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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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Sort 1633 results by
Recent activityNewest posts

@HarryH 

Last reply

HarryH

Part of a research trial for Teriflunomide, has anyone heard of this or been on it?

First posted on the Shift.ms app
3

@eficaribe70 

Last reply

eficaribe70

Question: Why there is not enough research, trials, opportunities options and Medication (DMTs) for PPMS? I know the PPMS is not as high as RRMS but everything is focus to RRMS. Eileen Figueroa Houston TX

First posted on the Shift.ms app
7

@Cojabri 

Cojabri

9 month Ocrevus?

At my last appointment with my neurologist she changed my Ocrevus infusions to every 9 months instead of every 6 months due to research indicating there is no difference in disease progression/lesions with the longer gap. Is anyone else on a 9-month infusion cycle?
First posted on the Shift.ms app

@watsoncraig 

watsoncraig

Research

https://multiplesclerosisnewstoday.com/news-posts/2025/06/25/3-progressive-ms-patients-see-lowered-disability-car-t-cell-therapy/
First posted on the Shift.ms app

@MarnieV 

Last reply

MarnieV

My doctor said if I didn't have any new lesions after my mri I could stop taking the Copaxone injection and take a pill. Does anyone know what pill that would be? Want to do some research before I get it. Oh yeah and there were NO NEW LESIONS!!!! After 15 years of injections I need a break

First posted on the Shift.ms app
9

@sharons 

Last reply

sharons

I've just been diagnosed even though I've been attending the MS clinic for a few years. My neurologist has suggested I research dmt on the ms website and look at the various treatments. Any advice on DMT?

First posted on the Shift.ms app
10

@RC83 

Last reply

RC83

What charities do you support?

Ive just started donating to Shift. This post is not to push others to do so - its optional. I went for just £1 per month to start with as there are 74,304 members here and if we all donated that it would total £1,114,560 per year inc. gift aid. Bargain compared to YouTube at £12.99/m. Many thanks t...
First posted on the Shift.ms app
22

@Sara05 

Last reply

Sara05

Has anyone got Arthritis and Ms?

Currently waiting on an appointment. Id put my stiffness & pain down to walking different with Ms but after some research its sound more like Arthritis on top
First posted on the Shift.ms app
2

@Phillip101 

Last reply

Phillip101

Don’t know what to do.

I joined this sight not to whine and complain about my symptoms. But unfortunately to find others that have similar stories and yes support from complete strangers. And you all can’t imagine the support that I have felt through throughout your replies and messages. It doesn’t seem real that so many...
First posted on the Shift.ms app
5

@MarieDate 

Last reply

MarieDate

Shift.MS Discovery?

What led you all here to Shift.MS? A friend whose daughter had just been diagnosed with MS happened to mention how she had a buddy through Shift.MS. Curiousity got the better of me and I researched Shift.MS 🙂The rest, as they say, is history. Did your MS nurse recommend the site? or perhaps yo...
First posted on the Shift.ms app
7
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