A place for facts and information about Chronic Thromboembolic Pulmonary Hypertension (CTEPH)
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The information provided on this site is intended for people living with CTEPH or those caring for someone with CTEPH
This site is intended for a US audience
Hear personal stories and real-life experiences of people living with chronic thromboembolic pulmonary hypertension (CTEPH).
People who've been treated for pulmonary embolism (PE) and still have symptoms after 3 months could have CTEPH.
Whether you're undergoing diagnostic tests or preparing for surgery, everyone's CTEPH journey can be different.
From diagnosis to recovery, pulmonary thromboendarterectomy (PTE) surgery for CTEPH involves a series of important steps and decisions.
Greg's shortness of breath eventually led to his diagnosis of CTEPH.
Harry's CTEPH was found after proper screening, starting with a ventilation/perfusion (V/Q) scan.
Arlene's symptoms were attributed to asthma, delaying CTEPH treatment.
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Site last modified 03/2021
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