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Ok so I don't know how you're dr. Explained what MS you have but mine all he did was tell me that my white blood seals ( amunsistam ) is attacking my body and I do apologize for the bad spelling I was told spell it like it sounds. So any way my question is how do some of you cope me I smoke weed to ...

Hello, I’m new here. I’m Susana, I was diagnosed in June 2024. During the last months I’ve been medicated to anxiety and, of course, having therapy. But, even I have support from my family, it’s a very lonely road where sometimes I’m ok, or even happy, and other times I just want cry and give up. I’...

In a world that spins a tad too fast, Where MS folks must break the cast, A funny poem to share the light, On how they live, both day and night. Awake at dawn with body guessing, “What today? A curse or blessing?” Coffee spills, a tremor’s greeting, Socks mismatched, but heart still bea...

I'm a brand new member here, and even if I end up not having MS I feel the most seen by Ms patients because of my symptoms so hopefully you all can give me wisdom. My whole life I have known there was something physically off about me. I couldn't do activities other kids could, random pains no one...

I feel my brain and body shaking. I see my whole body being in a tremor phase, I find it weird to do anything, my hands are shaking and I need to apply too much pressure to hold something like a fork and when I have to walk like stomp my feet... And my voices breaks , I can't find the words to say w...

I haven't been cold or flu sick in years. Wiping noses and catching my sick cubs puke. Nothing. I'm probably late in discovering this but I feel like fat serves as the canvas for germs and bacteria to stick to in your body. Vegan again, and staying that way (logic and common sense reasoning), but i...

I started intermittent fasting a few months after my diagnosis,my diet switched to heavy on the veggies,and i run away from any stressfull people and situations ,i work out and keep a positive outlook,at this point no one even beleives i have m.s,i do not know if everyones outlook is the same ,a bit...

I've been swimming down that river called denial. I was diagnosed in March. And not coping very well. Only my boss and a work bestie knows of my diagnosis. My family don't check in on me since they were told, my two friends i do have don't even ask about it anymore. My partner doesn't seem to a...

Hi brothers an sisters in MS 🤗 Yesterday an amazing things happened. I had more than 13000 steps, and I wasn't tired so much 😯 Last time when I could do that long distance was 3 years ago! So these steps are very important for me, the are the proof of my work,with my mind and body.🥺 Never give up...

Hey everyone, I have a question. I'm being forced to retire because of this disease. My walking isn't getting better, and it's really hard to do my job. I'm a technician in the aerospace sector. My question is, I'm 39 and have been doing this kind of work for almost 20 years. Has anyone had to chang...