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Hi all, I am 22 and was diagnosed with rrms in July after an attack in May. I’ve just started a dmd. Still have some symptoms - fatigue, feeling faint and I overheat quickly. My managers know, but they just don’t get it. My job is so fast-paced and they still think I can do anything and everything...

Hi Everyone I’ve had MS a while now but have recently noticed (probably as I’ve recently been walking slower and with a slight limp and have probably been looking more fatigued than usual) that people, who do know me, talk to me in the same way as they would a child and/or can be very patronising....

Hello. Just wondering what people's experience of fatigue following Ocrevus infusion was? We were planning on trying to take a trip away (in the UK) immediately after the second infusion. Trying to understand if that's advisable given energy levels? Thanks

Hi all, first post. I'm 22 and slogging through the long and troublesome diagnostic process to figure out what's going on. My strong suspicion is MS, but my objective clinical indicators are either barely there or nonexistent ⁠— I have small demyelinated lesions and speckled ANA blood titer, but tha...

Hi guys, please help. I did an MRI today and my result is no active lesions neither enhanced or added. So from November 2019(my last MRI) according to the radiology examination nothing is changed. But in reality I feel so much worse. I used to walk miles on november and now I cant walk even 100 mete...

I apologize in advance for the long post. I know MS is different from Person to person, My ms consists of numbness in my right hand and neurological pain in my abdomen and fatigue and I experience these symptoms on the daily. When I 1st knew something was wrong was my 1st clinical event that happe...

Hiya everyone 🙂 I have a lumber MRI this Thurs and I have been having symptoms again since May 2020. My symptoms started in May 2019 numb feet, pins and needles, ataxia and weakness on left side. I have brain fog, cant concentrate and struggle finding the right words. I was seen in Nov 19 by a ...

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 everybody I hope you are coping well with the lock down. Does anybody have a solution for extreme fatigue ? I am all day on a wheelchair I have SPMS

Calling all aspiring actors! I am casting the third series of a very successful Netflix show. Please do take a look at the brief below and get in touch if you are interested: Roland is in his 40s. Warm, cheeky, sharp, witty. He has MS with mobility and fatigue symptoms. He lives on his own with ...