Meet Camden and Mallory

To look at Mallory & Camden playing at the park or laughing with their friends at school, you would never know these happy, rambunctious 7 year-olds have a genetic, life-shortening disease.  Day in and day out, their lungs are slowly deteriorating.  In the past several years, there have been many advancements in CF research.  In the 1950s, a child with CF rarely lived long enough to attend elementary school.  Today, the median predicted survival age is close to 40, but that's still far too young. And there is no cure.   

There is no break from Cystic Fibrosis

To add insult to injury, CF never sleeps.  It's unpredictable and relentless, and there is no remission. CF never takes a vacation or holiday. Summer break, Christmas, birthdays - all of those mean nothing to the monster that is CF.  It's progressive -  Mallory & Camden will never outgrow it.  Rather, as they get older, their symptoms will increase and their lung function will decrease.  Disease progression is inevitable and all we can do right now is fight our hardest to slow it down.  We are buying time and hoping that it is enough.

Money buys science and science buys life

While we fight and raise money and wait desperately for a cure, others around us run out of time. Every day, another person is lost far too young.  We will not and cannot give up fighting for Mallory and Camden.  Please fight with us.