Last year I tried stand-up for the first time as a participant in LOL4CFF, and this year I'm continuing my support for the Cystic Fibrosis Foundation as a member of the event's planning committee.  And I need your support! 

When I started fundraising last year, I found out about a personal connection I have to CF - a little boy named Micah. Micah has benefitted greatly from current therapies available thanks to the work of the CF Foundation - work that donations make possible. I'm raising money in honor of Micah and two other local kids who fight CF, Tatum and Banks, who are pictured below.

There are a couple of ways to support me and the CF Foundation: 

1. Make a donation that will be credited to my fundraising efforts. Any amount you can donate will make a difference and be greatly appreciated!  

2. 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! 

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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.