There are many challenges faced by patients living with a rare, chronic illness like Myositis. These can include: medication...
Tag Archive for: myositis awareness
Diagnosed with Dermatomyositis in 2012, I was looking for an easy (and interesting) way to share my story with...
Jerry Williams shares his #MyositisLIFE living with Polymyositis and overlap syndromes
Myositis Support, , #MyositisLIFE, MyositisLIFE Story, MyositisLIFE VideoMSU Founder and President, Jerry Williams, shares his #MyositisLIFE. He shares his commitment to helping other Myositis patients...
I was diagnosed with Polymyositis in September of 2012. Before getting sick, I was always so busy working, running...
I am the their care giver you see me every where But what you don't see is just how I...
I have polymyositis , having been diagnosed 24 years ago. The diagnosis was confirmed after six months of testing. I...
I have been working on my cross stitch project for several months. Here is the first half.
I have Inclusion Body Myositis (IBM); a rare and degenerative muscle disease. It is an autoimmune disease with symptoms...
This is a glimpse of my simple but fulfilling life with Myositis.
In December 2003 I began complaining about a burning sensation in my lower legs, so bad that it would...
Emily Filmore, Vice President of MSU and author of "The Marvelous Transformation: Living Well with Autoimmune Disease" shares this...
Maureen, the Senior Group Administrator for MSU, and a patient living with Polymyositis, shares her #MyositisLIFE with MSU showing...
2015 - Photos and Video of Myositis patients, friends, and family supporting MSU and Myositis Awareness.
Before Dermatomyositis I was a pretty healthy guy. I was in good shape, went to the gym 7 days...
Myositis Awareness Day And My Husband’s Diagnosis by Guest Author, Barbara Naturally Speaking It’s been almost three years since...
Myositis Awareness Day 2015 video is a story in photos and music that shows the support that MSU fosters...