Connect with others who get what you're going through.

The thing with Shift.ms is the community reaches out to you in a way that is completely different from your consultant, GP, friend, family or loved ones.

@Dean

I was really lucky to be signposted to Shift.ms on the day of my diagnosis. I met with real people who were like me, were still working and were still ambitious.

@Cathy

Thank you Shift.ms you've been a life changer for me. People and community have saved me; but I never would have met those people had it not been for Shift.ms. It’s important to share where I’ve been, MS is a rough ride! But you enabled me get to where I am ♥️

@Donna

A lot of people assume Shift.ms is just there for people during their diagnosis but for me Shift.ms has given me a platform to talk about my experiences and in turn I hope I'm helping other people.

@Ellen

The sense of community that Shift.ms affords people of all ages, walks of life and from all around the world has made this big disease seem like a smaller part of my life.

@ChefTrevis