BENEFITING: Cystic Fibrosis Foundation
ORGANIZER: Cystic Fibrosis Foundation
Dear Family and Friends,
I am participating in the NYC Marathon Cystic Fibrosis Breathe Team to raise money for thousands of people with CF like my daughter Katie. Throughout her life, she has been able to do more than anyone expected due to breakthrough medications and treatments. In this photo, she had just finished a Half Marathon as part of a Half Ironman Triathlon relay team.
I raise money to help Katie and others continue to lead their best lives. Each mile of this marathon will be dedicated to a person I know with CF. Their stories will inspire me to run one more mile. I also hope their stories will inspire each of you to make a donation to help all people with CF continue to run, continue to breathe and continue to pursue their dreams.
Here is the names of all to whom I'm dedicating this race. When possible, I dedicated a mile that correlates to the person's age. Please consider making a donation to honor someone you love!
1 Katie; 2 Selah; 3 Van; 4 IV; 5 Allie;
6 Jozie; 7 Christopher; 8 Ryan; 9 Gareth;
10 Eve; 11 Michael; 12 Sage; 13 Silas;
14 Sandra; 15 Kelli; 16 Casey; 17 Katie V;
18 Alexis; 19 Diana; 20 John; 21 English; 22 Emily K-G;
23 Emily S; 24 Scott; 25 Howell; 26 Katie
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care.
The Cystic Fibrosis Foundation funds more CF research than any other organization, and nearly every CF drug available today was made possible because of Foundation support. Will you support my team and join us in Adding Tomorrows?