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 Coalition for Pulmonary Fibrosis
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Tools and Resources for Reporters and Editors

The CPF is available to the media as a source of unbiased, accurate, and timely information on idiopathic pulmonary fibrosis (IPF) and the latest research on the disease. Our CPF experts are available for interviews as well as to provide background information. You can also turn to us to arrange interviews with top IPF experts around the country.

To arrange interviews or for further information please contact:
Teresa Barnes
888-222-8541, ext. 702
tbarnes@coalitionforpf.org


Facts About Idiopathic Pulmonary Fibrosis
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Reporters' Guide to Idiopathic Pulmonary Fibrosis
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Patient Profiles

The Roney Family
Deirdre Roney's mother, grandmother, and three of her uncles died of idiopathic
pulmonary fibrosis (IPF). In this profile, she talks about the impact of IPF on her
family and about living with the threat of the disease. To read the Roney family
profile, click here.

Battling IPF For My Father, My Family, and Myself
By Teresa Barnes, CPF Vice President of Patient Outreach and Advocacy

Fibrosis Survivor Breathes Easy: A profile of CPF Advocate Frank Cabral

 
 
 
 

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Site Last Updated 8/4/08
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