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: MDS Caregiver #36707
    Carol Van Buren
    Participant

    I was my husband’s caregiver this past year. He just died last month. One of the most important things I learned is that you can’t be aggressive/assertive enough with asking questions. He had been healthy as a horse all his adult life and then last summer grew progressively short of breath and week to the point of having emergency hospitalization at which time he had bone marrow biopsy and MDS diagnosis along with pancytopenia. With pancytopenia he was low on all 3 cell types – white cells, platelets and red blood cells. He had transfusions 2-3 days a week – at first the doctors thought it was caused by latent Lyme disease and toxoplasmosis infections. IT took 2 months to treat those (which chewed up a lot of time). Then a months trial of prednisone – not benefit. Then 4 months on vidaza (chemotherapy) which just made him sicker. By the time we were finally referred for bone marrow transplant (the only cure) it was too late. He had over 10 hospitalizations and basically lived at the hospital most of the time any way with the need for such regular transfusions. Whenever we asked the doctor point blank his prognosis and specific MDS diagnosis (as you know there are many types) this issue was sidestepped as if walking on eggshells. More attention was placed on the possibility that this could progress to leukemia rather than going ahead and acknowledging how serious his MDS itself was – its cancer but they don’t call it that and it is every much as fatal. We were talked out of 2nd opinions when in fact if we had proceeded earlier on it would have been more likely that the bone marrow transplant could have been pursued and successfully achieved earlier in the process. My biggest recommendation is to really push on getting answers to your husbands specific diagnosis, prognosis and referral for second opinion by going to an MDS center of excellence. And, you don’t need a referral to do so you can look up the centers on line and reach out directly. I am finding I was very strong throughout the process, but now am having a lot of medical problems myself and have not decided yet if I really want to continue live without him. We had no children, my parents are both gone, and my supposed friends are very distant. So, the other advice is be sure to surround yourself with good support system – take friends up on any offers of help. Be sure to engage support early in the process – even if you don’t feel like you need it.

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