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, which has also affected other members of his family. Vazquez describes the important connection to the PF community that he found through the Pulmonary Fibrosis Foundation. Now, as a support group leader in the Chicago area, he encourages others to utilize the resources of the PFF.
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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.
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© 2019 Pulmonary Fibrosis Foundation
22 окт 2019
