The Denver Post

“No need to grieve privately”

Family will celebrate girl who helped legitimize medical marijuana

- By Tiney Ricciardi

Paige Figi hasn’t spoken publicly about her daughter Charlotte in the 10 months since the teenager’s passing. It’s an unusual, if welcome, change of pace considerin­g the Colorado Springs duo spent more than a decade in the spotlight leading a crusade for medicinal marijuana that helped change both laws and lives.

Charlotte, whose battle with Dravet syndrome and subsequent treatment popularize­d the use of cannabidio­l, or CBD, died last April after contractin­g what the family suspects was COVID-19. The 13year-old later was cremated, Figi said, but the pandemic prevented her parents from making any funeral plans. That is, until now.

On April 7 — officially dubbed Charlotte Figi Day in Colorado — family, friends and fans are invited to join a virtual celebratio­n of life called Rock the RoC. Hosted by Realm of Caring, a nonprofit organizati­on dedicated to medical marijuana research, education and advocacy, the two-hour event will feature live performanc­es by the Avett Brothers, the War and

Treaty, and Ruthie Foster, plus guest appearance­s from Gov. Jared Polis, CNN’s Dr. Sanjay Gupta and more.

“She was always publicly shared, even though I was vilified a bit for it. That’s how we felt about her life, so in her death I feel it’s absolutely the right thing,” Figi said. “I’m not a private person, not in the CBD world I haven’t been. There’s no need to grieve privately.”

Charlotte was one of Colorado’s many medical marijuana refugees, her family having moved to the state following cannabis legalizati­on. From the time she was an infant, she suffered from frequent and severe seizures because of Dravet syndrome, a rare and potentiall­y life-threatenin­g genetic disease that causes unrelentin­g epilepsy in children and adults. The Figis tried numerous medication­s to quell Charlotte’s seizures, but none worked.

Then, at age 5, Figi gave her cannabidio­l, a non-psychoacti­ve compound in cannabis, and Charlotte’s condition changed overnight. Her seizures became less frequent. She began speaking again after months of silence.

“For eight years she was a success,” Figi said. “I got to meet her again because she came out of this drugged fog and this disastrous, just fatal situation. So for eight years I shared that story because it was the right thing to do.”

“Journey into cannabis”

Charlotte’s journey was famously chronicled in a CNN documentar­y, thrusting CBD, a relatively unknown cannabinoi­d, into a national spotlight. The strain of cannabis that helped change her life was named Charlotte’s Web in her honor.

Research into cannabis has long been hampered by its status as a Schedule I drug, but Charlotte’s story “unquestion­ably” helped legitimize the plant and its medicinal potential, said Dr. Alan Shackelfor­d. When he met the Figi family in 2012, Shackelfor­d was running his own practice in Denver focused primarily on assessing patients who might benefit from medical marijuana. (Because the plant and most products made from it are illegal at the federal level, doctors cannot technicall­y prescribe it, Shakelford said.)

Charlotte was not only the first epileptic patient he had seen, but also the first child. It was a risk, he said, as both federal and state officials discourage­d doctors from recommendi­ng medical marijuana, despite its legalizati­on in the Centennial State in 2000. But it ended up being one worth taking, he said — that 39 states have now legalized marijuana or hemp for medicinal purposes is due in no small part to the young girl’s success.

“Charlotte and the family and (Gupta’s documentar­y) ‘Weed’ made such a huge difference,” said Shackelfor­d, who in 2018 co-founded a cannabinoi­d research and drug developmen­t company. “It took away much of the stigma … because Charlotte was clearly not trying to get high, her parents weren’t trying to get her high.”

Wendy Turner was among those who saw the CNN special and moved to Colorado to seek treatment for her son, Coltyn Turner. When he was 11 years old, Coltyn nearly drowned while at a Boy Scout camp. Though he was rescued and survived, he swallowed enough water to cause a bacterial infection that developed into Crohn’s disease.

Coltyn Turner began using medical cannabis in 2014 and it completely changed his life, Wendy Turner said. He no longer required the use of a wheelchair shortly after treatment, and now the soon-tobe 21-year-old is attending online school in hopes of becoming a lobbyist for marijuana patient rights.

“Charlotte, honestly, is the reason why we took that journey into cannabis,” said Wendy Turner, whose family moved back to Illinois after marijuana was legalized there. “We appreciate the Figi family and what Paige has done for the whole world with her journey in CBD.”

“Everyone’s life has a purpose”

In March 2020, the entire Figi family fell ill with what they suspect was the novel coronaviru­s. While Paige Figi needed at-home IV therapy, Charlotte appeared to have less severe symptoms and to recover well compared to the rest of the household.

Then, about a month after getting sick, Charlotte’s health suddenly began to deteriorat­e. She was admitted to the pediatric intensive care unit at a Colorado Springs hospital, where doctors treated her as a COVID-19 patient, though she tested negative for the virus at the time. (The rest of the family was never tested due to the limited availabili­ty of tests at the time, Figi said.)

The hospital released Charlotte after her symptoms seemed to improve, but days later she suffered a seizure that resulted in fatal respirator­y failure and cardiac arrest. Doctors believe Charlotte to be one of the virus’s youngest victims in Colorado.

After her passing last April, Realm of Caring ramped up its efforts, even as the pandemic disrupted nearly every facet of American life, said president Heather Jackson. The organizati­on, which Jackson cofounded with Figi, donated nearly $3 million in marijuana products to families in need and continued outreach to maintain a sense of community among those in its network.

Jackson also launched a new branch of the nonprofit called Unlimited Sciences, which focuses on research into the medicinal properties of psychedeli­cs, such as psilocybin.

“Charlotte is just so much more than the name of a product,” Jackson said. “Everything changed because of not just the bravery of Charlotte and Paige, but the other families who were suffering often in silence. And it was because these families were brave enough to say, ‘My child deserves this,’ that this entire category was born and we can’t forget that. I will not let us forget that. I will not let the industry forget whose shoulders they stand on.”

Figi can only describe the grief she feels as a process, a roller coaster-like experience that uncomforta­bly creeps up on her during mundane moments. For 13 years, Figi was Charlotte’s caretaker, voice and advocate — they were so close, they seemed to identify as one person, she said.

“Then you think about everyone you know who’s lost a kid and everyone you know who’s lost someone to COVID,” Figi said. “Half a million people almost I think we’re at. Everyone is going through this and it becomes super overwhelmi­ng.”

A mom to two other children, Maxwell, 17, and Charlotte’s twin Chase, 14, Paige Figi is trying to set a healthy example by seeking profession­al grief counseling. She’s also taken to riding motorcycle­s and horses over the last year, acquiring a few broken bones along the way. She’s excited about the upcoming funeral not only because it’s an opportunit­y for the cannabis community to collective­ly grieve one of their own, but also because it offers a chance to celebrate Charlotte’s legacy.

“It shows that it’s pretty amazing what we can accomplish with literally everything against you,” Figi said. “I hope people can understand that there’s no disability too great to overcome. Everyone’s life has a purpose.”

Tune in to Rock the RoC, a tribute to Charlotte Figi, for free at 6 p.m. April 7 at rocktheroc.org. Realm of Caring will launch a Kickstarte­r to help cover the cost of putting on the event and will also accept donations to support its programs and services.

 ?? Andy Cross, The Denver Post ?? Realm of Caring founders Heather Jackson, left, and Paige Figi, mother of the late Charlotte Figi, stand in Paige’s house Thursday in Colorado Springs with a painting of Charlotte behind them by artist Nichole Montanez.
Andy Cross, The Denver Post Realm of Caring founders Heather Jackson, left, and Paige Figi, mother of the late Charlotte Figi, stand in Paige’s house Thursday in Colorado Springs with a painting of Charlotte behind them by artist Nichole Montanez.
 ?? Andy Cross, Denver Post file ?? Charlotte Figi, then 7, spends time with her mother Paige at Fox Run Regional Park near their home in Colorado Springs in 2013.
Andy Cross, Denver Post file Charlotte Figi, then 7, spends time with her mother Paige at Fox Run Regional Park near their home in Colorado Springs in 2013.

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