Shift.ms
Donate
Learn about MS
MS symptoms
MS symptomsA guide to MS symptomsWhat are the early signs of MS?Understanding visible and invisible symptoms of MSMS HugMS and optic neuritis
MS diagnosis
MS diagnosisBeing diagnosed with MSWhat is MS?Different types of MSIs MS hereditary?Late onset MS and treatment
MS treatment
MS treatmentGetting treatment for MSCoping with MS fatigueExercising with MSUnderstanding MS relapseHSCT treatment for MS
Living with MS
Living with MSAfter diagnosis: living with MSMultiple sclerosis and mental healthWorking with MSMS, sex and relationshipsA guide to MS benefits in the UK
  • Forum
  • Learn about MS
  • MS symptoms
  • MS diagnosis
  • MS treatment
  • Living with MS
  • Find MSers
  • Buddy Network
  • Films
  • MS Latest
  • Get Involved
  • Volunteer
  • Fundraise
  • Donate
  • About us
  • Contact us
  • House rules
  • Terms of use
  • Privacy policy
  • Cookie policy
Sign in

We are a charity and rely on donations

Charity Number: 1117194 (England and Wales)

Registered Company: 06000961

Registered address:
Shift.ms, Platform, New Station Street, LS1 4JB, United Kingdom

London office:
Shift.ms, Somerset House, Strand, West Goods Entrance, London WC2R 1LA, United Kingdom

©2026 Shift.ms

Looking for
something specific?

  • Picked for you
  • Browse topics
  • Find MSers

Topics

  • Diagnosis
  • Symptoms
  • Newly diagnosed
  • Healthy living
  • Research
  • Disclosure
  • MRI
  • Browse all
Sort approximately 40290 results by
Recent activityNewest posts

@Truck 

Truck

t

Hello my name is Leonard and I've been diagnosed with MS for 20 plus yes and I wdould love to find a way to walk short distane
Sunshine, United States
First posted on the Shift.ms app

@mrsmagoo924 

Last reply

mrsmagoo924

This heat in New Jersey is insane…

Anyone else suffering.? Even with the air on, I’m struggling. I’m hydrating and resting. But can’t seem find anything to help.. suggestions?
First posted on the Shift.ms app
8

@Shonn 

EditedLast reply

Shonn

This is how I feel about taking medication

The way I believe is this the pharmaceutical industry are the richest people in the world so I try not to take as much medicine as they suggest or just things that they suggest. I just get an infusion every 6 months and I noticed that I don't get the same feeling that I have in the past from getting...
First posted on the Shift.ms app
12

@ilovems 

Last reply

ilovems

Everything trembles

Twitching, tremors, trembles. Arm trembles, the thighs twitch. It is never stopping. I think my limbs are morse code communicating 😵‍💫
First posted on the Shift.ms app
3

@thomassivems 

EditedLast reply

thomassivems

Did anyone ever have to wear a depends?

How did you feel afterwards?
First posted on the Shift.ms app
20

@itsemma 

itsemma

Time off

I’m trying to plan a vacation, get some sunlight and hopefully calm my nervous system. I don’t know where to go, for minimal stress, not super expensive and good for weather. Not too hot for my MS though
First posted on the Shift.ms app

@JoshuaOct2024 

Last reply

JoshuaOct2024

Feeling horrible like life is going on around me and I can't understand it. The way my body feels is like it is falling apart. I have been in the hospital. They do vitals, blood work had a MRI done. They always discharge me and say there's nothing wrong that they can help me with. I would like to get into a assistant living situation because I feel I need it.

First posted on the Shift.ms app
1

@thomassivems 

Last reply

thomassivems

Know what medication is being given to you.

Q drugs for multiple sclerosis (MS) are immunosuppressants used to treat highly active, severe, or relapsing forms of the disease by killing white blood cells that attack myelin. The primary, FDA-approved chemotherapy for MS is Mitoxantrone (Novantrone). Others, such as Cyclophosphamide (Cytoxan) an...
First posted on the Shift.ms app
1

@deano 

deano

The dreaded PIP review form arrived

17 pages , and you can't fill out online . I checked with DWP.

@SoniaG236 

Last reply

SoniaG236

Dear all, I have noticed that some people who say they have MS yet on their bios they leave the name of their DMT blank. Is it that some of you are genuinely not taking anything to help with the MS or are you using vitamins?

First posted on the Shift.ms app
66
PreviousNext page