Walk with our team to Cure Cystic Fibrosis

#HeIsAbel

Fundraising for Dallas Great Strides

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#HeIsAbel

Have you ever held a newborn baby? They are so tiny and have that baby smell and tiny fingers and toes, and oh that tiny little nose. Now imagine hearing that the tiny baby your holding has a life expectancy, and reaching age 50 is far fetched. Imagine being told that a simple respiratory infection could bring that life expectancy down to next week or maybe even tomorrow.

There is currently no cure for cystic fibrosis and too many people with CF die young. I'm walking to help change that reality.

CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.

Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. We need a cure so that everyone with CF has a better chance to live a long, healthy life.

Will you be the support we need?

Will you help us end cystic fibrosis?

By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.

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Attendance Policy

The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.