Supporting Shift.ms

Do you feel like you’re in a pretty good place or do you feel like you could do with more support? Even one year on, we’re conscious things still feel very uncertain, and many people are struggling more now, with the cumulative impact of social isolation and changes to healthcare and support, than ...

My blog post all about my MS! Shift.ms was always there for me from the beginning to now and will continue to be for hopefully years to come! Hope you enjoy it! https://shift.ms/blogs/how-shift-ms-helped-me-through

We want to share a blog post from the lovely @Jane_Watts that was published recently on our blog page: https://shift.ms/blogs/finding-shift-ms-a-new-lease-of-life Can relate to @Jane_Watts's story? What's your experience of trying to find support when you were first diagnosed?

I was in a complete state of shock. I was confused by the questions I already had, the answers I didn’t understand and the questions I didn’t know to ask. Shift.ms was the answer I was looking for. I’m proud to be apart of this campaign because I know how much shift.ms can help someone newly diagno...

Hi everyone I just wanted to share this video I was a part of recently. I remember when I was first diagnosed with MS, and I found shift.ms not long after. Shift has been a big part of my life since that diagnosis, and I want it to keep being here for other newly diagnosed people, which is why I’...

http://www.youtube.com/watch?v=Ep_fwJnC5I0&feature=youtu.be We’ve all experienced possibly one of the toughest years we’ve known. There has been a surge in new members turning to Shift.ms in greater numbers than ever before. Many will be people who have recently been told, “you have MS”. We all re...

https://www.youtube.com/watch?v=Ep_fwJnC5I0 Learn more here 👉 https://shift.ms/always-here