We are kicking off our Fifth fundraising event in Tiffin, Ohio. Last year with help from our
community we raised almost $50,000 that went 100% to Cystic Fibrosis Foundation. We are reaching out to you with hope that you will join us by Sponsoring our event. This revenue helps support our mission: To cure cystic fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatments, and ensuring access to high quality, specialized care.
JuNo’s Ark used to be called Noah’s Ark when our 10-year-old son Noah was diagnosed with
Cystic Fibrosis at two weeks old. When our second child Julia was born in 2017, we found
out that Julia in fact, does have Cystic Fibrosis as well and decided to change our team’s name
to JuNo’s Ark. While we had hoped for a different outcome, that will not stop our passion and determination to raise awareness and funds for the disease!
The money we raise for the CF Foundation goes directly towards research that makes it possible to find new drugs for this genetic disease, making it possible to treat our children. Did you know that Cystic Fibrosis research is solely supported through donations from individuals such as yourself, in addition to corporations? Cystic Fibrosis does not receive ANY federal funding for research towards new drugs to combat the disease.
Please support our cause!
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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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.