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CBD oil legislation passed South Carolina's House (92-5) and Senate (unanimous), and became law on May 28, 2014 when Gov. Nikki Haley did not veto the bill, making South Carolina the seventh state to legalize CBD oil. Th bill requires a clinical trial to be established at the University of South Carolina.
October 8 Andrew Tobey waits for Cody Morehead to catch up as they hang the drying poles during the Realm of Caring hemp harvest in eastern Colorado.
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July 9 Preston, his mother, Ana Watson, sister Sydney Watson and grower Jason Cranford take a first look at the plants, named “Haleigh’s Hope,” that will provide the oil for an attempt to control Preston’s seizures. “This is the plant that is going to help Preston,” Ana said.
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Preston resists his mother
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ViPova, owned by Lexaria, has created a CBD oil tea product that ranges in price from $20-$107. ViPova is a US based company that is utilizing lipid technology to make CBD more bioavailable. This happens because the endocannabinoid system is lipid based which could mean that your dollar goes further because you need less CBD to have the same effects as an oil based CBD products.The Medics is a Colorado based CBD oil company that has created two types of tincture products that range in price from $40-$196. The first and less expensive line, called “High Grade”, is made from European hemp. The second line, known as “Premium”, is made from 100% USA Colorado grown hemp and cost a bit more. This difference in price is probably due to the sheer cost of growing their own hemp.
“The big thing that parents are always saying,” Ana said, “is they want their child to say, ‘I love you.’?”
July 9 Ana Watson finally is able to get CBD oil for Preston. The journey hasn’t been without frustration. She has had to fill out many forms and file a change-of-patient record for the medical marijuana registry. She now is overwhelmed with worries: how much to buy and when; how strong it will be; how much to give Preston; whether to add THC.
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To Ana, it sometimes seemed as if what epilepsy didn’t take from her son, the drugs would. But she also knew that just one year of uncontrolled seizures meant a 1 percent chance of dying. The longer Preston’s seizures ran riot, the likelier epilepsy would kill him.
Ana Watson and nurse Chelle Bennett carry Preston
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May 8 The dregs of his afternoon seizure medications are still on his lips as Preston rests on his porch after a long day of school interrupted by numerous myoclonic seizures.
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It wasn’t until Preston was 6 years old that doctors finally put a name to his con***ion: Dravet syndrome. And in some ways, that was worse than not knowing at all because it meant there was no cure to find.
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