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After years of watching a cruel, incurable genetic disorder called Dravet Syndome rob their daughter of her basic bodily functions and send her into convulsions that caused head injuries and broken teeth, they had reached the end.
"We really thought, this is a horrible existence; she's not going to live much longer." Paige says. "This is not a life for her. This is torture. She is suffering all day. I'm not OK with this. She wasn't even human anymore. She'd lie in my arms drooling, seizing, screaming and crying."
Then, in an act of desperation, or inspiration - or maybe both - Matt called Paige from overseas, where he was working, and suggested a radical approach to Charlotte's treatment.
"We need to try cannabis for Charlotte," he told Paige. "We live in a compassionate state."
Fifteen months later, the little girl with the DNR order is standing in the kitchen of their Black Forest home with her mother getting her Pull-Ups changed, cuddling in the arms of a visitor, playing with toys and strategically pushing the buttons on her "talker," an electronic device that communicates when Charlotte can't.
Her seizures have dropped from 1,200 a month to three, and the ones she has are shorter in duration and less severe. She's off all the other medications with their troubling side effects. And, as one of the youngest medical marijuana patients in Colorado, her dramatic turnaround is starting to draw national attention, with a CNN report on the horizon.
Because they haven't figured out a way to tax it yet.
They will. Oh, they will.
Same with ecigs.
Our government couldn't care less if something is good or bad. All they care about is if it's taxable.
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