President, founder, and CF mom
We created the Violet Foundation to organize community events and activities to benefit people and organizations that are dedicated to helping those with cystic fibrosis. Our mission is to inspire communities to stand together with those who fight CF every day.
Cystic fibrosis is a life-threatening genetic disease that affects the lungs and digestive system, leading to decreased lung function, and the inability to absorb essential nutrients.
Read more about the disease at the Cystic Fibrosis Foundation's website.
LEARN ABOUT CF
Foundation inspiration and CF patient
in the fight to cure cystic fibrosis
May 22nd's open bar to benefit the Cystic Fibrosis Foundation was a huge success! Stay tuned for our next event!
Violet Foundation is a tax-exempt 501(c)(3) organization
All 2018 proceeds will be granted to the Cystic Fibrosis Foundation
Founder and CF dad
FIGHTFOR A CURE
We created the Violet Foundation to bring friends, families, and neighbors together in the fight to cure cystic fibrosis (CF). Our mission is to fundraise for organizations dedicated to curing CF and helping those affected by the disease. Our goal is to inspire entire communities to fight for a cure so that people with CF do not fight alone.
Bringing communities together to end CF