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I am by myself again at work. Started at 2:30 pm, was expecting someone to come in at 4-4:30, but they haven’t come in yet. I am fricken sick of my parents telling me to think positively when at work. It feels like anytime they say that shit, something decides to pull the rug from under me and flip ...

Hi All. Just wanted to share this article from The Telegraph that's been written by Bianca Wallace. Her ongoing openness about the challenges MS presents to her as well as her upbeat perspective is excellent. "I wrote the forthcoming film A Ray of Sunshine in the hope that it will help address the...

Since being diagnosed with MS in August 2021, which was 1 month before starting my final year at college (year 13), I had nearly lost all hope in my future and the goals I always wanted to achieve. I would always ask myself why now? A few weeks before starting the year with all its ups downs. Went ...

Hi my fellow MSers, Hope you are well. I work in marketing however as it's digital and CRM it's not as creative as people think. My work although unemployed currently consists of working with data, GDPR, analytics, writing data logic, buidling customer journeys, marketing KPIs (key performance in...

Hi MSers, Hope you are well. In the UK MS is a disability by law. Such as certain cancers and HIV, if you didn't know we are protected by the Equality Act. I have relapsing-remitting multiple sclerosis and I am not in a wheel chair. However, I have difficulties walking but you won't really notic...

My name is Rita I just joined this morning and I don't know what I am hoping for or what to expect from here? I was diagnosed with MS May 26,2021. That came as a bonus diagnosis to my presenting problem my now secondary diagnosis descibed as stable grade 2 spondylolisthesis with bilateral pars defec...

Hi MSers First of all hope you are all good as much as we can me. I write this as my body tingles. So today I had my appointment with my neurologist pharmacist and finally meet the MS nurse. From 9 am till 11:30 am and getting medicine for the body tingling. I also did blood tests and although mi...

I have tinitus. Really loud in one ear. I have a mri booked for this. The neurologist does not link it to ms. It started when the optic neuritis ended. I started ms treatment July 2022 and as per procedure I should have a further mri. The neurologist was not planning on doing this until she confirme...

So I just found shift.ms due to a intense match of scrolling through my Instagram feed while I should be going to bed. I am so glad this popped up. I can't stop scrolling throw everyone's post and just feel like I finally found a place to talk to people who understand what it's like. NOW I want to a...

I know there isnt a cure for MS yet (trying to speak positively and hopefully there will be one soon). But can your lesions heal/recover or disappear ? I’m very new to this MS life and im trying to learn more. Also with flare ups and relapses do those symptoms tend to stop at some point? I know ever...