MDS is a bone marrow failure disorder
MDS is a blood cancer
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Welcome to the MDS Patient Message Board. We hope that you will find this to be a very valuable resource in your journey. We have recently revised the format of our forum to be much more user friendly and pleasing on the eyes. Let us know if you have any problems, or if you have additional suggestions on how we might further improve our site.

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  • in reply to: Idarubicin and Cytarabine #66739
    Rosemary
    Participant

    The doctor now says that because of the TP53 gene the intensive chemo won’t work and so I’ll go on vidaza and venetoclax which will keep me going for 12 – 15 months. What is the end like?

    in reply to: Recent diagnosis of Mum (UK) #66645
    Rosemary
    Participant

    Hi Clare,
    I’m 72 and had the same diagnosis recently. I had the blood test because of extreme tiredness but now with regular transfusions I’m quite well and functioning normally. My doctor is expecting to see a progression to AML at my next bone marrow biopsy and it’s all downhill from there apparently. That may be what they’re expecting with your mother. I’m not having medication yet and frankly I’m wondering whether it’s worth it as there is no cure. Is your mother having any reaction to the azacitadine?

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