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Hello MS team! I am an actor writing a play which includes my experiences as an MS warrior. I wanted to know if anyone here has MS counselling experience or can recommend? I would love to have a chat with them by way of researching other perspectives of MS, rather than just my own. I'd also be ...

Hi. I have been searching for information on how MS looks in menopause. I mean for anyone who has/is with experience of this stage of life, can I just say it is difficult. I am finding it hard to pull apart what is symptom of MS vs menopause. I mean cog fog, fatigue, moods, joint pain, dizzines...

Hi! I<code>m not usually the one to write and ask, but there come moments like this when it</code>s just a natural action. So to the point...I understand your questions, life challenges, your ups, and down days. I`m an MS mom and have the disease for 17 years now. So the first time I met MS as a dia...

I have a conflict of interest to declare: I am on the UK MS Register committee. - The MS Register here struggles to get more sign-ups. Everything you share is to further the cause of MS research. Your data is secured properly and never ever shared, outside of the anonymised research data. - The Fre...

Hi anyone, I’m doing some research on folding electric wheelchairs. Ideally prefer if able to use both indoor &amp; outdoor, on grass for example. What’s people’s experience, Colette

Good short post and a film featuring several Shift.ms ers. https://multiple-sclerosis-research.org/2020/06/the-human-side-of-ms-and-research-a-short-film/ @longboat

He says, "I am interested to know if any of you who have COVID-19 are suffering from a persistent loss of smell and taste and how has it affected your life? Please let us know if smell training makes a difference." - Here is the full post: https://multiple-sclerosis-research.org/2020/06/mscovid19-lo...

Can someone help me? I’ve searched the web and all the MS sites and can’t find the answer. I would like to hear from someone who has symptoms daily that come and go. Like everyday. For instance I permanently have numb feet but sometimes in the day it travels up to my knees then goes away back to jus...

How much of your immune system do you think is not suppressed? If you know about some research or info I'd love to read. Perhaps 20-40% I'd guess is active seeing as treatment is labeled as causing a low immune system.

Hi all, Seeking advice. Has anyone been taken off Tecfidera due to developing lymphopenia? If so, which DMT did you try next, and did your lymphocyte count remain stable with your next choice of treatment for RRMS? Anyone had the same adverse effect happening repeatedly despite trying differ...