Danielle Falcone
This summer The Falcone Four hikes Mount Hood! I'm taking on 30+ miles of mountainous terrain for my siblings: in honor of Gabby and Nathan and in memory of Nick and Samantha. Donate to help me reach my $4,000 goal while I train for my hike with my loved ones in mind! Every donation makes a difference in advancing scientific research to find better treatments, more effective medications, and eventually a cure!
Those that know the Falcone family know our shared journey with cystic fibrosis all too well. For those that don't: I am one of six Falcone children, but one of only two that wasn't born with CF. My brothers Nick and Nathan and sisters Samantha and Gabby were diagnosed with this chronic illness in each of their childhoods. That's right--four siblings with CF. As rare as CF is, more than one sibling diagnosed is even more rare.
Sadly, Samantha and Nick have passed in recent years from complications related to CF. Nathan is under surveillance by his care team as he awaits his third lifetime liver transplant. Thanks to pivotal scientific research resulting in lifechanging medications--as a result of generous philanthropic support from donors around the country--Gabby and her husband are raising their three children while she no longer suffers the daily burden of symptoms she had when she was younger.
_ _ _
There is currently no cure for cystic fibrosis and too many people with CF die young. I’m hiking to help change that reality.
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.
Those that know the Falcone family know our shared journey with cystic fibrosis all too well. For those that don't: I am one of six Falcone children, but one of only two that wasn't born with CF. My brothers Nick and Nathan and sisters Samantha and Gabby were diagnosed with this chronic illness in each of their childhoods. That's right--four siblings with CF. As rare as CF is, more than one sibling diagnosed is even more rare.
Sadly, Samantha and Nick have passed in recent years from complications related to CF. Nathan is under surveillance by his care team as he awaits his third lifetime liver transplant. Thanks to pivotal scientific research resulting in lifechanging medications--as a result of generous philanthropic support from donors around the country--Gabby and her husband are raising their three children while she no longer suffers the daily burden of symptoms she had when she was younger.
_ _ _
There is currently no cure for cystic fibrosis and too many people with CF die young. I’m hiking to help change that reality.
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.
APR
27
27
APR
16
16
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