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Are you taking Cladribine for your MS. Turns out it is pretty decent stuff! - Another example of why we need everyone with MS to sign up to the UK MS Register. - https://ukmsregister.org/ - "Over half of MS patients analysed did not relapse or experience disability progression during 60 months of f...

I am wondering if anyone has seen either a geneticist or immunologist in the context of your MS. My brother is encouraging me to go, and he is also encouraging me to eat a keto diet. He doesn't quite articulate what he thinks these other doctors can do for me. My brother reads a lot of books about h...

Hi everyone, I am abit frustrated.. I can not find what l am looking for in any MS related sites. Do i have to have a relapse to get steroid injection in other words can i have steroids to dampen down the symptoms I have been experiencing? Thanks

Hey everyone, So since a relapse in Jan I started to get random muscle twitches anywhere, they didn't last long, say minutes. I do however get some that are lasting longer. The one today is twitching a fair sized area in my outer quad and it's...... um, getting me down. Is there a way to stop it ...

Hi all, I wondered if anyone could help answer some questions/give their experience.... I was diagnosed in May this year with rapid RRMS following loss of sensation/power in right leg/Side in December 19 and then optic neuritis in April 20. First MRI was in March 20. I was originally told I would r...

Hello everyone. A friend sent me this article. Early days of course, but hope springs eternal. I've ordered a bag of apples to my weekly delivery in case it comes true. Fingers crossed. Jon https://www.sciencedaily.com/releases2020/04/200406190436.htm (just in case this link doesn't work, it'...

What do we know about MS and menopause? How do symptoms change, Is there an increased risks of getting a relapse? How do the disability level change? Thanks ladies and sorry gents.

Hey there... New to this... I’m wanting to hear feed back from folks who have opted out of DMT... I was diagnosed 7 months after my son was born in 2010. I am currently having my 3rd relapse, though this one has required a 3 day dose of solumedrol. I completely changed my lifestyle after diagnosis, ...

Dear All, Hope you are all safe and remaining healthy in this lock down, I have a very strait forward question. Is there a period of time for a relapse to form or strike in other words, how long does it take for a relapse to occur? Three years later after having my first relapse, I started having...

Hi, I have rrms, diagnosed in 2010, symptoms since 2007. I started copaxone in 2018, had MRI new lesions. So started tecfidera in February this year. I just wondered as i have not been on dmds for 8 years after being diagnosed. Whether the dmds would be less effective going forward, I know t...