Life with Pulmonary Fibrosis | Portraits of PF - Valeria Hatcher
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- čas přidán 26. 04. 2020
- 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. While managing and advocating for her health, Valeria also attends several support groups which she refers to as lifesavers. She acknowledges the physical and mental challenges of PF and encourages others to reach out to the Pulmonary Fibrosis Foundation for information and support.
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.
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© 2020 Pulmonary Fibrosis Foundation
