Pulmonary Fibrosis Foundation Works to
Drive Awareness of Lung Disease
CHICAGO, July 25,
2024 /PRNewswire/ -- September is Pulmonary Fibrosis
Awareness Month, presented by the Pulmonary Fibrosis
Foundation (PFF) to drive awareness of pulmonary fibrosis (PF)
and interstitial lung disease (ILD). There are more than 200 types
of interstitial lung diseases (ILD), which are characterized by
varied amounts of inflammation, scarring, or both, that damage the
ability of the lung to absorb oxygen from the air. Pulmonary
fibrosis means scarring of the lung and can be seen in many types
of ILD.
More than 250,000 Americans are living with PF and ILD. With the
theme "Every Breath, Every Story," the PFF will highlight patient
journeys. These stories will mobilize family members and supporters
to spread the word about PF, which has no known cure.
"Pulmonary Fibrosis Awareness Month fosters a more informed and
engaged community through our efforts in educating the public,
promoting early detection, and advocating for those affected by
this disease," said Scott Staszak,
President and CEO of the PFF. "PF and ILD are serious, debilitating
conditions, and we are committed to ensuring that everyone has
access to the necessary resources, so no one has to face this
journey alone."
As part of Pulmonary Fibrosis Awareness Month, the PFF is
providing opportunities for dedicated individuals to raise
awareness and funds, amplifying the community's collective
impact.
Portraits of PF – Throughout September, the PFF will
post a daily story and photo from people living with PF and ILD,
caregivers, health care professionals, transplant recipients and
those who have lost a loved one to these diseases. These heartfelt
stories help others understand the many journeys people with PF and
ILD have experienced.
National PFF Walk Day – On September 28, supporters can unite with patients,
families, and friends across the country to walk together toward a
cure. Registration is free, and the virtual walk begins with
an inspiring Mission Moment from the PFF. In addition to National
PFF Walk Day, the Bay Area Walk will take place on Sept. 7, followed by the Chicago Walk on
Sept. 14.
30 Facts in 30 Days – The PFF will share medically
accurate PF and ILD facts every day on Facebook and Instagram to
educate the public about the impact of the disease. Supporters can
expand the reach of these messages by liking, sharing, and
commenting on the facts to their own groups of friends and
followers.
Strike the Lung Pose – The PFF invites the public to
take a selfie making the lung pose and submit it to the
PFF who will add the PFAM template. It will then be sent back for
use on social media to demonstrate support of the PF community.
ILD Day – On Wednesday, September
18, the PF and ILD community will recognize the fourth
annual ILD Day featuring a webinar called The Journey to
Diagnosis: Process, evaluation, and your care team.
Invite a Building or Landmark to #BlueUp4PF – Iconic
landmarks and buildings nationwide will shine blue during PF
Awareness Month. Invite a building in your community to go
blue and let us know so we can share the information on social
media.
Pulmonary Fibrosis Awareness Month is sponsored by Amgen Rare
Disease, MannKind Corporation and Trevi Therapeutics.
Donate and learn more about PF and ILD at
pulmonaryfibrosis.org.
About the Pulmonary Fibrosis Foundation
The mission of the Pulmonary Fibrosis Foundation is to
accelerate the development of new treatments and ultimately a cure
for pulmonary fibrosis. Until this goal is achieved, the PFF is
committed to advancing improved care of patients with PF and
providing unequaled support and education resources for patients,
caregivers, family members, and health care providers. The PFF has
a four-star rating from Charity Navigator and is an accredited
charity by the Better Business Bureau (BBB) Wise Giving Alliance.
The Foundation has met all of the requirements of the National
Health Council Standards of Excellence Certification
Program® and has earned the Guidestar Platinum Seal of
Transparency. For more information,
visit pulmonaryfibrosis.org or call 844.TalkPFF
(844.825.5733).
Contact: Dorothy Coyle
773-332-6201
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SOURCE The Pulmonary Fibrosis Foundation