Shift.ms

15 Jan 2013 19:22Last reply 15 Jan 2013 20:36

Linda111

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:

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@wellbelle

1 Nov 2023 22:49 EditedLast reply 2 Nov 2023 12:06

MS society Livingwell Virtual Book Club

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 ...

8

@EleanorAdmin

2 Nov 2023 11:49

One tap connection appeal - Supporter shout-outs!🥰🫵

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...

@lindhsie

13 Nov 2022 09:22Last reply 18 Sep 2023 13:57

HSCT

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

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@wellbelle

10 Sep 2023 12:18

MS society Livingwell Virtual Book Club

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...

London, United Kingdom

@monty1952

12 Oct 2019 05:11

Life and Times of an MS., Sufferer.

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...

@RickF

11 Mar 2018 04:23Last reply 6 Jul 2018 06:41

Lyrica 911 be aware everyone!!!!!!!!!!!

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...

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@Linda1983

20 Oct 2017 00:15Last reply 2 Apr 2018 00:16

New to all of this

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.

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@Lindaetob

6 Jun 2017 10:47Last reply 12 Jun 2017 07:30

Laser Therapy?

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...

7

@burninglegsalso

5 Apr 2017 14:35Last reply 6 Apr 2017 15:55

ms?

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...

3

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