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Well, besides I have ms and my legs have weakened on me, I now know where I stand in society. I will be living in adult foster care doing i am on ssi. Wow. Thanks society... I cant wait till I go. 😔

I can't do this anymore I just don't see a purpose in life anymore 😔

Finally starting to feel abit human again hoping to get back to normality ASAP 🙏 being ill is 💩💩💩

So what a few worldwind months I have had! Waited 6 months for my treatment and when I had my first full dosage afterwards instantly became 🤰 . I am nervous about what the relapse will/if do to me after the 👶🏻is born in November. I am excited but so so nervous & anxious because never for the life...

Hi-ho and hello. My name is Matthew, I was diagnosed with MS relapsed remitting 2016, and am currently doing the Ocrevus infusions. Whether I be lucky, lady fortuna has her eye on me, or what have you, I just wanted to share that I got my last advance for a memoirs piece I've been ghost writing. I'm...

Oh life!! You are so beautiful, a bit complicated but still beautiful!

The most hard time of having MS is when the symptoms start coming and working when having them, that is the hardest part

Yes MS makes our lives a living hell but since we must all contend with it we should all look at making, ourselves at least, at least a little happier. Drink what you like, as long as it does not conflict with your condition or meds. Listen to the music you like. Watch the movies/shows you like. ...

My marriage seems to be going to shit, I'm lonely, bored, unfullfilled and MS makes life even crapper! Covid really won this round and I need to have someone to really speak to and remember what the point of it all is

Well it’s been 3 years since my last relapse and now I feel I’m sinking into one again. Possible virus but no temperature, always a worry. I hate going into hibernation but more for my partner. I’ve had a great 3 years, Buckingham Palace and jumped 15,000 and raised £1700 for the MS trust and also I...