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3xBMT
I'm a 3 time BMT patient. I'm doing well thanks to some amazing science and research.
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Hi hope things are OK. I'm a 3 time bmt patient. Happy to talk about my experience if it helps.
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Hi Sean, MDS UK is probably the place you need to go. There is an MDS Community page where sufferers have just your sort of questions. For the record, I had MDS (RCMD) which became quite aggressive. In 2010 I had 3 bone marrow transplants. Today, I have a normal life and run the odd Marathon
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Thankful mine never progressed to your AML...
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I'm a 3x Bone Marrow Patient and diagnosed with MDS in 2009. Thankful that someone (Anthony Nolan! and others) is running a register!! And not forgetting the help and support from my specialist group - MDS UK Patient Support Group. The way those of us who've suffered a similar disease are able to help each other is amazing.