Looking for
something specific?

My very first MS Blog has been posted on MS Shift. So excited and happy to see it

This page is an index of my attempts to blog-diarize my journey with MS. https://team-gherkin.blogspot.com/2017/01/my-ms-journey.html

Hello fellow MSers! Do any of you blog about your MS? Or have you come across any blogs about MS that you've found helpful? The background behind the question is: My first clear symptom of MS was optic neuritis. When the hospital consultant diagnosed it, he simply said 'Don't Google it!'. I didn...

Hello all. So I'm starting a new blog on MS called ImmuneBliss (www.immunebliss.com)! Writing a blog about MS is something I have wanted to do for a long time; however, gathering the courage to do so has taken longer than expected. But now I finally feel ready to share my experiences with others...

I've just started an msblog - as if there aren't enough out there already 😉 https://aheartbreakingmsblogofstaggeringgenius.wordpress.com/ It's very much a work in progress and I'm figuring it out as I go, but I'd be grateful if you'd check it out, comment or don't! Cheers! xx

Hello all I have decided to create a blog to document my life with MS and my Journey if anyone would like to follow then please feel free to do so http://charliehine.wordpress.com/

NEW MS BLOG | "Get Better: Find your MS Hierarchy of Needs" by @HackMyMS Improving function starts with identifying lifestyle factors that affect your symptoms. Kristin Hardy, HackMyMS. Want to improve your function? Start by figuring out MS hierarchy of needs. No, not binge watching Killing Ev...

NEW MS BLOG | “When my career and my MS fatigue met” by @SHF1 I was diagnosed with MS in 2018, and because of a compromised left hand, I was unable to easily use my phone or any devices. Thankfully, my husband likes to do research and was very helpful in reading through articles and information a...

NEW MS BLOG | “Am I Invisible?” by @Rubysoho_87 Even prior to my diagnosis when I didn’t know why I was unwell, I was having to cancel plans more often. When I was feeling good, I’d do too much and burn out (which is something I can still be guilty of, but I’m much better than I used to be!) I w...

Hi all, - If you take ocrelizumab (Ocrevus) , as I do, and want to participate in a vaccine trial then have a read of this post on the Barts MS blog and get in touch with them via the blog. - https://multiple-sclerosis-research.org/2020/06/mscovid19-covax-or-coronavirus-ocrelizumab-vaccination-study...