Booked tickets to see a band called Pop will eat itself at Southampton, 1865 club at weekend. Was really worried as I cant stand or walk very far,(i use a cane) rocked up at venue and spoke to site and they showed me to the balcony and gave me a stool to sit on and a great view. ( I did reach ...

Struggling with mad fatigue the last few days and if one more person says yeah I’m feeling a bit tired too. I might just bop them on the nose ….. if I had the energy 🤣🤣🤣🤣. Hope all you guys out there are having a good week 👍.

High there, I have had benign MS for 32 years. Finally decided to stop pretending there is nothing wring with me. I take tablets and listen to my Doctors but tend to keep myself to myself re MS. So hello everyone. Gareth

As we gear up to witness amazing feats of athleticism and perseverance at the Olympic Games, let's take a moment to appreciate the incredible strength and determination of individuals living with multiple sclerosis (MS). These everyday heroes face unique challenges with unwavering courage and resili...

Cast your mind back to that moment when you were sitting opposite your doctor and told “it’s multiple sclerosis”. Three words that are nothing short of life changing. When we speak to MSers about their diagnosis appointment, it’s clear that how those three words are delivered, and the care that im...

A year ago Professor Gavin Giovannoni published a blog about a new group of treatments in development called BTK inhibitors (link in comments). With multiple trials ongoing, Gavin wondered if these treatments could “usher in the next generation of innovative MS treatments”. At the time, the post...

Hiya hope everyone is well, I just wanted to ask for some advice on how to handle being out in the sun apart from having ice drinks/ pops but what else I can do as I am terrified, also the same as going to the gym which I used to absolutely love doing before I got ill and I miss it but I'm also terr...

I got diagnosed in 2008 and always have been maybe scared to try medication but seem to manage it quite well with vitamins clean eating and exercise. Last year was my first relapse since then that affected my walking and then had to go on steroids for a week To help which it did. But wondering wha...

Hey 👋 Welcome to the Shift.ms community! Drop a comment below and let us know where you're from 👇 Whether you've got MS questions, you're seeking advice, or you just want to chat to other MSers, we've got you covered 💚 Take a minute to hear Sarah's MS story and learn how she gets the most out ...

Hi everyone I’ve been using Copaxone now for nearly 10 years with really good results, but I’m running out of skin to inject because of scar tissue and lose of fat around my stomach. I’ve been diagnosed as secondary progressive now so my MS nurse says I’m not eligible for Oral DMD’S has anyone else...