A MESSAGE FROM Molly's Fundraising Page
I am so excited to be running the 2024 TCS NYC Marathon with the Cystic Fibrosis Breathe Team! My niece and goddaughter, Nell Pritchard, was born with Cystic Fibrosis 33 years ago. Since then, our extended families and friends have been so supportive of Nell, her health journey, and the mission of the CF Foundation. Nell, who lives and works in NYC, is an inspiration to anyone who she meets! Her strength of body, mind, and spirit, is incredible!
Research and medical advances have made Cystic Fibrosis much more treatable in the last thirty years, which would not have been possible without raising awareness of this genetic disease, and public/private fundraising efforts. The end goal is to find a cure!
I am also running to recognize the amazing efforts of the doctors, nurses and researchers who are dedicated to these patients! Without them, none of this would be possible.
Please support my fundraising efforts for the 2024 TCS New York City Marathon Cystic Fibrosis Breathe Team. No donation is too small. Please click on the donate button!
