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
Register today: Fiona, living with Dermatomyositis for three years and ILD for two years, has realized the importance of being proactive about her lung issues. Some of the things she does are based on research, others are based on her personal experience. She is not a doctor but is delighted to share how she deals with it on an everyday basis. Join in this video chat session to hear Fiona’s experiences, ask questions, and share what works for you! Fiona led a video chat, “Myositis and Food with Fiona” that was excellent! You don’t want to miss this one.
Submit your personal Myositis story or video today! We learn through the experiences of others.
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