A recent study by the American Epilepsy Society shows that the cannabis component CBD is a safe and viable treatment for treatment resistant epilepsy.
Despite numerous states legislating for medical marijuana, the DEA refuses to remove cannabis from the Schedule 1 drug list, claiming it has no therapeutic value. This Schedule 1 classification means that scientists in the US struggle to study the possible clinical applications of the plant. And yet … in the areas where medical marijuana is allowed, one curative application stands out as being majorly successful and life changing. Children suffering from severe epileptic conditions such as Dravet’s Syndrome faced a life-expectancy of less than ten years, with the effects of multiple fits exponentially disabling them. Standard medical treatments did little to alleviate these conditions: but the discovery of “Charlotte’s Web” strain in Colorado, a high CBD, low THC cannabis strain made into an medical cannabis oil, did. Hundreds of parents flocked to areas like Colorado, and their stories reveal a hugely high success rate, with fits almost completely stopped.
Imagine the pain of being a parent to a child suffering such extreme torture, and knowing that there exists a successful treatment but your government agency refuses to acknowledge the weight of proof provided by anecodotal evidence – and at the same time, prevents science from researching this treament.
Read a mother’s story: Dravet’s Syndrome and high CBD here
That’s why this study by the American Epilepsy Society is so important. Conducted by a reputable agency concerned with promoting research and education for professionals working with epilepsy, its not shared social media of emotive memes but an impartial investigation of whether, and how, cannabidiol works.
But wait – I thought you said scientists found it difficult to study medical marijuana in the USA thanks to the DEA’s Schedule 1 classification of cannabis?
That;s still true. The reason why researchers were able to analyse the role of CBD in allieviating epilepsy is because they weren’t using cannabis itself. Instead they investigated the potential of EPIDIOLEX, a “proprietary oral solution of pure plant-derived cannabidiol, or CBD” produced by GW Pharmaceuticals. In other words: its OK to use cannabis if it comes from a drug company.
We have to ask ourselves: how long can governments deny that medical marijuana works in the face of increasing evidence? And if drug companies produce medications that we can grow and make ourselves (at much lower costs) how long can it be illegal?
taken from the American Epilepsy Society Please sign: this petition on Change – a mother from Northern Ireland is joyful to have used cannabis to treat her son – but now finds herself a cannabis refugee, unable to return home for fear of prosecution: The post American Epilepsy Society Study shows CBD can be best treatment for epilepsy appeared first on Growers Guide to Cannabis.EFFICACY AND SAFETY OF EPIDIOLEX (CANNABIDIOL) IN CHILDREN AND YOUNG ADULTS WITH TREATMENT-RESISTANT EPILEPSY: