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America, meet your LGBTQ Olympians proudly representing red, white, and blue.

Greg Louganis won Olympic gold medals for diving in 1984 and 1988. But he still wasn't quite enough to land a coveted Wheaties box.

And by "enough," I mean straight.

"[Wheaties'] response was that I didn’t fit their wholesome demographics or whatever," Louganis once explained of the cereal snub. "Basically, being gay, or being rumored that I was gay, [prevented me from being on the box]."


Photo by Pascal Rondeau/Getty Images.

If your blood is boiling at that, you're not alone.

When it comes to America's acceptance of LGBTQ athletes, clearly, a lot has changed since Louganis was given the cold shoulder two decades ago. But we don't need a cereal box to tell us that — just look at this year's Team USA roster.

America boasts seven out and proud LGBTQ Olympians competing in this year's games — and all of them are women.

These badass queer athletes are helping show young LGBTQ people around the world that, yes, they can play sports too — and be amazing at it.

1. Brittney Griner, basketball

When the 6'8" center isn't snagging rebounds, Griner's working on her mobile app, BG:BU, which helps young people fight bullying.

Photo by Jayne Kamin-Oncea/Getty Images.

2. Megan Rapinoe, soccer

Rapinoe helped the U.S. women's soccer team win gold against Japan at the 2012 games. Also, she can't travel without gum and a reliable neck pillow, in case you're wondering what she probably brought with her carry-on luggage to Brazil.

Photo by Harry How/Getty Images.

3. Ashley Nee, canoe/kayak

Nee — who's been on the world championship stage for the past three years — basically lives in the water. But she can have fun on land too. Her hobbies include street art and long boarding.

Photo by Ronald Martinez/Getty Images.

4. Kelly Griffin, rugby

Today, Griffin is a warrior on the field, but that wasn't always the case. She didn't start playing rugby until her freshman year of college.

Photo by Sean M. Haffey/Getty Images.  

5. Seimone Augustus, basketball

Augustus, who helped lead her team to gold in the 2008 and 2012 Olympics, started her own foundation to raise awareness around health and wellness.

Photo by Jayne Kamin-Oncea/Getty Images.

6. Jillion Potter,  rugby

Potter is a Coloradan (who's kinda obsessed with flossing) who helped her team win bronze in the world championships in 2013.

Photo by Sean M. Haffey/Getty Images.

7. Angel McCoughtry, basketball

McCoughtry has already set individual U.S. records at the Olympics for best field goal percentage and most field goals made. But she also wins brownie points for having a song available on iTunes called “Illusion."

Photo by Jayne Kamin-Oncea/Getty Images.

This isn't just a big year for queer U.S. Olympians either. Globally, there are more out LGBTQ Olympians than ever before.

There's a record-breaking 43 (and counting) out LGBTQ Olympians in total participating in this year's games, according to historian Tony Scupham-Bilton and Outsports.

And that's a huge flippin' deal (that diving pun's for you, Tom Daley).

Olympic diver Tom Daley (U.K.) made a splash after coming out in 2013. Photo by Clive Rose/Getty Images.

So is 2016 just ... gayer than years past?

I wish! Queer athletes have always competed in the Olympics, of course, but ever-evolving societal views have made more athletes comfortable competing as their authentic selves. What's even cooler about 2016 is that game-changing new policies are opening the door for more transgender Olympians to compete too.

While we certainly shouldn't ignore the fact that, in many regions of the world, progress on LGBTQ rights and visibility has been much slower — and in some places, legislation is even going backwardthere's no denying that the global trend is bending toward equality.

Nicola Adams is an out and proud boxer from the U.K. Photo by Jamie Squire/Getty Images for BEGOC.

Hudson Taylor, founder of Athlete Ally — a leading organization combating homophobia in sports — told Upworthy, "The progress is palpable."

"In the last year, we have seen more athletes come out, more allies speak out, and more teams and leagues take a stand than at any other time in history," he noted.

All of this progress surely puts a smile on Louganis' face. After all, he's been demanding change since his Olympics three decades ago.

“We’ve come so far, as far as marriage equality and so many things that I’ve really kind of fought hard for,” Louganis said. “I never thought I’d see the day that I would be able to get married.”

Oh, and that whole Wheaties fiasco? A popular online petition demanding Louganis get his cereal box got the right people's attention at General Mills earlier this year, and justice was finally served. He got his Wheaties box.

“It means more now than it probably would’ve then because they would’ve been celebrating the athlete [back then],” he recently told "Oprah: Where are they Now." “I’m a gay man living with HIV. I feel like I’m being embraced as a whole person and not just a part of me.”

Photo courtesy of General Mills, used with permission.

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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.

True

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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