The PFF Care Center Network

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  • čas přidán 20. 01. 2022
  • To find a Care Center near you, visit pulmonaryfibrosis.org/medicalcare or contact the PFF Help Center at 844.TalkPFF (844.825.5733) or via email at help@pulmonaryfibrosis.org.
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    People living with pulmonary fibrosis may struggle to identify the resources and treatments available to them. That's why the Pulmonary Fibrosis Foundation developed the PFF Care Center Network consisting of medical centers nationwide that provide care and support for those with PF and their caregivers.
    Your core Care Center team includes a pulmonologist, respiratory therapist, nurse, radiologist and others, who have extensive expertise treating adults with fibrotic lung disease. They meet to develop and discuss your diagnosis and individualized care plan. This may involve bringing in specialists, such as genetic counselors and lung transplant teams, to help you and your loved ones along your journey.
    The mission of the Pulmonary Fibrosis Foundation is to accelerate the development of new treatments and ultimately a cure for pulmonary fibrosis. Until this goal is achieved, the PFF is committed to advancing improved care of patients with PF and providing unequaled support and education resources for patients, caregivers, family members, and health care providers. 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.
    © 2022 Pulmonary Fibrosis Foundation
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