Dave Nessler

On March 27th, 2009, my son Morgan was born. About 6 weeks later, we found out that Morgan had Cystic Fibrosis. At the time, I really had no idea what CF was. I had heard of it in name only, and did not even know what CF could do to a person who had it. What I found out was something I was never prepared for. Cystic Fibrosis is a genetic, life threatening disease that primarily affects the lungs and digestive systems. CF has NO cure to date. In a nutshell, the body creates thick, sticky mucus that clogs the lungs and leads to life threatening lung infections. Today, life expectancy for a person with CF is around 37 years old. If you are one of the lucky ones.

The Cystic Fibrosis Foundation has made tremendous advancements in research and progress in the treatment of CF over the years. The Foundation is a non-profit organization, and relies on fundraisers like Great Strides to raise funds for continued research and education. CF receives NO government funding, so it is up to us to step up and do what we can to help ensure Morgan's future. Great Strides is the largest and most successful CF fundraiser of the year. I am asking that you please consider joining my team for the walk, and show your support for Morgan, and everyone else with CF. If you are able to sponsor my team with a small, tax deductible donation, that would also be greatly appreciated.

Morgan's life literally depends on the continued success of the Cystic Fibrosis Foundation. If you are able to help in any way, you can use this page to sign up, donate, or get involved by volunteering on walk day. If you have any questions at all, please feel free to ask.

Thank you.

Dave