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 Coalition for Pulmonary Fibrosis
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1659 Branham Lane
San Jose, CA 95118-5226
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announcments
bullet Co-Sponsorship of Pulmonary Fibrosis Research Enhancement Act Increases to 27 Members of Congress
bullet NIEHS Study Finds Healing Process Found to Backfire in Lung Patients
bullet CPF Publishes 4th Quarter, 2008 Action Alert Newsletter
bullet CPF Fall Fundraising Campaign Raises More than $500,000 to Benefit Patients and Researchers Fighting Pulmonary Fibrosis
bullet InterMune Reports Japanese Regulatory Approval of Pirfenidone in IPF
 

 
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


CPF in the News.
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Frequently Asked Questions About IPF
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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