Shift.ms

@bigdill306

22 Jul 2025 21:08Last reply 23 Jul 2025 15:59

Hey everyone 👋 I’m Dylan, a 38-year-old guy living with MS out here in Saskatchewan. I run a legal weed dispensary (yes, I’m that guy), and I use dark humor, sarcasm, and a whole lot of cannabis to get through the weirdness that is life with MS.I figured it was time to find a space with people who get it the fatigue, the brain fog, the “oh cool, my leg’s just doing its own thing now” moments. I’m just here to connect, share some laughs (the darker the better), and not feel like I’m the only one in the snow belt dealing with this.If you're in or around Saskatchewanor even if you're not say hi. I don’t bite. Unless it's a bad MS day and my jaw spasms. (Kidding. Mostly.)Looking forward to getting to know some fellow weirdos on this ride

Saskatoon, Canada

First posted on the Shift.ms app

28

@cazz174

23 Jul 2025 09:37Last reply 23 Jul 2025 15:21

Morning, I had a bad fall on Monday night,not bad enough for a&e. My leg has been either giving way or shooting out straight, any advice welcome. Thanks in advance.

First posted on the Shift.ms app

3

@amandalynn96

21 Jul 2025 22:07Last reply 23 Jul 2025 13:22

Has anyone else have a lot of trouble with their insurance companies denying medication that would help your MS? I've been waiting for what seems like forever and keep getting denied. New things have been starting that effect everything I do.

First posted on the Shift.ms app

15

@DruBlue107

22 Jul 2025 20:47Last reply 23 Jul 2025 11:58

NYC humidity hits my MS different than Caribbean humidity

First posted on the Shift.ms app

4

@sdown1970

16 May 2025 01:51Last reply 23 Jul 2025 11:27

Hi, I’m Shannon and new to the group. I’m 54 and was diagnosed with PPMS when I was 19. I’m wondering if anyone else feels that Menopause is making your symptoms worse? Thank you!

First posted on the Shift.ms app

29

@Debbie79

7 Jan 2023 19:22Last reply 23 Jul 2025 09:18

Trigeminal neuralgia

Has anyone els had to deal with Trigeminal neuralgia (TN) due to their MS ?

35

@LOUISEHOPKINS

20 Jul 2025 15:56 EditedLast reply 22 Jul 2025 23:12

Ocrevus Has anyone had this as I’ll be put on it next month

First posted on the Shift.ms app

17

@TracyD

17 Jul 2025 16:10Last reply 22 Jul 2025 19:35

I'm not sure how 6 years went by

It's been a long time since I posted here but I got a notification about getting fitter and since that's exactly what I'm doing right now I logged in for a read. After Lemtrada in 2015/16 I've been on Ocrevus for 5 years now, diagnosed for over a decade, I'm also 10 years no new activity on my MRI's...

Reading, UK

10

@sharons

21 Jun 2025 20:33Last reply 22 Jul 2025 19:35