August 26, 2026
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Max was a husband and a father with a big life: adventure, travel, laughter. At 18 he was prescribed Xanax for occasional anxiety, and for about a decade he used it at low, regular doses, mostly for sleep, prescribed by the same doctor the entire time. Around 2015 his body began to break down in ways no one could explain. Crushing stomach pain. Electrical sensations in his brain. Every test came back normal. Every doctor shrugged.
What Max had, and what he eventually diagnosed himself with after years of searching, was benzodiazepine-induced neurological dysfunction, a nervous system injury that can persist long after the medication stops. In this interview his wife Kelsi walks me through everything: the switch to Klonopin that made him worse, the four-week taper that should have taken years and sent his body into shock, the re-exposures and the Flagyl reaction that stacked injury on injury, the facilities that were not equipped for him, and the five years she spent keeping him alive with a faith and steadiness that left me in awe. Max died in April 2020. His letter, which Kelsi reads here, makes one thing absolutely clear: this was not a man who stopped loving his family. This was a man enduring neurological torture that nobody in his medical system could recognize, for four years, until he found the name for it himself on a patient forum.
That is why this story matters. Max's death was preventable. Not by willpower, and not by more medications, but by clinicians who recognize this injury, taper slowly, and take patients seriously when they say the drugs are hurting them.
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