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2023 HONOREE: JAMIE GILDERSLEEVE
Jamie Gildersleeve
Jamie Gildersleeve
Friends,
I'm excited to share that I have recently been nominated and granted an opportunity to make an impact as an honoree in the 2023 class of 'Pittsburgh's 50 Finest'!!!!
While the recognition is extremely humbling, I'm beyond excited to utilize this platform to push for a cure so very much needed by the Cystic Fibrosis community.
Change can be defined as, "making a significant difference." It's in those four words, that breathes life into my campaign to raise funds and awareness for those affected by Cystic Fibrosis. I've been a forever believer in the notion, that if you want to make a change, you need to be the change.
So YOU and ME, let's be the change. Make that donation. It's easy, secure and ensures that a change in the lives of those with Cystic Fibrosis is significant. We won't stop until CF means CURE FOUND!
What is Cystic Fibrosis, "CF"?
Cystic fibrosis is a devastating genetic disease that affects the lungs and digestive system. More than T E N million Americans are symptomless carriers of the defective CF gene. Advances continue to be made in finding a cure, but YOUR HELP is needed now -- more than ever -- to help keep up the momentum of this life-saving research.
Did you know?
Sixty years ago, children with CF usually did not live long enough to attend elementary school. That means kids like my littlest loves, Brooklyn (10) and Reese (7) would not be here! Today, because of Foundation-supported research and care, the median survival age of people with CF is about 40. Let me repeat. FORTY!! This is remarkable progress, but not good enough. We continue to lose precious lives to CF every day.
Your donations go directly to the research very much needed to find that cure. Let's do it. Together. Thank you for taking my mission in supporting the CF Foundation as your own. Love you all so much <3
I'm excited to share that I have recently been nominated and granted an opportunity to make an impact as an honoree in the 2023 class of 'Pittsburgh's 50 Finest'!!!!
While the recognition is extremely humbling, I'm beyond excited to utilize this platform to push for a cure so very much needed by the Cystic Fibrosis community.
Change can be defined as, "making a significant difference." It's in those four words, that breathes life into my campaign to raise funds and awareness for those affected by Cystic Fibrosis. I've been a forever believer in the notion, that if you want to make a change, you need to be the change.
So YOU and ME, let's be the change. Make that donation. It's easy, secure and ensures that a change in the lives of those with Cystic Fibrosis is significant. We won't stop until CF means CURE FOUND!
What is Cystic Fibrosis, "CF"?
Cystic fibrosis is a devastating genetic disease that affects the lungs and digestive system. More than T E N million Americans are symptomless carriers of the defective CF gene. Advances continue to be made in finding a cure, but YOUR HELP is needed now -- more than ever -- to help keep up the momentum of this life-saving research.
Did you know?
Sixty years ago, children with CF usually did not live long enough to attend elementary school. That means kids like my littlest loves, Brooklyn (10) and Reese (7) would not be here! Today, because of Foundation-supported research and care, the median survival age of people with CF is about 40. Let me repeat. FORTY!! This is remarkable progress, but not good enough. We continue to lose precious lives to CF every day.
Your donations go directly to the research very much needed to find that cure. Let's do it. Together. Thank you for taking my mission in supporting the CF Foundation as your own. Love you all so much <3
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