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The first U.S.-hosted Olympics was a disaster, but it had many silver linings.

First steps are always a bit shaky.

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The year was 1904, and it was the United States’ first time hosting the Olympic Games.

This should have been an exciting moment, but America’s inaugural games in St. Louis were actually kind of a mess.

St. Louis wasn’t even supposed to be the host city of the games — Chicago was.


The Windy City had won the bid to host the 1904 Summer Olympics, but the games’ time frame overlapped with the Louisiana Purchase Convention (also known as the 1904 World’s Fair) in St. Louis, a more popular and established event. World’s Fair officials were unwilling to allow a “rival” event to take place in another city, forcing Olympic officials to move the games to St. Louis. The games were no longer a standalone event.

[rebelmouse-image 19533892 dam="1" original_size="512x387" caption="1904 World's Fair. Photo via David R. Francis, "The Universal Exposition of 1904"/Wikimedia Commons." expand=1]1904 World's Fair. Photo via David R. Francis, "The Universal Exposition of 1904"/Wikimedia Commons.

To make matters worse, by July — less than two months before the games began — no invitations to other countries had been extended. But even if the invitations had gone out on time, it was unlikely Europe would make a strong showing due to political tensions back home and the considerable distance to travel. The result was an Olympic delegation that, by default, skewed heavily American, with only 42 of the 651 athletes coming from non-U.S. nations.

The games were also host to politicking, scandals, practical jokes, and bad luck — all of which made for a colorful retrospective, but a lackluster event at the time.

However, amid the chaos and countless obstacles the athletes faced in St. Louis, the event served as a showcase for many Olympic records and firsts.

The fact that the games served as a de facto American platform didn’t curb the competitive fire of the athletes who did show up; many had trained their entire lives for the opportunity.

One such athlete was University of Michigan runner Archie Hahn.

Having won events at the 1903 Intercollegiate Championships, expectations were high for the multitalented track athlete. Hahn didn’t disappoint, winning gold in all three of his events: the 60 meters, the 100 meters, and the 200 meters. In the latter event, Hahn set an Olympic record time of 21.6 seconds. His record stood for 28 years and endured better-attended games in the future.

Another was George Eyser, a gymnast with a wooden prosthetic leg who competed for the American team.

[rebelmouse-image 19533893 dam="1" original_size="512x377" caption="Concordia Turnverein Gymnastic Team, 1908. George Eyser is in the center. Photo by Louis Melsheimer/Missouri Historical Society/Wikimedia Commons." expand=1]Concordia Turnverein Gymnastic Team, 1908. George Eyser is in the center. Photo by Louis Melsheimer/Missouri Historical Society/Wikimedia Commons.

A German immigrant, Eyser had lost his leg in a train accident as a child, but he stood out as the premiere talent in his local St. Louis gymnastics team. And at the 1904 Games, he won six medals — five of them in a single day — securing his place in American Olympic history.

It would be over a century before the Olympics would see another amputee compete in the games.

While this Olympiad was far from flawless, it secured a place in athletic history not just with the individual athletic achievements it provided, but also the bevy of new sports it hosted.

Prior to the St. Louis Olympics, boxing, freestyle wrestling, and the decathlon had never been medal events. A century later, it’s hard to imagine the Olympics without them.

Other introduced events, such as tug-of-war, don’t feel quite so essential because, well, they didn’t stick around too long. The six-member event debuted in 1904 with the U.S. winning all three medals, but it lasted only through the 1920 Games before its elimination. Nonetheless, many modern fans have been clamoring for its return to the Olympics.

[rebelmouse-image 19533895 dam="1" original_size="640x363" caption="1904 tug-o-war game. Photo by Charles Lucas/Library of Congress/Wikimedia Commons." expand=1]1904 tug-o-war game. Photo by Charles Lucas/Library of Congress/Wikimedia Commons.

These new events and the athletes they featured may have been foreign to many at the time, but they quickly won the hearts of fans the world over.

The inaugural U.S. Games ultimately served as a reminder — albeit a rocky one — that the spirits of Olympic competition and unity persevere even under the most bizarre circumstances. An Olympic athlete is trained to be tenacious in the face of adversity, and nowhere have we seen this better than the sparsely attended, poorly planned 1904 St. Louis Summer Olympics.

These games may not hold a spot in the pantheon of legendary Olympiads, but they still highlight the accomplishments and spirit of the athletes who participated. The enduring and unlikely legacies stemming from these games remind even the most jaded fans that the Olympics exist as a platform for the athletes.

The chaotic affair also served as a pioneering event, paving the way for United States’ rich history in the games in both hosting and competing.

This story was produced as part of a campaign called "17 Days" with DICK'S Sporting Goods. These stories aim to shine a light on real occurrences of sports bringing people together.

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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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