Paul Rosolie, a seasoned conservationist and passionate advocate for the Amazon rainforest, embarked on an extraordinary and controversial mission: he attempted to be eaten alive by a giant green anaconda.
His goal? To raise global awareness about the alarming rate of deforestation and the destruction of one of the world’s most vital ecosystems.
Having spent years studying the Amazon’s rich biodiversity, Rosolie wanted to create a bold statement that would capture worldwide attention. Equipped with a custom-built carbon fiber suit designed to endure the crushing force of the snake’s coils, an integrated oxygen supply, and multiple cameras attached to document the experience, he approached the massive predator.
The entire endeavor was captured in a Discovery Channel documentary. Despite the advanced protective suit, Rosolie described the immense physical strain he endured as the snake began to constrict him. “I’m getting coils over me,” he said during the harrowing encounter. “She’s got my arms pinned. She knows there’s nothing I can do.”
As the snake tightened its grip, Rosolie’s breathing became labored, and his heart rate skyrocketed. Eventually, the monitoring team intervened and freed him from the snake’s crushing embrace before the situation became critical.
Reflecting on the experience in an article for The Guardian, Rosolie admitted feeling a mix of grim amusement and frustration over the sensationalized marketing of the documentary. The stunt sparked backlash from animal welfare groups and segments of the public, raising questions about the ethics of such an experiment.
“I was willing to try something risky and, yes, maybe ridiculous, to draw attention to a place and a species I deeply care about,” Rosolie explained. “If offering myself to a snake was the cost of bringing awareness to the Amazon’s plight, then I was prepared to pay it.”
For two intense hours, Rosolie remained trapped in the suffocating suit, experiencing the raw power of one of nature’s most formidable predators. His controversial experiment ignited global conversations about conservation, the fragility of the Amazon rainforest, and the urgent need for action.
Whether viewed as reckless or heroic, Paul Rosolie’s bold stunt undeniably succeeded in shining a spotlight on an environmental crisis that demands our immediate attention.
Céline Dion Shares Raw Video of Stiff-Person Syndrome Crisis in Never-Seen Footage from New Documentary
In a devastating moment from “I Am: Céline Dion,” the famous person battles through an unexpected and horrifying SPS episode.
Fans are getting an unheard-of glimpse inside Céline Dion’s tribulations during the last few years of her life.
After being diagnosed with stiff-person syndrome in August 2022, the 56-year-old superstar tentatively but proudly returns to the recording studio in a devastating sequence towards the end of her new documentary, I Am: Céline Dion (available for streaming globally on Prime Video).
Shortly after, as part of her continuous treatment regimen, she makes her way to physical therapy and her foot starts to hurt.
Dion’s body locks up, indicating that she is in severe agony while her care team gives her a diazepam nasal spray during the SPS crisis episode. One of her teammates says, “We’ll do a 9-1-1 if she goes back into a spasm.”
In the movie, Dion subsequently remarks, “Every time something like this happens, it makes you feel so embarrassed.” “I’m not sure how to say it. You know that you dislike losing control of yourself?
The five-time Grammy winner thought back on the horrifying moment that director Irene Taylor’s crew captured on camera during her PEOPLE cover interview.
“Overstimulation—whether it be happiness, sadness, sound, or a surprise—can put me into a crisis—that’s one part of the [SPS] condition,” Dion explains, adding that she “did not see” the crisis episode coming that day. “Before something triggered, I was fine.”
Taylor’s understanding of the condition deepened when she was “two feet away” from Dion during the crisis.
Taylor remarks, “That was really amazing, not just for Céline to go through it, but for me to see as well.” “I continued to film because that is how I work, and I thought we would decide later whether or not to incorporate that into the movie.”
Dion and Taylor had developed a close relationship by the time the movie was in post-production, and according to Taylor, “I knew that putting it in the film was really not a risk because she believed in me at that point.” “I really can only thank her for that because she is an open book, was there, and didn’t hold anything back.”
Dion is attempting to humanize the uncommon illness through the movie and contribute to fund-raising efforts for scientific studies in the pursuit of a solution.
Neuropathy has a very broad spectrum. For this reason, I’m making a lot of effort to raise money so that people can speak with their husbands, friends, or neighbors about it,” Dion explains.
Adds Dr. Amanda Piquet, the doctor who diagnosed Dion and director of the University of Colorado Anschutz Medical Campus’s program on autoimmune neurology: “There are many exciting things in store for SPS, and the future looks bright.”
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