Coalition for Pulmonary Fibrosis (CPF)

Coalition for Pulmonary Fibrosis (CPF) - Information

YOU'RE NOT ALONE!

Join the CPF Community

48,000 too many! Each year, over 48,000 Americans are diagnosed with Pulmonary Fibrosis. We think that's 48,000 too many. Join us in stopping PF!

The CPF needs you! Every individual reading this page can make an important difference in the effort to fight this dread disease. We are all, every one of us, at risk for Pulmonary Fibrosis, and we must join together as a chorus of voices working to bring about change.

Click here to go directly to the membership form!

Membership Benefits Include

E-mail updates on breaking pulmonary fibrosis news
Access to peer-reviewed educational materials authored by our world-class scientific advisory board
Access to the latest information on clinical trials
A free subscription to the CPF Action Alert Quarterly newsletter
Information on local education and awareness events
Opportunities to become involved in education and awareness efforts in your community
Recognition as a CPF partner (organizations only) in all public information and materials

Note - Membership in the CPF is open to all individuals and organizations interested in promoting awareness of pulmonary fibrosis and in helping to advance pulmonary fibrosis education, patient support, treatment, and research. No membership fee is required, though donations are encouraged.

Please Complete this form to Join *Required fields

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Please complete this portion of the form only if you are a patient or a family member of a patient with pulmonary fibrosis....

I am a Veteran or in active military service:
Yes No

Do you have IPF:
Yes No

Date of diagnosis:
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My diagnosis was confirmed by (check all that apply)

High-Resolution Computer Tomography Scan (HRCT)
Bronchoalveolar lavage
Chest radiography (x-ray)
Surgical Lung biopsy
Arterial blood gas (ABG)
Pulmonary function test (PFT)
Bronchoscopy

These Documents available to US & Canadian residents only.

I understand that all CPF educational materials and resources are available on the CPF Web page, however I do not have an internet connection that I can regularly access, and would like to receive the CPF's Resource Kit by mail.

I represent the office of a physician or healthcare professional, and would like to receive copies of "Let's Talk About IPF" brochure for our patients.