Myositis Support and Understanding announces reaching a milestone of giving $250k in myositis patient financial assistance.
Whether you missed it or want to watch it again, because it was that good, join your Myositis family...
To kick-off Spirit Week, join us LIVE on YouTube for an intimate discussion honoring the life of Stella Clapp...
Photos from the 1st Annual Myositis Empower Walk in Las Vegas, Nevada, by the Landman Family in loving memory...
Photos from the 2nd Annual Myositis Empower Walk in Las Vegas, Nevada, by the Landman Family in loving...
Third Annual “A Day of Remembrance” a video event to honor and remember those we have lost with myositis....
Learn how not forgiving others negatively impacts us, not the person we don’t want to forgive. We’ll look at...
Second Annual “A Day of Remembrance” a video event to honor and remember those we have lost with myositis....
Introducing the NEW Myositis Support Community! The Myositis Support Community is similar to Facebook, however, it provides a more...
Myositis patients have special needs when preparing for natural disasters. Learn more and be prepared with a plan
Living with, and trying to overcome, autoimmune diseases affect all the people we love. Those of us who have...
Learn more about the different types of Myositis Live Online Video Support, Education, and Activity Sessions we offer, how...
Mums journey was a very difficult one. I remember her first fall the day I gave birth to...
We hope that your involvement with Myositis Support and Understanding (MSU) has allowed you to feel more included and...
12 things your chronically ill friend wants you to know about feeling left behind, and what you can do to help!
, , Myositis, Myositis Life Hacks
One of the worst things someone with chronic illness can do is make a mistake in the balance between...
Hi, I’m Sage and I am nine years old. My mommy has dermatomyositis. I have a list about the...
