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

Positive acceptance of this monster

First time posting but have been reading the forums for a while now, so here goes. I was diagnosed in 2015 and it didnt really register and properly kick in...

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...

Decline in walking/standing

Okay while I now have an MS diagnosis from my GP (will see him later), still need the MS Neurologist to confirm this. They tried at first to say it's...

ppms

diagnosed in 1994 at 50 yrs old. On MS meds for about 6-8 yrs. Dealt with recurring loss of balance until 2013. Had CCSVI procedure in 2013 which made a...

Self confidence

Mine has disappeared. There is so much I can no longer do. I CAN walk but that is about it. My cognition is rapidly failing along with my ability to...

Exercise is nearly impossible

The only exercise I get is from walking, and I can't even do that if it's even slightly muggy out. When I sweat, I become dizzy and lightheaded. As soon...

Exercise

I go to the ymca, I go swimming to stretch all my muscles. I also use the hottub for a few minute to help my aching back. Also, I use...

How A Sport Changed My Life

I’m now an avid equestrian (dressage rider), which has given me not just joy, but physical rehabilitation, a social outlet, a purpose, and have goals. After I was diagnosed, I...

Good and Bad Days with MS

What does a good day with MS look like for you? What does a bad day with MS look like for you?...

Happy Thanksgiving!

Living with multiple sclerosis (MS) can present its own set of challenges, but even in the midst of those struggles, there are still things to be thankful for. Take a...

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