You Are Not Alone - Welcome Letter

Join the CPF for Education, Support and Hope

More than $2 million invested in PF research

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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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RECENT & UPCOMING EVENTS

  • July 26, 2014:
    2nd Annual Golfing for a Cure in Crete, IL
  • June 14, 2014:
    7th Annual NYC Run-Walk-Hike for Pulmonary Fibrosis
  • April 26, 2014:
    Pulmonary Fibrosis Patient Education Day-University of Minnesota
  • April 12, 2014:
    April 12, 2014 – 2nd Annual Jim Kelly Memorial Tournament
  • April 1, 2014:
    Memphis, TN Inaugural Support Group Meeting