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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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Found 165 results

@Melissa40

Last reply

Melissa40

MS warrior program

Hey guys, I saw in a post about weight lifting, someone mentioned MS warrior program. Can somebody explain this to me please😊
  • Symptoms
3

@Amy_Angelloz

Last reply

Amy_Angelloz

New ms warrior

I recently got diagnosed January 2021 after 10 years of symptoms and lost use of my legs. After a lengthy stay at the hospital and many pt appointments I can get around with my cane or walker.
  • Newly diagnosed
  • Diagnosis
  • Symptoms
  • Healthy living
  • Work and play
3

@Jhevon

Last reply

Jhevon

Hello MS Warrior's

Anti Inflammatory?
Pittsburgh, PA, USA
  • Symptoms
1

@Irene_Kostyk

Last reply

Irene_Kostyk

M.S. Warrior

I was diagnosed many years ago and the last 15 years have been really difficult. I continue and I do my share of complaining. But it does help having a place to go with questions. Thank you fellow warriors for your struggles are felt. Stay inside and keep hydrated.
  • Diagnosis
  • Newly diagnosed
2

@LumuniouslyImperfect

Last reply

LumuniouslyImperfect

Type 1 Diabetic & MS Warrior

Hello fellow Warriors! I’m one, like many others, who enjoy a variety of autoimmune afflictions; MS, Type 1 Diabetes, Fibromyalgia, Pernicious Anemia, Hypothyroidism and a bout of Autoimmune Gastritis. As a veteran diabetic (33 years) and an MS’r since 2010, I find that these two impact me the most ...
2

@Irene_Kostyk

Irene_Kostyk

M.S. Warrior

I was diagnosed many years ago and the last 15 years have been really difficult. I continue and I do my share of complaining. But it does help having a place to go with questions. Thank you fellow warriors for your struggles are felt. Stay inside and keep hydrated.
  • Diagnosis
  • Newly diagnosed

@Stacy_Chambers

Stacy_Chambers

MS Warrior

Hi! MS warriors...I'm Stacy new to the group

@StillAsleep84

Last reply

StillAsleep84

How to be an MS warrior...

Hello everyone, I wanted to ask you all what it takes to be a MS warrior? Now more than ever it seems we need to draw on all of our resources and wondered what these are? I'm newly diagnosed, new to this site and looking for some inspiration to help me cope over the next few weeks and months. Thanks...
  • Newly diagnosed
  • Diagnosis
  • Symptoms
7

@SLHL

Last reply

SLHL

#MS warrior

Hopefully many of you have seen my fellow MS team mate (from CPISRA World Champs) and all round inspirational girl Kadeena Cox breaking the World Record at the World Championships in Doha this week in the 100M sprint. Kadeena is an outstanding athlete and a most humble, caring and loving character t...
  • Healthy living
  • Exercise
  • Work and play
  • Family and children
1

@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

@Colleengresko

Colleengresko

MS Mommy

I recently decided to start telling people I have MS. I have been very private about my diagnosis since I was diagnosed about 3 years ago. I felt like a huge weight was lifted off my chest! My friends encouraged me to go further with sharing as a healing tool. I decided to create a blog about mother...
  • Diagnosis
  • Newly diagnosed
  • Exercise
  • Healthy living
  • Disclosure
  • Mental health
  • Symptoms

@Robbie

Robbie

My platform is growing

Hi everyone I wanted to invite you all to my Beneath the Tracksuit socials, as an MS Warrior, a published Author and now I'm an approved artist, I wanted to share it all with you https://instagram.com/beneath_the_tracksuit?igshid=ZDdkNTZiNTM= https://www.facebook.com/Beneaththetracksuit https://t...
London, United Kingdom
  • Research
  • Work and play
  • Healthy living
  • Symptoms

@Shiftms

Shiftms

How do you identify with multiple sclerosis?

Hey Shift.ms community 👋 We'd love to hear from you about how you identify with multiple sclerosis. Do you consider yourself a "person with MS," or do you prefer terms like "MS warrior" or "MS survivor?" How do these labels make you feel, and do you feel like they accurately represent your experie...
  • Work and play
  • Work and Study

@Mswarriorant

EditedLast reply

Mswarriorant

Hi there!

I stumbled across this on Instagram, I’m hoping to connect with others that have this illness. I share my journey on TikTok @mswarriorantonio if you’re interested :-) I’m hoping to hear back from you all!
Dearborn, United States
  • Treatment
1

@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

@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

@inozz

Last reply

inozz

Calling for MS Warriors

Hi everyone! My name is Alex. I'm an MS Warrior diagnosed in 2015. I'm sure you all understand these were not the easiest 7 years of my life. After getting my diagnosis, I was almost mindlessly trying every approach and solution I could find online. Different MS medications, homeopathy, countless di...
  • Symptoms
  • Diagnosis
  • Healthy living
  • Hot and cold
  • Work and play
  • Diet
  • Vitamins and supplements
  • Newly diagnosed
  • Mind and body
  • Research
2

@lmt4

Edited

lmt4

Shift in my world!

Hi everyone! I am a new member and I look forward to making connections here. I have been diagnosed with Primary Progressive MS just over a year ago. I used to work as a Dental Hygienist (DH) and a DH educator with a college downtown. Since my diagnosis I have noticed an increase lack of balance and...
  • Diagnosis
  • Work and play
  • Work and Study
  • Symptoms
  • Balance
  • Newly diagnosed
  • Money
  • Blurred vision
  • Primary progressive
  • Mental health

@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

@Vickyms

Last reply

Vickyms

The words we use to describe ourselves

Hi fellow MSers! I was recently introducing myself on a Facebook group for a course I am doing, and wanted to let them know about my MS as it's just as much a part of me as my job. I was going to write 'ms sufferer' but that sounds so selfpitying so I put 'ms warrior' instead, but I don't really lik...
  • Work and play
  • Work and Study
  • Symptoms
9
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