Life with Pulmonary Fibrosis | Portraits of PF - Jose Vazquez

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  • čas přidán 22. 10. 2019
  • 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.
    For more information, visit pulmonaryfibrosis.org.
    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 presentation 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.
    © 2019 Pulmonary Fibrosis Foundation

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