Edit in profile section

Azalea's Story

Patsy Black
Donate

Patsy Black

Little Miss Princess Azalea is a happy 5 year old girly at this time in her life. Life hasn't always been so shiny for her, being born with cystic fibrosis and prematurely. We were unaware that CF even existed before azalea came into our lives. After learning the many obstacles she may encounter in her life, we searched for information on how to keep her healthy, happy and safe. With the advancements in treatment for CF, azalea has made it 2 years without a hospital stay (for which we are grateful and pray for many more while striving for a cure). Joining events such as these help raise funds for those whose legacies we carry and the many people living with CF. 

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. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.

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.

Comments

$150
raised of $350 goal
 

Achievements

Leader

Team Azalea Squad

$150
$350

Recent Donations

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.