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 15 posts - 391 through 405 (of 429 total)
  • Author
    Posts
  • in reply to: George is being transfered to the Moffitt center #3439
    sarah
    Member

    Kate, keeping you and George in our thoughts and prayers. Keep us posted.
    Sarah

    in reply to: "Certified nutritionist"? #2669
    sarah
    Member

    Tahoedonner, was curious what your fairly normal counts are?

    in reply to: My father's MDS #3407
    sarah
    Member

    Andrzej,
    Dec 2001 my husband was told by his Dr he had 6 months to live without a bone marrow transplant. After 3 years he has not yet found a suitable donor, and is very much alive. This disease is so different for everyone. No two are alike. What is your Dads classification of MDS? Remember to think positive, and take it one day at a time.
    Sarah

    in reply to: mom had her hemo. appointment #3399
    sarah
    Member

    Jody, good news, hope she continues to do well. Enjoy your sunshine.
    Sarah

    in reply to: My BMT #3380
    sarah
    Member

    Marsha, so great to hear from you. We have been thinking of you. Glad things are going well. You hang in there and take things one day at a time.
    Take care,
    Sarah

    in reply to: rash after induction #3316
    sarah
    Member

    Pam, hope you are feeling better soon.
    Sarah

    in reply to: Vidaza has nearly killed my Dad #3360
    sarah
    Member

    Sarah9, prayers are with you and your family. So sorry to hear your Dad had such bad results with the vidaza.
    Sarah

    in reply to: Hello.I'm back!! #3353
    sarah
    Member

    Great Alexa, keep fighting and think positive thoughts.
    Sarah

    in reply to: Dealing with loss #3327
    sarah
    Member

    John, Sorry to hear of the sudden loss of your brother. Been wondering how you were doing.
    Sarah

    in reply to: We are so confused….. #3311
    sarah
    Member

    Good Morning Barb,
    I agree the up’s and down’s are mind boggling. Maybe you will know more after next weeks appointment. Take it one day at a time.Hope he feels better soon.
    Sarah

    ,

    in reply to: 4 donors 6/6 being tested further #3287
    sarah
    Member

    Pam, fingers are crossed for you. Hang in there. You are fortunate to have good matches. Its good you are not experiencing the nausea. Hope you are headed home soon.
    Best wishes,
    Sarah

    in reply to: New to MDS #3248
    sarah
    Member

    Hi Drew,
    Welcome to forum. Sorry to hear of your mothers diagnosis. As you can already tell you will find a wealth of information and support among everyone here. How are her current counts? Any blasts in marrow?
    Sarah

    in reply to: high wbc #3164
    sarah
    Member

    Eve, good news , glad you can relax for now. Next week after seeing specialist you should know more. Have a good weekend.
    Sarah

    in reply to: Dad is in the hospital (my heart is broke) #3214
    sarah
    Member

    I too am sorry to hear about your Dad. I pray he will not suffer. Will keep you and your family in my thoughts and prayers.
    Sarah

    in reply to: Decision time! #3138
    sarah
    Member

    Dave, That is my understanding also about the mismatch C antigen. Search continues after 3 years now for my husband a match. Nothing has even come close to date. Will keep you in my thoughts and prayers as you proceed with your decision. Speaking as a caregiver myself, when the time comes your wife will do just fine!
    Sarah

Viewing 15 posts - 391 through 405 (of 429 total)

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