Charlotte cannabis
Charlotte Figi, the year-old girl with epilepsy who helped ignite a medical-cannabis movement, has died from complications suspected to be coronavirus-related, according to a Tuesday Facebook announcement. On her Facebook page, Charlotte's mother, Paige, wrote that despite a previous negative coronavirus test, her daughter was "treated as a likely COVID case. Charlotte, her parents, and the Stanley brothers, who own a Colorado Springs medical-marijuana dispensary, worked together to create a cannabis strain that contained a high concentration of CBD, a nonpsychoactive compound found in cannabis, and a low concentration of the psychoactive component THC. Charlotte successfully used this strain, dubbed Charlotte's Web, to treat her seizures, and soon other people with chronic conditions got wind of her story and sought CBD treatments themselves. She rose every day, awakening others with her courage, and with that smile that infected your spirit at the cellular level.
Charlotte Figi, Poster Child for Medicinal Benefits of CBD, Dead at 13
By creating an account, you agree to the Terms of Service and acknowledge our Privacy Policy. Falling well underneath the. The life-changing benefits reported by those who rely on Charlotte's Web and the CBD oil it produces to manage seizures, anxiety and other symptoms have changed hearts and minds in the medical and legal fields, leading the way for greater access while playing a surprising role in the widespread acceptance of cannabis-derived medicine.
The strain's namesake, Charlotte Figi, became the poster child for the medicinal CBD movement, and a symbol of hope to thousands. Charlotte Figi, who was born with a rare form of epilepsy, helped inspire the CBD movement.
She died on Tuesday. In a tribute, drsanjaygupta says she changed his outlook on medical marijuana. While CBD products are commonplace today, public awareness around the non-intoxicating cannabinoid was low in when Charlotte had her first seizure at three months old. Her home state, Colorado, had begun their medical patient registry just six years earlier; less than ten states had legalized the sale of cannabis to qualified patients nationwide.
A frantic hospital visit led to few answers; blood tests, magnetic resonance imaging and recording of her brain wave patterns revealed nothing out of the ordinary. Over the next year, her seizures returned, lasting hours at a time and leading to frequent hospital stays and prescriptions to seven different drugs, including habit-forming barbiturates and benzodiazepines.
Despite the medication, the seizures always returned — and now, Charlotte was suffering status epilepticus , a condition where seizures last more than 30 minutes or come in clusters, with no time for her to recover between each electrical disturbance in her tiny body.
Seizures of this length carry a high risk for injury and death to neurons and neuronal networks, which can lead to developmental disability, permanent brain damage, and death. At two and a half, doctors confirmed, via tests for a particular gene mutation, that Charlotte was living with a rare, drug-resistant form of epilepsy known as Dravet Syndrome.
Her parents tried everything to manage the seizures, looking into experimental drugs and putting her on a ketogenic diet recommended by a specialist. When she was five, they decided to try medical marijuana. Getting two doctors to approve the youngest medical marijuana patient in the state was only the beginning of the challenge; they also had to find an appropriate product for such a small child. Meeting the Stanley brothers , the group behind a family-owned grow operation, changed the future forever: not just for one little girl, but for the brothers' business and the cannabis movement as a whole.
During her first years of treatment with cannabis oil, Charlotte went from having grand mal or generalized tonic-clonic seizures a week to only two to three a month, usually in her sleep.
She regained the ability to walk and feed herself. Frequent hospitalizations turned into days at school, horseback rides and games with her siblings.
Inspired by her progress, the brothers named the strain Charlotte's Web. After fifteen thousand families reached out in the next month, they decided to pivot their business away from medical marijuana and toward the production of low-THC industrial hemp. The company's fields in Colorado, Kentucky, and Oregon are subject to rigorous soil and water tests to ensure they're free from microbes, bacteria, and toxins before the first seed is planted. Farmers tend , plants by hand, testing phytocannabinoid levels every five days to ensure the plants are harvested at their peak.
While the company isn't allowed to make any medical claims, testimonials flood in from families dealing with conditions that lead to seizures including autism, chromosomal disorders and genetic conditions like tuberous sclerosis complex.
Studies have shown that cannabidiol, whether in the form of hemp oil or US Food and Drug Administration FDA -approved prescription treatment Epidiolex, can significantly reduce seizures resulting from treatment-resistant Lennox-Gastaut syndrome and Dravet syndrome by regulating neuronal hyperexcitability.
Evidence suggests that CBD activates and desensitizes ion channels known as capsaicin and vanilloid receptors. In healthy humans, these proteins detect temperature, respond to stimuli like spicy food, and transmit and modulate pain; in epilepsy, neuropathy and chronic pain patients, the receptors are overly sensitive, their response amplified.
For parents, like Charlotte's mother Paige Figi, accessing essential treatments for their children wasn't easy. She'd been lucky enough to live in a state with medical marijuana, but each day she heard from families who didn't have the same options. The Stanley Brothers established a non-profit foundation, Realm of Caring, to help such families access cannabis treatment.
Paige Figi's non-profit organization Coalition for Access Now worked with bipartisan representatives to introduce a federal bill, the Charlotte's Web Medical Access Act of , to remove CBD-rich plants from the legal definition of marijuana, thereby exempting it from classification as a Schedule 1 substance under the Controlled Substances Act CSA.
The group has also lent support in state legalization battles, sharing the story of not just Charlotte but many children like her to show skeptical minds the life-and-death urgency behind opening access to alternative treatments. In , patient advocacy groups found an unexpected success with a Farm Bill that reclassified hemp legally defined as cannabis sativa plants containing less than.
Department of Agriculture. Charlotte's Web Holdings, Inc. The fight is far from over; the sale of industrial-hemp derived CBD still faces federal legal challenges from the U. Food and Drug Administration which has not approved it as a medical treatment, dietary supplement or food additive as well as shifting regulation and enforcement in each state. Benzinga does not provide investment advice. All rights reserved. Email Address:. Leave blank:. Forgot your password? Contribute Login Join.
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Charlotte's Web CBD (cannabidiol) oils contain plant-based cannabinoids and other beneficial phytocompounds for a full spectrum of plant-powered goodness. Shop CBD. Charlotte's Web™ CBD products are rich in proprietary Charlotte's Web™ genetics containing an array of beneficial cannabinoids such as CBD .
The Colorado Sun — johningold coloradosun. Charlotte Figi, the Colorado Springs girl who, as a gleeful and fragile child, launched a movement that led to sweeping changes in marijuana laws across the globe, has died from complications possibly related to the new coronavirus. She is seizure-free forever. Paige Figi had posted in recent weeks on Facebook about a serious illness that sickened all the members of her family with fever, coughing and breathing difficulties and sent Charlotte to the hospital. The test result came back negative — though the coronavirus test has been beset with false negatives.
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By creating an account, you agree to the Terms of Service and acknowledge our Privacy Policy. Falling well underneath the. The life-changing benefits reported by those who rely on Charlotte's Web and the CBD oil it produces to manage seizures, anxiety and other symptoms have changed hearts and minds in the medical and legal fields, leading the way for greater access while playing a surprising role in the widespread acceptance of cannabis-derived medicine.
Girl who inspired Charlotte's Web marijuana oil dies after unspecified "virus" hits family
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Charlotte's Web CBD Empowered The Medical Marijuana Movement: Here's How
Don't have an account yet? Get the most out of your experience with a personalized all-access pass to everything local on events, music, restaurants, news and more. Charlotte Figi, the namesake of the Charlotte's Web CBD strain and the face of a nationwide movement toward medical marijuana acceptance and CBD use, has passed away at the age of thirteen, according to a post on the Facebook page of Charlotte's mother, Paige Figi. She is seizure-free forever. Thank you so much for all of your love. Please respect their privacy at this time," a friend of the Figis wrote on that page shortly after 9 p. April 7. Charlotte's passing was confirmed by the Realm of Caring Foundation , a medical marijuana advocacy group co-founded by Paige Figi.
She was Thank you so much for all of your love.
Charlotte Figi, the young Colorado girl who became a symbol of the medical benefits of CBD, which was used to treat her seizures, has died. Charlotte Figi — the young girl who became a leading symbol for the medical benefits of cannabis and CBD after it helped treat her rare form of epilepsy — died Wednesday. She was
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It does not induce the psychoactive " high " typically associated with recreational marijuana strains that are high in THC. Charlotte's Web is named after Charlotte Figi whose story had led to her being described as "the girl who is changing medical marijuana laws across America. Media coverage increased demand for Charlotte's Web and similar products high in CBD, which has been used to treat epilepsy in toddlers and children. It was originally called "Hippie's Disappointment" as it was a strain that had high CBD and could not induce a "high". While initially anecdotal reports sparked interest in treatment with cannabinoids , [9] there was not enough evidence to draw conclusions with certainty about their safety or efficacy. In , there was little evidence about the safety or efficacy of cannabinoids in the treatment of epilepsy. The Cochrane review suggests cannabinoids be reserved for people with symptoms that are not controllable by other means, who have been evaluated by EEG-video monitoring to confirm diagnosis, and are not eligible for better-established treatments such as surgery and neurostimulation. Three out of four trials reported some reduction in seizures, but no comparison with placebo was possible due to the small number of people in the trials. The drugs were well tolerated. Due to the anecdotal nature of the health claims being made medical bodies have published statements of concern. The recent anecdotal reports of positive effects of the marijuana derivative cannabidiol for some individuals with treatment-resistant epilepsy give reason for hope.
Charlotte's Web
Charlotte Figi, whose life-long battle with a rare seizure disorder led to medical marijuana reform , died Tuesday after members of her family contracted an unspecified "virus," according to a post on her mother's Facebook page. Figi was 13 years old. She is seizure-free forever. Thank you so much for all of your love," the post said. Realm of Caring, a non-profit that funds and conducts cannabis research co-founded by Charlotte's mother, Paige Figi, also shared news of her death.
