Hi, I am Jeanne.  My husband Bill was diagnosed with IPF in 2020 after 2 years of coughing.  He had no other symptoms.

 As many others, I searched the internet for information and arrived at the PFF website.  The wealth of information and support has helped us to navigate this journey through otherwise uncharted territory.  With your support we will find a cure.  

This card is a limited edition.  

I will sell 100 cards celebrating Pulmonary Fibrosis Awareness Month this September.  You may want to send congratulaions after a tough procedure or to celebrate a lung transplant, or just to let someone know that you are thinking of them.

To place an order, please contact me first to confirm availability: jeanneeq@gmail.com.  When I confirm your order with you, you can make your donation from this page, share your address with me, and I will ship them the next business day. 

Your donation makes a difference.  Please help change the outcome of Pulmonary Fibrosis one breath a time.

Thank you

I am proud to lead the way toward a world without pulmonary fibrosis (PF). Please join me as I raise funds and awareness to benefit the Pulmonary Fibrosis Foundation (PFF).

Pulmonary fibrosis 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. Over 250,000 Americans are living with PF today. Approximately 50,000 new cases are diagnosed each year.

Because of the work of the 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 support will make a difference in the lives of PF patients and their families, please visit www.pulmonaryfibrosis.org.