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If your MS is like mine, surviving a day is much like surfing. The ocean is an energy field and the waves come in, some higher and most with deep troughs. When I'm in between energy waves, down in the trough, I just dog-paddle along the best I can. When the wave crests, I feel like I'm surfing on a ...

Have you changed your outlook on life or your priorities in some way since being diagnosed with MS? We call this 'MS energy': it's the desire to do something - anything - positive following your diagnosis. It can happen right away or months or years after. We've launched a project to capture and s...

From myself and the rest of the Shift.ms team, we wanted to thank all of the men who continue to contribute to our MSer community. Statistically, there aren't as many of us, so thank you for speaking up and leading the way for others like me. Below is a list of posts and blogs by some of our male me...

Hi guys! Haven't been around here lately, as I was hard at work on the blog (linked in my profile). Hope everyone's OK and keeping up with their lives. Stories are a wonderful way to teach people anything. I believe them to be the best tool of raising awareness for Multiple Sclerosis and teaching ...

Hi there my name is Anna.I'm 35.i have two boys,Gabriel and Santiago.i was diagnosed in 2014 on the 8th with ms.everything is still new to me

Hi I'm Sara, and I have a rare form of MS called tumor reactive multiple scerlrosis that mainly attacks my brain and spinal cord. What do you guys recommend for energy. I just started treatment at the end of last year. An my next infusion is next month. But I need some information about what you gu...

I use to ride bikes all across town and now I look at my mountain bike as if I can’t do it anymore. Fatigue and depression are the worst parts of MS I feel like