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My Great Strides Story

Cassidy Aubin

Fundraising for Glastonbury Great Strides

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Cassidy Aubin

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

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.
MAR
26

Another great strides team did a photo shoot for their fundraiser. Jonas was so excited to participate and we are hyped for the upcoming walk! So close to our goal. Thank you so much everyone!

MAR
4

3/4 of the way to my personal goal. Long way to go as a team. If you’d like to purchase a shirt to go towards the fundraiser contact Cassidy!

FEB
24

Very thankful for our preventative medicine practices our team has in place. Jonas does breathing treatments twice daily and up to 6 times a day when ill. Let’s keep the fundraising going to help fund a cure for CF. Thank you!

JAN
7

Off to a great start! Jonas says “thank you”!!! 💜

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$1,400
raised of $1,500 goal
 

Achievements

Leader

Team Jonas Scott

$1,560
$3,000

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.