#think - Shift.ms

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I think might be having a flare not sure

So I was diagnosed on May 28 had a 5 day steroid treatment and I'm currently on dimethyl fumarate. I was out late last night had me two beers and barely got any sleep so I'm wondering did I push my body or are this side affects from the meds. Started the meds about 4 days ago and took one last nig...

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Whenever I go to big events like concerts, football games, church, etc… I ask myself “I wonder who here has MS too!?” Anyone else ever think that way?

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Found this MS cure being studied using micro particles not sure what to think of it?

https://www.hopkinsmedicine.org/news/articles/2024/02/tipping-the-balance-in-ms#:~:text=Although%20there%20currently%20is%20no,MS%2Dlike%20symptoms%20in%20mice.

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Q- I was thinking about smoking hash through a vape rather then smoking. I don’t smoke but it’s meant to relax me due to anxiety and help me relax before bed. What are you this?

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Anyone from Virginia USA thinking about relocating back home any good neurologist

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I know it's time to quit working and focus on my health, however, no one understands and thinks I'm giving up. I dont feel as though that I have a good support from my partner or family. How do I do this alone?

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Do anyone take Teriflunomide ? If so what you think about it ?

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Hello everyone 😊. A little about myself. I was diagnosed with MS (after experiencing a few different symptoms (🤔maybe in a period of 3 months or so 🤷🏼‍♀️). This happened November 2008 at the age of 30. After being discharged from the hospital, I went to see a neurologist who started me on daily injections. I don’t recall too much, however I remember the Dr telling me newly diagnosed patients will have a relapse in about 2 years. I was on injections (which injections 🤷🏼‍♀️) less than a year (due to insurance). About 2-3 years later, I again have insurance. I recall hearing anything you take or do to yourself can trigger your “MS”. So because of that, I refused to be back on meds/injections. My way of thinking (maybe not the healthiest) was “It’s been close to 4 years and I haven’t had a relapse or suffered from it. Fast forward ➡️, almost 16 years later I have never experienced anything to do with MS since the time I was diagnosed. I’ve doubted (and still do) of my diagnostic was correct. A few years ago I had some tests done on me and according to Dr- I still show cloudy patches bla bla bla. I’m very thankful and blessed with myself but I’ve also wished and prayed MS didn’t exist. I wish everyone the best, NEVER lose hope or faith and always be thankful you don’t have it worse 🥰.

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Newly diagnosed, I've had a lot of these symptoms going on for 3 years. Was made to think I was crazy. Well last week they thought I had a stroke. Did an MRI and found out that I have a so my journey is just starting

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I have had ms for half my life this year, and I still don’t get why there are so many people who have it and think they’re a warrior?! (esp females, sorry ladies no offence intended)yeah it’s life ruining and all that, but not once have I seen someone with a similar disease, or even worse someone with one even more brutal insist on being a Warrior, be quite then, you shear actual warriors constantgo on about their symptoms and how much they are being a warrior pls stop thinking we have this status and accept that this is not the right word I beg all of you to please tell me this get on someone else’s boobs in here who feels like I do ????

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