Announcement

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CHANGES AT MSWORLD - MSWORLD'S CLOSURE

We began with a mission and purpose to help others living with MS.

We were excited to get going!

And hit a few bumps along the way…

However, in all seriousness, we remain grateful for our amazing volunteers, members & all who have made MSWorld a valuable resource for all!

July 10, 2024, we celebrated the goodness of these past 28 years. With a heavy heart, we will be ending our services.

We need a financial miracle to keep going forward.

We thank all for your support.

MSWorld's website will close on October 16, 2024.

“I personally want to wish all of you the guidance to find this type of support, as so many do here. Also, my prayers and love extends beyond my understanding. It has been a pleasure to steward this journey.”

God Bless you, Kathleen

Kathleen Wilson
Founding President
❤️

we leave knowing that
we did our best and
stayed true to our mission and purpose.


Please visit our General Questions and Answers forum to read more.
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MSWORLD TALKS ON FACEBOOK!

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    #1

    MSWORLD TALKS ON FACEBOOK!

    Hi Everyone!

    MSWorld Talks is now on Facebook.

    You can watch by clicking the following link:

    https://www.facebook.com/MSWorld.Fan.Page/

    Check out our amazing event and please share!
    Last edited by Lolli_pOP; 12-27-2018, 02:03 PM.
    Lolli_pOP
    Creative Center Director
    Content Management Director
    Social Media Administrator
    Tags: None
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    #2
    Originally posted by Lolli_pOP View Post
    Hi Everyone!

    MSWorld Talks is streaming live today on Facebook.

    You can watch by clicking the following link:

    https://www.facebook.com/MSWorld.Fan.Page/

    Don't miss our amazing event and please share!
    Will this be available after the LIVE event?? If so, may I have a link? Thank you!!

    Not officially diagnosed due to non-MS-specific spots on MRIs, but the neurologists all agree it's MS.
    Frustrated. January 2019: finally saw an MS specialist worth seeing. Maybe we'll get to the bottom of this.
    EDSS of 5.5, sometimes 6.0

    Comment

      #3
      You can still watch on Facebook and we will have all videos on MSWorld in the near future.

      Thank you!
      Lisa
      Lolli_pOP
      Creative Center Director
      Content Management Director
      Social Media Administrator

      Comment

        #4
        Originally posted by Lolli_pOP View Post
        You can still watch on Facebook and we will have all videos on MSWorld in the near future.

        Thank you!
        Lisa
        Ok, thanks!

        Not officially diagnosed due to non-MS-specific spots on MRIs, but the neurologists all agree it's MS.
        Frustrated. January 2019: finally saw an MS specialist worth seeing. Maybe we'll get to the bottom of this.
        EDSS of 5.5, sometimes 6.0

        Comment

          #5
          MSWorld Talks is now on Facebook.
          As one of the millions of people who refuse to have Facebook or Twitter or those immoral for-profit corporations collect every word I type, analyze my text and then sell my private data and info to an unknown number of companies without my permission or knowledge, I won't be using MSWorld on Facebook.
          59M / RRMS / Dx1987 / Ocrevus

          Comment

            #6
            Originally posted by Golgotha View Post
            As one of the millions of people who refuse to have Facebook or Twitter or those immoral for-profit corporations collect every word I type, analyze my text and then sell my private data and info to an unknown number of companies without my permission or knowledge, I won't be using MSWorld on Facebook.
            Hello Golgotha ~

            You can view MS World Talks right here on our website.

            Just click on MS World Talks - top of page.

            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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