Emily Filmore shares her Beautiful Life for Myositis Awareness Month and MSU’s #MyositisLIFE project. 

Emily Filmore, Vice President of MSU and the author of “The Marvelous Transformation: Living Well with Autoimmune Disease” shares this glimpse into her #MyositisLIFE.

Here is the article her husband wrote about his life as a spouse of someone with chronic illness, referred to in the video: www.emilyfilmore.com/blog/chronicspouse

MSU note: Emily Filmore’s “The Marvelous Transformation: Living Well With Autoimmune Disease” is available for sale on our website here: Understandingmyositis.org/shop/marvelous-transformation/

Find Emily on our Myositis Network


 

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Myositis Support and Understanding Association (MSU) is a patient-centered, all-volunteer 501(c)(3) nonprofit organization Empowering the Myositis Community. Founded by Myositis patients, for Myositis patients, MSU provides education, support, advocacy, access to research and clinical trial matching, and need-based financial assistance.

View more information: Myositis Support

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