The Pulmonary Fibrosis Foundation (PFF) is hosting their biennial summit this November!
Pulmonary fibrosis covers 200 different conditions that include sarcoidosis, IPF, scleroderma and other rare diseases. The conditions are characterized by chronic fatigue, hacking cough, chest discomfort, and weight loss. Treatment should be personalized by patient, as everyone is different. They could have ebbs and flows of disease flares, others may experience a steady progression of the condition. There is no cure, but the PFF is working toward that.
The PFF is a reliable non-profit dedicated to supporting everyone in the pulmonary fibrosis community, from patients and caregivers, to medical professionals and researchers. They strive to promote collaboration between the medical community and patient community to achieve better standards of care and ultimately a cure for those battling PF.
The PFF Summit 2017 will seek to accomplish the PFF’s goals of better treatment and a cure through continuing medical education (CME) for health care providers and working sessions with patients, families and those who have been affected by PF. To learn more about it click here.
Who: The Pulmonary Fibrosis Foundation
What: The PFF Summit
Where: Omni Nashville Hotel, Nashville, TN
When: November 9th through the 11th, 2017
