.png){kind=logo}
Welcome to Karrin Russo's Page
Karrin Russo
Karrin Russo
Having been previously selected and recognized by the Cystic Fibrosis Foundation as a STANDOUT honoree was an incredibly rewarding experience. I have become well acquainted with the Foundation and the life-saving work the organization does for those with the cystic fibrosis. This year I have joined the leadership team for STANDOUT as a member of the committee. Our committee team will continue the momentum of the STANDOUT program and the CF Foundation, as well as help nominate and mentor the STANDOUT Class of 2024.
In support of my position on the committee, I am raising funds for cystic fibrosis (CF) research and care. I want to introduce you to one of the children I have an opportunity to help… this is Team CF Ambassador Chloe. Though she is doing well now, I want to make sure Chloe and all the other children living with this disease continue to grow and thrive. By supporting me, you can help us make a difference in Chloe’s life.
Know that your generous gift will be used efficiently and effectively— CFF is a careful steward of every dollar.
There are three ways to support me:
1) Make a donation that will be credited to my fund-raising efforts. Any amount you can donate will be greatly appreciated!
2) Purchase a ticket to join us for the STANDOUT event on November 7, 2024 at The Ruth in West Charlotte. Dinner and beer/wine are provided! (I would be ecstatic to have you at my table as I support the honorees!)
3) If you know others that would be willing and interested in joining our efforts please send them my link and invite your friends to support our effort!
Cystic fibrosis (CF) is a devastating genetic disease that affects the lungs and digestive system. More than ten 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.
To learn more about CF and the CF Foundation, visit www.cff.org. Together, we can make a difference in the lives of those with cystic fibrosis. Thank you for supporting the mission of the CF Foundation!
In support of my position on the committee, I am raising funds for cystic fibrosis (CF) research and care. I want to introduce you to one of the children I have an opportunity to help… this is Team CF Ambassador Chloe. Though she is doing well now, I want to make sure Chloe and all the other children living with this disease continue to grow and thrive. By supporting me, you can help us make a difference in Chloe’s life.
Know that your generous gift will be used efficiently and effectively— CFF is a careful steward of every dollar.
There are three ways to support me:
1) Make a donation that will be credited to my fund-raising efforts. Any amount you can donate will be greatly appreciated!
2) Purchase a ticket to join us for the STANDOUT event on November 7, 2024 at The Ruth in West Charlotte. Dinner and beer/wine are provided! (I would be ecstatic to have you at my table as I support the honorees!)
3) If you know others that would be willing and interested in joining our efforts please send them my link and invite your friends to support our effort!
Cystic fibrosis (CF) is a devastating genetic disease that affects the lungs and digestive system. More than ten 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.
To learn more about CF and the CF Foundation, visit www.cff.org. Together, we can make a difference in the lives of those with cystic fibrosis. Thank you for supporting the mission of the CF Foundation!
OCT
10
10
Comments