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CPF 'Living with IPF' Patient Seminar to be Webcast Live October 13, 2007
Date:10/8/2007

ilable for IPF patients and their families.

The CPF is unable to provide technical support for the event's Webcast. Technical Support is only available by email through Multivu at: webcast@multivu.com.

Minimum Computer Requirements to listen to broadcast:

The Windows Media Player software, downloadable free from http://www.microsoft.com/windows/windowsmedia/default.aspx and at least a 56Kbps connection to the Internet. If you experience problems listening to the Webcast, send an E-mail to: webcast@multivu.com.

For those who would like to attend the meeting in person, the physical location is:

Kane Hall, Room 110

University of Washington, Seattle

**The UW campus begins at the corner of NE 45th Street and

15th Avenue NE.

Seattle, Washington

For more information, visit http://www.coalitionforpf.org or call 1-888- 222-8541.

About Idiopathic Pulmonary Fibrosis (IPF)

IPF is a lung disorder characterized by a progressive scarring - known as fibrosis -- and deterioration of the lungs, which slowly robs its victims of their ability to breathe. Approximately 128,000 Americans suffer from IPF, and there is currently no known cause or cure. An estimated 48,000 new cases are diagnosed each year. IPF is difficult to diagnose and an estimated two-thirds of patients die within five years of diagnosis.

About the Coalition for Pulmonary Fibrosis

The Coalition for Pulmonary Fibrosis (CPF) is a 501(c)(3) nonprofit organization, founded in 2001 to accelerate research efforts leading to a cure for idiopathic pulmonary fibrosis (IPF), while educating, supporting, and advocating for the community of patients, families, and medical professionals fighting this disease. The CPF funds promising research into new approaches to tr
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SOURCE Coalition for Pulmonary Fibrosis
Copyright©2007 PR Newswire.
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