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SAVE THE DATE: Nov 6-9, 2025 / Puerto Vallarta, Mexico

The 20th Annual Hook the Cure is almost sold out, with only one or two rooms remaining. We've arranged for additional accommodations at Villa Premiere's sister property, Buenaventura Grand. We'll keep you updated on this situation.

Come and join our dynamic duo, Bob Huston and Jeff Jennison, as they take you on an unforgettable adventure in the stunning paradise of Puerto Vallarta.

🚀 Last year’s event was unforgettable, and we’re beyond excited to share that we’ve raised an incredible $10.85 million net since the beginning of this amazing journey! 🎉 This November, we’re heading back to Villa Premiere to mark 20 years of making magic happen with exceptional fishing 🎣 and golfing experiences ⛳, soothing spa services 🧖‍♀️, ALL-INCLUSIVE accommodations 🏨, celebrity guest appearances 🌟, headliner concert 🎶, and the formation of new friendships 🤝, we believe that our 20th event will sell out fast! 🚀 Register or donate HERE.

Hook the Cure is renowned for its incredible silent & live auction items 🎁, and we want YOU to be part of this unforgettable event as an auction donor. Some of our most popular items are local condo stays 🏖️ to gift cards 💳, tickets to sporting events 🏀, dazzling jewelry 💎, cutting-edge tech gadgets 📱, and so much more! By becoming an auction donor, you’ll play a pivotal role in the shared mission to find a cure for cystic fibrosis. 💖 Let’s unite and make a difference together! 💪✨📥 Download the auction form HERE or click the donate to our auction link above to get involved!

 

CELEBRITY GUESTS

In addition to headliner, Lucas Hoge, Hook the Cure continues to attract some of baseball’s greatest players including Roger Clemens, Rick Honeycutt, Orel Hershiser and Matt Young. Thank you for going to bat and helping raise over $10.85 million net for the Cystic Fibrosis Foundation.

 

PROUDLY SPONSORED BY:

 

 

OUTSTANDING CORPORATE PARTNER

 
 

WHAT IS CYSTIC FIBROSIS?

Cystic fibrosis is a progressive, genetic disease that affects the lungs, pancreas, and other organs. There are close to 40,000 children and adults living with cystic fibrosis in the United States (and an estimated 105,000 people have been diagnosed with CF across 94 countries), and CF can affect people of every racial and ethnic group.

In people with CF, mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause the CFTR protein to become dysfunctional. When the protein is not working correctly, it’s unable to help move chloride -- a component of salt -- to the cell surface. Without the chloride to attract water to the cell surface, the mucus in various organs becomes thick and sticky. In the lungs, the mucus clogs the airways and traps germs, like bacteria, leading to infections, inflammation, respiratory failure, and other complications. For this reason, minimizing contact with germs is a top concern for people with CF.

 
 

ABOUT THE CYSTIC FIBROSIS FOUNDATION

We are fueled by a dedicated group of scientists, caregivers, donors, volunteers, and people with CF and their families who are united by a common goal: to find a cure for this devastating disease and help those with CF live longer, healthier lives. We are driven by a dream that one day, not one person will lose a life, child, sibling, parent, or friend to cystic fibrosis, and we are determined to succeed.

The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care.

The CF Foundation is the world's leader in the search for a cure for cystic fibrosis, and nearly every CF-specific drug available today was made possible with our financial support. We are a donor-funded, 501(c)(3) nonprofit that is fully accredited by the Better Business Bureau's (BBB) Wise Giving Alliance program.

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