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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.

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.

Sensory Implications for Bi-Polar Disorder

June 10, 2010 in Insider Insight, Latest Articles by Susan N. Schriber Orloff, OTR/L

While Autism is very much in the current spotlight, the rate of children being diagnosed with Bi-Polar Disorder is even higher.

According to the National Institute of Mental Health over 1.5 million children under the age of 15 are severely depressed. And one major study (Child and Adolescent Bipolar Foundation) states that nearly half of those children who exhibit depression before puberty will be diagnosed with Bi-Polar Disorder before they are 20 years of age. Another study projects that there are at least 1 million children who are suffering with this condition who are “uncounted”. Symptoms can emerge at any time in the life cycle, cases have even been diagnosed in preschoolers.

Unfortunately, according to Dr. Terrence Ketter, director of the bipolar disorder clinic at Stanford University, “at least half of the people that have this disorder do not get treated”. Getting it treated early on is essential. Dr. Demitri Papolos, research director of the Juvenile Bipolar foundation says that the disorder grows “like a tumor” and that heaping the torment of this disorder on an adult is “bad enough, but loading it on a child it is tragic”.

The cause of the rise in the diagnosis of this disorder appears to be related to stresses in school and at home. The Centers for Disease Control note a 20% increase in (presumed bi-polar-related) suicides in children over the past ten years.

A child with one bipolar parent has a 10%-30% chance of becoming bipolar, and if both parents are bipolar the odds reach 75%. In the general population, 90% of all those diagnosed with bipolar disorder have at least one close relative with a mood disorder.

Treatment in the past has often been by trial and error. Protocols include drug regimens, lifestyle changes, individual and family therapy. Occupational therapists can play a major role in helping families with the necessary lifestyle changes as well as helping the child develop behaviors that allow them to gain some measure of self-control. OT’s can also help with parenting techniques and helping families develop routines that can help the bipolar child relate more successfully with unaffected siblings.

Learning to balance sleep, meals, play as well as school demands is extremely important for not only these children but also the whole family. The child can be taught to seek out their siblings and to use them as a sounding board, “trusted eyes and ears” for when their perceptions become distorted.

Often these children are also diagnosed with ADHD, and the very nature of the affects of bipolar disorder creates sensory distortions and unstable sensory processing abilities.
With the above in mind the occupational therapist can help provide assistance by:

  1. Helping to create fixed family schedules for bedtime, wake-up times, meals, etc., as well as helping families understand that “drug holidays” are both dangerous to the child as well negatively impacting therapy progress.
  2. Providing avenues for families to discuss, on a regular basis, problems within the home and at school to help resolve issues before they reach the crisis stage.
  3. Helping the family to find ways to reduce family and inter-sibling/parent bickering.
  4. Education for the family about the behaviors associated with the disorder.
  5. Participating with the psychologist in family therapy meetings.
  6. Increasing transitional tolerance when unexpected changes in routines occur by role-playing and other techniques.
  7. Providing evidence of successful completion of specific task demand situations and activities. (ADL’s, etc.)
  8. Provide routines that promote self-monitoring, behavior training, and daily structure that helps the child organize and monitor their behavioral reactions.
  9. Increasing gross and sensory motor proficiency in novel (supported) situations (such as the S.H.I.N.E. Sensory Program © (Socialization, Hiking, Integrative, Neuro-muscular Experience© part of Children’s Special Services, LLC)
  10. Supporting the parents and helping them understand that they can be active participants in the therapy programs, but most of all, as one parent put it, “..at least now I know I am not a bad mother”.
  11. Administer assessments that can realistically help set goals for self-care and community and academic situations.
  12. Increase self-esteem through relaxation and other techniques that reduce feelings of helplessness and inadequacy. These can include but are not be limited to:
  • •  breathing techniques
  • •  visualizations
  • •  journaling about moods; thoughts, ideas and feelings
  • •  utilizing structured and unstructured activities such as crafts, cooking, music, and drawing, to express moods constructively.
  • •  preventing further impairment through or loss of function through related activity based interventions.

While recent pharmacological advances have greatly increased the management of this disorder, OT’s working as a team member in conjunction with the physician can greatly contribute, by providing tangible task/activity/function-based successes, creating hope for the possibility of a normal life.

Susan N. Schriber Orloff, OTR/L, is the author of the book Learning RE-Enabled, a guide for parents, teachers, and therapists (and a National Education Association featured book), and the Handwriting on the Wall Program. Children’s Special Services, LLC is the exclusive provider of P.O.P.tm Personal Options and Preferences, tm social skills programs. She was the 2006 Georgia OT of the Year and the CEO/executive director of Children’s Special Services, LLC, which provides occupational therapy services for children with developmental and learning delays in Atlanta. She can be reached through her Web site at www.childrens-services.com or at sorloffotr@aol.com.

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