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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...

Hi everyone. My name is Kevin, and I was diagnosed with MS about a year and a half ago. What a whirlwind journey so far. I actually have a question for anyone thats felt this...i had a very serious bout of anxiety and stress in mid July; I've started yet another drug for that but does anyone have re...

Can I take sea moss capsules with my MS?

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.

Hi all, I'm a 52 year old male just diagnosed with Primary Progressive MS. It's mostly affecting my left leg so far, with foot drop, altered gait and weakness. I can no longer stand up from a squat on that leg, which is scary for a guy who's been healthy, strong and physically active his whole life....

...about MS. - This is v short notice for this afternoon - Wed 2nd September. I was only asked last night. - It turns out my GP is also the director of this program - https://www.ox.ac.uk/admissions/undergraduate/courses-listing/medicine-accelerated - and I have been roped into giving a last-minute...

Can this happen I lost so much weight it ridiculous first it was mouth ulcers got rid of them with zinc and vitamin c.hair loss, now weight loss l'm loosing muscle not fat scary. No ms nurse here seeing gp/ neurologist soon.

So my wife of 31 years was diagnosed with RRMS in 1995. In that time she has tried many many medications. Nothing has stopped or even slowed her progression into secondary progressive MS. We travelled to Poland 2010 for CCSVI treatment. Still her MS progressed. She has been using a wheelchair now fo...

I have RRMS/SECONDARY and at times, I, feel like I can't even walk, it hurts so bad to walk sometimes. I don't want to use a wheelchair because my independence is so important to me. Maybe, I am having a bad exacerbation, but if that is what it is, this would be one of the worst one's that I had. A...

Hi there, I was wondering if anyone in this community has used or heard about using RSO to treat MS, this is an oil derived from marijuana, I’ve heard a lot about it, just want some feed back the MS community, thank you.