We have been so blessed to get a front row seat to the approval of many ground breaking medications for our son. Years and years of work, sacrifice, fundraising, and medical advancements done long before Evan’s CF journey began, that he now gets to be on the cutting edge of benefiting from.
The Cystic Fibrosis Foundation (CFF) leads the charge in advancing new therapies for all people living with CF while continuing to aggressively pursue a cure. Without the CFF, the forecast for not only our son’s life expectancy, but the quality of that life would be much worse off. We owe much to the CFF.
We continue to dream a million dreams for our baby boy and wake up every day with the determination to do all we can to make those dreams his reality. Our dream for our son is a cure, and we believe that day will come sooner than we could have ever imagined because of your relentless support. We hope that you will continue with us in this journey.
All donations will go directly to the Cystic Fobrosis Foundation and are 100% tax deductible.
- McKay & Stacy Allen -