Life with Pulmonary Fibrosis | Portraits of PF - Dot Delarosa

After being diagnosed with pulmonary fibrosis, a disease she had never heard of, Dot Delarosa was told she had two to five years to live. With a lung capacity of 20 percent, Dot was referred for lung transplant. She received a transplant in 2010 and celebrates her lungaversary (anniversary of a lung transplant) every year. Dot describes her journey with PF and how she has devoted her life to giving back to patients and the community.
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