Who We Are
The Pulmonary Fibrosis Foundation (PFF) is a 501(c)(3) nonprofit organization founded by brothers Albert Rose and Michael Rosenzweig, PhD. Their sister Claire died from idiopathic pulmonary fibrosis (IPF), and they were both later diagnosed with the disease. Their goal was to build an organization dedicated to identifying effective treatments and providing support for those living with the disease. This vision shaped the PFF to become what it is today – the leading patient advocacy organization for the PF community. The PFF continues to be the foremost resource for our community by raising awareness, providing disease education, and driving research to find a cure.
What We Do
The mission of the Pulmonary Fibrosis Foundation is to accelerate the development of new treatments and ultimately a cure for pulmonary fibrosis. Until this goal is achieved, the PFF is committed to advancing improved care of patients with PF and providing unequaled support and education resources for patients, caregivers, family members, and healthcare providers.
Details
| (312) 273-4991 | |
| klynch@pulmonaryfibrosis.org | |
| Kelly Lynch | |
| Director, Development | |
| https://www.pulmonaryfibrosis.org/ |
