Life With PF: Lung Transplant

Are you thinking about lung transplantation for yourself or your loved one? Some patients living with pulmonary fibrosis may be eligible for a lung transplant, but it is a complex process that may not be right for everyone with PF.

Through the stories of three individuals who are lung transplant recipients or currently listed for transplant, discover how to best prepare for the physical and emotional experiences people with PF face as they undergo evaluation, transplantation, and recovery.

Dr. Marie Budev, Medical Director of Lung Transplantation at the Cleveland Clinic, recommends that patients remain positive, and stay as healthy and active as possible during the waiting period. The path and timing is different for each individual so it is important to remember that every day counts.

Learn more about the lung transplant journey in this informative video.
The Pulmonary Fibrosis Foundation (PFF) offers essential programs and resources for people with pulmonary fibrosis. The mission of the PFF is to mobilize people and resources to provide access to high quality care and to lead research for a cure so that people with PF will lead longer, healthier lives. Social media platforms - Twitter - @PFFORG Facebook - @PFFORG Instagram - @PFFORG LinkedIn- Pulmonary Fibrosis Foundation Please note that any information contained in this presentation is for informational and/or educational purposes only. It is not intended to be a substitute for professional medical advice. Always consult your personal physician or health care provider with any questions you may have regarding your specific medical condition. This video is protected by U.S. and International copyright laws. Reproductions and distribution of this presentation without written permission from the Pulmonary Fibrosis Foundation is prohibited. © 2021 Pulmonary Fibrosis Foundation