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I'm sure a few of you have now heard this name. Has she invited you to be a friend, whilst mentioning you in an update suggesting love? I've got my eye on her and I'm watching her activities....... You have been warned. :evil:

Every last Thursday of each month, MS society book club comes together for an hour to discuss a short story. Hosted by myself (Laura) and Lynda. We both have MS and the book club is aimed at people in the UK with MS. It is an opportunity to contact via books and discussion with other people with MS ...

A big thank you to Jackie, and EVERY donor who’s supported Shift.ms’s appeal so far! The total is now sitting at over £73,000 out of our £100,000 target 🤯 We’re shouting-out, high-fiving and celebrating all of our donors below ⬇️. Your donations will help transform the experience of MSers seeki...

Hi! I’m I’m Lindah from Sweden. I’m new here so haven’t really figured out what this is all about.

Every last week Thursday of each month, our book club comes together for an hour to discuss a short story. Books are picked from The Reading Agency's Quick Reads selection so are very reasonably priced. Hosted by our wellbeing volunteers, Linda and myself (Laura). We both have MS and the book club i...

Life & Times of an MS Sufferer….. By Roger Deuxmont · March 31, 2019 Life & Times of an MS Sufferer….. These pages are dedicated to the following people, my father Leslie 1911-1980, my father was an indirect casualty of the smoking lobby, succumbing to the effects of lung cancer at the ag...

Hi everyone my name is rick f. I've had ms rm since 2014. My neourologist is highly qualified at Lima Linda ca. Usa. I've done ok for the most part. On my 2nd ms med tecfedera 2. Years now. Had steroid treatment 2 years Ago for eye vision fine. My left hand. Been numb since I was diagnosed 3.5 yrs...

Hi I'm Linda McIntyre. I'm newly diagnosed in March and would like to know if there's any one on here from miramichi.

Hello, my name is Linda and I'm new to this forum, so please excuse me if I don't work it right. I have mild MS and am on a fairly mild 5000IU of Vitamin D daily. Also trying to do yoga, but it gets harder to balance each time I try. Then someone suggested to do laser therapy (course he has a vest...

Hi, I am confused whether or not my symptoms are of MS or Parkinsons Disease. My Neurologiest is not being helpful. He sent me to every medical profession the ends in a "ist" for months. Im getting tired of his avoidance, I would like to compare similarities with one that had/has the same. If you s...