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I was only diagnosed a week or two ago. I seem to be losing the ability to construct sentences when talking to people as I just can’t find the correct words which is really frustrating. I’ve just had to have a conversation with British Gas over the phone and I got so stressed as I had to navigate wh...

Is anyone from the midlands, Ireland? Looking to make connections with people going through similar stuff!

This is something I posted on my blog today. Normally I ignore my MS and concentrate on wildlife and gardening, but today I was tempted to share a little. Today is World Multiple Sclerosis Day. There is always a day for something or other and most of them pass us by unremarked. Unfortunately, rather...

Anyone from fife here? Would love to connect with others who are going through it all too

Hello! I'm new here, I am newly diagnosed with MS (March 2024) I've done a ton of research, and reading about MS, but, I still have lots of unanswered questions. I am looking forward to connecting with this MS community and hoping to form new connections with experienced MS-ers who would like to sha...

Hello community, Quick introduction... my name is Matt, i was diagnosed with PPMS in 2015. Life has been as tricky as you'd expect but i've soldiered on regardless. Now, however life has thrown me a few curve balls and im struggling to cope. 30+ years working in the hospitality industry as a chef w...

👋🏼 Hello! I joined Shift.MS when it first began and was very small. I’d forgotten tbh 🫣but having come across the site on FB lately, decided to sign up again. How gobsmacked was I that I HADN’T been forgotten and was greeted with welcome back FoxyLady!🦊 I really would like a few suggestions abo...

I was diagnosed 11 years ago. I've embraced the eyepatch that helps the optic neuritis. Once I got used to the change in depth perception, at least. The cane is fine. My biggest issue has been slowly losing the ability to do the things I love. I was a bicycle mechanic and messenger and played drums....

Hi folks! New member here. I'm really hoping to connect with people. There's lots of people where I live that have ms, but I would like spread out and make some new connections. Just for mindless chatting and some ranting 🤣

Hi all Did ppl cut friendships they had before ms off/out because of no longer feeling the support, understandin or a connection. & how did ppl come across meeting new better supportive friendships I have known some ppl since I was younger but I'm quite fed up of the ms judgement & just how closed o...