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The story behind Michelle Obama's state dinner dress makes it even more stunning.

For the very last time, President Obama and the first lady hosted a state dinner in Washington, D.C., on Oct. 18, 2016.

Photo by Shawn Thew - pool/Getty Images.

They graciously welcomed Italian Prime Minister Matteo Renzi and his wife, Agnese Landini, to the White House with open arms.

Photo by Yuri Gripas/AFP/Getty Images.


And the two power couples showed the world why diplomacy is certainly the most fashionable way to go about foreign policy, that's for sure.

Photo by Yuri Gripas/AFP/Getty Images.

Unsurprisingly, however, it was FLOTUS' dress that really got people talking.

Photo by Mark Wilson/Getty Images.

Because, yes, it was downright stunning.

Photo by Shawn Thew/Getty Images.

But the story behind why the first lady chose to wear it makes it an even more beautiful look.

The dress by Donatella Versace — who famously rescued her brother's company and turned it into a thriving Italian brand amid doubts she'd be able to do so — was a nod to the visiting prime minister and his wife. But Michelle Obama's choice to wear the rose gold shimmering waterfall of a gown had an even more underlying feminist message behind it, according to The New York Times.

Photo by Mark Wilson/Getty Images.

Michelle Obama's dress was made of chainmail — metal armor, essentially. And that speaks volumes about the type of message she wanted to send.

The gown was symbolic of female strength — a testament to the resiliency of a woman willing to fight for her beliefs and protect herself from bullies that might come along the way.

"When they go low, we go high," the first lady said on stage at the Democratic National Convention this past summer.

Her dress from Tuesday night summed that message up quite nicely.

Photo by Mark Wilson/Getty Images.

The first lady rocked the Versace gown in the wake of what's being called "the most powerful speech of the 2016 campaign" — an address she gave to voters in New Hampshire about the dire need to respect girls and women.

“I can’t stop thinking about this," she said during her speech, citing Donald Trump's discussion of sexual assault caught on tape. "It has shaken to me to my core in a way that I couldn’t have predicted.”

Photo by Joe Raedle/Getty Images.

"I have to tell you that I listen to all of this and I feel it so personally, and I’m sure that many of you do too, particularly the women," the first lady said. "The shameful comments about our bodies. The disrespect of our ambitions and intellect. The belief that you can do anything you want to a woman."

“I know it’s a campaign, but this isn’t about politics. It’s about basic human decency. It’s about right and wrong,” she concluded. “And we simply cannot endure this, or expose our children to this any longer — not for another minute, and let alone for four years. Now is the time for all of us to stand up and say enough is enough."

Photo by Nicholas Kamm/AFP/Getty Images.

Like other first ladies before her, Michelle Obama often wears gowns that send a message above and beyond aesthetics.

Her royal blue dress at the Democratic National Convention, for example, was designed by Christian Siriano, an artist recognized for body positivity and inclusiveness within the fashion industry. Its sentiments fell in line with her powerful speech illustrating the value of national togetherness.

Photo by Joe Raedle/Getty Images.

In 2009, when she wore a white gown by designer Jason Wu to the president's Inaugural Ball, it was chosen as a show of hope and refreshed optimism — turning the page, in a sense, as the country struggled to climb out of the Great Recession.

Photo by Saul Loeb/AFP/Getty Images.

Michelle Obama's last state dinner is a tough pill to swallow for the many Americans who saw her as so much more than your standard first lady.

Much like her dress for this last state dinner, Obama's time in the White House represents what many of us aspire to be: strong, hopeful, and, even in the face of the most difficult of circumstances, having the ability to stay true to yourself.

Writing for The New York Times magazine, Chimamanda Ngozi Adichie perfectly explained how the first lady's grit and resolve in the face of opposition shaped her into nothing short of an icon:

"The insults, those barefaced and those adorned as jokes, the acidic scrutiny, the manufactured scandals, the base questioning of legitimacy, the tone of disrespect, so ubiquitous, so casual. She had faced them, and sometimes she hurt and sometimes she blinked, but throughout, she remained herself."

Photo by Olivier Douliery-Pool/Getty Images.

So, yeah. After eight years of being the first lady, chain mail was the perfect choice.

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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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When it comes to babysitting, you can hit the jackpot with someone who not only enjoys hanging out with your kiddos but also cleans out of boredom. The only babysitter I've had that experience with is my mom, but I do hear they do exist. While walking into a spotless house after a much-needed night out would be amazing, it's not really part of a standard babysitting package.

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Obama clearly knows how to work his way up in the world.

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Obama is spot-on with his analysis. You can talk about things all day, but what really matters is taking action and making things happen. Maybe that’s why his campaign slogan in 2008 was a simple three-word phrase about taking care of business, “Yes, we can.”

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Photo by Andrew Gaines on Unsplash

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