Ella was diagnosed with Cystic Fibrosis when she was 3 weeks old. Now, more than two years after her diagnosis, we have been the beneficiaries of the work and research funded by the Cystic Fibrosis Foundation. She has been on a modulator drug for over a year, and we've seen the positive impact in images of her lungs and in how quickly she recovers from illnesses. Without progress and support of the Cystic Fibrosis Foundation, and generous donations from those who care about the CF community, Ella would not be as healthy as she is today.
We are supporting the Cystic Fibrosis Foundation, and I invite you to join us at the event or make a donation to this event.
The Cystic Fibrosis Foundation has fueled dramatic improvements in cystic fibrosis research and care. Because of the Foundation, people with CF are living longer and healthier lives. The outlook for people with CF continues to improve year after year.
Thank you in advance for your support and participation to this event. And thank you for adding tomorrow to Ella's life!
xoxo, Lauren, Bryan and Ella