PFF Videos

Diagnosed with pulmonary fibrosis in 2009, Valeria Hatcher describes that much of her life revolves around scheduling doctor visits and making sure she has an adequate oxygen supply every day.

After caring for his mother who lost her battle with pulmonary fibrosis while awaiting a lung transplant, Jose Vazquez received his own diagnosis of IPF. He shares his struggle to accept the diagnose and the reality of living with the disease.

Después de cuidar a su madre que perdió su batalla contra la fibrosis pulmonar mientras esperaba un trasplante de pulmón, José Vázquez recibió su propio diagnóstico de FPI (Fibrosis Pulmonar Idiopática).

Cindy Chandler became a PFF Advocate after losing her husband and her mother-in-law to pulmonary fibrosis. Now, she describes the effort to build a group of grass-roots advocates across the country as a calling.

Gary and Marianne were married just two and a half years when Gary was diagnosed with idiopathic pulmonary fibrosis. They found hope and inspiration in their local support group and are now leaders of the group.

Dot describes her journey with PF, her lung transplant, and how she has devoted her life to giving back to patients and the community.

Meet Heather Kagel, who was diagnosed with IPF five years ago experiencing breathlessness and a cough that wouldn’t go away.

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