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Hello everyone. I just wanted to say hello and maybe get any useful info from anyone who may have had similar experiences. Firstly I want to point out that I am not suffering badly and am well aware that I am more fortunate than many so really don't want any sympathy, just thought my story might be ...

https://www.youtube.com/watch?v=mzaidLfVgSY&feature=youtu.be The world 🌍 of health is adapting to an entirely new way of operating, including switching to digital delivery of care and telemedicine. But what does this mean practically for people with MS? 🤔💭 In episode 1 of this miniseries, we’re ...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

I was diagnosed about 9 months ago. I recently started coming to terms with my diagnosis, though most times i try to ignore it, it somehow stick its head in my business.

started one month ago and having some stomach/digestive issues. Posted list of side effects says this should pass in two weeks. Not my experience and asking others if they’ve experienced anything similar. thanks

Hello, was diagnosed in March after two surgeries. I’m learning everyday of what my body can do and cannot. Each day a lil different. My one leg does not follow”directions “ and quite often “drags” . Wondering if any body can suggest a brand or o line of shoes, that might help. Thank you

<p>Hi 👋 I completed my first round of Mavenclad in February of this year and received my letter from the Government asking me to “Shield” for 12 weeks in March, due to the risk of possible complications from COVID-19. At that time my lymphocytes were 0.8. Does anyone know what lymphocyte level we a...</p>

I'm going for a spinal tap in 6 weeks or so, been doing some reading about the procedure and after care, what has been anyone's experience after having one done. Seems to be alot of complain g of back pain and headache

Can someone please elaborate what are some of the early signs and symptoms of the disease? How do I approach the subject with my physician?

Hi all. Does anyone have any experiences of taking Amantadine for MS fatigue. I am currently taking modafinil x 2 100g first thing each day but still suffer from chronic fatigue in the afternoons. MS Nurse has recommended switching to Amantadine. I’m happy to switch but reluctant to give up moda...