Pulmonary Alveolar Proteinosis (PAP) is a life-threatening lung disorder that affects men, women, and children.
The PAP Foundation is a non-profit patient advocacy organization dedicated to finding a cure and to improving the lives of those affected by PAP.
Through advocacy and collaboration, we promote research on PAP and provide information and support for PAP patients, healthcare professionals, and the public.
We are pleased to be a resource of information about PAP. However, the information provided here is not, nor is it intended to be, medical advice and should never take the place of advice from your personal health care provider.
International PAP Scientific Research Meeting, May 15, 2010, New Orleans, LA, USA