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 501(c)(3) nonprofit organization with a mission to improve the day-to-day lives of Myositis patients. MSU is a patient-centered organization, founded by Myositis patients, for Myositis patients, and believes education, support, advocacy, and assistance are key to helping patients and caregivers. As a nonprofit, we rely on donations for funding and volunteers to help manage our fast growing organization.

View more information: Myositis Support

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PIONEER, Idera clinical trial for dermatomyositis

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