September 2014 PF Awareness Month

Quick Reference – Patient Access to Ofev (nintedanib) and Esbriet (pirfenidone):

You Are Not Alone - Welcome Letter

Join the CPF for Education, Support and Hope

More than $2 million invested in PF research


Old man smiling with his son and daughter in background

The CPF is here to support patients and caregivers through every step of their experience with PF — sharing resources, information and working to protect the rights of our patients. We serve the national patient and physician community by advocating for patients, funding research for treatments, building public awareness, and pressing for increased federal research funding. The CPF needs you on the team to help us conquer PF. Join now and help us find answers. There is no charge for any of our services.

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  • August 8, 2015:
    5th Annual Violet Rippy 5K for Pulmonary Fibrosis – Pittsburgh, PA
  • June 27, 2015:
    8th Annual Run-Walk-Hike for Pulmonary Fibrosis – New York, NY
  • April 23, 2015:
    Yale 8th Annual Fibrosis Symposium Session for Patients and Families
  • March 26, 2015:
    4th Annual Celebrity Bartending Event – Pittsburgh, PA
  • March 7, 2015:
    Understanding Pulmonary Fibrosis – A Seminar for Patients, Caregivers, and Families