You Are Not Alone - Welcome Letter

Join the CPF for Education, Support and Hope

More than $2 million invested in PF research

join now

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.


Spring newsletter just out - new research updates

Help pass the PFREA!

RECENT & UPCOMING EVENTS

May 19, 2012:
Patient and Family “Meet the Expert” Forum – San Francisco, CA

June 02, 2012:
Breathe Strong Pilates Fundraiser - Bethpage, NY

June 09, 2012:
1st Annual Vic Vittorino's Walk for Your Next Breath – Delanco, NJ

June 10, 2012:
02 Riding for PF – Raymond, ME

August 11, 2012:
Second Annual 5k Run/Walk for PF - Pittsburgh, PA