Looking for
something specific?

My name is Joe. Been diagnosed with MS since 2000. I’m fatigued all the time and I walk with a cane for balance I used to be a beer delivery driver. I suffer from fatigue and depression. Looking for new friends to talk to about life and how to cope with this disease.

Hi! My name is Cheyenne and I was officially diagnosed 2yrs ago but have had symptoms since 2019. Iv hit my crap gap for my treatment plan (ocrevus) and am struggling a hit to keep up with all the end of year things as a parent of an elementary school aged child, as well as her end of year wrap up w...

wondering if MS or Stormy Weather related, or both?...

Hi, today habe notices symptoms Pins and needles in face , watery eye headache and fatigue . Eyes hurt so blinds are down as hurting my eyes . ( feels like a relapse goimg to happen ) Weather hasnt been So great hear today no sunshine and cold / jumper weather . Has this affected anyone with sudden ...

What works for you with fatigue? I know we are all wildly different & one size does not fit all. But I'd love to hear some options of things to maybe try out. 😊

Ok, so how does everyone deal with their fatigue effectively? I just can't. I still work 30 hours.in care, and that still leaves things needing doing at home. So on m6 days off, I'm washing clothes, hoovering etc. I keep going until I'm worn out which has put me in a constant deficit. I try to slac...

Finally got my results, the MS is stable. I haven’t had any relapses since I started my meds a couple of years ago. However, I still feel terrible. The fatigue, the anxiety and the cog-fog is out of control. My body doesn’t feel right, something is off. I’m currently on a heart monitor to rule out a...

Good Morning All, I have been really struggling lately with feeling unwell daily and battling daily life. I find it really hard to get people to understand and get a lot of comments that are really.. annoying. So I sat and wrote the below. I hope no one minds me sharing it. Sam’s letter to MS...