Welcome to Eat, Drink & Breathe for CF

I proudly dedicate this site to my son Eric who in October, 1980 at 6 weeks of age, was diagnosed with Cystic Fibrosis. Although his older brother Billy and younger brother Christopher do not have the disease, they Eat, Drink and Breathe every day knowing that their brother has the disease. They have also motivated and inspired me to find new and creative ways to raise money and awareness for the support of family members and friends whose loved ones have Cystic Fibrosis.

- Anna Jenkin

Shop Our Store

Our store contains a collection of bracelets, necklaces, stamps, shirts, mugs and other custom items. Orders over $20 qualify for free shipping and 100% of the proceeds are donated to the Cystic Fibrosis Foundation.

May Special

In honor of CF awareness month, all items offered in purple are buy one get one free including Mugs, t-shirts, bracelets, CF headbands, etc. As always 100% of the proceeds are dontated to the CF Foundation! Please note, there is a $20 minimum purchase to qualify for free shipping. Purchases under $20 will be $5.

Learn more about Cystic Fibrosis

Cystic Fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide).

Attend a Cystic Fibrosis Event

CF has a number of events throughout the year including Great Strides walks, golf tournaments, a gala and other opportunities to attend an event or volunteer.

Great Strides 2017

Donate to Team Rock Solid's 2017 Great Strides campaign by clicking the Donate button.