


My Great Strides Story
Sue Barnes
Fundraising for Valley of the Sun Great Strides
Sue Barnes
There is currently no cure for cystic fibrosis and too many people with CF die young. My granddaughter, Jasmine, is three years old and was diagnosed with cystic fibrosis about two weeks after she was born. She is a warrior and is bravely fighting this disease with the help of the Cystic Fibrosis Team. I’m walking to help fight for a Cure.
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 for your support.
Grandparents,
Sue and Rick Barnes
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 for your support.
Grandparents,
Sue and Rick Barnes
MAR
4
4

Comments