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Question about colostony

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    Question about colostony

    We have a new member who posted a question on 10-15-2019. She posted it in an appropriate forum, so I don't want to move it. But, it might be more likely to be seen and responded to here, in the General Forum. Her question has only received one response thus far.

    Originally posted by marlie4334 View Post
    Have any of you with progressive disease had a colostomy and did it improve your quality of life ?
    Please respond here:
    ~ Faith
    MSWorld Volunteer -- Moderator since JUN2012
    (now a Mimibug)

    Symptoms began in JAN02
    - Dx with RRMS in OCT03, following 21 months of limbo, ruling out lots of other dx, and some "probable stroke" and "probable CNS" dx for awhile.
    - In 2008, I was back in limbo briefly, then re-dx w/ MS: JUL08

    - Betaseron NOV03-AUG08; Copaxone20 SEPT08-APR15; Copaxone40 APR15-present
    - Began receiving SSDI / LTD NOV08. Not employed. I volunteer in my church and community.