Eve was diagnosed with Juvenile Dermatomyositis (JDM) in September 2022. This is a rare disease that has no FDA-approved treatments and no cure. 

We want to solve that! Please join us on Sunday, July 2nd, as we walk to give back to CureJM (Time and Place TBD)! CureJM is a nonprofit organization leading the way in finding better treatments for JDM patients, advancing clinical trials, and funding grants to help find a cure.

Please consider donating to help Eve and kids like her in their battle with JDM (a single dollar would help)! This disease isn't going away, unless we help! Let's find a Cure with CureJM.

Thank you, The Brull Family