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Seven months and 1,600 miles after their journey began, Ana has finally given Preston his first dose of marijuana.
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The state health department, which manages the patient registry that all children using medical marijuana must join, offers almost no guidance.
The shaking calmed.
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At the North Carolina Children’s Hospital in Chapel Hill in May, Dr. Robert Greenwood hustled into the meeting room wearing a tie covered with Dr. Seuss characters.
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The hospital didn’t see any improvement in the before-and-after EEGs of four kids whose seizures appeared to lessen significantly. That may have been due to something called “electroclinical dissociation,” where the seizure still occurs but its outward indicators disappear. It also might be that parents can pick up on smaller improvements than an EEG can, said Dr. Kevin Chapman, a pediatric neurologist at Children’s who was a co-author on the study.
“Stop arguing with me!” Ana finally says. “Damn.”
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Ana Watson has decided to try adding THC
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Preston’s grandmother, Milly, thought he had the munchies.
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July 11 Sydney Watson, 8, tries to get older brother, Preston, to drink some sweet tea. Sydney was Preston’s little nurse when they were younger, helping her mother care for him. Preston hasn’t been eating very well or taking medications without a fight lately, and Ana asked Sydney to help.
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