Dr. David Lederer explains that each patient’s journey with PF is unique. When thinking about the future, your doctor may be able to give you an idea of what the progression of your disease might look like. In the early stages of the disease, people often have no symptoms. Learn about progression episodes and how your doctor will monitor disease progression.
The Pulmonary Fibrosis Foundation (PFF) offers essential programs and resources for people with pulmonary fibrosis. The mission of the PFF is to mobilize people and resources to provide access to high quality care and to lead research for a cure so that people with PF will lead longer, healthier lives.
For more information, visit pulmonaryfibrosis.org.
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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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© 2018 Pulmonary Fibrosis Foundation
29 май 2018
