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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

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...

A 20-minute test for MS is on the horizon. Check out the story and my pick for the book of the month at: https://lnkd.in/g34WvHeY.

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/...

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...

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...

Yes I don't understand how this invisible monster can invade my body like Godzilla invaded Tokyo it comes without warning with pain and a astonishing time warp feeding off of my brain I have lesions on my brain what on my spine for 13 years and I'm tired and depressed because on top of that I have t...

I was diagnosed in 2009 when I was 19 to 20 years old and I didn't know what to do so I locked myself up in the bedroom and started crying because I didn't want multiple sclerosis because I didn't want the pain now I am always in pain 24/7 none stop and sometimes two of my fingers on both hands go n...

I was diagnosed last year in July. I have to walk with a Walker. My hands went numb. I honestly can't take much more. If it wasn't for my two kids I don't know what I would do. I'm starting to think it never gets better

I have Multiple sclerosis son 2016 and Ive been working as an administrator for 12 years. I have changed department recently and have new management. Managers ghave known that I suffer with MS but dont do much to help me. My manager keeps auditing me everytime I do work wrong and keeps asking me t...