Friends of the Pulmonary Fibrosis Warriors Presents Music Bingo Under the Stars!

I am proud to be part of Team PFF, leading the way toward a world without pulmonary fibrosis (PF). I hope you will join me as I raise funds for the Pulmonary Fibrosis Foundation (PFF).

The Pulmonary Fibrosis Foundation is very near and dear to my heart. My father has this disease, and at this moment, there is no cure. Please help support the research to find a cure! My dad and I have met many wonderful, loving, and supportive people through the foundation and in my Dad's PF Warriors group. Without them, I don’t know where we would be! Please join us on September 14th at the Music Bingo Under the Stars event for a fun night with great prizes, all for a good cause!

Pulmonary fibrosis (PF) is a condition that causes lung tissue to become thickened, stiff, and scarred. The lungs eventually lose their ability to transfer oxygen into the bloodstream, making everyday activities such as breathing and walking extremely difficult. It is a progressive disease, which means it tends to worsen over time. Every individual diagnosed with pulmonary fibrosis has a unique experience with the disease, and there is no “standard” or expected clinical course. With no known cure,  the disease is often fatal within three to five years of diagnosis. There are over 250,000 Americans living with PF today. Approximately 50,000 new cases are diagnosed each year.

Because of the work of the Pulmonary Fibrosis Foundation (PFF), there is hope for those living with PF. Funds raised will support the PFF’s efforts to accelerate research, advance improved care for those living with the disease, and provide unequaled support and education resources for patients, caregivers, family members, and healthcare providers.

But we can't do this without you! Only with your support can we keep the PFF's mission active. Please click the "Donate" button to make your gift today. Thank you in advance for your generous support!

For more information on how your gift will make a difference in the lives of PF patients and their families, please visit www.pulmonaryfibrosis.org.

Thank you in advance for your generous support!

$3,602.07

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$250.00

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of your goal reached

My Supporters

  • Linda Kraemer 14 hours ago
  • Event Proceeds and Contributions 14 hours ago
  • Cheryl McMullan In honor of Dennis McMullan September 2024 $25.69
  • Beverly Ferrer August 2024
  • Anonymous I am hoping for a cure's discovery for Pulmonary Fibrosis Foundation. August 2024 $25.69
  • Cheryl McMullan In honor of Dennis McMullan September 2024 $25.69
  • Anonymous I am hoping for a cure's discovery for Pulmonary Fibrosis Foundation. August 2024 $25.69