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A Tribute to Mothers and Fathers of Bipolar Children

January 24, 2011 in Featured, Insider Insight by Admin Dawn

by Janice Papolos and Demitri F. Papolos, M.D.

In our book, The Bipolar Child, we talk constantly about the burdens that parents of children with bipolar disorder must shoulder and overcome, all the while attempting to make decisions with the clinicians who work in an area of medicine that is still in its infancy.

But we’ve never composed a stand-alone list that lets others look at what the parents must grapple with and withstand — in all its stark and disturbing reality.

This list, sadly, cannot even be described as “exhaustive or complete,” but the parents coping with a child (or children) with bipolar disorder deserve special recognition and honor for their enormous valor as they:

  • Look at a very young and much-loved child with a nagging fear that something is seriously wrong.
  • Feel the external world bearing down on them, advising them to take multiple parenting classes or to tune into Nanny 911. Feel infantilized and ashamed as people offer up criticism and advice.
  • Accept that they need help from a professional, but feel a stranglehold of fear.
  • Come to learn that there are only 4,101 child psychiatrists in the entire United States–many wary of making this diagnosis.
  • Watch their child and other siblings besieged by an illness for which there is little diagnostic or treatment consensus in the field of psychiatry.
  • Receive multiple diagnoses such as ADHD, OCD, ODD, PDD, anxiety disorder, or simple depression.
  • Come to accept that the child has a very serious psychiatric illness and make the agonizing decision to begin a trial of medications (if they can find a psychiatrist who can treat their child, or who has open hours).
  • Read the package inserts of medications which list possible side effects, as well as frightening black-box labels, and watch apprehensively for any signs of serious trouble such as lithium toxicity, tardive dyskinesia, Stevens-Johnson syndrome, new-onset type-II diabetes, or pancreatitis.
  • Attempt to explain to a child how the doctor is trying to help and what the medications are going to do; subsequently they watch their child experience distressing early side effects that include nausea and diarrhea and severe drowsiness; or worse, the paradoxical effects that produce the opposite reaction of what the drug is being used to treat.
  • Deal with the disillusionment of a failed medication trial and explain to that child why those pills didn’t work and tell him or her: “We’re going to try something else,” knowing that they may have to repeat that phrase a number of times and thus begin a new round of side effects.
  • Have to get a child who has a needle phobia to a lab for a blood draw to determine drug levels. (This experience alone could turn one’s hair grey.)
  • Watch children’s weight balloon upward and their self-esteem plummet as they take certain medications that can be very effective, but that may also cause weight gain.
  • Become an all too familiar face at the pharmacy, experiencing shock at the cost of each prescription.
  • Have to suffer the ignorance of people in the media, who–in a cavalier manner–discuss over-diagnosis and over-medication. Moreover, these parents hear certain clinicians in the field publicly utter insulting sound bites such as: “This is an easy way for parents to let themselves off the hook;” or “This is simply the diagnosis du jour.”
  • Have to listen to the word “No!” from a child one hundred times each morning, but be unable to assert the parental “No” as it will predictably trigger a meltdown.
  • Suffer the physical abuse of a child raging out of control, and experience crippling shame because they can’t manage their own child.
  • Are set adrift in a house that has become a war zone.
  • Deal with feelings that alternate from extreme anger at the child to the most unbelievable yearning to help that child, from anger at the outside world for failing to realize what is happening to them, to exhaustion in trying to deal with the child with some modicum of equanimity.
  • Become perplexed that their child often does well in the outside world, only to return to the safe harbor of home to rage at a parent (most often the mother), leading to the suspicions of outsiders that “Something must be going on in that household, and with that woman;” or “She seems so nice, but you never really know people;” or “He can keep it together at school, so he must be a very manipulative kid.
  • Have to mount a siege each school-day morning simply to get a child suffering a sleep/wake reversal up and out to school.
  • Hesitate to answer a phone, afraid that it will be the vice-principal in charge of disciplinary action calling to report an “incident” at school.
  • Come close to earning a degree in educational law so as to work with the school system. Keep in constant contact with the teachers and psychologist or aide in order to assess what’s working and where yet another accommodation may help.
  • Waylay careers and reduce household income so a parent can stay at home to deal with the child and spend hours at doctors’ and therapists’ and tutors’ offices.
  • Experience the heartbreak of knowing that their child is rarely invited to birthday parties. Conversely, if he or she is invited, the event might be overstimulating thus provoking some kind of meltdown, and effectively putting an end to any such celebrations in the future.
  • Fear that their child will become aggressive with kids on the playground or in the neighborhood, thus earning disdain and a cold shoulder from the other parents.
  • Want the world to understand, but fear that the stigma will further isolate the child and their family.
  • Attempt to explain the almost inexplicable to the siblings, and to help them cope with the chaos in the household. Feel overwhelming guilt that the family is always fractured as one parent goes to a soccer game while the other stays home with the unstable child; or that a rare dinner at a restaurant devolves into an embarrassing, abruptly-ended event as parents race the child and siblings home and away from disapproving diners.
  • Are paralyzed if a child becomes manic and hypersexual and says inappropriate things or makes inappropriate gestures.
  • See their marriages become shaky as the stress of coping with this illness leaves parents little time to relate to each other and most conversations begin to center around the problems of their ill child.
  • Listen with horror as their child screams, “I don’t want to live anymore;” or “I’d be better off dead.”

It is hard to fathom how these parents get through a day. Their reality is simply unimaginable to the outside world, and their lives–until their children are stable–are a virtual stew of guilt and powerlessness, anxiety, fear, uncertainty, confusion, blame, and shame. These are feelings that most of us would do anything to avoid, but all are feelings that a family who lives with bipolar disorder must endure for months and years at a time.

And yet, we see family after family find the help, learn to cope, steady their footing, and move on with their lives. And then we see them turn around and offer a lifeline of information and support to others who must walk the same path, only now no longer alone.

We celebrate these parents: their grit and their commitment, their love and their humanity….Parents who have never stopped trying to help their children — against seemingly overwhelming odds.

Demitri Papolos, M.D. is an associate professor of psychiatry at the Albert Einstein College of Medicine in New York City, where he is the co-director of the Program in Behavioral Genetics. In 2001, Dr. Papolos became the director of research of the Juvenile Bipolar Research Foundation (JBRF) where he established a consortium of clinical and basic researchers from medical centers across the country in order to focus on the root causes of childhood-onset bipolar disorder. 

Demitri F. Papolos, M.D. is one of a handful of psychiatrists in the world who began to see and to speak out about the possible deleterious effects of antidepressants and stimulants in the population of children within the bipolar spectrum. His extensive work with youngsters with the condition and their families, led him to team with his author wife, Janice Papolos, to write the first book ever published on the subject of early-onset bipolar disorder, The Bipolar Child. In its first and second editions, the book returned to press 23 times and third edition was published in 2006.

Dr. Papolos earned his undergraduate degree at Harvard and completed his medical training at New York Medical College and the New York State Psychiatric Institute at Columbia Presbyterian. He is in private practice in New York City and Westport, Connecticut.

This article originally appeared in his online newsletter, which you can subscribe to at his website BipolarChild.com.

Why Has Childhood Bipolar Disorder Become an Epidemic?

November 12, 2010 in Special Needs News by Admin Dawn

When a young child’s behavior problems go beyond mere toddler tantrums, parents face bleak choices about how to treat them. Should they seek psychiatric or psychological help? Should the child be put on medication or some other behavioral treatment? Should he or she be labeled with a psychiatric illness like bipolar disorder?

Slate had a compelling look at the question this week, which, unlike many previous articles on the topic, does not reduce parents who seek treatment to gullible victims of fad diagnoses who simply want to drug away any sign of individuality in their children.

read more at Why Has Childhood Bipolar Disorder Become an Epidemic? – TIME Healthland.

Welcome to our New Community Members

November 6, 2010 in Around the Site by Admin Dawn

We had a ton of people join our community this week so we wanted to do a quick weekend shout out to them in the order that they registered!

We also wanted to highlight our mission statement this week to make clear that we are an inclusive community and welcome diverse voices!

Special Needs.

It’s an all encompassing label, yet we let a diagnosis divide us among this powerful group of advocates and caregivers into categories of rare and not-so-rare diseases, genetic conditions, developmental delays and the unexplained afflictions. We have more in common than separates us and Support for Special Needs is the community that offers a chance to exchange wisdom and ideas among one of the most powerful group of people we know. Join us as we learn from each other about how to help our kids and ourselves.

Now let’s meet our new members! Click their names to reach their profiles and say hello to them! Ready? Set? GO!

Barbara – “Mother of 9 yr old child with special needs”

Linda

Heather Pierini – “I am the mom to two girls, almost 9 and 3 months.”

Karyn Climans

Jacki – “My daughter has ADD with Cystic Fibrosis and Cerebral Palsy”

Rachelle – “I am the mother to a wonderful most precious angel with special needs. My daughter Alyssa has OPCA (a degenerative brain disease), Cerebral Palsy, Microcephaly, ONH (optic nerve hypoplasia) Infantile Spasms (a form of Seizures), developmental delay (almost 2 and at a 6 month level) and has a G Tube. She is the happiest most beautiful baby girl I know. I was devastated at first but came to realize that God chose me to raise this blessing and I thank him every day for her. I stay strong so that she will stay strong. I used to pray for healing but them realize that in order for God to heal her he would have had to make a mistake when he created her. God does not make mistakes. Now I pray that he will just keep her happy and make her the best she possibly can be. I have my moments when I must cry and morn that child I dreamt of but I never let her see me. I use the shower for that release period. I know that for me to dwell in her short comings would only take away from the time I have her since with her degenerative brain disease I do not know how long God will bless me with her. She was born with 3 rare diagnosis so we say she is extra special 3x’s over. I love her more than anyone could ever know and I would not change her for the world. She is my precious angel.”

Keely Miller – “I am a Mom of 3 children with special designer genes. I have learned that “Variety is the spice of life” and we sure do have a variety of things going on in our family. Our Geneticist is working on finding the main ingredients! My youngest and I have been diagnosed with a duplication on our 13th Chromosome and my other two are in the process of diagnosis with Genetics.”

Lynne McKenzie – “Mum of two beautiful children. The youngest, my son, requires 24hr care.”

Julie

psmadel – “mom of child with EEC Syndrome”

Tanya Lewis

Alicia Harper – “Navy wifey; SAH mommy full-time to 3, part-time to 1; 2 year old son dx hydranencephaly; full-time psychology student; contact for the International Hydranencephaly Group for support/resources/information for families facing dx; and in love with my life!!”

Joy Owens – “I am a mother to a 10 year old boy who is living with a severe congenital heart defect. He has had 8 surgeries in the last 7 years with more in his future. It is a chronic and life threatning illness with no cure. In January of this year our 2 1/2 month old baby boy died because of a severe heart defect. all 72 days were spent in the hospital. We also have a healthy 11 year old boy and 7 year old girl.”

Caroline Callaway

Dan and Amy Stout

AidelMaidel – “I’m the 30something mom to a bunch of kids, including, but not limited by, one teenager on the autism spectrum, one 8 yo with Retinitis Pigmentosa, a visual impairment, ADD, APD, and some neurological impairments, and two more who are (seemingly normal). We’re orthodox Jews who live in NYC. :) I’m happily married and work a full-time, full-stress job.”

Lora Alexander

Nancy Powers – “Adoptive mother of two school-aged sons”

Jenny Fenner

Julie Renner

Cheryl Crisp – “I am the adoptive mother of a child who is medically fragile, ventilator dependent, and has multiple disabilities. In addition, I am the pediatric clinical nurse specialist at a diagnostic clinic for children with a wide variety of special needs including autism, developmental delay, mental handicaps, medical disabilities, and learning disabilities. Working with these children and families is my mission, and I will do anything I can do to help them in any way I can, because I know firsthand what having a child with special needs is like. I consider toys to be a very special type of assistive technology, because the allow children to communicate in a way that they otherwise might not be able.”

Laurie Sweeney – “I am 53 years old, working in a PhD in ED Psych. I have been an adoptive and foster mother for over 30 years. Most of my kids have been some combination of Bipolar, FASD, RAD, ADHD. GB is 7 and her parents’ TPR was approved on 7/28/2010. She will be finalized in a couple of weeks. She has FASD and Bipolar. I have an adult son, J, who is Bipolar and doing very well. I have 2 legally adult children, living at home, MK, who is Bipolar, FASD, EX-RAD and a new mother, and D, who simply isn’t functioning. We successfully adopted a 4 1/2 girl, Hope, on August 26, 2010 from a dissolution who is Bipolar, Rad, and had been diagnosed PPD-NOS (PPD-NOS has been removed). I will be a SAHM for a while, then finish my dissertation.”

Teens’ sleeping patterns a clue to mental health risk

October 28, 2010 in Special Needs News by Admin Dawn

The sleeping patterns of teenagers can provide a clue to their longer-term risk of developing depression or bipolar disorder, say scientists.

Erratic sleeping patterns were an often overlooked feature of “basically all mood disorders and all psychiatric disorders”, explained Naomi Rogers of the University of Sydney’s Brain and Mind Research Institute.

“In people who develop depression, often you can trace back and find they have had early sleep disturbance,” the Daily Telegraph quoted Rogers, as saying.

“We know that disturbed sleep occurs in basically all mood disorders and all psychiatric disorders, and the more disturbed sleep patterns are we tend to see worse mood symptoms.

“But whether (disturbed sleep) is an early sign, or risk factor, we are not yet sure,” she said.

Read more here: Teens` sleeping patterns a clue to mental health risk.

Meet Pierrette, living The Coffee Klatch adventure

October 20, 2010 in Around the Web, Resources by Admin Dawn

Can you introduce yourself and let us know your involvement in the special needs community?

My name is Pierrette d’Entremont. I am the mother of three girls, our middle daughter has Tourette Syndrome and sensory issues. I have Tourette Syndrome and I am bipolar. I have also had sensory issues my whole life. These diagnoses only came at the age of 19, after many awfully hard school years. As a result, I designed a special needs tool to help with sensory motor issues, the Kid Companions chewelry tool. It lets kids chew or fidget discreetly and can double as a parent-worn teether or nursing necklace for infants. This became clear while breastfeeding our yougest! (Note: Pierette sponsored one of our first giveaways! We are big fans of her chewelry!)

How did you get involved in The Coffee Klatch? Do you have a specific role there?

I got a Direct Message from Marianne Russo asking if I would be interested in such an adventure. It’s right up my alley since I communicate much better via “live typing” versus “live talking” ;) It comes as no surprise then, that my role is mostly behind the scenes. I helped design the logo and twitter background and tend to be online via tweetchat or the message board during blogradio sessions. This summer I was tremendously busy with our Kid Companions business and have had to take some time off, but with fall and back to school, I should be a more regular moderator.

What are your goals in your work at TCK? What do you hope people get out of it?

I hope that parents of special needs children can see that their child can have a succesful and productive life. If my own mother (@lornadent on twitter btw) had labeled me and put me in a special needs “box”, I may not be who I am today. I do have Tourette Syndrome. I have both motor and verbal tics. As a young adult this, along with an unmanaged bipolar disorder was intensely painful and difficult. Many times due to adults and peers misunderstanding my situation. These disorders do not affect me cognitively, in fact just the opposite, and this can make things challenging too. By educating and supporting parents, like we do via TCK, I hope to indirectly reach some of the kids out there. Children that are suffering with mental health issues and sensory issues that are often hard to explain and hard to understand.

How has being part of TCK changed your personal life? Do you have an anecdote to share about that?

I find that I can, by a few keystrokes, reach someone else in a similar situation. The world seems very small in our network and borders non-existant. Issues and challenges facing kids with special needs are certainly not unique to countries. Certainly our laws and school systems are different but we all have common ground and this parent forum alows us to share ideas and solutions that work (or don’t work) in our areas.

Is there a particular show you’d really like to call our attention to? Why was that one you want to make sure your readers don’t miss?

Well, the Temple Grandin blog radio interview was certainly a not-to-be missed edition. I listened to it with our 7 y/o daughter and she listened intensely ;) I liked the second session with Dr. Duncan McKinlay, perhaps because there were many people with Tourette Syndrome online at the same time and we could all communicate easily and quickly.That is often not the case with us, we tend to make each other tic ;) . It is also a relatively rare disorder, so speaking with others that have TS is always interesting. Dr. McKinlay is also very easy to speak with and has a wealth of readily available information. Many of the shows I’ve enjoyed the most are open actually forums. We have a set topic and then the ball rolls along with parents and health professionals joining in throughout the hour.

A simple solution to boys’ hyperactivity: Give them a break.

October 5, 2010 in Special Needs News by Admin Dawn

Lexington child psychologist Anthony Rao is author of “The Way of Boys: Promoting the Social and Emotional Development of Young Boys.’’

Q. You write that young boys are overdiagnosed much of the time and labeled with ADHD, bipolar disorder, and learning disabilities. That our problem isn’t always boys, it’s our expectations of them. Elaborate?

A. Because when boys enter into preschool or any learning situation, the expectations to succeed or perform don’t really match where they’re at. They don’t make eye contact very well. They don’t listen as well. Their hearing is not as acute as it is for girls, so they don’t develop language skills as quickly. And they have high motor activity. You have boys being asked to sit longer or be indoors, and teachers who are at the front lines saying your child is having a problem fitting in. That translates quickly into a diagnosis and a medication.

Read more here: Anthony Rao has a simple solution to boys’ hyperactivity: Give them a break. – The Boston Globe.

Weighing the risks of mental health drugs for children

September 21, 2010 in Special Needs News by Admin Dawn

It is not just transplant patients tapering off anti-rejection drugs who use medications in traditionally untested ways. WHYY’s health and science intern and University of Pennsylvania Bioethics graduate student, Alyssa Bindman, examines the issue.

Children often receive prescriptions for medications to treat conditions such as schizophrenia and bipolar disorder that have been tested only on adults, leaving a lot of room for questions about the short and long-term effects of using them.

“Children are not just small adults. They have different bodies, minds and brains. They undergo an enormous degree of development,” said Christoph Correll, a research psychiatrist at The Zucker Hillside Hospital and an associate professor of psychiatry at Yeshiva University’s Albert Einstein College of Medicine.

Clinical trials on children are notoriously challenging to conduct – and therefore scarce — in part because they are subject to high levels of scrutiny by review boards. The hesitance of some families to participate in studies out of fear or stress may create an additional barrier, Correll said. Some families and patients are overwhelmed and “don’t want to add any other iota of burden,” he said. They may be suspicious of research, feel exploited, or concerned their child will be used as a “guinea pig.”

Read more here: Weighing the risks of mental health drugs for children | WHYY News and Information | WHYY.

Child’s Ordeal Shows Dangers of Antipsychotic Drugs

September 8, 2010 in Special Needs News by Admin Dawn

At 18 months, Kyle Warren started taking a daily antipsychotic drug on the orders of a pediatrician trying to quell the boy’s severe temper tantrums.

Thus began a troubled toddler’s journey from one doctor to another, from one diagnosis to another, involving even more drugs. Autism, bipolar disorder, hyperactivity, insomnia, oppositional defiant disorder. The boy’s daily pill regimen multiplied: the antipsychotic Risperdal, the antidepressant Prozac, two sleeping medicines and one for attention-deficit disorder. All by the time he was 3.

He was sedated, drooling and overweight from the side effects of the antipsychotic medicine. Although his mother, Brandy Warren, had been at her “wit’s end” when she resorted to the drug treatment, she began to worry about Kyle’s altered personality. “All I had was a medicated little boy,” Ms. Warren said. “I didn’t have my son. It’s like, you’d look into his eyes and you would just see just blankness.”

Read more here: Child’s Ordeal Shows Dangers of Antipsychotic Drugs – NYTimes.com.

Growing up bipolar: ‘Nobody was on my side’

September 1, 2010 in Special Needs News by Admin Dawn

Jennifer Konjoian was 10 years old when she put a plastic bag over her head. She remembers doing it impulsively, for no other reason than to get attention.

For her mother, it was the last straw in a series of tantrums that led her to believe something was seriously wrong with Jennifer. After that incident, she took Jennifer to a psychiatric hospital.

But that was far from the end of the journey for this mother and daughter to understand what was making Jennifer feel so frequently frustrated and overwhelmed by daily life situations at home. It took a second hospitalization at a different institution before she received medication that worked — lithium — for a diagnosis that seemed to fit: bipolar disorder.

Read more here: Growing up bipolar: ‘Nobody was on my side’ – CNN.com.

Americans with Disabilities Act also applies to those with mental illnesses

August 2, 2010 in Special Needs News by Admin Dawn

This week, we celebrate the 20th anniversary of the Americans with Disabilities Act.The ADA is a broad civil rights law designed to provide a clear and comprehensive national mandate for the elimination of discrimination against individuals with disabilities.

Like the Civil Rights Act of 1964 that prohibits discrimination on the basis of race, color, religion, national origin, and gender, the ADA seeks to ensure equal opportunity for people with disabilities. It does not guarantee equal results, establish quotas or require preferences favoring individuals with disabilities over those without disabilities.

I am a person who experiences severe and persistent mental illness. I will not be cured. Although I am an advocate for recovery, I am not “in recovery” from my brain. I cannot abstain from “being bipolar” as one abstains from substance addiction behaviors. I am not defined by my illness, but it is a prism through which I experience the world. This is a fundamental part of who I am, as much as my ethnic heritage. It is a biologically based disease, like diabetes. I did not survive it, as some survive breast cancer. If I had breast cancer, I would receive substantially better health care and support services.

via Americans with Disabilities Act also applies to those with mental illnesses | newarkadvocate.com | The Newark Advocate.

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