The Win4Quinn Foundation, is a nonprofit founded in October of 2019 by Quinn Edgington’s family. Quinn is the reason for the foundation. Quinn is a 4-year-old fighting Cystic Fibrosis, which means she endures endless procedures, breathing treatments, and fights every day against CF, (a genetic disease that affects the lungs and digestive system). We are a collection of family and friends who are fighting to make the lives of CF families easier. Our board of directors is a group of CF parents, CF grandparents & CF friends and family. We are in this because we know how hard it is to be in the fight against CF.
The Need
There is a huge need in the Cystic Fibrosis community, because CF is an expensive, exhausting, and time consuming disease. From quarterly 4-hour clinic visits to daily breathing treatments, these regimens take a lot of time and a lot of money. CF effects not only the person with CF, but their family as well. Parents fight to take care of their child, provide financial support, and live a fulfilling life. Win4Quinn will help with some of the financial burden CF families endure. With your help, as a team we can help families NOW. There are other foundations that are tirelessly working to find a cure for CF, so lets help families until the cure is found.
How Can You Help?
- Every year we have two main fundraising events you can participate in. We are excited for our 4th annual Win4Quinn Summer Party, held in conjunction with the Utah National Association of Therapeutic Schools and Programs (NATSAP) Regional. If you are interested in sponsoring the party please contact us.
- The second fundraiser we do each year is bicycle kits — we work with DNA Cycling to design custom Win4Quinn jerseys and bib shorts. Each year is a new design, and we are excited to unveil the new 2020 jersey. If you would like to sponsor the kits please contact us.
- We hold these two annual fundraising events, but financial contributions are welcome year-round — visit our donation page today.