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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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@garzo68 

Last reply

garzo68

Has anyone tried ivermectin for there ms before I try it ?

First posted on the Shift.ms app
1

@autumnelizabeth 

Last reply

autumnelizabeth

Looking for a friend (:

Hi, I am currently searching for a MS friend(s) who can relate to the challenges and turbulences of being diagnosed in your mid 20’s. Support groups around me are awesome, but tend to have an older population (nothing wrong with it, just want to find my community too). Perks if you live in NorCal an...
First posted on the Shift.ms app
2

@MarrzRob 

Last reply

MarrzRob

Yup

MS sucks
First posted on the Shift.ms app
4

@mightykae 

EditedLast reply

mightykae

Walkin' to feel better.

Ok, so thanks to my pre-ms weak self I dontbhave a ton of muscle mass. And now apparently, on top of MS, and potential POTS, i am at risk for the diabetes. So, inspired by my mom ive started walking at local parks with a goal of hitting a mile a few times a week on good days. I do use a cane here an...
Millcreek, United States
First posted on the Shift.ms app
1

@Garytrente 

Last reply

Garytrente

Virus effect

Hello, recently I got a virus for about a week. I’m fine now but I feel my MS Progress after the virus. Does anyone know if a virus can cause an increase in MS symptoms.
First posted on the Shift.ms app
26

@Mrsjenks78 

Last reply

Mrsjenks78

MRI Results

Finally got my results, the MS is stable. I haven’t had any relapses since I started my meds a couple of years ago. However, I still feel terrible. The fatigue, the anxiety and the cog-fog is out of control. My body doesn’t feel right, something is off. I’m currently on a heart monitor to rule out a...
First posted on the Shift.ms app
4

@Spiderhack 

Last reply

Spiderhack

Normal medication

Hello fellow MS people I am currently on DImethyl fumarate (Tecfidera) and whilst it’s done its job as far as I am aware. Are there any other natural Meds people recommend and if so where you get them from ? I am in the UK I appreciate exercise is a great one which I do but sometimes I am too tir...
First posted on the Shift.ms app
4

@lailai93 

Last reply

lailai93

Has anyone ms had little affect to there lives? I’m just been dignosed but they think I had an attack in 2018 just before I found out I was pregnant

First posted on the Shift.ms app
17

@Carlos 

Last reply

Carlos

Hi I have rrms but latley I seem to be having more episides than usual , I am pretty used with tingling down one leg and regular pain in my sides which I believe is somthing called the ms hug which is reall annoying, but latley I have been experiencing servere pain in my lower jaw and teeth which happen when I touch a certain part of my bottom lip, even licking my lip can set it of, a few days ago it got scary when I was unable to talk due to the pain when simply trying to speak, I am currently on copaxone, this is the first time I have spoke about my ms on a forum apart from speaking to my long suffering partner ( who has to endure my whinging ) I just would like to know if anyone else has this sort of pain and any advice on how to deal with it . Thanks David

First posted on the Shift.ms app
3

@Sophieee 

Last reply

Sophieee

A relapse query

Hello! I’m sophs, I am 19 years old! And have been suffering with RRMS since I was 14. I was diagnosed with MS 2 years ago after I went blind in my left eye. In 2020 I was screwed over by Covid, i suffered my first relapse, I was 14 during this time. I selfishly went paralysed in my right hand. Whe...
First posted on the Shift.ms app
4
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