#be - Shift.ms

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We are a charity and rely on donations

Charity Number: 1117194 (England and Wales)

Registered Company: 06000961

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

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

©2025 Shift.ms

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Can your balance come back to normal? I can walk a lot better but when I come to stop to stand I feel like I’m swaying forward and backwards

First posted on the Shift.ms app

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

First posted on the Shift.ms app

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Hi everyone! I have been recently diagnosed with RRMS. My nurse has advised that I start a DMT - either Avonex or Plegridy. Is anybody on these or does anybody have any advice on which one I should go for? Thank you in advance

First posted on the Shift.ms app

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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

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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

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It’s my birthday today, MS has been part of my life for 22 years! OMG

First posted on the Shift.ms app

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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

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Hello all how are you all? One thing I’m proud about I’ve done over 3,930 steps today. But question how is everyone in the heat? It’s only been 22 degrees and I can’t cope. Upset stomach feel fatigue ahhh please tell me it’s not just me

First posted on the Shift.ms app

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Hi all, does anyone find being outside in direct sunlight or heat worsens there conditions/symptoms? I used to love being outside in the sun a few years ago but now I find within about half an hour out in the sun my legs are done for!! Not even in shorts or sunbathing?!

, United Kingdom

First posted on the Shift.ms app

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So since my diagnosis I seem to have lost all my friends 😔 not being able to do what I used to sucks, does anyone live in or around west Yorkshire I'm the UK? xx

First posted on the Shift.ms app