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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.

Developmental co-ordination disorder kids often troubled

November 3, 2010 in Special Needs News by Admin Dawn

They’re the clumsy children who can’t sit still in class and who trip when they’re walking across a room.

Even doing up a button and opening a milk carton can be difficult for them. Not only do they struggle in school, but their clumsiness can set them up as primary targets for being bullied and ridiculed.

Their condition — developmental co-ordination disorder – affects more than 5 per cent of children yet it continues to be the most misunderstood and misdiagnosed mental health syndrome among kids, said Dr. John Cairney, psychologist and researcher at St. Joseph’s Healthcare.

Cairney was one of three speakers at the Open Minds Across Canada Mental Health Symposia held Thursday night at St. Joseph’s Healthcare. Similar symposia were held across Canada all focusing on child and youth mental health.

via TheSpec – ‘Clumsy’ syndrome kids often troubled.

Doctor stresses need for sleep screening for children with learning disabilities

October 29, 2010 in Special Needs News by Admin Dawn

Doctor Louise Scott says there is a very good reason why humans spend one third of their lives asleep. Because it’s important.

That was the pediatric neuropsychologist’s message Saturday morning to a group of 25 parents and educators of children with learning disabilities.

Scott, who has a private practice, works at Grand River Hospital and has a learning disability of her own, was at Arc Industries to discuss the relationship between sleep, attention and memory and executive deficits associated with Attention Deficit Hyperactivity Disorder and other learning disabilities.

Scott said the learning disabilities affect sleep and sleep problems affect the learning disabilities.

“It can be any or all of the above,” she said when asked if one affects the other or if they go hand in hand.

Scott said parents who think poor sleeping habits are affecting learning and attention spans need to be screened using an overnight sleep study.

via GuelphMercury.com – News – Doctor stresses need for sleep screening for children with learning disabilities.

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.

‘Massive spin’ on child ADHD study

October 5, 2010 in Special Needs News by Admin Dawn

A high-profile child psychologist accused drugs companies and other scientists on Thursday of falsely claiming attention deficit disorder (ADHD) was a genetic disease in order to promote the controversial drug Ritalin.

Clinical child psychologist Dr Oliver James tore into a Cardiff University study on BBC Radio 4′s Today programme, accusing the university’s child and adolescent psychiatry professor Anita Tharpar of “putting a massive spin” on the research which claimed to prove that ADHD was a genetic disorder.

The study said it found that children with ADHD were more likely to have a difference in the brain caused by small pieces of DNA that were duplicated or deleted. But of the 336 children with ADHD in the study’s sample, just 16 per cent of them had such DNA.

Dr James said the study in fact disproved any link between genes and ADHD because almost nine out of 10 of the children did not have the gene supposed to cause it.

Read more here: ‘Massive spin’ on child ADHD study / Britain / Home – Morning Star.

Sensory processing disorder: Why it’s not just the diagnosis du jour for kids

September 9, 2010 in Special Needs News by Admin Dawn

Every classroom has one: the kid who bangs against things incessantly, won’t make eye contact and acts up whenever the school bell sounds. He or she may be autistic or in need of Ritalin. But there’s a chance such children are simply overwhelmed by their own senses.

According to Roya Ostovar, a neuropsychologist at Harvard Medical School, some children have problems receiving and organizing sensory input from the environment. Known as sensory processing disorder, the condition involves the visual, tactile, oral, auditory and olfactory senses, as well as the senses used to balance and locate oneself in space.

Read more here: Sensory processing disorder: Why it’s not just the diagnosis du jour for kids – The Globe and Mail.

Healing of students all in a day’s work

September 3, 2010 in Special Needs News by Admin Dawn

Sue Rys, a school psychologist for the East Greenbush Central School District, can have an agenda for the day that includes testing, meetings and sessions with students all laid out.

But it’s often subject to change as she meets the needs of kids who come to her in crisis.

“The school’s primary focus is to help the student be successful in school, so if it’s a big mental health problem, we’ll do the school piece and try to scaffold that student so they can get through the school day,” Rys said.

Studies show at least one in five children and adolescents have a mental health disorder, according to the National Mental Health Information Center, part of the U.S. Department of Health and Human Services.

Read more here: Healing of students all in a day’s work – Times Union.

Mother helped other parents come to grips with autistic children

August 31, 2010 in Special Needs News by Admin Dawn

CLARA Park, a pioneering American autism campaigner, author and teacher, best known for two books, The Siege and Exiting Nirvana, in which she described raising her daughter Jessica, has died at a nursing home in Williamstown, Massachusetts. She was 86.

Park was one of the first parents to have the courage to share her experiences with others and, through her books, provided families and professionals with a greater understanding of what it can be like to bring up a child with autism.

The Siege was published in 1967, when little was understood about autism, a developmental disability that affects how a person communicates with, and relates to, other people and how they make sense of the world around them. The common thinking at that time was based on the arguments of child psychologist Bruno Bettelheim, who advocated the idea that autism arose when mothers withheld affection, and of Leo Kanner, whose ”refrigerator mother” theory proposed that a cold and distant mother was central to a child’s autism.

Read more here: Affected mother helped other parents come to grips with autistic children.

Autism Pioneer Dies

August 27, 2010 in Special Needs News by Admin Dawn

THE MYSTERIES of autism remain a tangle. We have yet to map the inner world of a person with autism, much less find its precise cause.

Trumpet player benefits from treatment Lovaas pioneered.

Trumpet player benefits from treatment Lovaas pioneered.

But a powerful therapy is helping thousands of families: the intensive, near round-the-clock behavioral therapies that teach children with autism how to pay attention, listen to others and learn. Those therapies, and their central conviction that autism is treatable, were pioneered by Dr. O. Ivar Lovaas, the groundbreaking child psychologist who died earlier this month.

via NorthJersey.com: Breaking the silence.

Autistic kids targeted by bullies

August 24, 2010 in Special Needs News by Admin Dawn

UNPOPULAR, alone and unable to understand body language … autistic children are such an easy target for bullies.

A recent survey of 400 autistic children showed 90% had been bullied in the previous year – four times the rate of other children.

Professor Tony Attwood, clinical psychologist and leading author in the field, said autistic children often could not avoid becoming targets.

He says the real solution to the problem lies in educating schools, empowering other children to help and stopping the bullies themselves.

“We say that both parties are in need of rescuing,” Prof Attwood said.

via Autistic kids targeted by bullies | Coffs Coast Parenting | Parents and Children in Coffs Coast | Coffs Coast Advocate.

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