MDS is a bone marrow failure disorder
MDS is a blood cancer
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Viewing 6 posts - 31 through 36 (of 36 total)
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  • in reply to: Enlarged Liver now Spleen #51080
    Jimmy Greenhut
    Participant

    Ian Palanglo, I have it mild compared to you. I’m not a BMT candidate. I’ve gotten my 3rd shot of Luspatercept but my HB is not responding,along with side effects. I’ve had 26 transfusions so far. Procrit didn’t work for me @ 60k units. I wish you well & thank you for sharing your journey. My thoughts are with you

    in reply to: low WBC and alcohol, correlation #50689
    Jimmy Greenhut
    Participant

    My Dr told me awhile ago that alcohol suppresses the bone marrow. Don’t know about wine? Ask your Dr when you see him next.

    in reply to: Luspatercept #49980
    Jimmy Greenhut
    Participant

    April 20th. That’s what my Dr told me @ Moffitt a couple weeks ago

    in reply to: Has anyone seen Dr Alan List @ Moffitt Cancer Center #49917
    Jimmy Greenhut
    Participant

    Sad day Marge, I saw him in early Dec. I asked about Luspatercept, which he thought would be approved. I was there yesterday and met Dr Komrokji who is also versed in this field, currently taking part of his patient load. Knowledgeable & trustworthy, first impression. Will continue to seeing him. Brought up Luspatercept again because the procrit isn’t working for me. Great news!! End of April I was told. Ins will cover it too. Good luck Marge, things are looking positive for a change 🙂

    in reply to: MDS / MPN RS-T #48732
    Jimmy Greenhut
    Participant

    Ann,still doing Procrit once a week now 40k units. I’m sorry Luspatercept isn’t yet :(. The FDA has fast tracked it. My Hemo says maybe early 2020. I’m in Fl. My hemoglobin is 9 for the last month. Was bi-weekly now every week. It was to late for me to enroll for the study, as I was already on Procrit. I apologize that I didn’t make that more clear.

    in reply to: Fatigue and tiredness in MDS #48694
    Jimmy Greenhut
    Participant

    Haydee, I also have MDS/MPN RS T. I posted several months ago and no one replied. It’s a rare branch of MDS. My Hemo/Onc said the same. I’m 60, with iron overload too. I told him quality of life. My wife can’t understand why I have to rest for an hr or 2 a day. My hemoglobin was @ 10.8 last Dec 2018. And has been going down since. When it got to 9.6 the hemo started me out on 40k units of Procrit. I go every 2wks for blood work. If I’m 10 no shot. I’ve been on it for 3 months now. Took awhile for the levels to get to 10. Nothing above. 4 weeks ago I was 9.7 and need a shot. 2 weeks ago I slipped to 9. It might no be working for me?? This Tue I see him with current blood work in hand. the lowest was 8.9 for me and that was 4 weeks after I started Procrit. No side effects. My Hemo said the FDA was fast tracking a drug named Luspatercept which he said maybe early 2020 it will come to market? Aranesp might be the next option if my level doesn’t rise.Fingers crossed. You have to be your spokesman. Your living with this not the Dr’s… I was given 8yr survival As you know its only 30% odds to transform to leukemia. Please feel free to call me. 239-247-2982. I’m in Florida. And stay positive.:) Best Jimmy

Viewing 6 posts - 31 through 36 (of 36 total)

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