Looking for
something specific?

Hi, first time I have posted but am having tough day. Am 50 but don’t like to think I look it or feel it, in my head at least. Diagnosed rrms in Jan this year (2020). It was actually good to have reason for so many things gone wrong with my health over many years. Am generally not too bad, bladder ...

Hi, I'm Mammy to two wonderful little men, the youngest being 5.5 months. I was due to go back on Gilenya sooner but as I'm sure is the case for so many, restart was delayed because of Covid. I'm due to go back on in over 2 weeks but can't get my little one to take a bottle. I've tried different ...

I used to have really bad childhood tremors until the age of about 10, to the extent that I used to be laughed at by the other kids. They'd get worse if I had to do anything stressful: speak in assembly, climb up wall bars etc. Anyway, nearly 40 years on and I looked up the possible causes. Yep! Y...

From positive and active days to a day like this...more slow and feeling tired of everything. Sometimes I`m thinking and trying to understand is it just the case of MS. I somehow start to see correlations between my slow days and days where I feel active and positive! I have read and heard that foo...

During the lockdown I've been binge watching House. They mention MS as a possible diagnosis every other episode, but I'm half way through season 5 and I still haven't seen an actual case... I feel discriminated!

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...

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'...

You may have seen that Mike, Gemma and Zoe have been working through some ideas about building mental resilience with Neuropsychologist Jo Johnson… here’s the playlist in case you’ve missed the videos: https://www.youtube.com/playlist?list=PLm0sRroMtds267oPVxXSAR6bJEZ_Vr__f There are new episodes...

Long story..had mri Feb 2 non specific liasions on my brain and 2 non specific liasions on spine. My left leg and foot numb since Jan. My right leg and foot and my right toes numb last 4 weeks..so my mobilty gradually deteriorating last 14months..dreadful burning night pain in legs and feet burning ...

Hi all, I am supposed to be moving to Ocrevus soon. I have 1.44 JSV antibodies and the docs here are scared that I will get PML. My 2 years on Natalizumab (Tysabri) is up on 2 Oct 2020 and they want me off Natalizumab really soon. My problem is that I am allergic to many medicines and had 5 weeks...