My Great Strides Story
Karen Weaver
Karen Weaver
Hi. Welcome to my
Cystic Fibrosis Fundraiser Page,
in Honor of my Grandson Lukas.
Our sweet adorable Lukas was diagnosed with Cystic Fibrosis when he was just an infant.
Because there is NO CURE for Cystic Fibrosis (yet), far too many people with CF can die young. TO SUPPORT RESEARCH and HELP CHANGE THIS, I AM *FUNDRAISING* for WALKERS on LUKAS' LIGHTNING LEAP TEAM for The 2025 GREAT STRIDES WALK, on MAY 18th, in Williamsville, NY!
CF is a genetic, life-threatening disease that devastates the lungs, pancreas, immune system and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.
Each person born with Cystic Fibrosis is on their own *unique journey* and experiences this challenging disease differently. While much progress has been made, a long road still lies ahead for far too many people fighting this terrible disease.
WE NEED A CURE!!! SO THAT *EVERYONE* WITH CF HAS A FIGHTING CHANCE TO LIVE A LONG, HEALTHY and FULL LIFE.
THIS IS WHAT I'M PRAYING for
MY GRANDSON LUKAS and
EVERY CHILD and PERSON with CF!
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.
Cystic Fibrosis Fundraiser Page,
in Honor of my Grandson Lukas.
Our sweet adorable Lukas was diagnosed with Cystic Fibrosis when he was just an infant.
Because there is NO CURE for Cystic Fibrosis (yet), far too many people with CF can die young. TO SUPPORT RESEARCH and HELP CHANGE THIS, I AM *FUNDRAISING* for WALKERS on LUKAS' LIGHTNING LEAP TEAM for The 2025 GREAT STRIDES WALK, on MAY 18th, in Williamsville, NY!
CF is a genetic, life-threatening disease that devastates the lungs, pancreas, immune system and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.
Each person born with Cystic Fibrosis is on their own *unique journey* and experiences this challenging disease differently. While much progress has been made, a long road still lies ahead for far too many people fighting this terrible disease.
WE NEED A CURE!!! SO THAT *EVERYONE* WITH CF HAS A FIGHTING CHANCE TO LIVE A LONG, HEALTHY and FULL LIFE.
THIS IS WHAT I'M PRAYING for
MY GRANDSON LUKAS and
EVERY CHILD and PERSON with CF!
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.
JAN
16
16
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