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Hi. I was asked yesterday to document my idea of 'My Perfect Day'. I started to write...my perfect day certainly didn't include MS but my reality is that everyday includes something about MS. I'm tired, I'm sore and I don't want to play MS anymore. So back to my narrative. For every few sentences I...

I am look for something that I can do that will help me to not feel so worthless. ( I am67 years old and my ms Has me confined to a wheelchair. I was dx in 1981)

📢 Calling all US-based MSers 📢 Do you live in the US? Fancy helping Shift.ms with something? We have a new volunteer role available that is based around the US MS community. If you're interested please email sophie@shift.ms today 📨 Thank you.

Finding a way to get the human nervous system to grow back the myelin, the nerve covering that MS attacks and causes the symptoms, be they minor or major, we all experience is the next huge hurdle. - I link to a total science paper here: https://www.cell.com/cell-reports/pdf/S2211-1247(20)30611-2.pd...

Hello fellow Warriors! I’m one, like many others, who enjoy a variety of autoimmune afflictions; MS, Type 1 Diabetes, Fibromyalgia, Pernicious Anemia, Hypothyroidism and a bout of Autoimmune Gastritis. As a veteran diabetic (33 years) and an MS’r since 2010, I find that these two impact me the most ...

<p>Need some advice. I have had health issues half my life. First started when I was about 16. I’ve been trying to find answers for years. Just recently found out that Ms was put in my medical records 2 years ago, although the Dr never verbally told me this. I also have trigeminal, occipital a...</p>

HI, I have just written a piece on MS and assistance dogs on the Barts blog- and how they help hundreds of people with MS lead independent lives:https://multiple-sclerosis-research.org/2020/05/mscovid19-dogs-are-being-trained-to-sniff-out-covid-19/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign...

<p>I have been reading the posts about working as a nurse with MS, and have a quandary – I am a therapist, with RRMS, due to start Ocrevus post-lockdown.</p> <p>The MS does not interfere with my ability to work. A colleague (the only one who knows about the MS) is anxious as to whether my employers ...</p>

<p>Hi all i find im a morning person with my rr ms, by lunchtime my fatigue starts to set in and i feel like im done the day. Does anyone else feel like this?</p> <div class="i-support-link"> </div>

<p>Is it safe for someone with PPMS to holiday in Devon UK this July .. We are prepared to follow all the rules given out by the government. I know MS means a compromised immune system but not sure if MS is on the vulnerable list ?</p> <p>Thank You<br> Jenny </p> <div class="i-support-link"> &lt;...</div>