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Hello! I was diagnosed in 2015, although the first onset was in 2013. Still trying to wrap my head around it all after 5 years! Havent had a full blown relapse since April 16 but have the odd numbness etc. How do you finally come to terms with having this illness and not constantly worry about what ...

Join Roxy, Heather, Maytee, Katt and Dave as they agree and disagree with hot MS topics, opinions and share their multiple sclerosis diagnosis stories. Did you have a difficult diagnosis? Why not share the lessons you learned with the Community in the comments below 👇 https://www.youtube.com/watc...

Recently I’ve seen a fair amount of posts on the forum here talking about relationships. Some from partners of MSers wondering how best to lend support and some from MSers wondering how best to communicate their needs. Would love to start the conversation here from both sides. MSers, how do you b...

In this film six MSers talk about coming to terms with their MS and issues raised in our Shift.ms 'Belong'. What good out of bad have you found since your diagnosis? Share your experiences in the comment section below 👇 https://www.youtube.com/watch?v=Dk3ZwDFwR0A

Hello it's been too long since i last check in here. I was hit by hard relapses ever, i was hurt so bad, i couldn't operate normally with my hands. But i am 80%better now but this time was the hardest since i have MS. But it just motivate me more to fight harder with MS.

Hi, I am writing a book about living with MS. I remember when I was diagnosed that I didn't get information from people who have MS, and I wanted to hear at first hand that it was possible to live well with it. So I am interviewing people with MS, talking about their experiences, what they found mos...

Hi all! My name is Edward. I am new here but not new to MS. I'm 35 and have had this MS since 1996. At that time I was too small and did not know about my problems. I lived as usual until 2019 and I lived with all these problems, I thought it was normal. But at the beginning of 2019, my health...

Join Katt, Dave, Sarah-Kate, and Tia as they read through Shift.ms fitness questions, share their stories, discuss mistaken advice, and why they choose to exercise their way. What exercise works for you with MS? Share your approach with the rest of us below ⬇️ https://youtu.be/QRIYGrQMo7M

We’re back with part two of ‘Do All MSers Think The Same?’ Roxy, Heather, Maytee, Katt and Dave return to agree and disagree with statements about healthcare professionals, relying on Dr. Google and much more. Dr Google vs HCPs where do you draw the line and go to the pros? https://www.youtube.c...

Remember MS u need us but we don’t need u!!!!!!!!! https://youtu.be/ZXvzzTICvJs

How is everyone doing?

It has progressed slightly over the last year or so and after another particularly bad fall yesterday, I've decided to use my cane religiously now ..think I have been in denial for 23years. I realized yesterday after asking my 6yr olds Teacher to step in as my stunt double in the Mommy/ Child piggy...

Hi all, I am new here. I just wanted to introduce myself. I’m 36y/o from Brisbane, Australia. I was working as a registered nurse in hospital when I was diagnosed in 2019 with RRMS. I have since had to retire from my job, unfortunately. I have multiple spinal and brain lesions (interesting haha, Ofc...

Hey there! 36 yo mom of 2, married & from Ontario, Canada. Having lots of symptoms on and off for past 15 plus years. Nobody is interested in searching for MS. All specialists and Doctors say "that's not MS"; in the mean time, im on the hunt. I obviously don't want to be sick but I would love some a...

Hello All, We just premiered our new project called "What doesn't kill you..." about people and their true stories related to MS - In cooperation with Czech MS foundation. I am MS patient myself (still Rookie) and I wanted to create something I would like to watch. Something uplifting and relaxing b...

Do any if you experience insane itchy, pins and needles numbness in your feet? An itch you cannot stop, I lose my mind scratching so bad there are blisters in the morning. I have read that the more the scratch at a MS itch the worse it gets and you have to do your best to ignore but can't seem to do...