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Hey everyone, I’ve just joined and thought I’d ask when dating how do people bring this up? I feel like I’m going to be single forever haha

Hi there! Is anyone else struggling with your relationships after the diagnosis? I personally feel that Ms changed me a lot and my wife seems to miss the person I was… and that I will never be again. Also, sometimes I feel “flat” like my emotions are not fully out, I think Ms changed that too. Very...

I have been in a relationship with my partner for 9 years, we were together for about 1.5 years when the MS hit bad, he stuck through it, not without upset, but here we are 9 years later, when we get into arguments it always reverts back to “I stuck with you through your illness” which I take on bo...

I’ve gone from running marathons,going gym and playing football to having to use crutches to walk 100m , constant pain and numbness in my left side, the fatigue is ridiculous and enough powerful meds to knock out an elephant ,all in 5 years,how does everyone keep their relationships alive with the i...

Anyone struggling with keeping a relationship ? Every guy I talk to ends up leaving after realising how much of a responsibility I am during my bad days :/

Ever since diagnosis I have found that my nearest and dearest try to take advantage of my difficulties. My husband tries to take advantage of my poor memory. I had a massive argument with my mother, and I have argued with a friend for my husbands sake. I feel like I don’t want to suffer fools gladly...

Hey everyone 👋 Before reading on, can I ask a favour. Can you comment down below with your relationship status? (Just one word will do)👇 It’d be cool to know so we can make more podcasts focused on what you need! I recently guested on the MS Trust podcast which explored how MS affects dating, rel...

Has anybody experienced a relationship and they make it that is not the Ms,,, and being pushed to the point of making so uncomfortable for you

I was diagnosed with RRMS in March 2022, after having Covid-19, 6 times in 8 months. Since diagnosis, things are progressively getting worse, such as my cognitive function, speech, tiredness, and pain. My memory is terrible now to the point where I am repeating my sentences over and over again, and ...

I've had MS for about 9 years now and doing this for myself by myself isn't funny more it never was but it sucks even more without somebody there I've been single for a long time and I want to get out and talk someone I want to get out and find maybe my soulmate or find maybe the mother of my child...