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I need to transfer money to my friend account

Hi! I got diagnosed with MS 10 months ago and my life changed dramatically. I’ve been feeling lonely because no one understands what I have. I cry almost every day and I feel so bad for having this autoimmune disease. Other days are better than others of course, but I can’t help but feel vulnerable,...

Hi, I have had ms for the past 15 years and been through it all already...I just want to be me again Katja

Hi! I got diagnosed with MS 10 months ago and my life changed dramatically. I’ve been feeling lonely because no one understands what I have. I cry almost every day and I feel so bad for having this autoimmune disease. Other days are better than others of course, but I can’t help but feel vulnerable,...

I'm new to this site I have MS I've been diagnosed since 2017 and I'm here to listen to my Ms brothers and sisters on anything y'all can help me with

Sometimes I feel I don’t know much about MS there’s so much to take in I remember my first appointment with my MS nurse and I just shut her down I wasn’t interested in nothing she had to say maybe it’s time for me to get my head round it 😞

I think I'm experiencing ms I had symptoms along time ago went and went along time with out them now its come back and have new symptoms I think I had the ms hug like weird sensation like squeezing pressure now along with the hug I'm getting weird pain in my feet and legs sometime legs feal weak asw...

I just had a brain mri and ots concerning to me and I wonder if tgis explains all these symptoms ive had of and on for over a year. 8ve been trying to reach my doc for two days abiut my mri report, I asked my pain clinic when I went there and he refused.to read the report and now they want another ...

benefits of cannabis or sativex for m.s

Jan2004 is when my journey started

I am MS person for 20 years and still suffering from drop leg,spasm

I have MS disanosed when I was 24 Ms doc said I had since I was 9 n I'm 45 now with my 10 yr old son

Hi been seeing neurologist for 5 weeks, been suffering with double vision, pins/ needles,falls,headaches, no sleep, tired for last 22 months, had head scan which is clear, had spine scan but results shows bulging disks in neck and wear and tear on lumbar spine, I had lumbar puncture yesterday and lo...

So today I ask if anyone had a feeding tube called a peg but i got a comment about some drug I'm guessing i have appointment on the 2ed about a peg as i can't eat hard food at all so I'm on yougets up a goes jelly but most of the time i start feeling sick or gag I'm nerves as if there's anyone out ...

Hi ms shift I was wondering if any ms people had a peg feeding tube that's what the Drs are thinking of puting in I'll now buy 2ed of jun

I got ms since 04. It’s hitting me hard these days. Hard stuff!!!!

I hav has MS with seizures for about 17 years. I have techfidera and several other meds. They have slowed seizures, but I am dizzy and have walking and balance issues. Is anyone out there having similar issues and if so, is there a cure or am I getting ready to get worse? Thank you.

I'll keep on pressing!