An Updated Pulmonary Fibrosis Information Guide

The Pulmonary Fibrosis Foundation has released their new Pulmonary Fibrosis Information Guide.

From the presser:

The Pulmonary Fibrosis Foundation (PFF), the leading pulmonary fibrosis (PF) resource for patients, their families, and the medical community, has announced the publication of its new Pulmonary Fibrosis Information Guide. The guide provides patients and families with up-to-date information about pulmonary fibrosis, treatment options, and ways of maintaining one's health while living with the disease. "Pulmonary fibrosis can be a confusing diagnosis," said David Lederer, MD, the PFF's Senior Medical Advisor, Education and Awareness. "Information available online and through other sources is not always accurate. Our new Pulmonary Fibrosis Information Guide was designed to provide clear, accurate, easy-to-understand information for people living with PF and their caregivers."

Dr. Lederer, quoted above, has long been the go-to source for easy to understand information about pulmonary fibrosis and idiopathic pulmonary fibrosis. His blog is a great resource for all of us and he was very supportive during my own journey with IPF.

Here is the guide:

Pulmonary Fibrosis Information Guide by the Pulmonary Fibrosis Foundation

I've read it and it really is a great resource for anyone affected by pulmonary fibrosis.  Head on over to the Pulmonary Fibrosis Foundation to find information about support, finding care, and connecting with others who are walking this same path.