I was wondering if anyone could give me some feed back on this.Today I took my 20 month old who has Sickle Cell SS to her regular hemotologist appt and even though I have done my research her doctor has put he on Hydroxyurea.My baby eventhough she has minor aches from the sickle cell she has never had a crisis before and she appears to be doing good with the disease.So I have a few questions for anyone that can answer them.Has anyone seen a difference in their health while taking this drug? and does it really work in preventing fewer crisis?Also if anyone can give me some better info on this it will help. The doctors can explain things to you but it sounds different coming from people that really know! Thank you!
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