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Charity Number: 1117194 (England and Wales)

Registered Company: 06000961

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Shift.ms, Platform, New Station Street, LS1 4JB, United Kingdom

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Shift.ms, Somerset House, Strand, West Goods Entrance, London WC2R 1LA, United Kingdom

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@Stumbler 

Last reply

Stumbler

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:
4

@jumpingJacks 

EditedLast reply

jumpingJacks

28 Days Later, 28 Years Later: The MS Edition

They didn’t catch a virus. They caught MS. It started with a tingle. Then came the mysterious fatigue no one took seriously. By 28 days in, society hadn’t collapsed but a concerning number of people were falling over for no reason, losing feeling in random limbs, and quietly Googling “why does my e...
First posted on the Shift.ms app
19

@Linda1983 

Last reply

Linda1983

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.
  • Diagnosis
  • Newly diagnosed
10

@Gwenny 

Last reply

Gwenny

Possible scammer???

I received a Friendship request about 1 1/2hrs ago, from someone with a name that runs in my Family, but on accepting that request, I then received an e-mail with very dubious wording. I have now deleted that Friendship, as well as the email. The friendship request was for a John Miller, but the e-m...
  • Work and play
  • Family and children
9

@RickF 

Last reply

RickF

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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8

@wellbelle 

EditedLast reply

wellbelle

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 ...
  • Work and play
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  • Symptoms
8

@Lindaetob 

Last reply

Lindaetob

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...
  • Healthy living
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  • Balance
  • Treatment
  • Unlicensed
7

@burninglegsalso 

Last reply

burninglegsalso

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...
  • Symptoms
  • Fatigue
4

@lindhsie 

Last reply

lindhsie

HSCT

Hi! I’m I’m Lindah from Sweden. I’m new here so haven’t really figured out what this is all about.
  • Diagnosis
  • Treatment
  • Symptoms
4

@Xristov11 

Last reply

Xristov11

THE MS THERAPY CENTRES UK & IRE

A BACKGROUND TO THE MULTIPLE SCLEROSIS (MS) THERAPY CENTRES OF THE UK AND THE REPUBLIC OF IRELAND Christopher Fox-Walker BA(Hons) There are 65 hyperbaric facilities in the British Isles owned and operated by patients to provide treatment for multiple sclerosis. There a...
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3
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