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Chris Mula

Chris Mula

Hello Friends & Family,
Once a year, Vanessa and I ask you to donate to the Cystic Fibrosis Foundation. As you all know, our youngest daughter, Brooke; was diagnosed with Cystic Fibrosis shortly after she was born in 2014.
The mission of the Cystic Fibrosis Foundation is 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 treatment, and ensuring access to high-quality, specialized care.
Please join Vanessa and me for the Brewers Ball at the Wharf in DC in Washington DC on Friday, June 10th. This event raises hundreds of thousands of dollars every year that goes directly to research for treatments and medications that improve and extend the lives of people living with CF. If you are unable to join us, please consider making a donation to the foundation through my page. All donations go straight to the foundation and are used for valuable research to help those living with Cystic Fibrosis.

The Cystic Fibrosis Foundation has fueled dramatic improvements in cystic fibrosis research and care. Because of the Foundation, people with CF are living longer and healthier lives. The outlook for people with CF continues to improve year after year.

Thank you in advance for your support and participation in this event, you are helping to make a difference for people living with CF.!
Thanks for your support.
Chris & Vanessa



raised of $10,000 goal

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