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Jeanie shares her photo collage to show her awareness of Polymyositis for Myositis Awareness Month and the MSU #MyositisLIFE project.
Just a little collage to raise awareness. #polymyositis
Tags: myositis awareness myositisLIFE
My journey started in 2013. I was in the best physical shape in a long time. I started each...
Sarah shares her Appreciate Every Day video for Myositis Awareness Month and MSU’s #MyositisLIFE project.
MSU Founder and President, Jerry Williams, shares his #MyositisLIFE. He shares his commitment to helping other Myositis patients...
As you probably know, we have lost many of our MSU group members throughout the past couple of years,...
I have polymyositis , having been diagnosed 24 years ago. The diagnosis was confirmed after six months of testing. I...
Emily Filmore, Vice President of MSU and author of "The Marvelous Transformation: Living Well with Autoimmune Disease" shares this...
Stan shares his thoughts on his wife, Ellen, and her on-going battle with polymyositis.
May 26, 2017 3:00 pm - 4:15 pm
Join MSU for our Inclusion Body Myositis video chat support session discussing anything you wish that can help make life with IBM easier. Be a part of the conversation, share how you adapt, and anything else that is helpful to the IBM community. Open discussion. Meet Face-to-Face and share experiences in this non-medical conversation with other people living with IBM! Make new friends who understand! You don’t have to feel alone!
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