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




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


Leave a reply

Your email address will not be published. Required fields are marked *


This site uses Akismet to reduce spam. Learn how your comment data is processed.

© 2021 Myositis Support and Understanding Association (MSU). All rights reserved. | View our Privacy Policy, Terms, and Non-Discrimination policy. MSU is a charitable organization with 501(c)(3) tax-exempt status. Federal ID #47-4570748.

The best way to prevent catching or spreading coronavirus is thorough hand washing, social distancing, and social isolation. Should you begin experiencing symptoms of coronavirus, which include fever, cough, and shortness of breath, please contact your doctor immediately. View COVID-19 resources and updates, and stay tuned to your state, local, and federal health agencies, along with the CDC.

Log in with your credentials


Forgot your details?

Create Account

Send this to a friend