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Culture

Heroic woman who tried to stop Travis Scott's concert when it turned deadly shares her story

concert, Astroworld, Travis Scott

Seanna Faith McCarty screamed at a cameraman that people in the crowd were dying.

When you cram a mass of humanity onto a stadium floor, and those humans are fans of the performer on stage in front of them, anything can happen. People have been crushed in mosh pits before—the Who and Pearl Jam concerts have seen multiple fans trampled to death in a concert, for example.

So when eight people were killed and dozens more injured at rapper Travis Scott's Astroworld Musical Festival in Houston last Friday, it was definitely tragic but not totally unprecedented. What was hard for people to grasp was how the tragedy was handled in real time by the people with power to do something about it.

Viral video shows two young concertgoers desperately trying to get a cameraman to stop the show because people were dying. One of them, Seanna Faith McCarty, pleaded with him to tell someone to stop the show, pointing toward the crowd and saying that people were dying. Another concertgoer, identified on Twitter as Ayden Cruz, stood on the ladder of the camera platform and also yelled at the cameraman to stop the show.

Watch:


Here's another angle of the attempt to alert the crew member to the deadly situation on the ground.

However, no one stopped the show. According to Insider, at one point, Scott can be heard over the loudspeaker saying: "Who asked me to stop? You all know what you came here to do." Insider also reports that concertgoer Cody Hartt said he alerted security that people were being crushed, and they allegedly responded, "We already know, and we can't do anything to stop the show. They're streaming live."

McCarty detailed the story of how she ended up on the camera platform, desperately trying to get someone to stop the show and do something about the deadly conditions in the crowd.

She described how she and her friend had wanted to be close to the stage, but ended up a ways back, on the side near a walkway. They were surrounded by chest-high metal barriers, and she said after waiting two hours for the concert to start, "Every gap was filled. Where your feet were placed was where they stayed." The energy of the crowd rose as the start time neared.

"Within 30 seconds of the first song, people began to drown—in other people," she wrote.

"There were so many people. Tall men, women. Women and men where the only thing they could see was the back of the person in front of them. The rush of people became tighter and tighter. Breathing became something only a few were capable of. The rest were crushed or unable to breathe in the thick, hot air. My friend began to gasp for breath, and she told me we needed to get out. We tried. There was nowhere to go. The shoving got harder and harder. If someone's arms had been up, it was no longer a possibility to put it down. So, people began to choke one another as the mass swayed. It became more and more violent."

She went on to describe how people were screaming for help and begging security for help.

"None of that came," she wrote. "We continued to drown. More and more. One person fell, or collapsed, it doesn't matter how it started. Once one fell, a hole opened in the ground. It was like watching Jenga tower topple. Person after person were sucked down. You could not guess from which direction the shove of hundreds of people would come next. You were at the mercy of the wave. I watched my friend be dragged away from me and lost sight of her. I began to realize in that moment that there is a way to die that no many people know about. Being trampled to death."

McCarty described the "shrieks of animals" and "sinkholes of people" all around her. She was shoved toward the ground and saw the body of a man, followed by "layers of fallen people."

"I felt a primal fear rip through me, and I'm not sure anyone understood the magnitude of the situation below," she wrote. "I screamed there were people on the floor. There were people. Unconscious. Being trampled by every foot that slammed into the ground as each individual tried to keep themselves upright."

A man finally grabbed her and pulled her out and away from the sinkhole of people. She was able to make her way to the back of the crowd, where she found people "just standing there. Like nothing was happening. Like people weren't dead a few feet from them."

She spotted the cameraman on the platform and climbed the ladder to get his attention. She pointed to the hole, telling him people were dying. He told her to get off the platform.

"I screamed over and over again," she wrote. "He wouldn't even look in the direction, so I pushed the camera so it pointed toward where I had just come from. He became angry. He called someone else up. I told him the same thing. People were dying, we needed to stop the music, we needed help, we needed attention towards the mass because I thought if only these people were aware, maybe they would do something. The other man grabbed my arm, and told me he would push me off the 15ft platform with no sides if I didn't get down. I told him to help. I told him people were dying. I showed him where. He wouldn't look in the direction either. I was in disbelief. Here were two people that could actually do something. Had the power to do something. Cut the camera, call in backup, pause something. They did nothing."

Then the crowd started booing at her. "They pointed their fury at me, unleashed a rage," she wrote. "I screamed people were dying over and over. No one would listen."

Finally, she climbed down from the platform and called 911. The operator told her they were calling the medical team in. She told them over and over that the concert needed to be paused to give the crowd light and awareness of the deaths. Nothing happened.

Two medical workers arrived and McCarty explained what she'd seen. They said they'd gone in and seen nothing. Two girls who had also been in the pit were nearby and explained what and where it was and they all led them to it. They climbed over the barrier and went through the people.

In her post, McCarty reassured readers that her friend made it out okay. But at least eight concert-goers were killed in the melee and 25 were taken to the hospital, including a 10-year-old in critical condition, according to USA Today. The names of the victims has been released: Mirza Danish Baig, 27; Rodolfo Peña, 23; Madison Dubiski, 23; Axel Acosta Avila, 21; Franco Patino, 21; Jacob Jurinek, 20; Brianna Rodriguez, 16; and John Hilgert, 14.

Here's to the people like Seanna McCarty who did everything in their power to get help for the people trapped in and trampled by the crowd. In the face of a frenzied mob, keeping your head and having the courage to take action is admirable, especially considering how many people neglected their basic sense of humanity in this situation.

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Three women, three MS journeys: How multiple sclerosis looks different for everyone

Gina, Nathalie and Helga share their reactions to being diagnosed with MS and how they stay informed and positive in the face of ever-changing symptoms.

Courtesy of Sanofi

Helga, Nathalie and Gina all have MS, and their experiences show how differently the disease can manifest.

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It’s been 155 years since neurologist Jean-Martin Charcot gave the first lecture on a mysterious progressive illness he called “multiple sclerosis.” Since then, we’ve learned a lot. We know MS causes the immune system to attack healthy tissue, including damaging the brain and spinal cord. Resulting symptoms can be debilitating and include fatigue, blurred vision, memory problems and weakness. Huge advancements in our understanding of MS and its underlying causes, as well as treatment advances, have been made in the past few decades, but MS remains a complex and unpredictable reality for the 2.8 million+ people diagnosed around the world.

Ironically, the only real constant for people living with MS is change. There’s no set pattern or standard progression of the disease, so each person’s experience is unique. Some people with MS have mild symptoms that worsen slowly but sometimes improve, while others can have severe symptoms that drastically alter their daily lives.

All people with MS share some things in common, however, such as the need to stay informed on the ever-evolving research, find various lines of support and try to remain hopeful as they continue living with the disease.

To better understand what navigating life with MS really looks like, three women shared their MS stories with us. Their journeys demonstrate how MS can look different for different people and interestingly, how the language used to talk about the disease can greatly impact how people understand their realities.

woman with horse, woman riding horseGina loves riding her horse, Benita.Courtesy of Sanofi

Gina—Hamburg, Germany (diagnosed with relapsing multiple sclerosis in 2017)

When her youngest son was 4 months old, Gina started having problems with her eye. She’d soon learn she was experiencing optic neuritis—her first symptom of MS.

“Immediately after the diagnosis, I looked up facts on MS because I didn’t know anything about it,” Gina says. “And as soon as I knew what could really happen with this disease, I actually got scared.”

As her family’s primary income provider, she worried about how MS would impact her ability to work as a writer and editor. Her family was afraid she was going to end up in a wheelchair. However, for now, Gina’s MS is managed well enough that she still works full-time and is able to be active.

“When I tell somebody that I have MS, they often don't believe me the first time because I don't fulfill any stereotypes,” she says.

Overwhelmed by negative perspectives on living with MS, Gina sought support in the online MS community, which she found to be much more positive.

“I think it’s important to use as many positive words as you can when talking about MS.” It’s important to be realistic while also conveying hope, she says. “MS is an insidious disease that can cause many bad symptoms…that can be frightening, and you can't gloss over it, either.”

To give back to the online community that helped her so much, Gina started a blog to share her story and help others trying to learn about their diagnosis.

Though she deals with fatigue and cognitive dysfunction sometimes, Gina stays active swimming, biking, riding horses and playing with her sons, who are now 11 and 6.

Cognitive dysfunction is common in MS, with over half of people affected. It can impact memory, attention, planning, and word-finding. As with many aspects of MS, some people experience mild changes, while others face more challenges.

Gina says that while there’s still a lot of education about MS needed, she feels positive about the future of MS because there’s so much research being done.

woman in wheelchair holding medal, woman rowingNathalie is an award-winning rower with multiple international titles.Courtesy of Sanofi

Nathalie — Pennes Mirabeau, France (diagnosed with relapsing-remitting multiple sclerosis in 2002)

Nathalie was a teenager and a competitive athlete when she noticed her first symptoms of MS, but it would take four years of “limbo” before she was diagnosed.

“Ultimately, the diagnosis was more of a relief, than a shock,” she says. “Because when you have signs and you don’t know why, it’s worse than knowing, in the end, what you have.”

However, learning more about the disease—and the realities of disease progression—scared her.

“That glimpse of the future was direct and traumatic,” she says. Her neurologist explained that the disease evolves differently for everyone, and her situation might end up being serious or very mild. So, she decided to stop comparing herself to others with MS.

She said to herself, “We’ll see what happens, and you’ll manage it bit by bit.”

By 2005, Nathalie’s MS had progressed to the point of needing a wheelchair. However, that has not dampened her competitive spirit.

Nathalie began her international rowing career in 2009 and has won multiple world titles, including two Paralympic medals—silver in London and bronze in Tokyo. Now, at 42, she still trains 11 times a week. Fatigue can be a problem, and sometimes hard workouts leave her with muscle stiffness and shaking, but she credits her ongoing sports career for helping her feel in tune with her body’s signals.

“Over the years, I’ve learned to listen to my body, letting my body guide when I need to stop and take breaks,” she says.

Nathalie explains that she used to only look backwards because of the initial shock of her diagnosis. In time, she stopped thinking about what she couldn’t do anymore and focused on her future. She now lives in the following mindset: “Even when doors close, don’t miss out on those that open.” Instead of focusing on what she can’t do, she focuses on the opportunities she still has. Right now, this includes her training for the 2024 Paralympic Games in Paris, where she will compete for another rowing medal.

“I only go forward,” she says. “Well, I try, anyway…It’s easy to say, it’s not always easy to do. But that’s what I try to do.”

woman exiting water after swimming, woman with great daneHelga's Great Dane has become a helpful and beloved companion.Courtesy of Sanofi

Helga—Johannesburg, South Africa (diagnosed with relapsing multiple sclerosis in 2010)

When Helga first started having balance issues and numbness in her feet, she chalked it up to her training as a runner. But when the numbness moved to her face, she knew something was wrong. She never guessed it was MS.

“When I was diagnosed, I felt completely overwhelmed and clueless,” Helga says. “I felt that I had nowhere near enough information. I did not know anything about the disease…I had no idea that it was going to be a process of continually monitoring and adjusting your lifestyle.”

In the beginning, Helga’s symptoms developed slowly, and she didn’t appear ill to others. She was even able to run for a few years after her diagnosis, but she couldn’t do marathons anymore, and she began to fall frequently due to balance issues and right-foot dragging. Then her cognition issues became more problematic, especially in her job as a trainer in a printing company.

“My executive function, decision-making and short-term memory were affected to the point that I was eventually medically unfit for work,” she says. She stopped working in 2017.

However, she didn’t stop living life. Even though she could no longer run, she continued to swim competitively. She got a Great Dane puppy and trained him as a service dog to help her walk. She also serves as vice chair of the patient support organization Multiple Sclerosis South Africa, and she advises others who have been diagnosed to join a patient advocacy group as soon as possible to get reliable information and meet others with MS.

Helga says she is “hopeful” about the future of MS. “I must say that I am so grateful that we have all the new medications available, because my life would not be the same if it wasn't for that,” she adds.

Part of how she manages her MS is by looking at the positives.

“If I could tell the world one thing about MS, it would be that MS is an incurable disease of the nervous system, but it's also the greatest teacher of valuing your health, family, friends, and managing change in your life,” she says. “My life is diversified in a way that I never, ever thought it would, and MS has been honestly the greatest teacher.”

Each MS journey is unique – with each person impacted experiencing different struggles, successes, and feelings as they manage this unpredictable disease. But the common thread is clear – there is a critical need for information, support, and hope. We are proud to participate in World MS Day and share these incredible stories of living life while living with MS. To learn more about MS, go to https://www.sanofi.com/why-words-really-matter-when-it-comes-to-multiple-sclerosis.

MAT-GLB-2301642-v1.0-05/2023

This article was sponsored by Sanofi. Participants were compensated when applicable.

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