Janet I. shares “Cross Stitch” for Myositis Awareness Month and MSU’s #MyositisLIFE project.
“I have been working on my cross stitch project for several months. Here is the first half.”
Tags: myositis awareness myositis story
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
Sage Filmore, 10 years old, interviews her mom, Emily Filmore, about MSU and what it is like to live...
Join us on January 18, 2018 for this patient-led online video education session. Fiona will share the exercises she does, based on research, and more specifically on the Helene Alexanderson exercises (Functional Index 2), while others are based on her personal experience (stretching). You will be able to share what you do, ask questions, and meet other myositis patients face-to-face.
Free Laughter Yoga live online video session with Laughter Yoga instructor, Lynn Lizarraga. Laughter is not only good medicine emotionally, it also works muscles. Join us on the date and time listed and have fun while getting active.
Submit your personal Myositis story or video today! We learn through the experiences of others.
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