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Having issues with drop foot..I've had to use a walker for stability and strenth..getting a brace for my left leg...and an Orthodontics...I'm having a hard time accepting this next stage...I've always been very strong and have gone through alot..but for some reason this is really bothering me...caus...

Losing my balance is the worst when it happens. I try to stay home and mind my business. Ocrevus has helped a lot.

I was wondering if anyone here has started on HRT in their mid 40s and found it helped with MS symptoms at all, along with other things (please feel free to share 'other things' if you are comfortable as I have read HRT can help with issues such as loss of libido and with pain and dryness you-know-w...

Hi I hope everyone is well, I have a random question, does anyone know if it is safe to use an electric sander?

I was diagnosed in 2005. I have relapsing remitting MS. I was in and out of the hospital quite frequently the first 3 to 5 years maybe. Have brain, neck and spine lesions. I am currently on a Aubagio and have been for the past 5 years. I have my ups and downs since my diagnosis. Just reaching out to...

Savvy Cooperative is looking for people who have been diagnosed with relapsing-remitting multiple sclerosis (RRMS) for a Paid Online Interview-US only DETAILS 1-hour virtual interview REQUIREMENTS Diagnosed with relapsing-remitting multiple sclerosis US residents 18+ $110 USD Total Compensati...

Share Your Experience with Relapsing-Remitting Multiple Sclerosis Savvy Cooperative is looking for people who have been diagnosed with relapsing-remitting multiple sclerosis (RRMS) DETAILS 1-hour virtual interview REQUIREMENTS Diagnosed with relapsing-remitting multiple sclerosis US residents ...

Share Your Experience with Relapsing-Remitting Multiple Sclerosis Savvy Cooperative is looking for people who have been diagnosed with relapsing-remitting multiple sclerosis (RRMS) DETAILS 1-hour virtual interview REQUIREMENTS Diagnosed with relapsing-remitting multiple sclerosis US residents ...

I was diagnosed with Relapsing Remitting MS in 2004. I am only taking Betmiga for my bladder control. I suffer with foot drop, poor balance, terrible fatigue, memory problems, vision issues, cognitive problems, dizziness. I feel like I have been forgotten! I’m due to see the MS nurse in April, so...

I've just been diagnosed with relapsing remitting ms, so far I'm doing oka, ice been accepted for limiting capability what else am I best of applying for x