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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

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Found approximately 14188 results
Deleted

@Coopsms

Coopsms

https://youtube.com/watch?v=H9QsAO4BU28&feature=share

Y
  • Symptoms
  • Treatment
  • Work and play

@billyshift

Last reply

billyshift

What makes your eyes roll with MS?

I want to hear everyone's little frustrations that come with life with MS. Laughter is the best medicine so I thought this would be therapeutic 😂 I'll start in the comments, add yours below! 👇
  • Blurred vision
  • Symptoms
  • Diagnosis
  • Work and play
66

@Smurfbythebay

Last reply

Smurfbythebay

What supplements are y'all into?

Hoping this will be a fun, informational thread! They may not have the same effect (or no effect 😅) on everyone, but I'm curious of people's experiences. So besides the good ol' vitamin D, what supplements strike your fancy?
  • Healthy living
  • Vitamins and supplements
  • Diet
  • Work and play
  • Treatment
5

@kellpage

EditedLast reply

kellpage

Hello! I’m Kelly (going on year 7 with MS)

Hello. I just joined and I’m excited as I’ve never talked to anyone else that has MS (I have an estranged aunt that has it but we don’t speak). I’m a 27 year old interior designer and set designer for film and television productions from Colorado, which has an unusually high number of people diag...
  • Newly diagnosed
  • Mental health
  • Diagnosis
  • Symptoms
  • Work and play
  • Healthy living
  • Going out
  • Family and children
2

@adamslilith

Last reply

adamslilith

"MS isn't your friend but it's not your enemy either"

New video online! Today I talk about my story... about the things MS has taken away from me and how I adapted to being chronically ill and STILL doing what I love. Yes, its motivation wednesday 😄 Check it out 🧡 https://youtu.be/clIF5jOVu0c
  • Symptoms
6

@Lowlander

Last reply

Lowlander

Just wondering what's your thoughts are?

Have you ever felt like you've backed your self into a corner with no way out? I've been officially told I'm now spms...no great shock I have been for years but neuro always told me I was rrms so I could still have DMT (tec). I've been NEDA since I started, now that mayzent has been approved he wan...
  • Diagnosis
  • Disclosure
  • Treatment
  • Which DMT
  • Relapsing remitting
  • Work and play
  • Secondary progressive
  • Accessibility
  • Work and Study
5

@Snowbirds

Snowbirds

Diet and yoga will help to reduce symptoms

Hope healthy eating and daily 1-2 hours yoga will improve this Heath issues suffering
  • Healthy living
  • Symptoms
  • Mind and body
  • Diet
  • Work and play
  • Exercise

@Yorete

Last reply

Yorete

Your MS patient pack - I got your back 😄

Hello my fellow MSers, I thought it would be useful to do a MS patient pack. You know my experience has been the NHS leaving me to die and then bully me. No one bullies me & Londrina! So check this out- Listen you are disabled, you have MS and depression lives with us please deny it BUT you are ...
London, United Kingdom
  • Work and play
  • Accessibility
  • Symptoms
  • Balance
  • Travel
  • Money
  • Exercise
17

@Darinka

Last reply

Darinka

Raise your hand if you feel victimized by insurance

I have been waiting and calling almost every week to see if my kesimpta has been approved. Apparently my insurance didn't receive the Dr form to approve this medication and I can't get a hold on the patient program. I have been crying for the past couple of hours lol I don't know when this finally ...
  • Copaxone
  • Treatment
  • Symptoms
  • Work and play
1

@billyshift

Last reply

billyshift

Which MS symptom impacts your daily life the most?

Introducing this month's MS poll 👇 *brownie points if you comment below with your number one tip for dealing with your symptom 🍫
  • Symptoms
63

@Mvsaccomanno

Edited

Mvsaccomanno

Hello everyone I am new to This club iam from Buffalo New York

Hello everyone I am New to this group I am from Buffalo NY 35 years old I was diagnosed August 2012 joining to build a support system and a better understanding of Ms to help now and in the future!
  • Newly diagnosed
  • Diagnosis
  • Work and play
  • Healthy living

@jamoranto

Last reply

jamoranto

A great glide. Wish you all the best

https://www.instagram.com/reel/Cp_kIb3DIr_/?igshid=YmMyMTA2M2Y=
  • Healthy living
4

@billyshift

EditedLast reply

billyshift

How long did it take you to get diagnosed with MS?

We’ve just launched Shift.ms polls! Take part in the first poll below👇 *Bonus points if you can leave a comment and let me know: are you happy with how long it took?
  • Newly diagnosed
  • Diagnosis
  • Symptoms
  • Work and play
186

@MSWarrior84

Last reply

MSWarrior84

I was diagnosed with Primary Progressive MS a year ago if anyone would like to talk...

No new lesions at my last scan after two full treatments of Ocrevus
  • Diagnosis
  • Newly diagnosed
  • Ocrevus
  • Treatment
  • Primary progressive
  • MRI
5

@Mrsadams1129

Mrsadams1129

Anyone get diagnosed years after being told it’s not MS?

To begin, I had a craniotomy in 2014 to remove a benign brain tumor from the left frontal lobe that was causing vision loss, the worst migraines I’ve ever had, and many other issues. Since 2020, I’ve noticed random nerve pain in other places on my body outside of my head. Random hot spots that feel ...
  • Symptoms
  • Diagnosis
  • Pain
  • Blurred vision
  • Numbness
  • Work and play
  • Brain fog
  • Spasticity
  • Healthy living
  • Hot and cold

@Mrsadams1129

Mrsadams1129

Anyone get diagnosed years after being told it’s not MS?

To begin, I had a craniotomy in 2014 to remove a benign brain tumor from the left frontal lobe that was causing vision loss, the worst migraines I’ve ever had, and many other issues. Since 2020, I’ve noticed random nerve pain in other places on my body outside of my head. Random hot spots that feel ...
  • Symptoms
  • Diagnosis
  • Pain
  • Blurred vision
  • Numbness
  • Work and play
  • Brain fog
  • Spasticity
  • Healthy living
  • Hot and cold

@MonikaPawelec

Last reply

MonikaPawelec

What do you think about CBD?

What do you think about CBD? Is it really helping for MS symptoms? I wonder if it really affects or is it just marketing?
  • Symptoms
7

@Drago

EditedLast reply

Drago

What R the craziest MS Symptoms you have had

Before diagnosis i thought i was going mad with some of my crazy symptoms. Whats are your craziest symptoms. I will start ... Not being able to blink my left eye lid while right eye lid closed 😜
Birmingham, United Kingdom
  • Symptoms
  • Diagnosis
  • Mental health
56

@Poppetkara

Last reply

Poppetkara

How am I supposed to cope with waiting a year to find out if I have MS

I have been told I may have MS but after seeing a neurologist he told me I need to wait a year before having another MRI scan. I don’t feel I can talk to anyone (I’ve told a couple of old friends…one who has Parkinson’s and was very understanding. I feel I’m slipping into a depression with the heav...
  • Disclosure
  • Diagnosis
  • Mental health
  • Symptoms
  • Family and children
  • MRI
  • Work and play
11

@shiftms-films

EditedLast reply

shiftms-films

Have you experienced loneliness because of your MS?

In this episode of MSers React Dave, Roxy, Katt and Heather respond to posts on Shift.ms about loneliness. Have you experienced loneliness because of your MS? If so you’re not alone! If you have an experience to share, or a way that you’ve learnt to adapt then please share your story in the comment...
  • Healthy living
  • Diet
  • Exercise
  • Research
  • Relapses
  • Mind and body
  • Symptoms
  • Newly diagnosed
  • Diagnosis
23
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