Huddy’s Buddies
We'd love to have you on our Huddy's Buddies team. Whether you provide support through well wishes and prayers, wearing a Huddy's Buddies shirt, joining us at the walk, or making a donation to further CF research.... YOU make a difference!
We would love to celebrate the GREAT STRIDES we've made in CF Research at the CF Walk on May 16th. Not only do we get a few extra steps in, but we have the opportunity to spend time together supporting Hudson and all of those affected by Cystic Fibrosis. By walking with us, you’ll see firsthand the important impact we are making together.
While the CF Foundation has made incredible progress, not everyone with CF can benefit from existing therapies, and we still need a cure. In recent history, many years have been added to the CF life expectancy, but no number of years is ever enough when it comes to fighting for your child's length and quality of life.
We remember our despair on diagnosis day, the terror in the hospitalizations that followed, and the HOPE we experienced as Hudson slowly began qualifying for different medicines, treatments, and therapies that decreased his hourly burden of living with CF. We are wholeheartedly committed to ensuring that someday soon, no family will feel helpless when they receive a diagnosis call because there will be a one-time cure for Cystic Fibrosis.
#UntilCFStandsforCureFound #UntilItsDone
Salty Since 2019,
Team Huddy's Buddies
We would love to celebrate the GREAT STRIDES we've made in CF Research at the CF Walk on May 16th. Not only do we get a few extra steps in, but we have the opportunity to spend time together supporting Hudson and all of those affected by Cystic Fibrosis. By walking with us, you’ll see firsthand the important impact we are making together.
While the CF Foundation has made incredible progress, not everyone with CF can benefit from existing therapies, and we still need a cure. In recent history, many years have been added to the CF life expectancy, but no number of years is ever enough when it comes to fighting for your child's length and quality of life.
We remember our despair on diagnosis day, the terror in the hospitalizations that followed, and the HOPE we experienced as Hudson slowly began qualifying for different medicines, treatments, and therapies that decreased his hourly burden of living with CF. We are wholeheartedly committed to ensuring that someday soon, no family will feel helpless when they receive a diagnosis call because there will be a one-time cure for Cystic Fibrosis.
#UntilCFStandsforCureFound #UntilItsDone
Salty Since 2019,
Team Huddy's Buddies
APR
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