Leticia Calderon

As many of you know, my niece Laila, was diagnosed with Cystic Fibrosis shortly after birth. 

Now 13 years, Laila is amazing and thriving. Except this past March she had to be hospitalized for 13 days due to a pesky lung infection. This was the first time since birth that she required hospitalization. Not something that was easy for her or for her loved ones. Laila had always been healthy enough to avoid being hospitalized like so many others living with Cystic Fibrosis but this time it was needed.

The Cystic Fibrosis Foundation has been amazing in finding new medications, treatments and research that will continue to help so many living with Cystic Fibrosis, like Laila. 

On May 21st, I will join Laila, family and friends in the annual 5K walk for a cure. But we NEED YOUR HELP! Please consider donating to this cause. Any amount will help us get closer to finding a cure. 

Thank you in advance. 

Leticia Calderon 

Team L.O.L