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I was diagnosed a little under two years ago; At 16. When I was released from my lengthy hospital stays I had appointment after appointment and I’m finally been able to go far in between. See less doctors and it feels so freeing.

Well after a few near breakdowns and a boat load of stress finally been given a solid diagnosis (rrms) last mri shows no signs of activity and also been told I’m going to be starting my Ocrevus treatment in January! Buzzing does not even come close! Today is a good day 🤙🏻

Add a few greens to my diet trying to get off this MS medication about to lift some weights Instead more positive you may not be able to control a lot of things but you can’t control what you think and what comes out of your mouth.

Last month we reached out with an opinion check and asked you if healthcare professionals should discuss progression at diagnosis. While 17% of you said you’d prefer to be told later on, around 75% said yes, you would prefer to be told about progression at diagnosis. In the second of our progressi...

Hi everyone My name is Jenny and I'm a high school student. After seeing two of my teachers struggle with a loss of control after they lost the ability to walk at the age of 27, I decided that I will create an app that will help them with understanding their gait progression. With a team mate, we d...

So I was reading my neurologist report on my last visit and instead of rrms he used the name progressive relapsing ms. So just a question cause Google just makes it harder to make sense of, what exactly is that? And anyone here have that diagnosis?

I recently had an appointment with my neurologist, sadly new lesions have appeared for the first time in years (I knew it would happen at some point but still upsetting to hear). I’m currently on Tysabri which I think neutralised the symptoms of a relapse luckily but has anyone else had a similar ex...