Help us give children hope for a brighter future.

Hello friends and family! We need your support! Will you donate and join Harper’s team this May to raise funds for JM? As many of you know, our little Harper was diagnosed with a very rare autoimmune disease last year called Juvenile Dermatomyositis or JM for short. JM affects 1-3 in every million children and currently there is no cure. Children with JM rely heavily on daily, high doses of steroids, chemotherapy injections and immune globulin infusions. Harper and kids like her, need better and safer treatments for JM. This is only possible through funding critical research with donations from friends and family. Please consider donating to her team and if you live nearby, join us for the event on May 19th! Her team will be adorned in unicorn horns and/or Tutus - Two of her favorite things :) Bring your pups! We have Curly Tail Cakes joining us with “pupcakes” for every 4 legged team member. We’ll have raffles for fun activities like Hapik, Lego Discovery Center and Monster Mini Golf. A live DJ, bounce house and magician. Plus DoughNation pizza truck will be joining us with their incredible wood fired pizzas. Please join us Sunday to walk for a Cure!

Every dollar makes a difference to improve treatments, care, and support for juvenile myositis.  

Juvenile myositis is a life-threatening disease which causes children to miss out on the best part of being a kid.

There are currently no approved treatments.  Current treatments save lives, but have devastating side-effects.  Together we can change that.  

Please make a donation to help me reach my goal.  Your generous donations can allow us to advance the fight against this disease.  

Want to help me fundraise?  Click "Join My Team!"

It is only with your support, we can get to the finish line.  

**If you wish to send a check, please make payable to Cure JM and mail to:

Cure JM, P.O. Box 45768, Baltimore, MD 21297, with our family's name in the memo

Thank you!