Diagnosed with Dermatomyositis in 2012, I was looking for an easy (and interesting) way to share my story with...
Archive for category: #MyositisLIFE
This is a collection of user submitted content designed to promote awareness and education about living with the rare disease, Myositis and its subtypes of Polymyositis, Dermatomyositis, Inclusion Body Myositis, and the Juvenile forms of Dermatomyositis and Polymyositis.
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...
Sage Interviews Emily about Life with Myositis and why #MyositisAwareness is important
Myositis Support, , #MyositisLIFE, MyositisLIFE VideoSage Filmore, 10 years old, interviews her mom, Emily Filmore, about MSU and what it is like to live...
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...
We know we cannot avoid stress; it is simply a part of everyday life. Whether it is stress over...