#n - Shift.ms

@SugaBug1971

Last reply

These flare ups are the worse I notice when I turn my heat up I get one easily

First posted on the Shift.ms app

3

@bpapi22

EditedLast reply

Need a friend

I’m 52 have SPMM with rapid progression of disease last 5 yrs. I’m almost wheelchair bound and can barely speak. I live alone in small town but need move city for best treatments but can’t afford. I very discouraged and am start suicidal ideation. Please help me 😢

First posted on the Shift.ms app

27

@Tcowart21

Last reply

No medicine

I have stop the zepoisa to treat the ms because my insurance wants 500 dollars for. That was 2 months ago. I have noticed some things happening. Now I’m worried

First posted on the Shift.ms app

9

@delki

EditedLast reply

I am not getting any thoughts about my situation right now. I cannot comprehend on what’s happening. It’s just scary and frustrating. I am so lost and I feel like no one understands me. I just had another episode of ON nearly after a year. I am just scared. I am an international student in WA and it’s so expensive. The tests and everything. I cannot keep going. I am just so so so lost.

First posted on the Shift.ms app

6

@Oine

Last reply

Thank you for having me here. I was diagnosed with MS last year 2024 December. Had brain lesions and tremors and a few other things. Still hoping God would make the diagnosis wrong. Started some treatment. Helped a while then didn't. Changed doctors new meds very caring team but symptoms are becoming more pronounced. Feel sad and down alot. Wonder if I did wrong by seeking better help and why the symptoms are getting more obvious

First posted on the Shift.ms app

5

@greenmoose_

Last reply

does anyone in England know if having ms will entitle me to free prescriptions. I've been paying for years and nobody told me this was a thing!?

First posted on the Shift.ms app

12

@jbharris1356

Last reply

Any one have trouble with numbness and tingling in the feet and hands from MS.

First posted on the Shift.ms app

12

@JenniferWoods

Last reply

I'm new here

Hello everyone! I'm new here I was diagnosed with MMS back in 2022 and progressed to RRMS and I've definitely had some eventful twists and turns through my MS journey so far but I'm glad to be able to find a community of people who are going through something similar to myself. I hope everyone is ...

First posted on the Shift.ms app

3

@mrym4444

Last reply