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Chelsea Clinton has an important message to people criticizing Barron Trump: Stop.

One 'first kid' stands up for another.

Chelsea Clinton was just 12 years old when her family moved into the White House.

On Jan. 20, 1993, the daughter of Bill and Hillary Clinton joined an exclusive club of "first kids" that included Amy Carter, Susan Ford, Luci Johnson, Caroline Kennedy, John F. Kennedy Jr., and a handful of others.

It's hard to imagine what it must be like to grow up with the spotlight of the highest office in the land fixated on you, but for a select group of presidential children, that's life, and it's not always easy.


The first family waves to the crowd at President Bill Clinton's first inaugural in 1993. Photo by Tim Clary/AFP/Getty Images.

With a new member entering the exclusive club last week, the former first daughter shared an important request with the public.

On Friday, Donald Trump became the 45th president of the United States. The real estate tycoon-turned-leader of the free world has five children: Donald Jr. (39), Ivanka (35), Eric (33), Tiffany (23), and Barron (10). And it's fellow White House tween, Barron, that Clinton's advice concerns.

Barron Trump deserves the chance every child does-to be a kid. Standing up for every kid also means opposing POTUS policies that hurt kids.

Posted by Chelsea Clinton on Sunday, January 22, 2017

Even if you disagree with a president's actions, words, or policies, there's no reason to take it out on a child.

Just days after her father was elected in 1992, conservative commentator Rush Limbaugh attacked Clinton on his somewhat short-lived TV show, comparing her to Millie, the outgoing White House dog.

In 2014, Elizabeth Lauten, then-communications director for Rep. Stephen Lee Fincher (R-Tennessee), took a swipe at Malia and Sasha Obama (ages 16 and 13, respectively) for their appearance during the White House turkey pardoning ceremony. "I get you're both in those awful teen years, but you're a part of the First Family, try showing a little class. ... Dress like you deserve respect, not a spot at the bar."

President Obama (R) stands with his daughters Sasha (L) and Malia during the White House turkey pardoning ceremony in 2014. Photo by Mark Wilson/Getty Images.

Those attacks were wrong when they were directed at the children of Democrats, and they're just as wrong when they're directed at the children of Republicans — like Barron Trump.

On Friday, SNL writer Katie Rich tweeted (and quickly deleted) a joke about the youngest Trump, writing, "Barron will be this country's first homeschool shooter."

In November, Donald Trump's longtime nemesis Rosie O'Donnell tweeted a message suggesting that Barron was autistic: "Barron Trump autistic?" she wrote. "If so — what an amazing opportunity to bring attention to the AUTISM epidemic." Days later, after much criticism, O'Donnell issued an apology to Barron's mother, first lady Melania Trump.

Barron and Donald Trump appear together at the 2016 Republican National Convention. Photo by John Moore/Getty Images.

This goes beyond slogans like Michelle Obama's "When they go low, we go high." This isn't about "winning" elections or losing. It's about treating others how you'd like to be treated.

Barron didn't choose to be born into the Trump family any more than each of us chose to be born into our families. In many ways, to be sure, he lives a charmed life — riches beyond most of our wildest imaginations and the son of one of the most powerful people in the world. But he's not responsible for the type of campaign his dad ran or the types of policies that will be implemented under his dad's watch.

Not only is it wrong to attack an innocent child, but as Clinton's Facebook post suggests, we must not get distracted from what really matters: how Trump plans to run the country.

There are many valid criticisms to be made about any politician — whether you're discussing Donald Trump, Barack Obama, or anyone else — but taking aim at their young children should not be among them.

Barron Trump arrives at the U.S. Capitol on Jan. 20, 2017. Photo by Win McNamee/Getty Images.

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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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