MDS is a bone marrow failure disorder
MDS is a blood cancer
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Viewing 8 posts - 391 through 398 (of 398 total)
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  • in reply to: Can I share my dad's story with you? #2653
    Jimbob
    Member

    Lisa, I am sorry for your loss but you have shown us that even in the tie of such a great loss there can be many gains. I am thankful that you have shared with us. Jim

    in reply to: bloodwork #2693
    Jimbob
    Member

    Jodi, when my doctor first saw something was wrong but he didn’t know what, I went through 3 CBCs and 2 BMB in a week. After they were pretty sure it was CMML, I had a CBC every week for about 2 months. They then decided that it was pretty stable and put me on a schedule for once a month. It is more likely that doctors will test less often than more often than what may be best for the patient. I almost wish they had kept it on a weekly basis. I was almost in the normal range on all areas the first week of December 2003 but had an extreme leukemic event on January 2, 2004 with a WBC count of 385,000.
    Everyone is different and reacts differently to various treatments.

    in reply to: Thank you to all participants #2678
    Jimbob
    Member

    Although I am not able to reply or post as often as I would like, I do read severral times a week an I am VERY thankful for the info and support that is given here. Even when there is something that I don’t agree with, it gives me something to check out. I hope and pray that 2005 will be a better year for all of us. Jim

    in reply to: Dad a "rainy day", searching NBMR for donor #2508
    Jimbob
    Member

    As soon as I was diagnosed with CMML, my supervisors and the HR people insisted I go on short term diability (at 65%) and six months later set me up for long term disability (at 60%). I am very lucky because it will continue until I am either able to go back to work or for the rest of my life – with full benefits of any other employee. Jim

    in reply to: New red blood building drug? #2549
    Jimbob
    Member

    I was on aranesp after I had a SCT. Doctor said that I no longer had CMML and needed to start building new cells asap. I got it once a month for 3 or 4 months. Jim

    in reply to: Somebody mentioned a nutritionist, his name was… #2516
    Jimbob
    Member

    Without good nutrition, the body hass trouble fighting most diseases. With MDS, we have to give ourselves every advantage we can get. Jim

    in reply to: Happy Christmas news #2466
    Jimbob
    Member

    Carrie, Congratuations and best wishes for you – and, of cpurse, your father, too. Jim

    in reply to: CMML-2 #2471
    Jimbob
    Member

    Edith, I was diagnosed with CMML in Feb 2003. I used alternative methods of nutriton and supplements mostly overseen by a Naturpathic/acupunturist. It did help me to cleanse and strengthen my body. Unfortunately, I overstressed myself during the last 5 weeks of 2003 and ended up in the hospital the beginning of 2004 after and extreme leukemic event. WBC of 385K with 95% blast and 85% leukemic. In March 2004, I had SCT with brother as donor. Now no CMML found in bone marrow or blood. I am cured but working my way through the side effects of treatments. Jim

Viewing 8 posts - 391 through 398 (of 398 total)

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