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 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...
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...
I feel like the past 2 months have been a real struggle for our relationship. We have been together a year January 4th and not had a flare up until October 20th. Been in and out of the hospital 3 times to get the steroids pushed through since October 28th. He has been more distant lately and he is ...
Evening all,
Without going into my whole life story ( it would take a while, and I don’t want to push you all over the edge..😂). But let’s say, my family was never functional, but guess, whose is?
That said, I lost my father a few years before diagnosis, and I have never been close to my mother. ...
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...
Good morning everyone 👋 Billy here. I'm going to be a guest on the MS Trust podcast soon. We're going to be talking about relationships & MS; dating, marriage, friends etc. Any topics you'd like us to cover or questions you want to ask? Let me know below👇
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...