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@Sammy33 

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Sammy33

New to MS

Hi everyone. I'm 33 years old and not so long ago I been diagnosed with RRMS. It took me a while to accept it and figured out what's happening with me. Still very new to it, trying to get as much information as possible. Thanks to everyone for sharing their stories, it's really helps.

@MiaPi 

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MiaPi

Copaxone switch to Tecfidera

Hello all, So I have been on Copaxone for 3 years. 1st year all good no relapse or new MRI lesions. Second year I got one new lesion but since it was also small my dr said let’s stay on Copaxone. Now my latest MRI showed one new lesion but at the same time I got lipoatrophy on my thigh from the Cop...

@NicciS 

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NicciS

In need of some positive words!

Hi, feeling fed up. I'm just about to move on to my 4th DMT in 5 years. So far I've done Tecfidera, Gilenya, Aubagio and now on to Ocrevus. Any positive stories anyone can throw at me would be gratefully received right now!

@Aaron_Holden 

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Aaron_Holden

Recent diagnosis

Hello everyone. I just wanted to say hello and maybe get any useful info from anyone who may have had similar experiences. Firstly I want to point out that I am not suffering badly and am well aware that I am more fortunate than many so really don't want any sympathy, just thought my story might be ...

Welcome to Shift.ms

Hello, I'm the Community Intern here at Shift.ms! I'm here to listen to your stories and share them across the site in the hope that they'll be helpful to other MSers. #MSstories Just testing the @ function by tagging @poleyjo :)
Leeds, England, United Kingdom

@Sophietest 

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Sophietest

VOTE for Shift.ms - pls 🙂

Please VOTE for Shift.ms to win ➡️ https://buff.ly/2CcRgUc ⬅️ 'Best non-fiction' at Webfest Berlin. The 'Animated Symptoms' series has been nominated - a series that shows real stories & experiences told by people living with symptoms of MS. You can watch it here: https://www.youtube.com/playli...

@Aimee 

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Aimee

New to the Shift.ms team

Hi! I’m Aimee and I’m new to Shift.ms, I’ve just joined the team as the Community Intern. I’m here to listen to your stories and hopefully share some of them through various media across the site. If you’re up for a chat, please feel free to drop me a message- it would be great to get to know you ...

Lemtrada, covid and MRI

So at the moment I am about 16 months post r2 of lemtrada, and my MRI was due in April, but it has now been postponed until ... further notice... This gave me immense anxiety and I’ve been having panic attacks for over a month now. I don’t know how to deal with this because even though I appear st...

Is my MS progressing?

https://www.youtube.com/watch?v=MM-6kNE4YYw&list=PLVUOB-ZqvZOGuy6t95B67vi5A6nQTY0BS Progression is often the elephant in the room, serving to build fear and trepidation for people who are living with MS. Through investigative conversations that unpick the human side of the topic, ‘Is my MS progres...

@Aiga_Akmentina 

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Aiga_Akmentina

What`s your well-being story

Hi! I<code>m not usually the one to write and ask, but there come moments like this when it</code>s just a natural action. So to the point...I understand your questions, life challenges, your ups, and down days. I`m an MS mom and have the disease for 17 years now. So the first time I met MS as a dia...