Coalition of Participating CF Nonprofits
"The following organizations participating in Warrior Wednesday represent tens of thousands of CF families around the globe. Each organization has a unique mission that brings incredible value to the CF community".
Warrior Wednesday leads the charge for Giving Tuesday in the cystic fibrosis community. Show your support and donate to your favorite CF charity below.
Scroll down to learn more about each charity. Click the links to donate.
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Boomer Esaison
(NY, USA)
Mission Statement: The Boomer Esiason Foundation is a dynamic partnership of leaders in the medical and business communities joining with a committed core of volunteers to heighten awareness, education and quality of life for those affected by cystic fibrosis, while providing financial support to research aimed at finding a cure.
CF Fighters
(MI, USA)
MIssion Statement: CF Fighters is a 501(c)(3) non-profit organization composed of volunteers dedicated to raising awareness, and helping Michigan CF patients and families who need our assistance.
We provide care packages, gift cards, gas cards, meals, and bill pay assistance. We also adopt families for Thanksgiving and Christmas each year.
CF Warriors
(Wales, UK)
Mission Statement: Our mission is to raise awareness for the importance of sport & exercise to the whole cystic fibrosis community across the globe, through events, research funded by the charity, and Warrior Packs we send out to children with CF, which are designed to help inspire them and make them feel like part of a team.
Claire's Place Foundation
(CA, USA)
Mission Statement: The specific purpose of Claire’s Place Foundation is to provide heartfelt help to children and young adults diagnosed with Cystic Fibrosis, as well as their families, for the purpose of improving their quality of life. We hope to accomplish this by heightening awareness and providing education, skills, financial and emotional support.
Cystic Fibrosis Lifestyle Foundation
(FL, USA)
Mission Statement: The CFLF assists in providing avenues toward healthy and active lifestyles through recreation, thereby empowering and educating people with Cystic Fibrosis on the critical psychological, social, and emotional connections between their lifestyle and their health.
Mauli Ola Foundation
(CA, USA)
Mission Statement: Dedicated to providing hope and confidence to individuals living with genetic diseases. Harnessing the healing powers of the ocean, we introduce surfing and ocean-based activities as natural therapies. We are honored to share our knowledge of the ocean, family values and community — May the wave heal us all.
MOF Surf Experience Days: Mauli Ola takes kids with CF surfing to experience what natural therapies can do for their lungs. The saline content in the ocean air and water breaks down the congestion in their lungs. Exercise helps to strengthen their lungs and expel mucous. With natural salt water treatments, their hospital visits are significantly reduced and they are exposed to the outdoors leading to healthier and more fulfilling lives that all kids should experience.
Piper's Angels Foundation
(FL, USA)
Mission Statement: To support and improve the lives of families in the cystic fibrosis community through grassroots advocacy and socially innovative programs, raising awareness through education, offering life-expanding activities, providing urgent financial support, and funding critical developments.
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The Bonnell Foundation
(MI, USA)
Mission Statement: To give emotional and/or financial support to parents who have a loved one with cystic fibrosis. Our hope is one day no CF parent will experience the pain of losing a child to this disease. Live – Breathe – Inspire
The purpose of The Bonnell Foundation is to provide tools to navigate the difficulties of living with CF. We strive to connect families with education resources through their CF journey. The Bonnell Foundation offers college scholarships to those affected by CF, financial assistance and lung transplant grants. We hope to equip families with a roadmap to
guide their way and to educate the community around them about cystic fibrosis.
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