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Support Rhonda's LOL4CFF Campaign!
Rhonda Cato
Rhonda Cato
I am trying stand-up comedy for the first time (!!). And I need your support! I am participating in an upcoming event, LOL4CFF, where I’ll be part of a comedy competition among first-time stand-up comedians. To cheer me on and support the Cystic Fibrosis Foundation, I'm raising funds and performing a five-minute set for the show. Every laugh (and donation) makes a difference!
Along the way, we're getting to know CF ambassadors, local kids fighting cystic fibrosis who need our support to help find a cure. Below are brothers Tatum and Banks, who live in Charlotte. I'm raising funds in their honor.
There are three ways to support me:
Cystic fibrosis is a genetic disease that causes a thick buildup of mucus in the lungs, pancreas and other organs. In the lungs, mucus clogs the airways and traps bacteria, which can lead to infections, extensive lung damage and respiratory failure.
Recognized globally, the Cystic Fibrosis Foundation has led the way in the fight against cystic fibrosis, 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.
Our vision is a cure for every person with cystic fibrosis and a life free from the burden of this disease. We will not leave anyone behind. You are an important part of our progress. Together, let’s make CF stand for Cure Found.
To learn more about CF and the CF Foundation, visit www.cff.org.
Along the way, we're getting to know CF ambassadors, local kids fighting cystic fibrosis who need our support to help find a cure. Below are brothers Tatum and Banks, who live in Charlotte. I'm raising funds in their honor.
There are three ways to support me:
- Make a donation that will be credited to my fundraising efforts. Any amount you can donate will make a difference and be greatly appreciated!
- Purchase a ticket for LOL4CFF and see this all go down! The event is on Friday, October 3, 2025 at The Big Chill in Charlotte. Tickets include a seated dinner, hosted beer & wine, and if you’re there, you can vote for me to win!
- If you know others that would be willing and interested in joining our efforts please send them my link and invite your friends to support our effort!
Cystic fibrosis is a genetic disease that causes a thick buildup of mucus in the lungs, pancreas and other organs. In the lungs, mucus clogs the airways and traps bacteria, which can lead to infections, extensive lung damage and respiratory failure.
Recognized globally, the Cystic Fibrosis Foundation has led the way in the fight against cystic fibrosis, 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.
Our vision is a cure for every person with cystic fibrosis and a life free from the burden of this disease. We will not leave anyone behind. You are an important part of our progress. Together, let’s make CF stand for Cure Found.
To learn more about CF and the CF Foundation, visit www.cff.org.
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