Nutshell88 16/08/18hello everyone worst thing for me is talking even to myself about how MS makes me feel I havent had any sensation of the invader MS untill July I had a symptom now I noticed recently Im having another invader sensation I hope its just worrying its like tidal wave in the bottom back of my brain is i…
JayJay10 16/08/18That feeling you get when you stand and those wobbly legs start rattling leading you to the ground. The WonderCore Smart is a good piece of equipment, however I’ve been unable to get much use out of it as my legs just don’t want anything to do with exercise right now. Shall I up my dose…
eilidh24 16/08/18Hi all I don’t often post but have been a member from right at the beginning as i was diagnosed at the same time you launched this wonderful helpful site. My little moan is out of frustration really I’ve had a dead arm for over a week now and nothing seems to easing it the pain is reall…
Nutshell88 15/08/18not released yet hi all, I heard on Franch24 Arabic channel about a new treatment stops MS from progressing 100% they tried it on rats this years they said it needs couple of years to be released they said they need to try it on humans first. anyone heard anything about it.
Julesds1977 16/08/18Hi everyone, Hope you are all doing ok. Ive been getting a lot of random aches and pains lately, mainly in my legs, bum and lower back. They never stay longer than a day, and seem to move about my body! As I’ve mentioned before in another post I was only diagnosed in June. I’m strugglin…
pikilily 16/08/18Hiya… I am in a bit of a quandary. I am experiencing what I think is Hug along with other symptoms..but I am also doubting myself. So a description, does this sound familiar?? I have a spot in my back that is numb but sore (just between my shoulder blades to the left of my spine) Inside my c…
curious.one 08/03/18Hope everyone’s doing well 🙂 Was wondering how many here have had lumbar punctures and have been cleared of the oligoclonal bands? If so, how has your journey through MS been in terms of treatments and progression? Read an article about OCB negative MSers potentially having better outcomes…
dannibrett 16/08/18Morning All, I’m now on day 4 of tecfidera and apart from a few hot flushes on the first day everything has been fine so far 🙂 I saw my neurologist yesterday as I’m currently having another relapse (which began before I started the treatment) and they’ve given me a hefty dose o…
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