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    #1

    Phone Number

    Hi!

    It's Diamond. Haven't been on here for a very long time. I am so confused. What number do I call to speak to a specialist on the National MS phone line. The one I've looked up is not the same number. My phone went 100% dead and they could not retrieve any numbers and I've had to begin by scratch. It's a real job. Is it possible for you to help me and list all the numbers or is it on here. I like the look of the new format but took me forever how to post. I hope everyone is doing as good as can be. Since 2015 I've been promoted to secondaryRMS. Many changes but I'm back on to check things out. Thank you in-advance for any help with numbers.

    Take good care...........
    Diamond


    Diagnosed 6-28-14
    RRMS
    Alone we can do so little; together we can do so much. ~Helen Keller~
    Tags: None
    #2
    Originally posted by Diamond57 View Post
    Hi!

    It's Diamond. Haven't been on here for a very long time. I am so confused. What number do I call to speak to a specialist on the National MS phone line. The one I've looked up is not the same number. My phone went 100% dead and they could not retrieve any numbers and I've had to begin by scratch. It's a real job. Is it possible for you to help me and list all the numbers or is it on here. I like the look of the new format but took me forever how to post. I hope everyone is doing as good as can be. Since 2015 I've been promoted to secondaryRMS. Many changes but I'm back on to check things out. Thank you in-advance for any help with numbers.

    Take good care...........
    Diamond
    Hi Diamond

    Here is the Contact Us link for the National MS Society, including the phone number:

    http://www.nationalmssociety.org/Hel...nks/Contact-Us

    What other numbers were you interested in?

    Let us know if this is what you are looking for.

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

    Comment

      #3
      Thanks alot!


      Diagnosed 6-28-14
      RRMS
      Alone we can do so little; together we can do so much. ~Helen Keller~

      Comment

        #4
        Originally posted by Diamond57 View Post
        Thanks alot!
        You're Welcome, Diamond57!

        Here is another support resource from the National MS Society:

        http://www.nationalmssociety.org/Res...ers-One-on-One

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

        Comment

          #5
          There are also local branches of NMSS. Depending what information or support you are looking for, they may be an even better resource for you. Their national number could tell you how to connect with your local branch, if you wish.

          MS News and Views is another agency that is good at support. The service is free of charge to the MS community and can connect you to MS support groups, drug assistance programs, financial resources, education, information, counseling, transportation, etc.
          1-888-871-1664 to connect to an MS News and Views Social Worker.


          There are other resources here: http://msworld.org/resource-center/c.../patient-care/
          You can click on the various links to find the resources in the category you are looking for.
          ~ 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.

          Comment

            #6
            Thanks Faith.............

            Nice to see your face again.


            Diagnosed 6-28-14
            RRMS
            Alone we can do so little; together we can do so much. ~Helen Keller~

            Comment

              #7
              Originally posted by Diamond57 View Post
              Thanks Faith.............Nice to see your face again.
              Awww; thanks. I was on vacation for 2+ weeks. And then was busy with playing catch-up on my To-Do list. It's good to be 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.

              Comment

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