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Read conversations, start a discussion, and connect with others about multiple sclerosis.

So much for family support

Living with for 20+ years and when you say you can't do something due to fatigue taking all ur energy and ur an emotional wreck and they say oh wise...

Losing independence

I’m 47 yo and was diagnosed 14 years ago. I was in grad school and finished my Master’s (MS, haha). I was an elite swimmer since I was a kid...

Mental Health and MS

How has your MS impacted your mental health? Do you ever experience anxiety, depression, or catastrophizing? What has helped you cope with it all?...

loneliness, isolation

All of us strongly disabled are affected personally, including 73-year-old me. I detect no discussions here dealing with psychic crises. All I hear is "Get help" yet neither society nor...

Managing fatigue

My fatigue is getting worse. I don’t know what else to do. I’ve talked to my neurologist couple times she doesn’t feel it’s related to my MS, which I don’t...

Hitting a Wall with Fatigue…😔

I was spinning all the plates, feeling ahead, and then I crashed. Beginning the uphill climb back to functioning, which is at least a few days. Hoping to return on...

Employment for ms patients

I’m reaching out for my wife who has ms. She’s fully functioning but is having a difficult time finding employment. My question is, is there resources available to her to...

single demyelination

I had one lesion that left right side of me numb and left side of front face. The doctors said I had single demyelination, which is going on 6 years...

Disability Drama

Hi everyone! I'm Jen...diagnosed with MS 11/2019. I just turned 50 last month. Last November I experienced Shingles (for the first, and hopefully last time) along with Meningitis at the...

Who has utilized stem cell?

Stem cell work has come a long way. Looking for your experience with it. Plus, on a different aspect of this type of procedure, does it in any way affect...

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