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Support my LOL4CFF Campaign!
Rachel Guzman
Rachel Guzman
My Mom and my 3-year-old think I'm the next big thing in comedy. But before I quit my day job and start touring the world, I thought I'd test my comedic chops at LOL4CFF, a comedy competition in support of the Cystic Fibrosis Foundation.
Yes, I'm diving headfirst into the world of stand-up comedy, and I need your help to make sure I don't bomb harder than a bad knock-knock joke. I'll be performing a five-minute set, hoping to bring the house down with laughter and raise some serious funds for a fantastic cause.
So, if you want to see if I can make a whole room laugh as much as I make my Mom and toddler giggle, please think about supporting my journey to the stage. Because who knows, maybe my Mom was onto something when she said I missed my calling as a clown.
Let's turn my nerves into laughter and make a real difference for those fighting cystic fibrosis!
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.
Yes, I'm diving headfirst into the world of stand-up comedy, and I need your help to make sure I don't bomb harder than a bad knock-knock joke. I'll be performing a five-minute set, hoping to bring the house down with laughter and raise some serious funds for a fantastic cause.
So, if you want to see if I can make a whole room laugh as much as I make my Mom and toddler giggle, please think about supporting my journey to the stage. Because who knows, maybe my Mom was onto something when she said I missed my calling as a clown.
Let's turn my nerves into laughter and make a real difference for those fighting cystic fibrosis!
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 through this link for LOL4CFF to see the live show and vote for me to win!!! The event is on August 9, 2024 at The Big Chill in Charlotte. Tickets include a seated dinner, hosted beer & wine. -because let's face it, I'm bound to be funnier after a glass or two!
- 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.
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