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 6 posts - 31 through 36 (of 36 total)
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  • in reply to: MDS with Sweets Syndrome, lung nodules #45777
    Rose eden Guanzon
    Participant

    Praying for both of you…

    in reply to: Bone Marrow Biopsy question #45772
    Rose eden Guanzon
    Participant

    My husband is the one with MDS. He wants me to respond to this. He has undergone 8 bmb since he was diagnosed last year. No sedation is done on him. The doctors does not just get fluid, +hey also get a bone chip when they do a bmb. He swears he does not feel pain and that the injection hurts more than the actual aspiration. So i guess every person is different. But if it is any consolation, i know he is telling the truth. I could not really see any pain on his face.i have been with him on every one of those bmb procedures.

    Rose eden Guanzon
    Participant

    Thank you John. If you are Caucasian you have a good chance of finding a match. I understand that a younger donor is better. However if your sibling is in good health that can work well too. You are in my prayers. We have decided to go ahead with the transplant. It might be this 3rd week of March. I will keep everyone updated.let us all pray for each other.

    Rose eden Guanzon
    Participant

    Bridgette from what I have read your type of mds has a very good prognosis. Stay hopeful. You will be alright.

    in reply to: On Dacogen and Needing Blood #45150
    Rose eden Guanzon
    Participant

    My husband has RAEB II.before we started Dacogen, his platelets were at 12000. At one time it was at8000. His WBC was at. 5 – .8. But the.8 was already on the 4th decitabine cycle. It went as low as.3 at one time.he started responding on the 4th cycle.for the last 6months, he had not needed a blood transfusion anymore.

    Rose eden Guanzon
    Participant

    Thank you to everyone who responded. Amy you have been so informative. It is now clear to me that i do not know enough. For example, i did not even know that i should be aware of the mutations. All i know is that my husband has RAEB II. I have also been such a coward and never even asked about the prognosis. I hope more people will continue answering in this forum so i will learn more. I will pray for all of you. I am very good with that.

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

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