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

How do you react when friends and family compare MS to other health conditions?

What works for prickly sensation and numbness relief?

I am 62 and diagnosed one year ago. Taken Copaxon for 8 mos. I was very active and exercised on regular basis. I have numbness and prickly sensation in palms...

When will I EVER get an answer!?

Progressively over the past 18 months, I have been losing fine motor skills. Have had horrible aching, sharp pain and loss of sensation in my fingers. I can't preform the...

Does anyone else get frustrated at people thinking we have Myalgic Encephalomyelitis (ME)?

When I say MS, people I think don't realize MS is very different from ME (Myalgic Encephalomyelitis, commonly known as Chronic Fatigue Syndrome, or CFS). They treat me like I...

Flexible Jobs for Chronic Conditions

Here is an episode of the FUMS Podcast Show that deals specifically with finding flexible employment opportunities that work well with our ever-changing disease burdens! http://fumsnow.com/fums-023-flexible-jobs-for-chronic-conditions-with-brie-reynolds. At the end, they...

Has anyone else become disinterested in things that used to be exciting?

No excitement no nothing. I'm wondering if there is anyone out there who has experienced an absolute disinterest in about nearly everything that used to be exciting to them?...

Has anyone else lost 'connection' with the left side of their body?

I seem to have mentally 'lost' the left side of my body. It still works fine, but I favour my right leg and lean to the right. Mentally if I...

Can anyone help me?

I've never been diagnosed. I've been looking for answers for two months now. Some of my symptoms I've had for over five years I just learned to live with. I...

Does anyone deal with MS sweats?

Aging with MS

I am 67 years old and I have relapsing/remitting MS. I've had MS for 25 years. I feel very fortunate not to have progressive MS at this point. As I...

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