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Height/Growth??
Quote: jdjd said:
Hi, My child has just started Focalin. He has been on various meds.for 5 years. I can't judge his reaction to the Focalin yet as it's only been 2 days and he has a bad cold. I noticed that the pamphet for the drug stated that height can be affected by taking the drug.Prior to this I don't remember any of his meds stating the possibiliy of stunted growth so definately. My son is small for his age. I'm wondering if anyone has an update on this and also I'm curious how all you children are fairing height wise on their meds. Do other Moms see that their children on meds are smaller the most others in their classes
My daughter at 9 years old and is 4ft 5in. and 62lbs (which for height is the 75th percentile and weight around the 50th), most of her life, she has been above the 95th for both height and weight, before and during the meds, she has been on meds since she was 7, she's been on Adderall, Concerta and Daytrana. She is the 3rd tallest in her class, but definitely one of the thinner kids in her class too.
My son, at 5 years old is currently 4ft 3in and 59lbs, which for both are off the charts (above the 100th), my doctor says that the medication hasn't either hindered his growth nor his appetite (which has always been pretty bad), so far, he's only been on Vyvanse. He is the 2nd tallest in the class and definitely the thinnest!
I don't think that my kids are necessarily the norm though. Our doctor says that if my son keeps growing at this rate, he'll be 6ft 5in by the time he's 16 (although he expects that he'll slow down soon, I'm not so optimistic), in the last two years, he's grown two sizes per year and several shoe sizes. I expect that by the end of this year, he'll be at least two shoe sizes bigger, he always is.
Just monitor it and try not to worry too much. All of the medications that my kids have been on have had the Long-Term Suppression of Growth (which has the information about stunted growth) paragraph on the product insert (which I read all of them from top to bottom, no matter how long they are). All of the stimulants seem to have the same risks - as well as the NON-stimulants. I have noticed that my daughter since being on the Daytrana patch, has had a lot less of all of these side effects. But has stomach aches all the time, the doctor says that this is a normal side effect and I just give her tums for it and it seems to help.
I learned a while ago, if I let myself worry about everything that they say about the medication, that's all I'll do is worry (tics, aggression, growth issues, loss of appetite, mood changes, headaches, stomach aches, etc...it's enough to drive you insane). Just be sure that the doctor is checking all vitals on a regular basis - my son goes every two months (because he's only 5) for a developmental and my daughter every 3-4 months. They check ALL vitals, including BP. I used to think that it really stunk going back and forth to the doctor all the time, but now I know that it's really necessary to do it.
Overall, my children are doing way better on the meds than off, but there are always unfortunately going to be the side effects.
Hope this helps
Lori
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