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.
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.
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 ♥️
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.
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.
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