Our Great Strides Story
Our beautiful Molly Grace was diagnosed with cystic fibrosis. Cystic fibrosis is a progressive, genetic disease that affects the lungs, pancreas, and other organs. Thanks to our early diagnosis, medications, and therapies we are fighting to slow the progress of the disease. However, there is no cure for cystic fibrosis and we face the sobering prospect that Molly’s life may be cut short.
Our Molly is full of moxie despite her diagnosis. She loves playing with her big sisters, singing, and dancing. This year we have made so many awesome memories, from horseback riding to family movie nights. We walk in hopes of making more memories in the years to come.
We are raising awareness and money for the CF Foundation so Molly, and every other CF warrior, can reach these milestones.
How can you support Molly?
- Pray! We are so thankful for the friends and family who have kept Molly and our family in their prayers.
- Share Molly’s story! Sharing our social media posts allows others to see and possibly join us in our fight!
Buy a shirt! Molly's Moxie shirts are available through May 20. https://mollys-moxie-crew.printify.me/products
- Walk with us! Join Molly’s Moxie Crew on June 1 as we walk for a cure!
- Donate! By supporting the CF Foundation we have the opportunity to be a part of ending this disease.
Connect With Us
IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.