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    Hi everyone, my name is Julia and I’m from the Lake District in Cumbria, UK
    i was diagnosed with RRMS 5 and a half years ago. Just gon

    #2
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    Originally posted by Foxy1967 View Post
    Hi everyone, my name is Julia and I’m from the Lake District in Cumbria, UK
    i was diagnosed with RRMS 5 and a half years ago. Just gon
    Hi and welcome to the boards I hope you meet some amazing people on here that you can relate to and be able to help each other out.

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      #3
      Originally posted by Foxy1967 View Post
      Hi everyone, my name is Julia and I’m from the Lake District in Cumbria, UK
      i was diagnosed with RRMS 5 and a half years ago. Just gon
      Hi Julia and welcome

      If you have any questions, just ask and we'll be glad to help, if we can.

      Feel free to share what's going on, how you are doing, or how you are feeling.

      Looking forward to seeing more of your posts!

      Take Care
      PPMS for 26 years (dx 1998)
      ~ Worrying will not take away tomorrow's troubles ~ But it will take away today's peace. ~

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        #4
        Hi Julia. Welcome to MSWorld. I hope you'll keep coming back.
        ~ 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.

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