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Over the years a number of strange things happened physically that could not be explained. I survived them but a couple eyars ago I was told I did have MS and probably had it quite a long time. At my age, I am told there is nothing to be done, no meds so I take everyday as it comes. I paint. I plann...

Just joined and thought I’d say hi 👋 I was diagnosed with ms in April 2008 , after I had my eldest son. My relapse effected my eyes and my face and mouth where numb, I was given a course of intravenous steroids and that seemed to make a difference, but within 4 weeks I had another relapse that al...

Ms is such a funny desease to have I use crutches to walk as my right leg is badly affected ive has surgery on my ankle to straighten foot, stop drop foot and waiting surgery on all toes now have clawing on right foot, people say was it worth having the surgery in first place . Well yeh I wouldn't ...

Hello you lovely lot. I was diagnosed with RRMS on July 24 over the phone and have my first phone appointment with my MS nurse next week. I’m not a huge fan of phone appointments - would be so much nicer to meet face to face - but covid means it’s all by phone. Anyway I want to make sure I make the ...

Nicked this link from a post over on the M S Society forums......................... https://www.youtube.com/watch?v=mlQ9AFjsVK8 Just watched this documentary and I can't believe I have not seen this before. Alright it was first made approx 4 years before MS came into my life but I think it is rea...

Hello All I was diagnosed with MS back in 2003 I’ve had my ups and down I’ve never been on any forums like this before so all new to me after pushing my doctor I’ve managed to have another MRI after 17 years to see how my MS has progressed and awaiting results next week @ 39 now I am worried to be h...

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...

Hi everyone I just joined I was wondering if any of you have multiple auto immune disorders? I found out I was diabetic (type 1) when I was 20 and recently at 36 diagnosed with MS last year. Now knowing that a lot of what I was experiencing for years had to do with the MS it explains a lot. I actual...

Hi everyone, I keep getting stomach pains, pressure down below. Sure it is uti. I keep on getting these. I must admit, I don't drink water really. Are people with ms more acceptable to uti ? Does anyone else get this ? Thanks.

Can I take sea moss capsules with my MS?