The Second Wind Foundation for Pulmonary Fibrosis is a non-profit organization of volunteers with a mission to increase the awareness, help fund research, and provide for the common good of individuals affected by Pulmonary Fibrosis. We were established in 2010 and intend on being an organization constantly striving to raise the level of awareness of this incurable disease. Pulmonary Fibrosis affects more that ¼ of a million people in the United States. However, if you ask the person standing next to you what is Pulmonary Fibrosis, they probably will not be able to tell you.
Pulmonary Fibrosis (PF) is a debilitating disease—marked by progressive scarring of the lungs—that gradually interferes with a person’s ability to breathe. Pulmonary Fibrosis belongs to a family of approximately 100 related diseases, called interstitial lung diseases, which have similar characteristics and can result in lung scarring. This scarring is most often referred to as Pulmonary Fibrosis.
We will strive to help educate, provide for research to find a cure, and assist individuals afflicted by this disease.
Please take a few moments to search our site and understand our cause.
Thank you for you time. If you wish to donate to our cause please feel free to send you donation to:
Second Wind Foundation for PF
P O Box 80
Auburn, NH 03032
Ron Geoffroy Sr.
President, Second Wind Foundation for Pulmonary Fibrosis