The CF Wind Sprint video series offers quick tips for living with CF. Topics include traveling, nutrition,exercise and treatments.
Every day, researchers around the world come one step closer to discovering a cure for cystic fibrosis. In the meantime, the CF drug “pipeline” ensures therapies are moving from the laboratory to the marketplace. We keep an eye on medical news sources from around the world and report on these developments as they occur.
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New Podcast Discusses Being a CF Parent

07/05/2011

The Boomer Esiason Foundation has posted a new video podcast featuring Megan Mollahan, a parent in New York who has two children with cystic fibrosis.

Megan's daughter, Maureen, is 20 years old and was diagnosed at age eight. Her son, Jack, is 10 and was diagnosed at two months. Megan discusses what it's like to wear "many different hats" as parent, caregiver, friend, advocate, etc.

Click here to read more about Megan and to listen to Podcast 104: Being a CF Parent and Caregiver.

This “LIVING. BREATHING. SUCCEEDING.” Podcast/Vodcast is made possible through an unrestricted educational grant from Genentech to the Boomer Esiason Foundation.

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