Charlotte Figi Bio
Charlotte Figi is the young girl whose battle with Dravet syndrome inspired changes to medical marijuana laws, died of complications from the coronavirus, according to a nonprofit organization co-founded by her mother. She died when she was 13 years old.
Charlotte Figi Age
Figi died when she was thirteen years old. She had not disclosed her exact date of birth and it is also not known when she used to celebrate her birth. However, this information is still under review and will be updated as soon as it is available.
Charlotte Figi Height and Weight
Figi appeared to be quite short in stature if her photos, relative to her surroundings, are anything to go by. However, details regarding her actual height and other body measurements are currently not publicly available. We are keeping tabs and will update this information once it is out.
Charlotte Figi Education
Details concerning her journey of education are unknown. This information will be updated as soon as it is available.
Charlotte Figi Family
Figi is the daughter of Paige Figi. After doing our research, details about her parents are not available and it is also not known if she has any siblings. However, this information is still under review and will be updated as soon as it is available.
Charlotte Figi Facts and Body Measurements
Here are some interesting facts you don’t want to miss about Figi:
- Full Name: Charlotte Figi
- Age/ How Old?: 13 years
- Date of Birth: Not Available
- Place of Birth: Not Available
- Education: Not Available
- Birthday: Not Available
- Nationality: American
- Father’s Name: Not Available
- Mother’s Name: Paige Figi
- Siblings: Not Available
- Height/ How tall?: Not Available
- Weight: Not Available
Charlotte Figi CBD
Figi’s mother, Paige Figi, began calling medical marijuana shops in Colorado. This was after doctors had exhausted all other options. Surprisingly her symptoms largely disappeared after she began taking oil infused with a strain of cannabis low in THC. The plant’s psychoactive ingredient, but high in the compound cannabidiol, or CBD. The oil’s name, inspired by her story, was changed to Charlotte’s Web.
Charlotte’s success led other families with children suffering from seizures to move to Colorado, where marijuana was legalized much earlier than other states.
Charlotte Figi Health Problems and Death
Figi had her first attack when she was three months old. When she was three years old, Charlotte had up to 300 Grand Mal attacks each week, this was too sad to the parents. She was diagnosed with Dravet syndrome and began to lose her ability to walk and speak. Her parents looked for medication all over that didn’t seem to help. Her mother found a cannabis dispensary in Denver that had a cannabis extract. It was said to be low in THC but high in CBD. She gave Charlotte a small dose., after paying $ 800 for two ounces of oil,
“When she didn’t have those three, four seizures that first hour, that was the first sign,” Paige later told CNN. “And I thought well, ‘Let’s go another hour, this has got to be a fluke.’
But the seizures stopped for a week and then dropped to just two or three a month, and Charlotte was allowed to discontinue her other seizure medications. The Figi family began working with the Stanley brothers, six Colorado-based brothers who grew cannabis and were working on a strain high in CBD and low in THC. Extracts from those cultures were used to treat Charlotte and other seizure patients. The Stanley brothers called the Charlotte’s Web strain to honor the girl who inspired it. The Stanley brothers also established a nonprofit organization, the Realm of Caring Foundation, which donates cannabis to adults and children suffering from a variety of diseases and ailments.
Realm of Caring, the nonprofit that focuses on medical cannabis research and education, attributed Figi’s death to “COVID-19 complications” in a Facebook post. A message posted to the Facebook page of Charlotte’s mother, Paige Figi, on behalf of the Figi family says, “Charlotte is no longer suffering. She is seizure-free forever.”
Neither El Paso County nor state health officials have publicly announced the death of a 13-year-old Coloradan due to COVID-19; Charlotte would be the youngest person to date to die in Colorado in connection with the coronavirus.
Charlotte was one of Colorado’s many medical marijuana refugees, whose family moved to the state following the legalization of cannabis. From the time she was an infant, she suffered from frequent and severe seizures because of Dravet syndrome, including many that required hospitalization. But at age 5, Paige Figi gave her cannabidiol, the non-psychoactive compound in cannabis known more commonly as CBD, and Charlotte’s condition changed overnight.
“Charlotte slept soundly for the first time in years. She went seven days without a seizure. Over time, the seizures dropped from thousands a month to just a few. After not speaking for six months, she started talking again,”
Frequently Asked Questions About Charlotte Figi
Who is Charlotte Figi?
Charlotte Figi is the young girl whose battle with Dravet syndrome inspired changes to medical marijuana laws, died of complications from the coronavirus, according to a nonprofit organization co-founded by her mother. She died when she was 13 years old.
How old is Charlotte Figi?
Figi died when she was thirteen years old. She had not disclosed her exact date of birth and it is also not known when she used to celebrate her birth. However, this information is still under review and will be updated as soon as it is available.
How tall was Charlotte Figi?
Figi appeared to be quite short in stature if her photos, relative to her surroundings, are anything to go by. However, details regarding her actual height and other body measurements are currently not publicly available. We are keeping tabs and will update this information once it is out.
Which school did Charlotte Figi attend?
Details concerning her journey of education are unknown. This information will be updated as soon as it is available.
Is Charlotte Figi dead or alive?
Figi is dead.
“Charlotte slept soundly for the first time in years. She went seven days without a seizure. Over time, the seizures dropped from thousands a month to just a few. After not speaking for six months, she started talking again,”