Name one thing you miss about yourself before your diagnosis?

Finding community on this site has been a constant uphill battle. No conversation seems to last, and unfortunately no community either. Not for me at least. And especially when I'm stuck in the middle of Nowhere, NC. Hopefully something gives here soon and I get to make a major change in my life- bu...

My stomach has been off the past few days. Crampy, bloated, and dark 💩. Some issues with urgency. I was taking an iron supplement but stopped in case that was the cause. I haven't taken any Pepto or Pepcid in the past 24 hours. My stomach can be quirky at times, but I am also feeling generally off ...

Most of the time I have a bunch of symptoms but every time I have a good MRI. Like, I'm so happy the MRI looks good but why do I always feel so crappy? Just complaining

It’s officially been one year since MS barged into my life completely uninvited. Worst. Houseguest. Ever. While this disease has tested me in more ways than I can count, it hasn’t taken my humor, my stubbornness, or the people I love. So here’s to another year of doing life anyway - even if MS insis...

I absolutely hate living with an invisible disease!! With an invisible disease, people don't your ill (disabled), because they can't always see symptoms unless symptoms are present. Like the other day a lady gets on the bus and says "if people have nothing wrong with them they should give up their...

Im struggling so hard. Like im going round in circles. Everything I try just ends up with zero results. How do you all do this? I am struggling. I dont wanna fight this anymore

Ive been on the sunbed this morning the first time since being diagnosed in may. I loved it. I felt calm, relaxed, happy. I drifted off to sleep.I love the sunbeds, they are my happy place and ive been really nervous about giving them up. Im going to take it slowly and start maybe once a week slower...

I live in the north west england UK and I was diagnosed with RRMS in 2022. Since then I have been denied DMTs despite requesting every time I see my Nuerologist. Since diagnosis I have decorated ALOT I have had quite a few attacks (each has gave me a lovely new symptom). But when ever I see my neuro...