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Hello! I’ve been diagnosed this year with highly active RRMS . My last relapse was July 2024 with a lesion showing as active at C1/C2 level of the spine. It was only sensory (pins and needles neck down) and slowly improved over the months. I still get pins and needles intermittently in the hands. ...

When I was 28 I found out I had MS, I've had optic neuritis, my left leg has weakness, numbness in different areas. I have been on different treatments, my treatment is being changed as I was taken Aubagio but had problems taken that one, will see what treatment is next.

Hi I just wondered what I should expect on my first neurology appointment, will it be to discus/ start treatment? They diagnosed me only by MRI and said I had multiple many lesions on brain and neck. Any advice please thankyou. X

I was diagnosed in 2022 aged 35, it then took another year to get onto treatment. My consultant believes ive actually had Ms since the age of 20 & was misdiagnosed. Still figuring out spotting relapses- i get the whole symptoms lasting 24hours or longer. But i have most of the symptoms daily to some...

Hey there, newly diagnosed and awaiting starting treatment. I have been reading some of the posts here and it's really nice seeing others who understand how it feels to be in pain all the time and all the other feelings that come with MS. Thank you

Hey there! Newly diagnosed this summer and have been putting off starting a treatment out of anxiety and fear. I’m trying to determine which is better, Tysabri or Zeposia. Anyone have any input on either medications? Curious of side effects, efficacy, etc. Thank you!

I was on tysabri injections every 4 weeks but I have now become JC virus positive so they switched me to every 6 weeks I have opted to switch treatment (can't remember the name) but I injections myself it's every month & I no longer have to go to the hospital which is a bonus!! I know I can't rememb...

Hi everybody. I'm new here. I'm currently on tysabri but my consultant has advised me that should my MRI show any changes that he will be stopping my infusion and that there is no treatment available for SPMS. My question is are any of you with SPMS on any disease modifying treatment and if so which...

Hi all. I'm thinking about asking my neurologist about doing this treatment. Has anyone done it and if so has it been successful?

Ever wonder why popping meds and following conventional treatments isn't enough to fix your midlife health issues? That's because there's a deeper story happening inside your body – one that connects your gut directly to every single symptom you're experiencing, even ones that seem completely unrel...