Join to explore more

Shift.ms is better if you're logged in

Join the communityOr find out more

By signing in to Shift.ms you agree to our terms of use and privacy policy.

Already have an account?

Sign in

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

  • Picked for you
  • Browse topics
  • Find MSers

Topics

  • Diagnosis
  • Symptoms
  • Newly diagnosed
  • Healthy living
  • Research
  • Disclosure
  • MRI
  • Browse all
Sort 1355 results by
Recent activityNewest posts

@ElizabethAnd 

12 Dec 2024 21:48 EditedLast reply 15 Apr 2025 19:38

ElizabethAnd

I wish i could make my brain turn off … just for a day and not worry or stress about a damn thing !! I am so damn depressed and everything and eveyone around me just doesn’t get it !! I am TIRED AND WORN OUT AND SAD AND CRYING AND CANNOT KEEP A SANE THIGUHT WHY WHY WHY I HATE THIS AND no one not even the one I should be able to depend on … anyway it doesn’t matter no one here cares or in my normal life this is just a venting app to get it out .. but alas nothing no one not even me cares to be on this planet anymore i just want to stop being so sad and like I’m a damn burden ….. stories multipolar surgeries having to learn to walk eat shit stand alllllll that and still no one helps !!! I’m expected to still be normal !! I am not normal anymore I can barely do the things unused too without 1,000000000 BREAKS !! It annoys my soul …. I JUST WANT ME BACK

Lafayette, United States
First posted on the Shift.ms app
7

@Maryam4887 

12 Apr 2025 08:04Last reply 13 Apr 2025 08:06

Maryam4887

I was diagnosed with Multiple Sclerosis (MS) back in 2018. Since then, I’ve been managing my condition with medications, specifically Baclofen and Pregabalin. Fortunately, I don’t need any other treatments at the moment. While the right side of my body remains weak and I walk with a cane, I am able to carry out all of my daily activities, including driving, spending time with friends, and fully enjoying life—ups and downs included.I recently started exercising, and I feel much better. I truly believe that with consistent physical activity, I can return to a more normal state, though I know I have a long road ahead of me.Thank you for your ongoing support. I’m grateful for the strength and progress I’ve made and look forward to the journey ahead.

First posted on the Shift.ms app
3

@TomDonahue 

6 Apr 2025 12:31

TomDonahue

https://www.foxnews.com/health/vitamin-d-supplements-could-reduce-multiple-sclerosis-symptoms-study-suggests

First posted on the Shift.ms app

@oldmanjenks 

10 Feb 2025 14:06Last reply 3 Apr 2025 19:26

oldmanjenks

Now, what is one good thing that has come from having Multiple Sclerosis?

First posted on the Shift.ms app
215

@heidi2sisterms 

30 Mar 2025 07:55

heidi2sisterms

Hi have many ? Ms can you tell me dry skin on face/ numb same time ? Legs in morning feel like I wore too small socks. Ice pick headache multiple time a week Is this MS symptoms(?)

First posted on the Shift.ms app

@Scrivie 

10 Feb 2025 14:48Last reply 13 Mar 2025 09:28

Scrivie

Hi everyone, I have a question how many times are we supposed to have contact with our Ms nurse, I have got primary progressive multiple sclerosis and in the last four years I have only seen my ms nurse for five minutes and had one phone call, is this right xx

First posted on the Shift.ms app
29

@not2bMSdwith 

1 Mar 2025 16:24 EditedLast reply 1 Mar 2025 21:37

not2bMSdwith

March is Multiple Sclerosis Awareness Month!

Happy March! Happy MS Awareness Month! 🧡
First posted on the Shift.ms app
2

@jilliantoye 

17 Feb 2025 21:39Last reply 17 Feb 2025 21:52

jilliantoye

Hi everyone... I'm new to the group, and so thankful to be here. I'm from Nicholasville, Ky. and was diagnosed with Multiple Sclerosis in 2005. My disease is progressing and I need help getting things like a shower chair, rails, etc. Unfortunately, I'm not able to financially afford these things on my disability. Any suggestions?

Nicholasville, United States
First posted on the Shift.ms app
3

@Sureth1 

5 Feb 2025 14:43

Sureth1

Multiple sclerosis is a terrible disease in the scenes that you look fine. Nobody sees it but back up the road it’s terrible. m

First posted on the Shift.ms app

@isaactoll17 

28 Jan 2025 12:17Last reply 3 Feb 2025 21:39

isaactoll17

Multiple Sclerosis Patients, I need some feedback.

Hey everyone I'm Isaac - a UCL student passionate about learning more about MS and how we can work together to help each other. I'm not currently diagnosed, but am working to build something to really help people impacted. by chronic diseases. Would love to chat with you guys about your experience...
17
PreviousNext page