Rare Disease Month
February is Rare Disease Month. A month dedicated to raising our voices to the world through advocacy, awareness, and education. Since juvenile myositis is a rare disease, we would like to recognize the warriors and families who battle courageously every day.
During February, we will share different ways for you to help support our rare cause. Will you join us in making your voice heard for better treatments and care on our journey toward a cure?
Meet Our Rare Disease Warriors
Since it is Rare Disease Month, we would like to take a moment and shine the spotlight on some of our amazing JM warriors.
Click the link below to read their stories and updates.
Help Find A Cure
Raising funds for juvenile myositis helps drive research toward better treatments and a cure for this rare disease. Every dollar supports vital medical advancements, patient support, and awareness efforts. Together, we can bring hope and progress to those affected.
Rare Disease Advocacy
Cure JM has been selected as a nonprofit keynote speaker at NIH Rare Disease Day 2026, where we will share how collaboration between Cure JM, the NIH, and NCATS is helping drive meaningful progress in juvenile myositis research.
Read the full story and learn how you can sign your name to our Proclamation of Thanks.
Make a Gift to Cure JM
Join us in supporting pivotal JM research, new clinical trials, and empowering educational programs, all with the goal of improving the lives of our JM kids and their families.
No gift is too small and in fact, could be game-changing for our rare disease families.
Thank you for joining our fight and making an impact that can change lives.
