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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! 👇

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?

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...

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

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...

Hope healthy eating and daily 1-2 hours yoga will improve this Heath issues suffering

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 ...

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 ...

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

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!

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?

No new lesions at my last scan after two full treatments of Ocrevus

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 ...

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 ...

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

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 😜

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...

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...