Learn about the rights of Cystic Fibrosis Foundation donors.
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We are excited that this spring, in Washington, DC, from March 13-16, 2024, there will be an enriched conference experience that combines March on the Hill (MOH) and our Volunteer Leadership Conference (VLC) into one extraordinary event for our leading volunteers with the theme of Hope in Action.
National Teams raise awareness about cystic fibrosis, and raise funds to support the Foundation's mission to find a cure for CF.
Being a parent with cystic fibrosis can be difficult, but a strong support system can help. By learning more about what to expect as a parent with CF, you can find new ways to balance your own health with the time it takes to care for your child.
By understanding the effects that different forms of contraception can have on people with cystic fibrosis, you can choose the method that is right for you.
Many people with CF choose surrogacy or gestational carriers as a family building option. By learning more about surrogacy and its potential challenges, you can ultimately assess whether it is right for you.
Our corporate champions are an important part of our progress — with corporate supporters by our side, we continue to advance our goal — to make CF stand for Cure Found.
Working alongside the CF community, the Foundation has fostered the development of more than a dozen CF treatments — an unprecedented number in a short span of time — and helped add decades of life for people with CF. And while therapies such as Trikafta® have had an incredible impact on the lives of those with CF, there are still many people with this disease who do not benefit from existing treatments. Our goal is to cure cystic fibrosis.
The Drive is the Cystic Fibrosis Foundation’s ultimate golf experience, held in the fall at renowned golf courses around the United States.
When you have cystic fibrosis, there are potential complications related to pregnancy. But as part of the planning process, you can learn more about these complications and how to partner with your CF care team to evaluate these risks based on your personal situation.