance companies that result in the untimely
deaths of so many of our peers and consumers.
So
let's get cracking, folks. Are we going to let the discrimination
continue? Are we going to sit on our posteriors and do nothing while
there are children, like Timothy O'Clair, taking their own lives?
Or are we going to sit right down and write the governor a letter
urging him to sign the mental health parity bill? I hope and pray
that the answer to the last question is a resounding yes, yes and
once again yes.
June
C. Gundersen
Watertown
Troubled Children - What’s Wrong With a Child? Psychiatrists
Often Disagree. By Benedict Carey
The New York Times, November 11, 2006
Paul
Williams, 13, has had almost as many psychiatric diagnoses as birthdays.
The
first psychiatrist he saw, at age 7, decided after a 20-minute visit
that the boy was suffering from depression.
A
grave looking child, quiet and instinctively suspicious of others,
he looked depressed, said his mother, Kasan Williams. Yet it soon
became clear that the boy was too restless, too explosive, to be
suffering from chronic depression.
Paul
was a gifted reader, curious, independent. But in fourth grade,
after a screaming match with a school counselor, he walked out of
the building and disappeared, riding the F train for most of the
night through Brooklyn, alone, while his family searched frantically.
It
was the second time in two years that he had disappeared for the
night, and his mother was determined to find some answers, some
guidance.
What
followed was a string of office visits with psychologists, social
workers and psychiatrists. Each had an idea about what was wrong,
and a specific diagnosis: “Compulsive tendencies,” one
said. “Oppositional defiant disorder,” another concluded.
Others said “pervasive developmental disorder,” or some
combination.
Each
diagnosis was accompanied by a different regimen of drug treatments.
By
the time the boy turned 11, Ms. Williams said, the medical record
had taken still another turn — to bipolar disorder —
and with it a whole new set of drug prescriptions.
“Basically,
they keep throwing things at us,” she said, “and nothing
is really sticking.”
At
a time when increasing numbers of children are being treated for
psychiatric problems, naming those problems remains more an art
than a science. Doctors often disagree about what is wrong.
A
child’s problems are now routinely given two or more diagnoses
at the same time, like attention deficit and bipolar disorders.
And parents of disruptive children in particular — those who
once might have been called delinquents, or simply “problem
children” — say they hear an alphabet soup of labels
that seem to change as often as a child’s shoe size.
The
confusion is due in part to the patchwork nature of the health care
system, experts say. Child psychiatrists are in desperately short
supply, and family doctors, pediatricians, psychologists and social
workers, each with their own biases, routinely hand out diagnoses.
But
there are also deep uncertainties in the field itself. Psychiatrists
have no blood tests or brain scans to diagnose mental disorders.
They have to make judgments, based on interviews and checklists
of symptoms. And unlike most adults, young children are often unable
or unwilling to talk about their symptoms, leaving doctors to rely
on observation and information from parents and teachers.
Children
can develop so fast that what looks like attention deficit disorder
in the fall may look like anxiety or nothing at all in the summer.
And the field is fiercely divided over some fundamental questions,
most notably about bipolar disorder, a disease classically defined
by moods that zigzag between periods of exuberance or increased
energy and despair. Some experts say that bipolar disorder is being
overdiagnosed, but others say it is too often missed.
“Psychiatry
has made great strides in helping kids manage mental illness, particularly
moderate conditions, but the system of diagnosis is still 200 to
300 years behind other branches of medicine,” said Dr. E.
Jane Costello, a professor of psychiatry and behavioral sciences
at Duke University. “On an individual level, for many parents
and families, the experience can be a disaster; we must say that.”
For
these families, Dr. Costello and other experts say, the search for
a diagnosis is best seen as a process of trial and error that may
not end with a definitive answer.
If
a family can find some combination of treatments that help a child
improve, she said, “then the diagnosis may not matter much
at all.”
A
KALEIDOSCOPE OF DIAGNOSES
The most commonly diagnosed mental disorders in younger children
include attention deficit hyperactivity disorder, or A.D.H.D., depression
and anxiety, and oppositional defiant disorder.
All
these labels are based primarily on symptom checklists. According
to the American Psychiatric Association’s diagnostic manual,
for instance, childhood problems qualify as oppositional defiant
disorder if the child exhibits at least four of eight behavior patterns,
including “often loses temper,” “often argues
with adults,” “is often touchy or easily annoyed by
others” and “is often spiteful or vindictive.”
At
least six million American children have difficulties that are diagnosed
as serious mental disorders, according to government surveys —
a number that has tripled since the early 1990s. But there is little
convincing evidence that the rates of illness have increased in
the past few decades. Rather, many experts say it is the frequency
of diagnosis that is going up, in part because doctors are more
willing to attribute behavior problems to mental illness, and in
part because the public is more aware of childhood mental disorders.
At
the playground, in the gym, standing in line at the grocery store,
parents swap horror stories about diagnoses, medications or special
education classes. Their children are often as fluent in psychiatric
jargon as their mothers and fathers are.
“The
change in attitude is enormous,” said Christina Hoven, a psychiatric
epidemiologist at Columbia University. “Not long ago people
did all they could to hide problems like these.” Attention
deficit disorder is perhaps the most straightforward diagnosis.
Elementary school teachers are often the ones who first mention
it as a possibility, and soon parents are answering questions from
a standard checklist: Does the child have difficulty sustaining
attention, following instructions, listening, organizing tasks?
Does he or she fidget, squirm, impulsively interrupt, leave the
classroom?
These
behaviors are so common, particularly in boys, that critics question
whether attention disorder is a label too often given to boys being
boys. But most psychiatrists agree that while many youngsters are
labeled unnecessarily, most children identified with attention problems
could benefit from some form of therapy or extra help.
They
are less certain about the children — perhaps a quarter of
those seen for mental problems, some experts estimate — who
do not fit any one diagnosis, and who often go for years before
receiving a satisfactory label, if they receive one at all.
These
youngsters collect labels like passport stamps, and an increasing
number end up with the label Paul Williams received: bipolar disorder.
AN
ILLNESS UNDER DISPUTE
Until recently, psychiatrists considered bipolar disorder to be
all but nonexistent in children under 18. Today, it is the fastest
growing mood disorder diagnosed in children, featured on the cover
of news magazines and on daytime talk shows like “The Oprah
Winfrey Show.”
The
explosion of interest in bipolar disorder came after the approval
of several drugs, called antipsychotics, or major tranquilizers,
for the short-term treatment of mania in adults.
Beginning
in the 1990s some researchers began to argue that bipolar disorder
was underdiagnosed in adults. Soon, several child psychiatrists
were arguing that the illness was more common than previously thought
in children too.
Some
experts who made those arguments had ties to manufacturers of antipsychotic
drugs, financial interests disclosed in professional journals. But
the message struck a chord, particularly with doctors and parents
trying to manage difficult children.
Parents
whose children have been given the label tend to adopt the psychiatric
jargon, using terms like “cycling” and “mania”
to describe their children’s behavior. Dozens of them have
published books, CDs, or manuals on how to cope with children who
have bipolar disorder.
A
recent Yale University analysis of 1.7 million private insurance
claims found that diagnosis rates for bipolar disorder more than
doubled among boys ages 7 to 12 from 1995 to 2000, and experts say
the rates have only gone up since then.
Katherine
Finn, a 14-year-old who lives in Grand Rapids, Mich., said she was
grateful for the growing awareness of the disease. Possessed by
feelings of worthlessness as early as the fourth grade, Katherine
said that by the sixth grade she “threw my sanity out the
window.”
She
became impulsive, loud, and abrasive, she said, adding, “I
would blurt things out in class, I would moo like a cow, act like
a little kid, just say the most random stuff.”
A
psychiatrist promptly diagnosed the problem as bipolar disorder,
after learning that there was a history of the disease on her mother’s
side of the family. Katherine began taking drugs that blunted the
extremes in her mood, and she now is doing well at a new school.
“It
hit me like a Mack truck when I heard the diagnosis, but I knew
right away it was correct,” said her mother, Kristen Finn,
who is writing a book about her experience.
Still,
many psychiatrists believe that, although childhood bipolar disorder
may be real in families like the Finns, it is being wildly overdiagnosed.
One of the largest continuing surveys of mental illness in children,
tracking 4,500 children ages 9 to 13, found no cases of full-blown
bipolar disorder and only a few children with the mild flights of
excessive energy that could be considered nascent bipolar disorder
— a small fraction of the 1 percent or so some psychiatrists
say may suffer from the disease.
Moreover,
the symptoms diagnosed as bipolar disorder in children often bear
little resemblance to those in adults. Instead, the children’s
moods seem to flip on and off like a stoplight throughout the day,
and their upswings often look to some psychiatrists more like extreme
agitation than euphoria.
“The
question with these kids is whether what we’re seeing is a
form of mania, or whether it’s extreme anger due to something
else,” said Dr. Gregory Fritz, medical director of the Bradley
Hospital, a psychiatric clinic for children in Providence, R.I.
Dr.
Ellen Leibenluft, a research psychiatrist at the National Institute
of Mental Health, argues that children who are receiving a diagnosis
of bipolar disorder fall into two broad groups. The children in
one group, a minority, have mood cycles similar to those of adults
with bipolar disorder, complete with grandiose moods, and a high
likelihood of having a family history of the illness. Those in the
other group have severe problems regulating their moods and little
family history, and may have some other psychiatric disorder instead.
“It
is a mistake to lump them all together and assume they are all the
same,” Dr. Leibenluft said. “It may be that the disorder
has different dimensions and looks different in different kids.”
For
parents with a child who is frantic and possibly dangerous, these
distinctions may be academic. The medications may blunt their child’s
extreme behavior, which may be all the confirmation they need.
For
others, though, the uncertainties about childhood bipolar disorder
loom larger. They wonder whether mania really explains what their
child is going through, and if not, what it is that is being treated.
Evelyn
Chase of Richmond, Va., said that a neurologist drove home his diagnosis
of bipolar disorder in her 10-year-old son by pulling out “a
copy of Time magazine and slamming the article in front of me.”
Ms.
Chase said her son seemed to react most strongly to abrupt changes
in the environment and to certain dyes and chemicals. “I used
the bipolar diagnosis for school and getting services, but I don’t
think it covers his behaviors,” she said.
For
Paul Williams, the diagnosis simply feels like a temporary stop.
In his short life, Paul has taken antidepressants like Prozac, antipsychotic
drugs used to treat schizophrenia, sleeping pills and so-called
mood stabilizers for bipolar disorder, in so many combinations that
he has become nonchalant about them.
“Sometimes
they help, sometimes they don’t,” he said. “Sometimes
they make me feel like another person, like not normal.”
In
recent months, his mother said, Paul seems to have improved: he
visibly tries to control himself when he is upset and usually succeeds.
He is an eager Mets fan who loves reading Harry Potter and the Goosebumps
series. He gets out and plays baseball and football, like any 13-year-old
boy.
But
he has grown tired of telling his story to doctors, and neither
he nor his mother expect that bipolar disorder will be the last
diagnosis they hear.
IN
SEARCH OF CLARITY
The specialists who manage children’s psychiatric disorders
are trying to bring more standards and clarity to the field. Harvard
researchers are completing the most comprehensive nationwide survey
of mental illness in minors and hope to publish a report next year.
And a recent issue of the journal Child and Adolescent Psychology
was entirely devoted to the subject of basing diagnoses in hard
evidence.
Given
the controversies, one of the articles concludes, “we acknowledge
that tackling the issue may be tantamount to taking on a 900-pound
gorilla while still wrestling with a very large alligator.”
Dr.
Darrel Regier of the American Psychiatric Association, who is coordinating
work on the next edition of the association’s diagnostic manual
for mental disorders, due out in 2011, said that researchers would
focus on drawing distinctions among several childhood disorders,
including bipolar disorder and attention deficit disorder.
“We
wouldn’t disagree that criteria for these disorders currently
overlap to some degree,” Dr. Regier wrote in an e-mail message,
“and that a significant amount of research is under way to
disentangle the disorders in order to support more specific treatment
indications.”
Until
that happens, parents with very difficult children are left to read
the often conflicting signals given by doctors and other mental
health professionals. If they are lucky, they may find a specialist
who listens carefully and has the sensitivity to understand their
child and their family.
In
dozens of interviews, parents of troubled children said that they
had searched for months and sometimes years to find the right therapist.
“The
point is that not everything is A.D.H.D., not everything is bipolar,
and it doesn’t happen like you see in the movies,” said
Dr. Carolyn King, who treats children in community clinics around
Detroit, and has a private practice in the nearby suburb of Grosse
Pointe Farms.
“Kids
often have very subtle symptoms they can mask for short periods
of time,” Dr. King said, “and the most important thing
is to observe them closely, and get a complete history, starting
from birth and straight through every single developmental milestone.”
She
added, “A speech delay can look like anxiety,” an obsessive
private ritual like mania.
Or
struggling children, in the end, may look only like themselves,
with a unique combination of behaviors that defy any single label.
Camille Evans, a mother in Brooklyn whose son’s illness was
tagged with a half-dozen different diagnoses in the last several
years, said she concluded, after seeing several psychiatrists, that
the boy’s silences and learning difficulties were best understood
as a mild form of autism.
“That’s
the diagnosis that I think fits him best, and I’ve just about
heard them all,” Ms. Evans said.
The
label is not perfect, she said, but it is more specific than “developmental
delay” — one diagnosis they heard — and does not
prime him for aggressive treatment with drugs like attention deficit
disorder or bipolar disorder would. He has not responded well to
the drugs he has tried.
“Most
important for me,” Ms. Evans said, “the diagnosis gives
him access to other things, like speech therapy, occupational therapy
and attention from a neurologist. And for now it seems to be moving
him in the right direction.”
Insurers Blamed for Crisis in Health Care. "The paper
pusher . . . is making all the money," says former banker.
By James T. Mulder
Syracuse Post-Standard, November 12, 2006
William
Mooney used to think chronic financial problems plaguing New York's
hospitals were symptoms of bad management and inefficiency.
"When
you put doctors who really don't know a lot about business together
with mismanaged hospitals, what do you think you're going to get?
A mess on your hands," said Mooney, president of the Westchester
County Association, a business/public policy group based in White
Plains.
The
former banker, however, changed his mind after he and other business
people from his association spent a year studying the health-care
crisis in his county, where in recent years two hospitals have closed
and another has flirted with bankruptcy. The biggest problem, they
concluded, is too many health-care dollars are going to fatten the
profits of health insurers and the salaries of insurance company
CEOs.
"The
hospitalsand the doctors are not making any money to speak of, but
the person in the middle, who is the paper pusher, is making all
the money," said Mooney, who's coming to Syracuse Monday to
address local hospital trustees and business people.
Mooney
has been traveling around the state trying to rally support for
reforms he believes will help correct the health-care crisis. He
wants the state to set up a health-care reinvestment fund. A portion
of insurance company profits would go into this fund to help hospitals
and doctors pay for electronic medical records and make other improvements.
He
also wants to restore the state Insurance Department's authority
to regulate health insurance rate increases. Insurers in New York
have been free to boost rates without regulatory review since 2000,
when a state law requiring state Insurance Department approval of
rate increases expired.
"With
my car insurance, the premiums are regulated. My property and casualty
premiums are regulated but my health insurance premiums are not,"
Mooney said. "That made no sense to us."
Mooney
said he typically opposes price controls, but believes they are
necessary in health care, where the traditional laws of supply and
demand don't work.
Leslie
Moran, senior vice president of the New York Health Plan Association,
an insurance trade group, said Mooney's proposals would increase
health insurance costs.
"Everyone
agrees there is some need to look at the New York health-care market
and ways to reform it and make it work better for everyone, but
you can't just tinker around with one player and one piece of that,"
she said.
The
reinvestment fund would be a new tax on insurers that would increase
premiums, she said. The state's health insurers already pay $1.5
billion a year in surcharges and assessments that are used to pay
for hospital charity care and graduate medical education, she said.
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