About Cystic Fibrosis... 

Why are we doing this?  To add tomorrows and healthy days to the more than 70,000 people worldwide living with Cystic Fibrosis, like Mallory.  See the links below to learn more about Cystic Fibrosis and ways to help.

• Cystic Fibrosis Foundation 
• Center for Orphan Disease Research & Therapy 
• Million Dollar Bike Ride
• ​Cards For Humanity - CF Edition
• Team Rare Disease Cycling
• Mallory's CFF Great Strides Page
• Kaitlyn Broadhurst’s documentary Catching Air
• Racing to Breathe
• Register as Organ Donor
• Thriving with Cystic Fibrosis
• Spinathon Info
• One Republic's "I lived"
• Gunnar Esiason "Cystic Fibrosis doesn't have to define you"
• "They Put A Price on My Life": Cost of Cystic Fibrosis Drugs is Sky-High