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Welcome to Laura Gregory's Page
Laura Gregory
Together, our efforts will continue to advance the Cystic Fibrosis Foundation's mission of finding a cure for CF in order to provide people living with CF the opportunity to live a long, healthy life. Any donation made to my page (small or large) is truly appreciated. In September I will be honored by the Cystic Fibrosis Foundation at a special event recognizing outstanding professionals in my community. If you would like to join me you can purchase a ticket to the event and 100% of tickets is donated to my CF campaign! I am currently working on my first event in June and will be sharing the details in the upcoming week or so!
With my commitment of raising awareness I’ll be hosting a few fun events this Summer, stay tuned for the details!
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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