It appears you have not yet Signed Up with our community. To Sign Up for free, please click here....

Myositis Message Board

Myositis Board Index
Board Index > Myositis | 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

My daughter was diagnosed in August of 1996 with JDM.She has been in remission for 6 years.She is now 13.She was 4 at diagnosis.It changed our life , there were a lot of ups and downs.Like you we were devastated everything changed and my poor helpless daughter this wasnt her fault or ours.I kept asking myself why why her.I will never forget how helpless I felt.At that time her and only a few others had this in the whole state of Florida.It was scary.My daughter was started immediatley on solumedrol IV.Within a couple of weeks she was getting her strength back,but we were far from being done with this disease.I planted myself at the library, internet and anywhere else I could find info on dematomyositis. With the high dose steroids there came problems.She was emotional, she got huge,she grew hair everywhere,then she started getting fractures,apparentley the steroids softened her bones up so it started out with a hairline fracture in her knee from just being a kid and running around and then a couple of weeks later she had back pain.She started kindergarten wearing a backbrace.The steroids also caused high blood pressure .She was started on rocaltrol wich is a calcium supplement for her bones.She developed a kidney stone from the build up of calcium in her kidneys.I took her for a second opinion but we ended up staying with our doctor and he took her off of steroids because of the problems and we started her on methotrexate(which is a drug for cancer)but the benefit of this drug outweighed the risks of not being on it.They also added naprosen for her arthritis symptoms.She did good and everything was looking up.We slowly took her off all meds and shes been in remission ever since.She now is so atheletic you would never know she had this disease.She still goes in once a year for bloodwork and a checkup.She has however been comlaining of arthritis like symptoms lately and she goes back to the specialist in November.Im praying its just growing pains but I always wonder in the back of my mind if it will come back,the doctor said there was a very slim chance it would.Anyways Im sorry for ramblin on I just wanted to let you know it isnt the end of the world,there is remission and when children are diagnsed with this , it usually does go into remission and you will have your happy healthy daughter back.
Hi serinity
I saw my daughter's doc the other day and she said that she rung her specialist and had a talk to him, he told her he does not think it is Derma........ but thinks that she does have a muscle prob, but does not know what.
I think this guy is nuts, how can it be that all her test show Derma and he is still saying no, i'm at my wits end. The test from Aussie has not come back yet, it sux living in a small country sometimes. You have to deal with Doctor's that dont know what they are doing.
Thanks for listening

All times are GMT -7. The time now is 07:24 AM.

© 2020 MH Sub I, LLC dba Internet Brands. All rights reserved.
Do not copy or redistribute in any form!