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Hi everyone! I’ve had MS for a long time (relapses started in 2011 and was officially diagnosed in May 2012) but I’ve literally only just joined here! I’m glad to be able to make connections with others who ‘get it!’ Enjoy your evening and take care of yourselves. Jen xxx

Hi everyone, just wanted to put a small post out to say connection with others is such a good way to gain support or give support to those of us no lucky enough to have someone close to them. I have a wonderful amazing wife who is truly supportive at every step of the MS journey and it is as much ...

Y'all, I've been hit on quite aggressively three times just today. Not a single man read my bio to understand that I don't tolerate that crap in my DMs - nor am I open to random connections! I didn't think this type of behavior was allowed on this platform? I changed my pfp to discourage this type ...

I don't want to ramble on a lot like my last posts but they could be helpful to understand the basics. I'm in 7+/10 pain everyday, I'm always nauseous, I always have some kind of headache, fatigued; too much to list. I have to restart my pip and uc to get what I should be receiving, so right now I ...

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...