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  "documentTitle": "Inspire Medical Systems, Inc. (INSP)",
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  "authorName": "Wolfpack Research",
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  "presentationDate": "2020-04-22 00:00:00",
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      "text": "Our research shows that Inspire’s management exaggerates its TAM by at least 50x in order to sell investors a growth story they must know is fictional.",
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      "text": "We also found a growing list of customer complaints, with terrifying descriptions of the potential downsides to Inspire's invasive procedure, such as “drooling, facial paralysis or drooping, slurred speech”.",
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      "text": "Two of the Inspire patients we spoke to allowed us to share their stories. We will refer to them as “Patient A” and “Patient B.”",
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      "text": "Inspire's real-world FDA submitted adverse event reports include horror stories of surgeons lacerating the patient’s jugular during surgery and patients nearly dying on the operating table.",
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      "text": "Inspire's own studies show that the unhappy patients we spoke to were not outliers. During Inspire's self-funded Stimulation Therapy for Apnea Reduction (“STAR”) study, the key to its FDA approval, 85% (107 out of 126) of patients suffered at least one adverse event.",
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      "text": "We reached out to several Inspire patients who had written about their experience online and spoke to four who were willing to share their story with us in detail.",
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      "text": "Patient B was nearly 80 years old when she had Inspire's device implanted. She complains that the constant electrical shocks feel like someone is “tugging and twisting” her tongue.",
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      "text": "“vehemently denied it could have happened.” — Inspire (regarding Patient A's claim); “tugging and twisting” — Patient B (describing tongue sensation); “ruined her life.” — Patient B (describing the device)",
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