
The Myositis Empower Walk Newsletter – Edition 1
Introducing the Myositis Empower Walk Newsletter (MEWN)! Meet Angela, Holly, and Ashley!
Introducing the Myositis Empower Walk Newsletter (MEWN)! Meet Angela, Holly, and Ashley!
Our dad's time with dermatomyositis was only a small portion of his life, although a very monumental time in our life.
We need plasma donors or we face a shortage of life-saving immunoglobulin therapy used to treat myositis and many other diseases. Join the #ItsMyTurn campaign.
Ryan demonstrates what he has learned living with myositis to help to rise from a low toilet using some practical tips and tricks.
Check out some photos we captured participating as a sponsor of the 2019 TMA conference. Find information about our sponsors and partners that also attended....
Ryan demonstrates what he has learned to make getting up from a seated position or a wheelchair easier with myositis.
I am not a vampire. However, at the direction of my dermatologist, I am living a “full vampiric life.”
We explain and highlight a personal account of how one patient fought the insurance company trying to deny a medication for myositis.
"Save Me" by Alyssa Smith is a song about myositis, released on Rare Disease Day 2019.
Any interaction with the outside world is fraught with danger when other people in the world are not careful, because of the insidious and invisible...