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Support Renee's Cystic Fibrosis Campaign!

Renee Freyer
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Renee Freyer

I'm Raising Money for the Cystic Fibrosis Foundation... and Trying Stand-Up Comedy for the First Time in a comedy competition.

My reason for participating is much bigger than a five-minute stand-up set. My cousin, Teresa, passed away from CF in 2004 at just 19 years old.

Teresa had a larger-than-life personality and an unforgettable sense of humor. More than twenty years later, I can still hear her infectious laugh. She had a remarkable ability to make an impression on everyone she met, and her spirit continues to live on in the memories of those who loved her.

I'm proud to participate in LOL4CFF in honor of Teresa, the Truxillo and Whitacre families, and anyone whose lives have been touched by cystic fibrosis.

The fight against CF has seen incredible progress. Groundbreaking therapies, including Trikafta, have transformed care for many people living with the disease. These treatments can benefit approximately 90% of people with CF, and life expectancy has increased dramatically over the past several decades. For children who begin these therapies at a young age, there is growing hope for even longer, healthier lives.

How You Can Help
  • Make a Donation - Every contribution, regardless of size, makes a meaningful impact and helps advance the mission of the Cystic Fibrosis Foundation.
  • Attend the Show - Join me at LOL4CFF on Friday, October 2, 2026, at The Casey in Charlotte. Your ticket includes a seated dinner, hosted beer and wine, and the opportunity to vote for your favorite comedian. (I hope that's me!)
  • Donate an Auction Item - Support the event through the silent or live auction.  Learn more:  Auction - LOL4CFF 2026
  • Spread the Word - Share this page with friends, family, colleagues, and anyone who may be interested in supporting this important cause.

Every dollar raised helps support the research, care, and innovation that continue to improve lives and bring us closer to a future where no family loses a loved one to cystic fibrosis.

Thank you for helping me honor Teresa's memory and support everyone affected by cystic fibrosis!  Learn more at www.cff.org.
MAY
29

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