Cast your mind back to that moment when you were sitting opposite your doctor and told “it’s multiple sclerosis”. Three words that are nothing short of life changing. When we speak to MSers about their diagnosis appointment, it’s clear that how those three words are delivered, and the care that im...

Suffering from depression due too ms. People are mean and dont understand what i go through, going on dates ends up being ignored, friends turning their backs on me and co worker thinking i am just using my ms as an excuse too not lift heavy😞

From BBC Sounds, for anybody who may want to have a listen https://www.bbc.co.uk/sounds/play/w3ct5xh0

Are you the type of person who wants to know all of the facts about progression as early as possible, or would you rather cross that bridge when you get to it? There can be a lot of disparity surrounding the topic of progression, so let us know your thoughts down below 👇 Sharing your opinions c...

Hi all, it's been a few months since I was last on this site. There is no excuse, no reason but all the same I am still on Kensimpta and the walking hasn't really improved. My memory is still a blur and understanding of others is not always clear. There are options but it is taking the right one kno...

Hi, calling all MSers!! My brother in law is running the London Marathon to raise money for the MS society because of my MS diagnosis. Amazingly the bank he works for is also match funding every donation which is brilliant! If anyone has a spare few pounds and wants to support him to help the MS Soc...

I keep feeling like I need to take a deep breath and yawn. My chest doesn’t hurt. But I just have this strange feeling like I need to do this deep breath all the time. Is this a symptom?? Thanks

What can we eat and what cant we eat i love food im not a big take out person but i have a family who likes homemade fried chicken peppered steak fry ups probably all the things i shouldnt eat we also eat healthy veggies fruit the normal but certain foods wipe me out more

Hi all, Hope you’re all ok. Question.. my MS nurse has asked me to have the puemonococal vaccine before I have my infusion, however has mentioned it’s only advisory and not something mandatory to prevent me having the infusion. Just wondered if some of you have had this, and is it better to do...

Has anyone else had a meningioma found incidentally when having an MRI scan to look for leisons?