Guest guest Posted January 13, 2008 Report Share Posted January 13, 2008 Hi, I've peeled through the archives on this site and would like to bring up the colchicine & have a few other questions. This weekend we met with a Rheumatologist from NIH. My son has not been diagnosed , just PFS for now. We are still awaiting Gene DX test results. So far his only syptoms are fevers like clockwork, loss of appetite durning an attack, and suspected body pain (just a guess from how much crying he does). We went over 's symptoms with the Rheum and she wrote us a script for Colchicine. She stressed that this drug has been around for decades and is very mild and should cause no serious side effects and not to worry. HOWEVER I really am usure of this is the right course of action for a small toddler. She even said he did not need monitoring while on it, which is contrary to what I've read. She seemed fairly casual about the drug and from what I'm reading, one should not tread so lightly. 1. His bloodwork showed slight tendancy to anemia. Do your kids exhibit the same? The warnings on colchicine say it can cause anemia. I think it unwise to give a child who already has low iron something that could make it worse. Anyone's kids here on colchicine develop iron problems? 2. Anyone have thoughts on giving a 20mos old this drug? Given that there are warnings against giving it to growing childern, I am not convinced that the risk/benefit is worth it. Now, if he ever showes protiens in his kidneys, I would definitly say, yes, the risk IS worth it. 3. Looking at the archives, I'm not seeing much success w/this drug. Anyone have a success story? 4. Everything I've read says that this drug is mainly for FMF. Anyone using it with success who has not been diagnosed with FMF? Thanks! Mom2 born 5/11/06 Fevering since February 07 Quote Link to comment Share on other sites More sharing options...
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