My Great Strides Story
Jackson Miller
Fundraising for Lancaster Great Strides
Jackson Miller
Hi! My name is Jackson. My brother Jacob and I were diagnosed with Cystic Fibrosis in early 2013. There is currently no cure for cystic fibrosis and far too many people with CF still die young. I'm walking to help change that reality.
CF is a genetic, life-shortening disease that affects 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. My brother and I also have cystic fibrosis related diabetes (CFRD).
Will you help us end cystic fibrosis?
My family formed the J Team in May of 2013. Participating in Great Strides has given us a way to educate others about Cystic Fibrosis while raising funds to make a difference in the lives of those living with CF. Over the last 12 years, our team has raised over $370,000 to support the mission, and we will continue until CF stands for Cure Found!
YOU have the power to help advance the research and science needed to drive our dream forward. Please consider making a donation and adding tomorrows for all of us living with Cystic Fibrosis.
CF is a genetic, life-shortening disease that affects 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. My brother and I also have cystic fibrosis related diabetes (CFRD).
Will you help us end cystic fibrosis?
My family formed the J Team in May of 2013. Participating in Great Strides has given us a way to educate others about Cystic Fibrosis while raising funds to make a difference in the lives of those living with CF. Over the last 12 years, our team has raised over $370,000 to support the mission, and we will continue until CF stands for Cure Found!
YOU have the power to help advance the research and science needed to drive our dream forward. Please consider making a donation and adding tomorrows for all of us living with Cystic Fibrosis.
Comments