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Ten-year-old Aurora Husk right reacts after taking a dose of hemp oil administered by her mother Megan Vaughan outside the Bristol Cannabis Oil Cures Cancer Child Elementary School on Friday October 2 2015. Husk who has intractable epilepsy is not allowed to consume the oil on school property. Her mother comes to the school twice a day to give her two of her three daily doses.
Supporters of the hemp oil law say the slow start could be caused by a lack of familiarity with the program. The oil hasn’t yet been sold in Missouri and won’t be available until this fall. But some of the blame for the slow start has fallen on the medical community. One of the sponsors of Missouri’s law singled out BJC HealthCare the St. Louis region’s largest medical system for having reservations about the hemp oil treatment.
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Vaughan drives to the school to pull Aurora out of class and walk her cbd oil kansas city around the block where she administers the dosages. The oil has to be administered two hours before or after Aurora takes her seizure medication so the time that Aurora gets her hemp dosages is important Vaughan said. The process takes about 15 minutes Vaughan said which amounts to nearly half a class. Some days Vaughan can’t make it to the school on time or even at all due to work commitments. Vaughan’s mother helps out or Aurora has to miss a dose. Karen Richards executive director of the Vermont Human Rights Commission said a student’s need for hemp oil could fall under the public accommodations act assuming the student has a disability. The commission makes recommendatios as to whether they believe discrimination occurred in a particular case.
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The commission makes recommendations as to whether they believe discrimination occurred in a particular case. The department has yet to investigate the hemp oil issue but Richards said she has heard of the problems parents are facing. The real issue is the difference between federal and state law regarding hemp and medical marijuana she said pointing to the memo from the attorney general’s office.
And though he applauded SSM for supporting the program he said patients should be able to get authorization from their own neurologist and not have to doctor-shop to access the oil. What I didn’t want to have happen is this niche market? he said. But the niche market may be the only hope now for Lucas and other Missouri children.