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

It's getting harder instead of easier....

I'm Rose. I was diagnosed with M.S. back in 1990, when there weren't a lot of treatment options. My diagnosing neuro had me on a constant low-dose steroid, plus a...

My journey with MS

I've had MS for a long time. December. 2022 will be 22 years. I live a great life. Positive attitude every day. Get up not in a hurry to start...

long wait to see neurologist

I have a new, tentative diagnosis of MS. My neuro-opthalmologist said that I meet criteria and they've found a few active demyelinating lesions on my MRIs that I am currently...

Yeah, Covid AGAIN

I am wondering if others have problems since getting Covid. I have had Covid three times and I am doctoring with a pulmonologist because I have lung issues. Never had...

Need some helpful advice!

Hey! I am not sure if I should be posting as I am not diagnosed with anything, but I am very worried and feel the healthcare system is neglecting me...

Millennials Living with MS

To the millennials living with MS on the site, we want to know: How has MS impacted your life?...

Parents with Multiple Sclerosis

School has started up again for most kids, which means an insane amount of running around, extra-curricular events, organizing breakfasts while getting kids ready for school, trying to get lunches...

HMO or PPO

I have been on a PPO plan for last ten years. This has allowed me to travel out of my small county and see Drs of my choice at the...

Friends/Family

What’s the best way to deal with friends/family thinking that you are just being lazy or making excuses, when you have heat issues and energy issues? I don’t think they...

Ms and mental illnesses

I was wondering if my Ms is causing my add and anxiety to become more intense. Seams to be worse than it was before....

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