shift.ms

Hello, My name is Jessica, i was diagnosed in 2015 with ms. I was just told in 2017 that i have an aggressive case, and all this time i have been alone it feels like. I mean i have my family but no one truly understands what ms is or does or what i go through so i feel alone.

This isn’t about MS,I just need a rant because I’ve seen something that has really grinder my gears. I was annoyed when they banned plastic straws and instead we have to have paper ones that go mushy,then they took away drinking coke in cafes and restaurants, that’s fine I’m confused but Iâ…

Flashback to the year 2003: I was 23, going on 24 and pregnant with my first (only) child. I was working in a Fedex Ground warehouse and I was 6 months along when during a shift, my right eye went blind! Oh how fun it was, I’m sure you can imagine!? What followed was literally the worst 3 mon…

Hello everybody! My name is April, I just learned about this site and am hoping to make some friends. I was diagnosed in 2007 after being misdiagnosed a few times. MS reared it’s ugly head in my last semester of law school but stubborn old me would not drop out of law school, and I don’t regret…

Well had a chat to the nurse today to ask about the impending start of Dmt. She was helpful with stuff but I did mention that in the recent scan I did nothing had changed. She was lucky enough to catch the Neuro and ask him bout the results. She said treatment will not happen at the moment. As the…

hey there all, I know its been talked about before. Suddenly I decided to have cupping treatment for MS heard it helps blood cerculation and other suff and honestly I feel my body flaoting beneath my skin not knowing where to go lol and because Im a muslim and an islamic treatment. but I have lil q…

Hey there! I’m just a small town girl living in a lonely world, who took a midnight train to tacoooo bellllll! That’s my attempt at humor, LOL but seriously just wanting to check this site out. It’s really nice, all the great support that I have within my family and friends. It’s just hard…

Has anyone else lost sensation full function of thumbs (mainly) /hands? It’s really bizzarre I can use my hands but my grip has gone slightly and I have permanent pins and needles in my hands that gets worse throughout the day. Would love to know if this is MS and not something more sinister x

hi guys , i have to have a DVLA medical check by my GP do any off you know what is involved in the test and what i should expect ? yours hank

Hello everybody. I have been away from this site for the past 3 years. My eyesight packed up and I couldn’t use a computer. Thankfully my left eye has returned to normal. right eye is still burred. Has anything happened in there MS world in my absence? I am reaching out to friends. new and ol…