#n - Shift.ms

28 May 2025 01:16

Believing in conspiracy bs

The doctors could not figure out what was wrong with me. I had an eye patch because I had a wondering eye while driving equipment at a warehouse. They diagnosed me and then I had too re learn how to walk. What did they put in my body. I am confused are you?

Round Rock, United States

First posted on the Shift.ms app

@Lynzielue

28 May 2025 01:11

Visible band

Hi I was just wondering if anyone has used visible band for pacing themself on their energy. If so was it worth it or not? I been seeing this all over the internet and was just curious if it would worked or not!

First posted on the Shift.ms app

@Sheilamarie26

27 May 2025 22:29Last reply 28 May 2025 01:02

How did you find out?

Hi everyone! I have RRMS and I found out that I had MS after going completely numb on my left side. Even then the Doctor was still uncertain and chose to call it Tranverse Myelitis. 5 years later, same symptoms. Only this time, I was sensitive to hot and cold. I had an MRI, Spinal tap, and evoked po...

First posted on the Shift.ms app

@Belledefluff

27 May 2025 21:24Last reply 27 May 2025 23:16

Teaching & MS

Hello, Has anybody here changed from teaching career to something else? I've recently gone back full time as I can't afford to be part time but I am *struggling*. I'm tempted to try starting an online tutoring business but I'm nervous about the fluctuations in income and not having the same sala...

First posted on the Shift.ms app

@angela79

27 May 2025 19:55Last reply 28 May 2025 01:17

Im currently waiting to see a neurologist.

For those of you in the days before diagnosis did you ever have mild optic neuritis or eye problems My GP suspects i have Ms I have a pulling type of pain in one eye alongside blurred vision and peripheral vision loss and dull colours and face pain. The pain has never been severe but the symptoms ...

Birmingham, United Kingdom

@Girathina

27 May 2025 18:26Last reply 27 May 2025 20:30

New here

Hey everyone! I'm kinda brand new here. Just seeing how this is. I haven't yet got an official MS diagnosis, but the MRI scans of my brain shows demyelinating disease.i do have a lot of the symptoms for MS. Im going back to neuro on the 9th.idk just scared of it all. Idk if my wife really quite unde...

First posted on the Shift.ms app

@vjm028

27 May 2025 18:26 EditedLast reply 27 May 2025 21:59

Hi everyone , new to this , just joined today. First diagnosed in 2008, managed well until about 4 years ago. Most recently this awful disease is trying to take my legs and I just need people to talk to who understand how soul destroying it can be to be honest. Talking to friends and family helps but they don’t understand , no matter how much they try to 😥.

First posted on the Shift.ms app

@missyt

27 May 2025 16:38Last reply 27 May 2025 23:54

I don't want to be a complainer

I don't want to be the person who complains all the time, so I just don't say anything..but then people expect me to just be normal. I haven't been complaining so I must feel fine right? I look fine..but I'm not fine! Does anyone else feel this way??

First posted on the Shift.ms app

@Gee18

27 May 2025 15:17Last reply 27 May 2025 21:00

Hey Everyone

Hope your all well.Does anyone live in the United Kigdom? I'm in the Midlands. Would love to meet other people with MS. I have such a big family and alot of friends, but as most of you must know it can be a lonely place when nobody truly understands. Would love to meet others on this path, Drop me ...

First posted on the Shift.ms app

@dom1975

27 May 2025 13:43

ephaptic transmission in MS.

My Neuro report came back thankfully but has described some symptoms shortly after my last vaccination as ephaptic transmission in MS. It was a written report so unable to ask what that means? Any of my MS family heard of it? Thanks in advance 👍

Carluke, United Kingdom

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