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Welcome to Rose Mongillo's Page
Rose Mongillo
Rose Mongillo
I am truly honored to have been selected by the Cystic Fibrosis Foundation as a 2024 Honoree. Along with the other 2024 honorees, I will be recognized by the Cystic Fibrosis Foundation at a special event recognizing outstanding professionals in my community. In accepting this distinction, I have committed to raise money to help the Foundation realize its mission of curing cystic fibrosis (CF) and providing all people with CF the opportunity to lead long, fulfilling lives.
I first learned about the CF Foundation 8 years ago when my son (8yo at the time) and I participated in a local "Great Strides" walk to support a very special family friend and CF Fighter! It has been an educational and rewarding experience to become involved in an organization with such an intense level of energy and commitment to advocating for patients and for bringing new life saving treatments to market. I feel incredibly grateful for this opportunity to help in the fight and passionate about patient access and affordability to treatments and an eventual cure.
Please help me meet my fundraising goal by making a donation and /or consider attending this very special event. By supporting my fundraising efforts, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.
Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is over 50. Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.
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!
I first learned about the CF Foundation 8 years ago when my son (8yo at the time) and I participated in a local "Great Strides" walk to support a very special family friend and CF Fighter! It has been an educational and rewarding experience to become involved in an organization with such an intense level of energy and commitment to advocating for patients and for bringing new life saving treatments to market. I feel incredibly grateful for this opportunity to help in the fight and passionate about patient access and affordability to treatments and an eventual cure.
Please help me meet my fundraising goal by making a donation and /or consider attending this very special event. By supporting my fundraising efforts, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.
Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is over 50. Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.
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!
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