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I was made redundant in 2020 and after spending some time thinking about my future I wrote a book. It comes out in May. Will be available in paper and digital. Is called Diagnosis Multiple Sclerosis. Is about my journey.

I published a book called MULTIPLE SCLEROSIS:Cause and Effect. How Stress Impacted My Thirty Year Journey With Multiple Sclerosis. AMAZON.COM, BARNESANDNOBEL.COM or fine bookstores everywhere! This tells my story, and what I went through to bring on the ‘GIFT’! By Peter J. Licari

MySclerosis' looks at how Multiple Sclerosis affects day-to-day life, told through the lens of Stash Capar, a film director who’s living with MS 📽️ If you don't talk about MS, it can be hard to know what your dealing with😖 It's ok to not be ok. Talk about it 💬 Stash opened up about his experience...

I recently posted as I am in limboland, waiting to see a neurologist. However, I was also referred to a rheumatologist due to a positive ANA and a mix of symptoms. The rheumatologist I saw was excellent and incredibly thorough. He obviously confirmed that seeing a neurologist is the next step, but ...

Last month I was on a panel with Dr. Amit Bar-Or and Dan & Jennifer Digmann. We discussed precision medicine and what the future holds for MS patients. You may enjoy hearing what the cutting-edge research is up to and how it will affect treatment in the future. Is a cure around the corner? https://...

Hey Shift.ms community 👋 We'd love to hear from you about how you identify with multiple sclerosis. Do you consider yourself a "person with MS," or do you prefer terms like "MS warrior" or "MS survivor?" How do these labels make you feel, and do you feel like they accurately represent your experie...

Hi everybody, I'm just wondering how many of us deal with MS in addition to other chronic illnesses? For the most part, I'm very positive, but it gets challenging at times. I have rrms, and was diagnosed with Cancer about a year ago. I also deal with anxiety and depression. Both are unde...

Check out the Multiple Sclerosis Explainer video: https://youtu.be/9Za00sVenro Check out more education resources at https://ms.stanford.edu

We are seeking people with MS to be part of a study investigating the effects of lifestyle recommendations delivered through an online learning platform! Developed by the University of Melbourne, this 6-week online course will give you the opportunity to connect with other people with MS and play ...

The perfect storm . X

I was told to download the NHS app to help understand Multiple sclerosis by my Neurology consultant. Connection Plus App store. Is a brilliant arsenal of information towards many common things. One place with everything you need to know and with videos. Download test for yourself and i bet. You...

I have recently been reading into the HPV vaccine in the school system. Now that I have been diagnosed with Ms my concern is triggering something in my daughter's immune system due to this vaccine. I feel like auto immune issues are strong in my family as now a 72 year old uncle has just been diagn...

I get a newsletter from MS News Today - it's American but has some useful information in it. I thought this might be of interest for those considering a change in their diet: https://multiplesclerosisnewstoday.com/expert-voices/2021/12/15/expert-voices-diet-nutrition-supplements-multiple-sclerosis/...

Eat a healthy, well-balanced diet by following "Eating Well with Canada's Food Guide" This will help you to meet your nutrition needs and keep your immune system healthy. There are many "alternative" diets, such as very low fat, allergenfree and gluten-free diets, that claim to help decrease symptom...

Hello fellow MSers, I know that I haven't posted anything before, despite been a member since 2015, but I have something special that I would like to share with you. It's MS TROLL. The idea "erupted" when I was talking with my "MS Buddy" -which I met thanks to Shift.ms, about our anecdotes with M...

https://www.youtube.com/watch?v=jl58eYFEJqU ‘My Sclerosis’ is the first film Shift.ms has shared that is fully written, produced and directed by an MSer, Stash Capar. Based in Toronto, Canada, Stash was diagnosed with multiple sclerosis in 2011 and had a few very rough years early on, but slowly, ...

'My Sclerosis' is a compelling Shift.ms film highlighting the daily struggles people living with MS go through, and the impact that this has on relationships and everyday routine - tasks that many people without MS take for granted. We’ve all told people we’re “fine” when we are not and know it’s ...

Over the last 2 weeks i've started to notice a lot of MS symptoms, like muscle twitching, spasms, weakness, fatigue, pins and needles, numbness. Most of them appeared in the first week and are now slowly getting a bit worse. I wanna know what was your experience of first getting MS symptoms and in w...

I have aggressive onset multiple sclerosis. It's crippling in every way!! It's not an option to pick when you get asked what kind you have. When you put it in a search engine, it brings up stuff about automotive!!! Some call it end stage or malignant. I'm 55, live in an assisted living home. Most of...