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Hi, I have been diagnosed with RIS (Radiologically Isolated Syndrome) - basically I have quite some lesions that I accidentally found out about, but never had any symptoms (female, 29-years old). I have a 6-month old daughter and about 3 months ago I started to experience some kind of numbness in ...

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...

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....

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.

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

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.

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...

Hey guys, I've been diagnosed with Ms since I was 13 and had lots of scarring before then, had nearly 10 years of treatment. However, my Ms keeps becoming active. The next and only drug they are suggesting is cladribine /mavenclad. So taking it for the short amount of time over two years. I'd lik...

Hi all, I am new to this site. I am currently in limbo. I do not have a diagnosis, although the neurologist felt it probably is MS. Limbo is difficult because I do not fit in with any group. One minute I am up, and then I am down. This is uncertainty. I guess a lot of people out there have experienc...