My CF Cycle for Life Story
Corey Keifetz
Fundraising for Metro DC CF Cycle for Life 2026
Corey Keifetz
My grandson Shane is now 15 years old...! It always amazes me how quickly time goes by and see your family grow and succeed in life...With Shane however, his life isn't like other kids his age as he was born with Cystic Fibrosis a terrible debilitating disease...He continues to go through twice daily chest compressions and lung inhalers plus Diabetes shots...
Shane has responded well to new medications but is far from living a normal "kids" life...he is growing into a handsome young man...soon he will be taller than me...! However, he has difficulty in gaining weight which is of great concern...
Cystic Fibrosis is a constant worry for us, especially for his parents David (my son) and Lorie...
There is currently no cure for cystic fibrosis and too many people with CF die young. That's why I'm volunteering to help with the next fundraising event on October 10th in Manassas...
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 Shane and all living with Cystic Fibrosis find a cure...? I hope you do...
Please click on the Donate button on this page...any amount is most appreciated...
Thank you from my entire family and especially Shane...
Corey and Ellen
Shane has responded well to new medications but is far from living a normal "kids" life...he is growing into a handsome young man...soon he will be taller than me...! However, he has difficulty in gaining weight which is of great concern...
Cystic Fibrosis is a constant worry for us, especially for his parents David (my son) and Lorie...
There is currently no cure for cystic fibrosis and too many people with CF die young. That's why I'm volunteering to help with the next fundraising event on October 10th in Manassas...
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 Shane and all living with Cystic Fibrosis find a cure...? I hope you do...
Please click on the Donate button on this page...any amount is most appreciated...
Thank you from my entire family and especially Shane...
Corey and Ellen
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