Twitter | Search | |
Search Refresh
Scott Mills 3h
Excited to announce I’m running for on 7 October! Please sponsor me on the link below or text SCMI88 £3 (or whatever you’d like to give) to 70070 to help stop
Reply Retweet Like
lomelindi12 17h
May I ask my friends a Q? When you were told you had progressed from RRMS to SPMS (if that’s how it happened to you) - did it feel as bad as/worse than your original DX?
Reply Retweet Like
Janice Dean 9h
Replying to @JaniceDean
Please watch the video of you can. All of us who have need support groups to get us through the toughest days.
Reply Retweet Like
Lisa 👢 Sep 20
💉 I am so done with Tummy Thursday, Stomach Saturday & Tummy Tuesday! I guess my fat moves too much cos this hurts like a #&×*%!
Reply Retweet Like
Bev Wright 22h
Another night dreaming I could run 😳 I hope it’s an omen 🤞
Reply Retweet Like
CNHS 10h
What do diet, lifestyle, & a healthy gut microbiome have to do with management & progression? Come to our 1 day educational seminar in Halifax to hear the latest research on these topics & more! Entry by donation; lunch included. Registration & info:
Reply Retweet Like
Hamish Bode Sep 19
Reply Retweet Like 14h
A little bit about me - I’m 32, I was diagnosed with RR MS in May2016, I try to make light of my MS where I can because I’d rather laugh than cry
Reply Retweet Like
MS:Spread Love 38m
When U apparently start loving everything around 😅 ⠀⠀⠀⠀⠀⠀⠀⠀⠀
Reply Retweet Like
Bruce Gann Sep 16
Completed our first MS walk we only raised $210 this year but it was a good time
Reply Retweet Like
National MS Society 15h
Funding MS priorities is critical to help those affected by to live their best lives. Urge your U.S. Representatives to pass the LHHS/Defense minibus spending bill next week!
Reply Retweet Like
kenthemser Sep 13
I once read that a person with primary progressive MS lives an average of 20 years from date of diagnosis. I'm at 27 years since diagnosis, and counting! And I sure as hell don't plan on exiting stage left anytime soon. Rock on, MSers!
Reply Retweet Like
OhioHealthMS 6m
Check this out! Using virtual reality to learn neuro-immunology! Amazing!
Reply Retweet Like
Kelli Butler🎶#OperaGeek Sep 18
When I was a kid I thought love was stupid & silly. Then, I met my husband, who I love immensely. When I was a kid, I thought I knew what hating something meant. Then the husband I love was diagnosed with . And now I know what & really are.
Reply Retweet Like
Cammie LaValle Sep 20
Replying to @SenTinaSmith
Theres a whole side of opioid ( fentanyl, heroin & illicit use) crisis u have not touched on. Over 100 million Americans suffer from acute,chronic or intractable pain; whether from severe injuries, combat wounds, , . Millions r being denied vital medication.
Reply Retweet Like
Leena Fayed Sep 15
An MS myth : MS is the same for everyone. That’s not true because MS can attack different areas of the brain, spinal cord, or optic nerves, symptoms can vary from person-to-person.
Reply Retweet Like
Ade Couper 9h
Replying to @LexusBradbury
Not too bad thanks- keeping going (despite the !), running a stall at tomorrow! Be good to catch up sometime xxx
Reply Retweet Like
NFNicole🐢🐘🐆🐾 2h
Replying to @Not_Interesting
My MRI so I can get treatment for this occipital neuralgia problem more! When I can’t move I can’t be on hold for 4 hours and then speak coherently. Where’s the advocate or organization that wants to help me? I’m a face of too.
Reply Retweet Like
Patty Long Sep 20
Today is 9-Ball night. Yay!! I’m finishing laundry waiting on the last load to dry. Should I take a walk or take that dreaded shower! I feel like a little kid, ‘No Mommy. I don’t wanna take a bath.” I think I’m going walking. 😆🤣🤣❤️❤️❤️
Reply Retweet Like
Gennaro D'Anna, MD Sep 17
Poster printed! Now it’s all ready for !
Reply Retweet Like