Published on: 11/4/16
Collective evolution covered the remarkable story of the Lambert family from Australia recently. The family had to make a very profound and life-changing decision on cannabinoid oil for seizures a few years back when their baby Katelyn, then only six months old, was diagnosed with the rare genetic disorder Dravet Syndrome.
Some Dravet Syndrome sufferers can experience up to a thousand fits a day. These seizures can last hours at a time and cause severe damage to the brain. To see a little baby suffer like this is unthinkable to most people, and as Joy Lambert, granny of Katelyn says, who do you love even more than your own children? Only your grandchildren…
This must have been an unbearable situation. Katelyn was on every imaginable kind of medication doctors could put her on to try and stop the seizures, but nothing helped. These medications not only didn’t improve Katelyn’s situation, but also had some severe side effects.
No easy decision
The Lambert family had to decide what to do next after an exceptionally traumatic seizure, which lasted two hours, that ended in Katelyn having to be rushed to a specialist hospital in a helicopter. This was when the family decided to consider alternative treatments, and Michael, Katelyn’s dad, discovered the documentary made by CNN on Charlotte Figi, a Dravet child whose seizures ended after using cannabinoid oil for seizures.
The cannabis that was given to Charlotte was not psychoactive. It has been called Charlotte’s Web, but it might as well have been called “hippie’s disappointment” because it has no narcotic value and won’t get anyone stoned. It improved Charlotte’s condition radically, and today she is a happy little girl who lives a normal life.
But despite its lack of psychoactive effects, the cannabinoid oil is technically illegal in Australia. Would you be prepared to break the law to save your child’s life? This was the question the Lambert family had to ask themselves.
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Taking the plungeThey decided to give it a try, and ordered cannabinoid oil for seizures from Endoca. The effect was immediate. Katelyn has not had a single seizure in a year, and her granny considers it a miracle for a Dravet Syndrome sufferer.
Joy says she can see such a difference in Katelyn, she is alert and goes to preschool, she is happy, and they don’t have to worry whether she will have a seizure during the day. The Lambert family is over the moon, and extremely grateful they made the decision that saved Katelyn’s life.
Grandpa Barry Lambert donated $33.7 million to cannabis research so that other children can also be helped. The Lambert Initiative at Sydney University will explore the potential of cannabinoids as a treatment in a wide spectrum of disease, not just for epilepsy.
Positive effects of researchHe is positive that very soon cannabis will be used for many ailments, and he hopes their unprecedented donation could be a real game changer in the world of medicinal cannabis research. Luckily laws are starting to change, and medicinal cannabis use is allowed in more places for specific medical conditions.
Barry Lambert says, “I think there’s a lot riding on this Sydney University research, and hopefully the scientists will prove what we believe to be true beyond doubt. I think the cannabis plant will be proven to be the wonder plant of this century. I know it’s been around for previous centuries, but I think scientists will discover what a wonderful plant it is and it will be of great benefit to mankind.”
Cannabinoid oil for seizures could save livesMany believe that cannabinoid oil for seizures has saved lives, and will continue to do so, with people like Barry Lambert and his family helping to bring about change and a greater understanding of this miracle plant.
Disclaimer: Views expressed here do not necessarily reflect those of Endoca and its staff. This article is not intended to provide medical advice, diagnosis, treatment or cure. Endoca CBD products have not been approved by the US Food and Drug Administration (FDA).