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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

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Sort 18 results by
Recent activityNewest posts

@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

@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

@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

@RobbiHall 

Last reply

RobbiHall

#MultipleSuperbness God's Way

40 years singing & telling story songs about NOUNS. Over 1 Million students, in schools, communities, languages, locations resulted inmy showing up. Quite a few folks with MS in the "entertainment" industries overcome like Montel, Terri Garr, Selma Blair, Annette Funnicello & Pryor stressed & miffe...
Portland, United States
  • Diagnosis
  • Disclosure
  • Symptoms
  • Mental health
  • MRI
  • Relapsing remitting
1

@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

@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

@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
Deleted

@Mwsurviver 

Mwsurviver

Instagram

Follow me on Instagram, for us people with ms. https://instagram.com/mswarrior2023?igshid=ZGUzMzM3NWJiOQ==
Deleted

@Mwsurviver 

Edited

Mwsurviver

Follow me on Instagram

I have created an Instagram, just for us with multiple sclerosis, https://instagram.com/mswarrior2023?igshid=ZGUzMzM3NWJiOQ== Thank you! 🎗🧡 We are Warriors
  • Diagnosis
  • Symptoms

@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
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  • Brain fog
  • Disclosure
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12
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