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 8 posts - 1 through 8 (of 8 total)
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  • in reply to: MY DAD IS GONE #12402
    hope&faith
    Member

    Sherrygal,

    I am sorry for your famlies loss and you and your family are in our prayers.

    Jeff

    in reply to: Hans is gone #12090
    hope&faith
    Member

    Esme,

    I am so sorry for your loss, but at least Hans pain is over and he’s in a better place

    in reply to: What is a normal Paletlette count #11236
    hope&faith
    Member

    He’s being treated at UCSF by a Dr. Damon. They said that they will give him a transfusion before he goes for chemo…

    in reply to: interesting protocol differences #11045
    hope&faith
    Member

    The doctors for my dad in UCSF have said that he needs intense chemo first week of january. Everyone is saying that he has not progressed to AML, but they want to move onto the 1week chemo with 3wks in the hospital for recovery. He went for a second opinion at stanford with DR. Greenburg and he concured. I am so confused the last appt. he had they said he did not need a transfusion, so what is the rush for chemo???

    in reply to: Season'sGreetings from a newby! #10976
    hope&faith
    Member

    Merry Xmas and I wish you a wonderful 2006. God bless you. My DAD is going in on the 2or3rd of jan. at UCSF. So, please pray for him as I will pray for you.

    Hope&Faith

    in reply to: Chemo now or in three weeks? #10553
    hope&faith
    Member

    The chemo is 1 week with a 3 week hospital stay afterwards

    in reply to: Hard not to be so sad #10380
    hope&faith
    Member

    Patti,

    I’m so sorry, it’s selfish because I know in the future I will be going through it with my father. Stay in the fight… Dont give up…

    jeff

    in reply to: Just Found out my dad has MDS #10331
    hope&faith
    Member

    Thank you all for the prompt responses and the wealth of info. I need to talk with my dad and his doctor to determine what type of MDS. The DR did use a term called displasyia. Any advice…

Viewing 8 posts - 1 through 8 (of 8 total)

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