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Breath of Life Gala & Auction - Cystic Fibrosis Foundation

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we would like to introduce you to some <strong>of</strong> the faces <strong>of</strong><br />

cystic fibrosis (Cf). They all wear the same smile and<br />

in their eyes you see reflections <strong>of</strong> hope and optimism<br />

for the day when a cure for their disease is found. with<br />

your help—one day soon—we will find a cure and then<br />

cystic fibrosis won’t have a face at all.<br />

whaT is CysTiC fibrosis?<br />

<strong>Cystic</strong> fibrosis is a life-threatening genetic disease that<br />

affects the lungs and digestive systems <strong>of</strong> approximately<br />

Jude Small<br />

30,000 children and adults in the united states. more<br />

than 10 million americans are symptomless carriers <strong>of</strong><br />

the defective cystic fibrosis gene. The disease occurs in one <strong>of</strong> every 3,900 live births,<br />

and about 1,000 new cases <strong>of</strong> Cf are diagnosed each year.<br />

when the <strong>Cystic</strong> fibrosis foundation began, few children<br />

with Cf lived to attend elementary school. Today, thanks<br />

to the efforts <strong>of</strong> scientists, caregivers and the development<br />

<strong>of</strong> new treatments supported by the foundation, the<br />

median age <strong>of</strong> survival for a person with Cf is 37 years.<br />

a remarkable improvement—although it is not good<br />

enough as we continue to lose at least one precious life to<br />

cystic fibrosis every day.<br />

who is The CysTiC fibrosis<br />

Brady Schroeder<br />

foundaTion?<br />

since 1955, the mission <strong>of</strong> the <strong>Cystic</strong> fibrosis foundation is to assure the<br />

development <strong>of</strong> the means to cure and control Cf and to improve the quality <strong>of</strong><br />

life for those with the disease. The foundation tirelessly pursues this mission by<br />

supporting innovative research dedicated to discovering and developing new therapies<br />

and by funding and accrediting specialized care centers to treat people with the<br />

disease.<br />

The <strong>Cystic</strong> fibrosis foundation is one <strong>of</strong> the most efficient organizations <strong>of</strong> its<br />

kind. it has received a four-star rating for sound fiscal management from Charity<br />

navigator, the largest independent charity evaluator in the united states, and is an<br />

accredited charity <strong>of</strong> the better business bureau’s wise Giving alliance.<br />

Emma Jefferson<br />

The faCes <strong>of</strong> CysTiC fibrosis<br />

never before in the history <strong>of</strong> the <strong>Cystic</strong> fibrosis<br />

foundation has the feeling <strong>of</strong> optimism for defeating<br />

this disease been so great. Progress has been made<br />

because the foundation has seized every opportunity<br />

to support the best minds in science and to recruit the<br />

finest team <strong>of</strong> caregivers to the Cf cause.<br />

when you support the <strong>Cystic</strong> fibrosis foundation, you<br />

are investing in the lives <strong>of</strong> those with cystic fibrosis.<br />

working together, we can give children and adults with<br />

Cf the quality <strong>of</strong> life and the future that they deserve.

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