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
Author: Myositis Support
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
In March 2012, after several days of low-grade temperatures and muscle aches, I noticed heaviness in my legs, like...
Register today for the MSU Caregivers, Family Members, and Friends online video support session in celebration of our Myositis Caregivers and National Family Caregivers Month. Tuesday, November 28th @ 6:30PM EDT. Join Barbara and Betsy for a discussion about Myositis and Caregiving. Ask questions, share your experience, or just listen and watch. Event is free!
IBM patients, mark your calendar and join us for this free video support session with Mary Jane on Nov. 30th, 3PM Eastern Time. Share experiences, ask questions, compare notes, and make new friends. This session is tailored to those diagnosed with, or suspected of having, Inclusion Body Myositis.
Submit your personal Myositis story or video today! We learn through the experiences of others.
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