Pulmonary Fibrosis Awareness Month: Raising Hope and Understanding Nationwide

September: Pulmonary Fibrosis Awareness Month

As September approaches, recognized as Pulmonary Fibrosis Awareness Month (PF Awareness Month), the Pulmonary Fibrosis Foundation (PFF) is gearing up for a nationwide effort aimed at raising awareness about pulmonary fibrosis (PF) and interstitial lung disease (ILD). With over 250,000 Americans affected by these progressive, life-threatening diseases, this campaign is crucial for fostering understanding and support among communities.

Pulmonary fibrosis and ILD are characterized by scarring and inflammation of the lungs, which significantly hampers the ability of patients to absorb oxygen efficiently. This often results in severe health consequences, making it imperative to spotlight their challenges and needs.

This year's theme, "Every breath of the way," not only emphasizes the resilience of those living with PF and ILD but also commemorates the 25th anniversary of the PFF. Dr. Amy Hajari Case, Chief Medical Officer for the PFF, stated, "Pulmonary fibrosis is a life-threatening condition with limited treatment options and no cure. Our organization is dedicated to improving awareness, which in turn drives investment in research and fosters stronger support systems for patients and their families."

Throughout the month of September, the PFF will engage its audience on social media, offering daily content that showcases patient narratives, educational facts about PF and ILD, and actionable ways for individuals to contribute to the cause. The foundation encourages everyone to interact with these messages, as likes, shares, and comments can amplify the reach of awareness efforts across various platforms. Follow along with their updates on Facebook, Instagram, and YouTube at @pfforg.

In addition to online initiatives, the PFF has organized numerous community events both in-person and virtually, such as the PFF Walks taking place in several key cities: the Bay Area on September 6, Chicago on September 20, and Washington, D.C. on September 27. These events aim to unite patients, caregivers, and advocates while raising essential funds for PF research and support services. A virtual National Walk Day is also scheduled for September 27, allowing even more participants to join the movement.

Moreover, notable landmarks across the country will illuminate in the PFF's signature blue on September 10, symbolizing hope and drawing national attention to the disease. On the same day, the foundation, in collaboration with ten partner organizations, will celebrate ILD Day with a free webinar titled, "Genetics and Beyond: Exploring Interstitial Lung Disease in Families and Individuals."

This dedicated month not only serves as a platform for education and advocacy but also empowers patients and caregivers to voice their experiences, promotes earlier diagnosis, and generates momentum for enhanced care solutions. By increasing visibility, the journey toward finding a cure progresses, ensuring that no one faces pulmonary fibrosis alone.

For those wishing to learn more or engage with PF Awareness Month, the PFF invites you to visit their website at pulmonaryfibrosis.org or contact them directly at 844.TalkPFF (844.825.5733). Join the collective movement in advocating for those living with pulmonary fibrosis as we strive for brighter days ahead and a future without this debilitating disease.

About the Pulmonary Fibrosis Foundation

The Pulmonary Fibrosis Foundation is dedicated to accelerating the development of new treatments and ultimately finding a cure for PF. Until that goal is reached, the PFF focuses on enhancing patient care and providing unparalleled support and education resources for individuals affected by this condition. Holding a four-star rating from Charity Navigator, being accredited by the Better Business Bureau (BBB) Wise Giving Alliance, and meeting the standards of the National Health Council, the organization stands as a beacon of hope for all impacted by pulmonary fibrosis.