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The Show Goes on for Pulmonary Fibrosis Patient Jerry Lewis
Date:9/4/2009

al professionals fighting this disease. The CPF funds promising research into new approaches to treat and cure PF; provides patients and families with comprehensive education materials, resources, and hope; serves as a voice for national advocacy of PF issues; and works to improve awareness of PF in the medical community as well as the general public. The CPF's nonprofit partners include many of the most respected medical centers and healthcare organizations in the U.S. With more than 19,000 members nationwide, the CPF is the largest nonprofit organization in the U.S. dedicated to advocating for those with PF. For more information please visit www.coalitionforpf.org or call (888) 222-8541.


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SOURCE Coalition for Pulmonary Fibrosis
Copyright©2009 PR Newswire.
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4. FDA Approves TYVASO (Treprostinil) Inhalation Solution for the Treatment of Pulmonary Arterial Hypertension
5. NHLBI stops study of pulmonary hypertension treatment in sickle cell patients
6. CPF Announces Dates for Seventh Annual National Pulmonary Fibrosis Awareness Week
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8. Scienceroll.com on an iPhone Application for Cardiopulmonary Resuscitation Training
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10. CPF, Pulmonary Fibrosis Experts Guests on Sirius and XM Satellite Radio Show June 16th
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