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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

The annual
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.

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Get Involved

Help Someone Breathe a Little Easier Today ...

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Volunteer to:

  • Help with an event

  • Help with administrative duties

  • Help with support group meetings

  • Help with hospital visits

email : volunteer@pfassociation.org to volunteer

Knowledge, like air, is vital to life.
Like air, no one should be denied it.
Alan Moore

 

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Get Educated

Educate Patiently                Advocate Passionately 

Inspire Consistently

Make a Difference. . . 

DONATE

A tax deductible donation provides life-saving oxygen to patients .

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MEMORIAM

Honor a loved one lost to PF with a note on the Memoriam page and/or a memorial donation

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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.

Healthcare Heroes

Honor a Healthcare Hero that's been part of your  PF journey.

FRAMING FIBROSIS

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The Founders

AND THEIR JOURNEY

Pulmonary Fibrosis Association was founded by John & Jan Orndorff.

Read their story here.

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Pulmonary Fibrosis Association

Need more information?

Email: info@pfassociation.org

Phone: 281.348.0802

Address:  1525 Lakeville Drive Suite 101, Kingwood, TX 77339

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