Read the results from the 2024 cost burden survey
Earlier this year, the Cystic Fibrosis Foundation and Dartmouth College, asked you to share your experiences with health care costs and how they may impact you and your family. You generously shared your experiences, and the results are now available.
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The survey, Cystic Fibrosis Outcomes, Social Factors, Tradeoffs Due to Cost and Financial Burden (COST-CF), revealed that while each person’s experience with CF may vary, the burden of the disease can be felt regardless of geography, employment status, or insurance coverage.
The Cystic Fibrosis Foundation uses this valuable data to shape support programs and tools designed to help the community navigate the challenges of health care costs. Our goal is to ensure that no one has to make difficult tradeoffs when managing their disease.
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We acknowledge that conversations around financial hardships are sensitive and the Foundation thanks those in our community who graciously shared their experiences to help inform how we can better serve you and your needs.
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www.cff.org
4550 Montgomery Avenue, Suite 1100N | Bethesda, MD 20814 US
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WE WILL NOT REST UNTIL WE FIND A CURE
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