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Barbara Gass

Fundraising for Annapolis Great Strides 2026

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Barbara Gass

From my niece directly:

"When I was born, the average life expectancy for someone with CF was just 13 years old. That’s middle school. Growing up, I spent a lot of time in and out of the hospital. I did two breathing treatments a day, each about an hour, took 30 to 40 pills daily, and watched friends undergo lung transplants or, unfortunately, pass away far too young. My lung function dropped as low as 56%. I lived with a constant fear of time running out.
If you want to know what it feels like to have low lung function, try breathing through a straw. That’s what it feels like to breathe on a daily basis with CF.

In 2019, everything changed and many of my prayers were answered. A new medication called Trikafta was approved. Within weeks of starting it, my lung function jumped 38%, eventually reaching 106%, the highest it’s ever been. For the first time, I could breathe freely. And because of that, I was able to do something I never thought possible: I became a mom. Today, my husband and I have two healthy kids, Liam, age 5 and Lucy, age 3, and because of the kindness of donors like you, they have a healthy mom. Your donations have helped the advances in treatment which have increased the average life expectancy for people with CF. It is now 65. But our mission isn’t over. Trikafta, unfortunately, doesn’t work for everyone, about 10% of people with CF still don’t have a treatment that works for their mutation.

If you ever wonder whether your donation makes a difference I am here to tell you, it does. I’m living, breathing proof that it does! You’ve changed my life! Together, we can keep pushing forward until CF stands for Cure Found."


 

There is currently no cure for cystic fibrosis and too many people with CF die young. As her proud Aunt, I am asking for your support 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.

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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.