PFA Operations will be closed until
October 1, 2022
Our Mission . . .
Provide assistance primarily for obtaining prescribed supplemental oxygen and medical equipment to under-insured, non-insured and acutely ‘in need’ Pulmonary Fibrosis Patients; and
Promote public education and awareness of the disease, its effects and the need for early detection and treatment; and
Establish and promote an area PF Patient Support Group and helpline and to encourage formation of affiliated support groups in other cities, giving patients and their families face-to-face encouragement in their common battle with this disease through information sharing;
As funding allows, support medical research programs and other similar 501(c)(3) entities working for the discovery of the cause, treatment and cure of Pulmonary Fibrosis
It Takes Your Breath Away
Shine a Light
Candle Lighting for
Pulmonary Fibrosis Awareness
with the Breathe Support Network.
Every year in September, the PFA has sponsored the candle lighting event. This year, we are working together to bring this event to you on Saturday, September 17th, at 8:00 pm local time.
We encourage everyone around the world to light a candle for your loved who has battled Pulmonary Fibrosis. Please share a photo and brief story on the special public post that will be set up for this event on the BSN business page at www.facebook.com/breathesupport.
We would love to see our entire PF community lighting candles around the world.
Help Someone Breathe a Little Easier Today ...
Knowledge, like air, is vital to life.
Like air, no one should be denied it.
Make a Difference. . .
Honor a loved one lost to PF with a note on the Memoriam page and/or a memorial donation
Add a picture and memory of your PF journey as a patient, caregiver or family member to share with our PF community for unity, hope and community.