When Jayce was diagnosed with Cystic fibrosis at 4 months old & it changed our family. We worried all the time about how things were going to go for him. I personally refused to give up hope. Jayce began taking Kalydeco in 2012 & he has been so much better. I felt like it was a miracle, yet we also felt guilty as all CFers couldn't have Kalydeco. I've kept it in my head & refused to believe that he's going to die from CF. There are so many more new drugs being developed through generous donations. Please help us as there is NO government funding for a cure. I've met so many others with CF online through the years & I've learned so much more from them. People with Cystic Fibrosis are really the bravest & strongest people that I've ever met.
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. I walk for them and hope you will support me in my efforts.
Real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease. By walking today, I am helping add tomorrows to the lives of people living with cystic fibrosis. Will you join me? Support me by making a donation to my Great Strides fundraising campaign today!
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
Please support me!
Help me reach my fundraising goal by donating to my Great Strides fundraising campaign. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting life-saving research and medical progress. Your gift is 100-percent tax deductible.
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Updated June 15, 2022. To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
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