Welcome to the Pulmonary Fibrosis Foundation's on-line Caregivers Support Group. This will be a safe place where the family and friends who take care of and support their loved ones who have been diagnosed with idiopathic pulmonary fibrosis or pulmonary fibrosis can share their stories, concerns, fears with each other. The diagnosis of pulmonary fibrosis not only affects the patient; it's a diagnosis that affects the whole family.

This is your support group. Ideally this will be an outlet where you can express your thoughts and feelings whatever they may be. Please remember this is a public domain and being respectful of each other is foremost.

The Pulmonary Fibrosis Foundation's mission is to find a cure and raise awareness of pulmonary fibrosis. We are devoted to improving the quality of life for those diagnosed with pulmonary fibrosis. The Foundation provides hope and inspiration for patients through education, advocacy and funding for clinical research.

If you would like to receive more information about pulmonary fibrosis, please contact Leanne by e-mail at pulmonaryfibrosisinfo@yahoo.com or phone 312.587.9272.

Debra Beck - Moderator
Teri Marietta - Vacation Moderator
Leanne Storch - Owner