Movin’ for Mallory – Cure Cystic Fibrosis

Movin' For Mallory Giving Page

Who is Mallory?
Mallory…

…loves to dance, to play softball, and is bright, funny, and kind.

… but she was born with a life shortening disease called Cystic Fibrosis (CF). Thanks to the Center for Orphan Disease Research & Therapy along with the support of friends and family at events like Spinathon, Mallory has access to medications to help keep her healthy and make her feel better when her CF gets her down. CF affects the lungs and digestive systems of people living with the disease, but it doesn’t have to hold them back!

Team Movin’ for Mallory is a group of family and friends who love and support Mallory, as well as others living with Cystic Fibrosis. Please join us in raising funds for research to help Mallory and the 70,000 people worldwide living with CF! Help add tomorrows and keep them healthy!

What is Cystic Fibrosis: https://www.cff.org/What-is-CF/About-Cystic-Fibrosis/

For more information visit:  http://www.movinformallory.org

 



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