Anyone in the UK with SAA
Hi I was diagnosed SAA in October 2010 and had ATG in November. I have heard today that ATG and Ciclosporine have failed and I am back at same low levels as before I started treatment. I am in the UK and my consultant is going to speak to the team at Kings and am back on transfusions. All seems a bit hopeless and they don't tell me a lot other than I have had some cyto genetics done which have shown up a clone and a genetic abnormality but not apparently one that is indicative of Hypo MDS. Don't see Consultant until another six weeks and find it very hard to know what is happening other than I am v. fatigued.
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