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

©2025 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 39 results by
Recent activityNewest posts

@jess555 

jess555

Jcv test negative result !😌

Mri pml surveillance was done today ..and my jcv test came back jcv Negative tnk god 😌 so relieved it’s de best news I could hope for so unless it changes I will continue on tysabri . #grateful #greatnews #happyout #mswarrrior
  • Diagnosis
  • Treatment
  • Tysabri
  • MRI

@wxrmthinthesun 

EditedLast reply

wxrmthinthesun

How do you live with your MS?

I'm just sharing some thoughts here and I'm curious about other people's opinions! So, we may all know that Christina Applegate did a red carpet in the past couple days with a cane that had "FUMS" all over it. Which I respect but it's not for me. The "MSWarrior/Fighter" and the " FUMS" mentality isn...
Scotland, UK
  • Diagnosis
  • Work and play
  • Symptoms
  • Positives of MS
  • Brain fog
  • Disclosure
  • Balance
  • Healthy living
  • Work and Study
  • Family and children
12

@LuLuu 

Last reply

LuLuu

MS Warriors🤩

Hey everyone! 🌟 Just wanted to share a little bit about my journey with MS. Despite the challenges, I've come to see it as my very own superpower. It's a reminder that staying positive and resilient can truly make a difference. Let's keep pushing forward, supporting each other, and spreading hope. ...
  • Work and play
  • Positives of MS
  • Healthy living
  • Symptoms
  • Mental health
First posted on the Shift.ms app
7

@Vpinnow 

Last reply

Vpinnow

New to the Community - Daughter of a Warrior

I recently found this group and am happy to be part of a community who will understand the every day life of MS. I am the daughter of an MSWarrior. My father has had MS as long as I can remember (27 years +) and I am the only support system he has. I have been struggling for the past few years as hi...
  • Family and children
  • Work and play
  • Symptoms
  • Diagnosis
  • Relationships
7

@MrWash 

Last reply

MrWash

Iron sharpens Iron

I accepted the diagnosis in 2021, I processed all the whirlwinds of emotions, prayed to God, then jumped into the gym to craft my body for the ongoing WAR! What the mind commands the body shall follow! As the great CT Fletcher says “I COMMAND YOU TO GROW” #MSWARRIOR
First posted on the Shift.ms app
5

@PaulGriffiths 

Last reply

PaulGriffiths

Your opinions please

Hi guys and dolls, having RRMS at an advanced stage my disabilities are quite severe although my sense of humour and fun and love of life drive me thankfully. I've recently started a website called, www.mswarriorsandtalkmatters.com where I like to post info on my own experiences and relevant informa...
  • Diagnosis
  • Relapsing remitting
  • Research
4

@Jen009 

Last reply

Jen009

13 years ago today I was officially diagnosed . . .

13 years ago today I was officially diagnosed with MS. I acknowledge this day every year for two reasons. The first is so I can say a massive thank you to the friends and family who have been there since the beginning (or joined me on the way) in supporting me on my journey living with this disease....
First posted on the Shift.ms app
4

@Rosie_Dee 

Last reply

Rosie_Dee

Post Surgery

Good afternoon everyone! So day 4 after my gallbladder removal, tubal ligation and endometrial ablation I say I am doing a lot better. Still have a few gas pockets but after I was able to have a BM I felt so much better. Still have some pain and soreness but its nothing I can't handle. My kids and h...
  • Symptoms
  • Pain
  • Work and play
  • Family and children
  • Relationships
3

@Redvariant 

Last reply

Redvariant

Motivation

If you’re struggling, just remember we are at civil war with our ms, so don’t let your ms win!! #mswarriors
First posted on the Shift.ms app
2

@MSwarriorMummy 

EditedLast reply

MSwarriorMummy

My MS story (in great detail)

So in Nov 2021 I woke up with a numb bottom and foot, brushed it off that I had slept funny. Next morning symptoms worse so went to Doctors, sent to my local hospital and given an mri they did no see Anything and sent me home. Next morning woke up wobbly legs pins needles in legs, went back to hospi...
  • Symptoms
  • Steroids
  • Diagnosis
  • Disclosure
  • MRI
  • Family and children
  • Treatment
  • Numbness
  • Work and play
  • Hot and cold
1
PreviousNext page