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Meri T!
It is great to read that you are doing so well post transplant!
I am also an old timer here, although I rarely check in these days.
It has been almost 17 years since I got ATG/Cyclosporine for my AA/MDS diagnosis! I am still Cyclosporine dependent but at a very low dose. I am grateful to be leading a very full life!
To all those new to this forum -
Keep hope alive regardless of the route that you choose - IST or transplant. They are learning more and more how to best treat this disease with each passing year!
Wishing you well!
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58 yo female, dx 9/08, AA/hypo-MDS, subclinical PNH, ATG/CsA 12/08, partial response. small trisomy 6 clone, low-dose cyclosporine dependent
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