good afternoon everyone it's been a while since I last posted anything! My neurologist didn't give me anything new to help my ms she still prescribed me copaxone and she said to stop taking it for a few months and then start taking it again! Since I stopped taking it I have been feeling great having...
Hi I have been diagnosed with RRMS a couple of weeks ago. I am 41 and it would seem that I have had MS for years, although I haven’t been aware of symptoms until April. My MS is very active with a lot of inflammation. I have been recommended cladribine, which seems very good and not intrusive. I jus...
Hello people I am a little new at this posting questions. But I thought I’d give it a go. Who better to ask than the ma community. I was diagnosed with ms after having optic neuritis
About 8-9 years ago. Since then I have very few symptoms. I do suffer what I Describe as a ice cold feeling/ pain ...
Hi everyone, I am new to this, I am just wondering if anyone suffers with leg cramps through the night and what medication they are on to help these, I have tried lots of things but nothing seems to be helping. 😀
Hi all, hope you are keeping well and safe in these unusual times. I am newly diagnosed in March, first symptoms 18 months ago and 1 minor relapse 6 months ago. Other than that I am lucky not to have any symptoms of note. I discussed with my MS nurse DMT drugs early March and my neurologist recom...
Having a flare up with all my old symptoms , been going on for the last month or so , have had 2 bouts of new symptoms since round 2 of lemtrada 15 months ago , no new lesions on my
Last mri
Just feeling pretty down about Feeling like I’m
Getting worse and struggling doing simple things
There are ...
Diagnosed in December 19, after private MRI, as a result of my acupuncture Dr recommending it. Went into hospital with suspected tumour on the spine. Another MRI and CT and just before I left, the Consultant told me that I had MS. I left hospital in a daze, thinking of wheelchairs, dribbling and bl...