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Additional testing?
I was wondering how often all of you out there with MAA or SAA get tested for MDS or PNH? Do you get BM biopsies done every few years or anything to see if something has changed? I only know of one person on here who has been tested for a TERC mutation, anyone else?
Thanks!
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~Dee~  ) 29yr, wife and mom of 3 :: Dx Moderate AA 9/09, treated with IV iron, currently "watch and wait" :: RBC,Platelets "ok" - low WBC and ANC
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