Has anybody ever heard of, or tried “ProdromeGlia Plasmalogen Supplement”? Literature looks interesting, but so can my resume-haha!

So I get looks everywhere I go due to me using a mobility scooter sometimes when I go places that require long distance walks or a lot of standing. MS makes it hard enough but add Lupus and POTS to it and omg Im over the judgment of people who don't even know me or what I go through everyday....it's...

I had a breakdown this morning hysterical crying. I had a fall last night getting off my electric recliner didn’t feel right and I lost my balance and fell on the floor and now I can’t get up on my own so I’ll call the ambulance. in the last couple of weeks that has been happening a lot falling one ...

I feel really weird at the minute, think I am in denial or something but my recent diagnosis doesn't feel real. I get the random numbness and tingles but I still make excuses and blame it on sitting too long or my circulation being bad. I know it isnt that but its like my brain won't allow me to sa...

Things seem to be getting worse, maybe? Yesterday I had to use a power scooter when I was shopping. I have a cane now. Two weeks ago I ended up in a wheelchair. I can’t keep up with my home. My husband is in the NVARNG (Army NG) and keeps getting activated for weeks at a time for these awful wildfi...

What are some of your favorite Videos online to follow to get exercise? I regularly have Gretchen Hawley or the MS gym on but wanted to see what everyone else uses as well

Hi all. Have started cladribine cycle 1 week 1 - just took one dose yesterday and within a few hrs- nausea +++ and abdominal pain. Also, feel so exhausted. Please tell me it gets better soon. Feel miserable 😞

Good morning, I had my first dose of Kesimpta yesterday. The nurse came to my house and showed me how to do it, she was lovely and it was easier than expected. Last night was awful, headaches like I’ve never had before, chills, nausea, weakness, just feeling generally unwell, and I’m pretty sure I s...

A little while ago I threw an idea out on here. What if there was something where people with MS could just talk honestly about what living with MS is actually like? Not doctors. Not neurologists. Not someone reading a leaflet explaining fatigue to people who've been fucking exhausted since Tues...

What are good meals that everyone makes to not over work your body.?