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Pop Culture

Wrongfully convicted man proves his innocence using an episode of 'MythBusters'

John Galvan was only 18 years old when he was arrested for a crime he did not commit.

mythbusters

Justice (and scientific education) served.

The Discovery show “MythBusters” delighted investigative junkies and movie buffs alike in the years following its launch in the early 2000s. The stunt-filled show featured special effects experts Adam Savage and Jamie Hyneman testing out the validity of everything from duct tape islands to mechanical sharks using scientific methods.

Back in 2007, 39-year-old John Galvan was 21 years into serving a life sentence for a crime he didn’t commit, when he caught a rerun of “MythBusters” on the prison television.

The episode, “Hollywood on Trial,” which originally aired in 2005, shows Hyneman and Savage failing to light a pool of gasoline using a cigarette—a classic action film trope.


Not even a rolling fully lit cigarette could ignite a flame. In other words, the myth was officially “busted.

This bit of information immediately caught Galvan’s attention, for it would be the very catalyst needed to prove his innocence and reclaim his freedom.

In September 1986, a fire broke out in a two-flat apartment building in southwest Chicago, killing two brothers—one of whom was suspected to be involved in a gang called the Latin Kings. Their siblings managed to escape and told police that a female neighbor had threatened to burn the building down as retaliation for her own brother’s death, an act supposedly committed by the gang.

The woman denied involvement and instead pointed the blame at Galvan, along with other neighbors interviewed by the police. Although Galvan had been asleep at his grandmother’s the night of the fire, he had no other evidence proving his innocence, and was arrested. He was only 18 years old.

Using violence, torture and deception tactics (which remain legal in 46 states), Detective Victor Switski eventually coerced Galvan into signing a confession after threatening that he could face the death penalty and end up “laying next to” his late father.

mythbusters sets man free

A photo of Galvan as a child.

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Galvan’s signed statement claimed he had started the fire by throwing a bottle filled with gasoline at the building and then tossing a cigarette into the pool of gasoline on the porch to ignite it. Which, again, is scientificallyimpossible.

Galvan immediately called his lawyer Tara Thompson, who had serendipitously been watching the same episode. Thompson and Galvan had been working on his third post-conviction petition, and both were thrilled to have stumbled upon some compelling evidence in the most unlikely of places.

“I remember I was excited, I was extremely happy because that just added to the other things that were coming together at that time. I felt like finally this is starting to all come out,” Galvan recalled.

Thompson added, “It was honestly shocking to me … I feel like all of us have seen movies — like Payback is a famous one — where they light the gasoline in the street with a cigarette and a car explodes, and I really had never given much thought to whether or not that might be real.”

“When I watched this MythBusters episode, as a lawyer, it made me realize that there are things you have to look deeper into — you can’t assume that you understand the science until you’ve looked into it,” she added.
innocence project

Tara Thompson (left) and John Galvan (right).

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The show’s findings were echoed by experiments conducted by the U.S. Bureau of Alcohol, Tobacco, Firearms and Explosives (ATF). It made more than 2,000 attempts to ignite gasoline with a cigarette under various conditions and every attempt failed.

It wouldn’t be until 2017 that Galvan got his evidentiary hearing on his post-conviction claims. Thompson not only presented their findings, but also seven witnesses—including those who attested to also being tortured by the same detective who had interrogated Galvan, and an arson expert who testified that what Galvan falsely confessed to was scientifically impossible.

Despite the overwhelming evidence, prosecutors still denied that the science was correct.

“Even then, they really did not want to accept that this was not possible,” Ms. Thompson recalled. “I find that very telling about the state of science and the law … that these things that we probably should accept as true in the legal space, the system does not always want to accept.”

Galvan would have to wait until 2022—and after several appeals—to gain his freedom. He was exonerated largely based on the fact that he was abused into involuntarily signing his confession, rather than any changes to the science of the case.

Rebecca Brown, director of policy for the Innocence Project, says it speaks to “the critical importance of establishing mechanisms for people to get back into court when science changes or evolves, or when experts repudiate past testimony.”

“A ‘change-in-science’ statute here would have allowed for a presentation reflecting those changes in arson science and could have likely expedited Mr. Galvan’s exoneration,” she explained.

good news

He'll never get those 35 years back, but he's going to make the best of the time he has left.

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Adjusting to a new life outside the prison walls after 35 years has been no easy task, but Galvan is nonetheless taking his newfound freedom in stride. He’s most looking forward to having his own space to call home and getting back to drawing and painting. If you would like to support Galvan, check out his Amazon wish list.


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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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