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.




Help pass the PFREA!

RECENT & UPCOMING EVENTS

June 08, 2013:
*NEW DATE* 6th Annual NYC Run-Walk for Pulmonary Fibrosis – New York, NY

August 10, 2013:
3rd Annual Violet Rippy 5K for Pulmonary Fibrosis – Pittsburgh, PA