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Ryan Berrigan
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Ryan Berrigan

I am being honored by the Cystic Fibrosis Foundation at a special event recognizing outstanding professionals in my community. In accepting this distinction, I have committed to raise money to help the Foundation realize its mission of curing cystic fibrosis (CF) and providing all people with CF the opportunity to lead long, fulfilling lives.

Please help me meet my fundraising goal by making a donation. By supporting my fundraising efforts, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.

Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is over 50. Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.

My Story:

28 years ago, my parents learned that my sister Olivia will be a fighter for the rest of her life. Knowing that their daughter would never live a normal life as a little girl was unfathomable. As her younger brother, I never fully understood why she had to miss hanging out with her friends after school to do her treatments, or wake up extra early every morning to hold a strange mist pipe in her mouth, or why she takes several pills before eating. To me, that was just Olivia. But as I grew older, it finally occurred to me the sacrifices she’s made for years.

This was important to me because seeing her fight allowed me to understand two critical life lessons at a young age. 1: Just because you don’t live a normal life, doesn’t mean you can’t live a successful one. 2: When you feel like you might be losing control in life, your best and only countermove is to keep pushing no matter how hard, or how weak the push may be. Any forward push is still a progression.

As for Olivia, she has made remarkable progress. But when it comes to Cystic Fibrosis, progress is something you can never have too much of. The CF community has made great strides, but we will continue the fight until we find that cure.

All I ask is that you join the fight with me, my sister, my family, your neighbor, and the whole Cystic Fibrosis community. Whether it’s $1, $5, $20, or $200, let’s make a little bit of progress today.


To learn more about CF and the CF Foundation, visit www.cff.org. Together, we can make a difference in the lives of those with cystic fibrosis. Thank you for supporting the mission of the CF Foundation!

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$3,900
raised of $5,000 goal
 

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