Sponsorship Opportunities
Partner With Us
Our sponsors help us provide essential information to patients, caregivers, and healthcare professionals, support dynamic events that bring together the community, and fund research to better understand and treat pulmonary fibrosis (PF) and interstitial lung disease (ILD).
Interested in joining these industry leaders? Learn more about how you can contribute below or contact Jennifer Mefford at partnerships@pulmonaryfibrosis.org for more information.
PFF Corporate Committee
Industry leaders—pharma, biotech, and others developing solutions in PF and ILD—engage meaningfully with the Foundation’s leadership and volunteer network. For more information, visit the PFF Corporate Committee webpage.
PFF Events
We host fundraising and educational events, including:
PFF Walk: Held across the country as well as virtually to unite everyone impacted by PF and ILD.
Broadway Belts for PFF!: Our biggest fundraising event includes performances by Broadway stars.
PFF Summit: The largest healthcare conference for PF and ILD in the world.
PFF Education Symposium: Focused on the latest advances in research and patient care, our symposium is created specifically for patients and caregivers.
Pulmonary Fibrosis Awareness Month
Every September, we post daily content on social media to educate, inform, and shine a light on the many faces of the PF and ILD community. Our social media campaigns include the “30 Facts in 30 Days” series, the "Portraits of PF" series, and #BlueUp4PF.
PFF Patient Programs
We provide patients and their loved ones with educational resources and support to cope with their diagnosis and live with this disease:
Educational Materials: Booklets, brochures, guides, and fact sheets available in print and digital versions, free of charge to the community. Topics covered include general disease information, supplemental oxygen, clinical trials, caregiving, and more. This program also includes the PFF Help Center which offers one-on-one support to find resources and disease education.
Webinars: Live and recorded disease education events led by specialists in PF and ILD. Offered 6-8 times per year and recorded for on-demand viewing.
Support Groups: Virtual and in-person opportunities for patients, caregivers, and lung transplant recipients to connect with others, share practical information and resources, and find support along their disease journey.
PFF Ambassadors: Patients, caregivers, lung transplant recipients, and those who have lost a loved one serve as spokespeople for the community. Trained in public speaking and storytelling, they share their personal experience and a message of hope with different audiences.
PFF Registry
The PFF Registry is a nationwide research program that collects data from patients living with PF or ILD as well as their caregivers and family members. This information will help researchers find answers to key questions about PF and ILD.
Care Center Network
Our Care Center Network allows those living with PF and ILD to find experienced medical professionals who understand their disease and support services to improve the quality of their lives. Care Centers offer access to clinical trials and patient education with a patient-focused delivery of care.
Meet Our Sponsors
Thank you to our partners for their generous support.
Sponsors
