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    Preston hides from his mom
    Seven months and 1,600 miles after their journey began, Ana has finally given Preston his first dose of marijuana.
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    “Time to get up, Boo-Boo,” Ana said to him. “Come on.”
    Ana doesn’t remember what Preston’s first word was. What she does remember is that first word arrived right on time. As did his first crawls. And his first steps.
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    “Colorado represents hope at this point,” she said. “This is the state of hope.”
    The doctor continues down the list of anti-epilepsy medications, collecting the medical history of Ana’s 12-year-old son, Preston, whose seizures cause such unrelenting brain damage that he functions at the level of a 2-year-old. The doctor ticks through 13 different medicines, but Preston has already tried each one, to little effect.
    Ana eventually calls a friend, who suggests giving the medicine in emptied pill capsules delivered as a suppository. She grimaces. But she has already been at it for an hour. The odds that seizures will kill Preston increase every year; the damage in his brain may soon be permanent. She is compelled to try.
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    Poceta says in extreme cases, it may be reasonable for patients to consider trying CBD after consulting their doctor.
    “It smells like marijuana,” she laughed. “I didn’t think it would.”
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    “Open up,” Ana coos.
    So now Ana is sitting in the hospital whose doctors have been the most outspoken in Colorado in urging parents not to use marijuana to control seizures — it’s too risky, they say; there are too many unknowns — and she is hoping for advice on what to do.
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    “Silly mommy,” he says to Ana, as she snuggles into a single hospital bed with him.
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