This was more like "A Month in the Life" since I filmed almost every day this month for Myositis...
Archive for category: MyositisLIFE Video
This is a collection of user submitted content in the form of videos 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.
Sarah shares her Appreciate Every Day video for Myositis Awareness Month and MSU’s #MyositisLIFE project.
I have heard so many stories of how those diagnosed with a chronic illness, like Myositis, have lost their...
Charlie Jester shares his #MyositisLIFE as a spouse and caregiver
Myositis Support, , #MyositisLIFE, MyositisLIFE VideoAs Jerry’s partner of 13 years, and spouse of 3 years, I think I have witnessed just about everything...
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...
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...
This is a glimpse of my simple but fulfilling life with Myositis.
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...