Welcome to Qing Tiffany's Page
Qing Tiffany
Qing Tiffany
Hi! My name is Qing and I'm being honored by the Cystic Fibrosis Foundation at a special event recognizing outstanding professionals in our community. In accepting this distinction, I have committed to raise funds to cure Cystic Fibrosis (CF).
As the Community Engagement Director for a Detroit nonprofit and Board Member for another organization, I work every day to connect people, build partnerships, and advocate for meaningful change locally and across Michigan. While I'm passionate and committed about many causes, my fight against CF is deeply personal.
My uncle, Scott Carmona was diagnosed with CF in 2002 at the age of 35.
Cystic Fibrosis is a progressive, genetic disease that affects the lungs, pancreas, and other organs, causing serious breathing and intestinal problems, chronic infections and lung damage. Today, more than 40,000 people in the United States live with CF.
Not long ago, most children with CF rarely lived long enough to attend elementary school. Thanks to groundbreaking research and care funded by the Cystic Fibrosis Foundation, the median life expectancy is now over 50.
My Uncle Scott is currently on the drug Trikafta, and is living an active and healthy life at the age of 59!
While treatments like Trikafta have transformed lives, many people with CF do not benefit from them due to their specific gene composition. That's why the Cystic Fibrosis Foundation remains dedicated to find a cure for every person with CF, and a life free from the burden of this disease.
Your support can help make that vision a reality. Every donation drives research, advocacy, and innovation that brings us closer to that cure. By donating, you're providing HOPE to parents with a newly diagnosed child that they can live a long fulfilling life and to young adults that they can dream big, build a career, and even plan for retirement.
Thank you for supporting me and this mission! To learn more about CF and the Cystic Fibrosis 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!
As the Community Engagement Director for a Detroit nonprofit and Board Member for another organization, I work every day to connect people, build partnerships, and advocate for meaningful change locally and across Michigan. While I'm passionate and committed about many causes, my fight against CF is deeply personal.
My uncle, Scott Carmona was diagnosed with CF in 2002 at the age of 35.
Cystic Fibrosis is a progressive, genetic disease that affects the lungs, pancreas, and other organs, causing serious breathing and intestinal problems, chronic infections and lung damage. Today, more than 40,000 people in the United States live with CF.
Not long ago, most children with CF rarely lived long enough to attend elementary school. Thanks to groundbreaking research and care funded by the Cystic Fibrosis Foundation, the median life expectancy is now over 50.
My Uncle Scott is currently on the drug Trikafta, and is living an active and healthy life at the age of 59!
While treatments like Trikafta have transformed lives, many people with CF do not benefit from them due to their specific gene composition. That's why the Cystic Fibrosis Foundation remains dedicated to find a cure for every person with CF, and a life free from the burden of this disease.
Your support can help make that vision a reality. Every donation drives research, advocacy, and innovation that brings us closer to that cure. By donating, you're providing HOPE to parents with a newly diagnosed child that they can live a long fulfilling life and to young adults that they can dream big, build a career, and even plan for retirement.
Thank you for supporting me and this mission! To learn more about CF and the Cystic Fibrosis 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!
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