Busy trying to find a flat to buy so have been foot slogging as best I can around various Leeds suburbs. At the end of the day I found myself actually flexing my toes when “walking” and moving more fluidly, exercise seems of benefit RE the MS, even managed to stand with my crutches off…

I am in a state of confusion right now over dmt’s. I have quit Copaxone, it didn’t seem to be effective anymore and i couldn’t do the shots every day and had a couple of those scary reactions that make you feel like you are having a heart attack. My neuro has suggested Mavenclad…

Hello, name is Anne, have had MS since xmastime 2013 Merry Xmas to me hey! My profile pic is from NYE this year, it’s the best i have looked all year. I am in the process of stopping Copaxone because it doesn’t seem to be doing anything good for me. I am tired of the painful needles and…

Hi, I just wondered how long people have waited to see a Ms consultant and for there medication, I’ve been told I can be waiting months and already been 3mths as I’ve opt for Cladribine and only the consultant can sign it off and there’s a long waiting list.

After waiting over a month for results, hot a cll today from ms nurse, asking how I was, and that the results showed significant changes to mri and to go to the clinic as they need to change my meds, I am currently on Avonex, has anyone else changed treatment. I have tried plegridy and tecfidera i…

Hello everyone As a new member I’ve been reading some of your experiences and getting much comfort from realising that there’s a lot of support available. I’ve been diagnosed for 9 years but so far my problems have been limited with a couple of episodes, along with bladder, sight and balance …