Marijuana has been associated with reducing seizures in people with epilepsy for years, but only now is the topic getting more of the scientific scrutiny it deserves. In a recent study, cannabidiol (CBD) reduced the number of seizures by half in a substantial number of children and adults with Lennox-Gastaut syndrome (LGS), a severe form of epilepsy.
GW Pharmaceuticals, a developer of cannabidiol, sponsored the study.
On September 26, a marijuana-based childhood epilepsy drug took a step closer to winning approval when its maker announced promising phase 3 clinical trial results. [1]
Justin Gover, CEO of the British biotech company GW Pharmaceuticals, said that the children participating in the trial had previously tried 10 other anti-epileptic drugs. Despite using the medication, the young participants still experienced 3 seizures a day, approximately 90 a month. Said Gover:
Researchers are continuously finding that an oil derived from the cannabis plant is actually incredibly effective in treating and controlling a rare form of epilepsy. Since an estimated 30,000 Americans live with the particular form of this disease, this relatively recent discovery brings new hope to tens of thousands of people in helping them to regain control of their lives.
What would you do if your child had a serious form of epilepsy that was resistant to treatment by conventional methods? If a form of liquid cannabis was available that had proven results for reducing your child’s debilitating and painful seizures by 53%, wouldn’t you obtain that medicine by whatever means possible? Here’s the only problem – it still isn’t legal in many states.
