Our team walks enormous strides for our mother, wife, daughter, sister, friend, and co-worker Breann who always persevered in any situation that was sent her way. Breann has lived with cystic fibrosis her entire life and spent most of her childhood in the hospital like it was clock work. When she was younger doctors told her she wouldn't even live to see her 20's but despite the odds almost two years ago, family and friends got together and celebrated a fabulous 40th birthday with her (she doesn't even look a day over 30 still).
No one knows what path life will bring anyone at this point after living through a global pandemic but we all plan on celebrating ATLEAST 20 more birthday's with Breann and loving every minute of it.
Join our team and help us add more tomorrows for not only Breann but all Americans living with cystic fibrosis – a rare, genetic, life-shortening disease that makes it difficult to breathe.
To participate, just click on the "Join our Team" button. From there, you can make a donation and start fundraising!
With supporters like you by our side, the Cystic Fibrosis Foundation continues to lead the way in the fight against CF, fueling extraordinary medical and scientific progress. The life expectancy of someone born with CF has doubled in the last 30 years. Despite this progress, many people with CF do not benefit from existing therapies either because their disease is too advanced or because their specific genetic mutations will not respond.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated June 15, 2022. To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
To minimize the risk of COVID-19 infection, we ask that attendees at CF Foundation events follow these steps:
FOR YOUR SAFETY AND THE SAFETY OF OTHERS: