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 610 results by
Recent activityNewest posts

@MarindaBrent 

Last reply

MarindaBrent

Grateful

Great evening everyone how’s you all day going ??❤️❤️
First posted on the Shift.ms app
2

@nicholas97 

EditedLast reply

nicholas97

Grateful

This may seem like an odd post but I want to THANK everyone on this page for sharing their experiences good and bad with MS!! Before I found this site I truly felt alone in what I was experiencing with my everyday life with this invader that has demolished my life. I have cried reading several post...
First posted on the Shift.ms app
6

@dkon 

dkon

Grateful

I just received my diagnosis last Friday and even though the news itself is unfortunate I feel so grateful for how the discussion was handled. I was called to the hospital’s immuno-neurology unit and two neurologists and the MS nurse gave me and my partner 1.5 hours — as much time as we needed to ex...
  • Diagnosis
  • Relationships
  • Family and children
  • Work and play
  • Treatment
  • Which DMT
  • Relapsing remitting
  • Symptoms

@HerStrength 

Last reply

HerStrength

Grateful

Hey guys! We go through soooo much having MS and many people can’t relate and it is so frustrating. However, we are still here my loves. WE HAVE LIFE!!
  • Work and play
  • Symptoms
2

@Marz 

Marz

Grateful

Hi everyone, I’ve had RRMS for over 20 years. I was diagnosed during a time when Australian TV was flooded with commercials of young women with MS in wheelchairs. So, when I was diagnosed naturally I assumed this was what my future held. Thankfully, I had a tribe of supporters who would not allow ...
  • Balance
  • Symptoms
  • Diagnosis
  • Newly diagnosed
  • Healthy living
  • Exercise
  • Brain fog
  • Fatigue
  • Relapsing remitting
  • Work and play

@Irene_Kostyk 

Last reply

Irene_Kostyk

Grateful

Does anyone suffer from wearing the wrong pee pad? Nothing seems to work. Please, let me know.
  • Work and play
1

@Erusha 

Last reply

Erusha

Grateful

Good day all, Just want to say this site has really helped answer questions others couldn't also just having a platform to share with people who understand. I'm sure I'll have more comments and questions on the future but thanks to everyone for all the help thus far 🙂
2

@PoppyJo 

Last reply

PoppyJo

Cladribine/Mavenclad Year 1. I took my first week or Y1 last week. I don't feel sick or have a headache today but I am absolutely exhausted. My bones feel tired and I'm moving around in slow motion. Did anyone experience this in the week after your first round? I'm working from home but it is taking a herculean strength of mind. I've had interferons and dopamine years ago, azathiapron for 8 years and then 4 months of Tysabri (until I had an allergic reaction). All this to say, this isnt my first treatment experience but this one seems to have wiped me out. Is it just me or are there any other kindred spirits out there? I'd be really grateful for any shared experience and also experience of managing work through treatment weeks.

First posted on the Shift.ms app
3

@Niccole 

Niccole

🎄 Happy Christmas Eve, everyone! I'm so grateful everyone is here.😉

First posted on the Shift.ms app

@JeffT 

Last reply

JeffT

I miss me. The me from just a few years ago. I see Facebook Memories or pics of me in my phone and it is clear the toll my PPMS has taken on me. I used to look quite young for my age. Not anymore. I’ll get past this feeling. I’m grateful to be alive and still mostly enjoying my life. But…I still miss me.

First posted on the Shift.ms app
18
PreviousNext page