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Does any information on the effectiveness of intravenous Prednisone therapy for Crohn's Disease in kids?


My 14-year-old daughter is having a flare-up of her Crohn's Disease. Her G.I. doc is interested in putting her on intravenous Prednisone therapy to get it under control, since the oral dose doen't seem to be doing the trick, at this time. Yuck, for many reasons, including hospitalization for days to weeks, (according to the doc) in a facility far from home. (Yes, I know that can also result from a full-blown flare.) Does anyone have info or personal experience on the effectiveness of I.V. Prednisone therapy? Thanks!

hi Elisabeth, I am a female crohn's pt. dxed at the age of 12.My heart goes out to your daughter. I can understand the pain she is going through plus the questions you may have.

Is she a candidate for Remicade to get things under control or possibly Humira? Most GIs tend to stay away from steroids just because they have life long side effects if some has been on them for years. I was on them for 13 yrs. and weaned off and put on 6MP for a while then Entocort came out (it's a steroid BUT doesn't have any of the bad side effects like prednisone--it doesn't get absorbed into the blood stream at all) and I've been on it ever since.

Have you attended a local Crohn's & Colitis Foundation of America chapter meeting near you? go to the site and click on events/chapters, then click on the state you live in and the info will come up. My parents went to the meetings when I was 1st diagnosed to educate themselves. That helped out alot. CCFA has a live chat as well as a hotline that is run by healthcare professionals well versed in IBD M-F 9 am - 5 pm (EST). Give them a call. They also have meetings that are geared toward kids so they have someone their age to talk to.

I know it's scary, frustrating, and a very emotional time right now. I've been there many times myself. I went through missing alot of school in 11th and 12th grade, being in constant pain 24/7, canceling appts. w/my friends due to not feeling well, etc. Just know that you and your daughter are not alone in the battle.

Feel free to email me if you have questions. I have included some sources for you as well as a site that is for parents with kids who have IBD--dragonpack.

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