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My Great Strides Story

Dorine Fabio

Fundraising for Buffalo Great Strides

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Dorine Fabio

There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking to help change that reality. I am walking in Buffalo Great Strides this May. I walk for my daughter Ashley who has Cystic Fibrosis. She is currently 36 years old and thanks to all the research that has been done she is currently on the drug Trikafta! This is has been a game changer for her! It has helped reduce lung infections and kept her out of the hospital. Thanks to Trikafta she currently has 2 beautiful healthy active daughters. She is married and works full time. We need your help as there are still people with CF that don’t have any medications to help them, so more research needs to be done! Please help me to raise money for research to help those that need it. You can click on my link to donate. 

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.
Thank you!!

Comments

$650
raised of $500 goal
 

Achievements

Leader

Team Ashley’s Angels

$1,150
$1,000

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.