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I was diagnosed March 31st, 2025, And I don't know how to get my family to realize I might never be better... I understand that it's only been a few months, the first year of diagnosis is the first, and this is hard on them too. I am blessed to have a family who can assist me and help provide for ...

They didn’t catch a virus. They caught MS. It started with a tingle. Then came the mysterious fatigue no one took seriously. By 28 days in, society hadn’t collapsed but a concerning number of people were falling over for no reason, losing feeling in random limbs, and quietly Googling “why does my e...

First post, new to the "scene" 😅 I've heard lots of stories of people being diagnosed with MS and using language such as "finally being diagnosed" etc.. but i haven't heard a story similar to mine before.. so A) i wanted to share that for those who may have experienced similar. And B) it's wild.. ...

I recently had my MRI results and (as I kinda suspected after a rough few months) had new lesions. I'm currently on Plegridy (moved from Tecfidera as I'm JCV positive and my lymphocytes lowered a lot). Tecfidera worked ok for me, but Plegridy obviously hasn't been as effective. Due to the hard fe...

Hey everyone! I'm kinda brand new here. Just seeing how this is. I haven't yet got an official MS diagnosis, but the MRI scans of my brain shows demyelinating disease.i do have a lot of the symptoms for MS. Im going back to neuro on the 9th.idk just scared of it all. Idk if my wife really quite unde...

So it's been like two to three months so far since I've been diagnosed and throughout that time everything just feels fake, like I don't know how to put it I feel kinda detached kinda like first person Sims basically, here's my question, has anyone else experienced this fakeness feeling and if so, h...

How does everyone cope with having MS? I spend alot of time alone and even though that's been most of my life, it's become alot more difficult to deal with it. When I talk to people about it, I know they are trying to help but at the same time they always seem to kinda brush it off with some simple ...

I'm scheduled to establish with a neurologist in early July, however, right now my feet feel like their always waking up from being asleep. Kinda like ever so light fluttering that feels like they are moving when laying or sitting. Anyone else experience this? What helps?

I have no new lesions on my brain. Yay. Sad update: my brain is apparently smaller than average. In the 26th percentile. Idk if it’s MS related or not. But the amount of brain excercise I am doing now is kinda tiring. I don’t really discuss this last part with anyone. I don’t want people to comm...