#y - 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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How many of you have been married or together after dignosed?

I’ve Been with my husband 12 years but married for 7. I was just wondering how did everyone else marriage went after being dignosed?

First posted on the Shift.ms app

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Hi how are yall doing? Ok this might sound kinda dumb question but I always get ask what stage of ms is at im like huh? I just no I have ms but no idea about stages or anything like that. I forget everything all the time. I no my neurologist ask me if I have any relapses so I say no thats another thing I have no idea what are they talking about.. yes I have ms for 6_7 years and still no idea what they trying to bask ne if anyone can help would be supernawesome

First posted on the Shift.ms app

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Scarred to do something that would have effect on you finances.

Hello everyone I am very lucky at this present moment with my MS, as it is staple 🤞 I go to the gym each week when I have time in my day, but the one thing that I would like to start doing is running with my wife, as she has just started a few week ago. But, I am scarred to partake, as there was ...

First posted on the Shift.ms app

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I am not getting any thoughts about my situation right now. I cannot comprehend on what’s happening. It’s just scary and frustrating. I am so lost and I feel like no one understands me. I just had another episode of ON nearly after a year. I am just scared. I am an international student in WA and it’s so expensive. The tests and everything. I cannot keep going. I am just so so so lost.

First posted on the Shift.ms app

"Suddenly you realize....."

https://www.facebook.com/share/r/1BYdajAjU9/?mibextid=wwXIfr

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Thank you for having me here. I was diagnosed with MS last year 2024 December. Had brain lesions and tremors and a few other things. Still hoping God would make the diagnosis wrong. Started some treatment. Helped a while then didn't. Changed doctors new meds very caring team but symptoms are becoming more pronounced. Feel sad and down alot. Wonder if I did wrong by seeking better help and why the symptoms are getting more obvious

First posted on the Shift.ms app

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does anyone in England know if having ms will entitle me to free prescriptions. I've been paying for years and nobody told me this was a thing!?

First posted on the Shift.ms app

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Anyone else diagnosed with Spinal MS? I had never heard of it until I was diagnosed a year ago. I have cists from my C1 to C7 of my spine. Causes paralysis on my right side and severe nerve pain that is like seering burning needle like pain in my left. My eyes, hearing and memory has been greatly affected too.

Whittier, United States

First posted on the Shift.ms app

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Is it ms or the meds that make you feel like you have the flu??

First posted on the Shift.ms app

Hello. I'm new to this site but didn't know where else to go. If you are on Medicare and taking Betaseron, what plan D do you have?

Monterey, United States

First posted on the Shift.ms app