.png)
Support Krissy's LOL4CFF Campaign!
Krissy Fox
Krissy Fox
I have officially lost my mind and am trying stand-up comedy for the first time (!!). I am participating in an upcoming event, LOL4CFF, where I’ll be part of a comedy competition among first-time stand-up comedians.
I’m doing a five-minute set for the show, all for the Cystic Fibrosis Foundation and to raise money and bring awareness to this great cause that has made it possible for my son Louie to have a future.
In 2020 my joy at finding out I was pregnant with my first child quickly turned to panic as we learned our son would be born with CF, a genetic illness with no cure. Thanks to the CF foundation and our team of doctors we were able to quickly educate ourselves on how to best care for Louie and he has thrived.
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.
I’m doing a five-minute set for the show, all for the Cystic Fibrosis Foundation and to raise money and bring awareness to this great cause that has made it possible for my son Louie to have a future.
In 2020 my joy at finding out I was pregnant with my first child quickly turned to panic as we learned our son would be born with CF, a genetic illness with no cure. Thanks to the CF foundation and our team of doctors we were able to quickly educate ourselves on how to best care for Louie and he has thrived.
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.
JUN
12
12
Comments