Plus BreatheCon, the O'Donnell's family story, and more on lung transplant


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Register for BreatheCon!

Come together with other people living with CF to discuss topics unique to you! BreatheCon is a free, online event just for adults with cystic fibrosis. Join us Friday, Sept. 20 and Saturday, Sept. 21 ([link removed]) for keynotes, workshops, group chats, and more.

Sign me up» ([link removed])

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Is Lung Transplant Right for You?

Early discussions about lung transplant as a potential treatment can extend and improve the quality of life for people with CF. Newly expanded lung transplant content on cff.org ([link removed]) outlines the emotional, financial, logistical, social, and physical aspects of the transplant experience.

Explore my options» ([link removed])

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Fueling a Family Legacy

Father-daughter duo Joe and Kate O’Donnell have made the fight to cure CF a driving force in their lives ([link removed]). Joe and his wife, Kathy founded The Joey Fund in 1986 in honor of their son who had cystic fibrosis. Today, Kate runs The Joey Fund with her sister, Casey and co-chairs the Tomorrow’s Leaders program in Massachusetts. Together, the family has raised hundreds of millions of dollars toward a cure for CF.

Hear their story on the Breaking Through podcast» ([link removed])

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Get your IPC Passport

You can help educate health care providers about how to reduce the risk of cross-infection among people with CF. Download a pocket-sized Infection Prevention Control (IPC) Passport Card and see 7 Ways to Guard Against Germs in Health Care Settings ([link removed]) on cff.org.

Print my passport» ([link removed])

DONATE ([link removed])

Cystic Fibrosis Foundation

4550 Montgomery Ave, Suite 1100N

Bethesda, Maryland 20814

www.cff.org ([link removed])



4550 Montgomery Avenue, Suite 1100N | Bethesda, MD 20814 US

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