Smash CF Yall

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Serving up Hope, one Smash at a Time

 

Get ready to serve, rally, and make a difference! Join us for an unforgettable evening of pickleball, community, and fun as we rally together to support individuals and families living with Cystic Fibrosis.

 

When: August 15, 2026, 5:00 PM
Where: Austin Pickle Ranch
Contact: Mirandaromkema@gmail.com

 

Whether you're a seasoned player or just love being part of a great cause, this tournament is for everyone!

Every serve, every volley, and every point played helps bring hope through research, care, and support.


 

Expect:

🏓 Competitive & recreational play
🎉 Music & entertainment
🎁 Raffles and prizes
🍔 Food & drinks
💜 Supporting cystic fibrosis research and care


 

Grab your paddle. Bring your friends. Let's Smash CF together! 💜💚

 

🎟️ Event Tickets:
 

$5,000 - Presenting Sponsor
Recognition as the Presenting Sponsor on all event materials
Opportunity to set up a table at the event
Entry for 5 teams of 2 in the tournament
Dinner and drink tickets for 10 at the event

$2,500 - Gold Sponsor
Recognition as the Gold Sponsor on all event materials
Entry for 3 teams of 2 in the tournament
Dinner and drink tickets for 6 at the event

$1,000 - Silver Sponsor
Recognition as the Silver Sponsor on all event materials
Entry for 2 teams of 2 in the tournament
Dinner and drink tickets for 4 at the event


Youth Ticket - $60
Age 12-17
Entry for 1 individual in the tournament 
Dinner ticket

Team Ticket - $200
Entry for 1 team of 2 in the tournament
Dinner and drink tickets for 2 at the event

Individual Ticket - $110
Age 18+
Entry for 1 in the tournament
Dinner and drink ticket for 1 at the event



 

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. 💜