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Hi! I’m Kathy Reagan Young, founder of FUMSnow.com and the FUMS Podcast Show. I’m interested in interviewing English-speaking MS’ers from several different countries about your diagnosis and treatment experiences in your country. I think it will be really interesting to see the difference in care...

I've decided that I am going to to get involved with the whole blogging and Twitter thing and finally get out of my head the things that I would like to say to my MS if it were a person. Thinking about this, it has become clear that everything that I would want to say basically fits under the title ...

When my #MS says "No" today... fishtank cleaned happily. #FUMS ➽ Thoon & Katia - My Goldfish 🐠 Simple yet keeping me happy → https://rebrand.ly/Thoon ← #Goldfish #Aquarium #Pet

I'm just sharing some thoughts here and I'm curious about other people's opinions! So, we may all know that Christina Applegate did a red carpet in the past couple days with a cane that had "FUMS" all over it. Which I respect but it's not for me. The "MSWarrior/Fighter" and the " FUMS" mentality isn...

I used to play quite badly i must admit lol https://www.youtube.com/channel/UCGvb6zzPd7SqWLeY2wPtxSw trying to learn all over again purely to shove fingers up to the MS FUMS

Hey guys, I am just curious: what are you going to plan on world ms day on 31th of may? Are there any cool meet ups or activities you're joining? Hence I live in Germany, I will meet up with my F.U.MS group. I guess we will go out for food, drinks and fun – as usual :) Cheers, Tina

End of Year 1 MRI - First review results are in. It's bloody awesome news !!!!! NO progression No new lesions Existing damage less conspicuous I swore from the start I would kick this shitty illness in the nuts and teach it who was in charge of my immune system. At half time I'm winning and it'...

I started getting random dizzy spells about 2 months ago after i got a cold, just feels like the room is spinning. They are now more frequent and aggressive. I'm struggling at work to not fall, it's getting increasingly more difficult to read. I'm so over this.

Hi, I just wanted to make an introduction post. My names Allina, I was diagnosed with rrms at the end of September in 2022, right before I turned 18. I've been on treatment for roughly a year now, trying to slow the fast progression I was having. I'm a mother of two beautiful babies, a nursing stude...