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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Viewing 4 posts - 16 through 19 (of 19 total)
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  • in reply to: WONDERING— #46981
    Dale Frank
    Participant

    Thanks for feedback. My port is installed under the skin to reduce infection rate. Flushing with Heparin avoids clotting in the catheter. Nurses adjust the mix and low rate to optimize Vidaza efficacy. I’ll report after first round with port.

    Be well.

    in reply to: Is Vidaza worth it? #46980
    Dale Frank
    Participant

    Misty, I have had 3 rounds of Vidaza. Nausea is manageable by spacing meals and with some ginger fruit chews my doc gave me. I have had some blistering at injection sites but Kathy and others have posted suggestions. Other than this, I have felt as well during the 5 day injection period as before and after the 5 day period.

    Pat Lawson, thank you for sharing your husband’s experience. His disease sounds similar to mine. I will look into Veneteclax trials.

    in reply to: 5.5 months post transplant #46963
    Dale Frank
    Participant

    Joey,

    Great news for your dad. Fingers crossed here. How old is your dad? I’m 71 with low WBC, RBC and Platelets and considering bone marrow transplant, but scared of the ordeal. Thx.

    Dale

    in reply to: WONDERING— #46962
    Dale Frank
    Participant

    Hi. I have had 3 cycles of Vidaza injections in tummy and had bad blistering during/after cycles 2 and 3. Dangerous since my WBC count is 1.0. I had a port installed in my chest and will start my next Vidaza cycle by injection through the port.

Viewing 4 posts - 16 through 19 (of 19 total)

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