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39 of the best celebrity responses to Keaton Jones' powerful video about bullying.

People of different backgrounds came together in support of one courageous boy.

Last week, a Tennessee woman named Kimberly Jones posted a video of her son Keaton online. It went mega-viral.

The video, which has been viewed on Facebook more than 20 million times since posting, shows Keaton in tears over being bullied at school. There's a sense of despair and helplessness in his voice that no child should have to feel, but too many have.

"Just out of curiosity, why do they bully?" a distraught Keaton asks his mom. "What's the point of it? Why do they find joy in taking innocent people and finding a way to be mean to them?"


The video clearly resonated with people — some who have been bullied, some who have been the bully — and within hours, words of support began to roll in from around the world, including some notes from some high profile people.

Hollywood has Keaton's back.

Avengers Chris Evans and Mark Ruffalo came up big for the little guy.

As did Eleven from "Stranger Things," offering her friendship.

The delightful Tom Cavanagh of "The Flash" voiced his support  for Jones and against bullies everywhere.

Same with Beth Behrs of "Two Broke Girls."

He got some love from members of "The Walking Dead" cast.

Even Gaston and LeFou (a couple of fiction's most famous bullies) weren't having it.

Broadway star Ben Platt offered a few words of support.

And so did voice actors Susan Eisenberg and Kevin Conroy, who provided the voices for Wonder Woman and Batman, respectively, on the animated "Justice League" TV show.

"Coco" director Lee Unkrich and "Ghostbusters" mastermind Paul Feig stepped up.

Some of the biggest stars in professional sports showed up, as well.

LeBron James called bullies "straight up wack, corny, cowards, chumps."

Cubs slugger Anthony Rizzo and Pirates outfielder Andrew McCutchen both offered words of kindness and comfort.

Former Green Bay Packers cornerback Bernard Blake urged Jones to "never be ashamed of who you are." Former NFL star Antonio Cromartie stepped in to say that bullies are often just insecure about themselves, asking him to be strong.

Former NFL wide receiver Donté Stallworth urged caution for people suggesting that the bullies be confronted with hostility, asking people who really want to make a difference to try to do it through lessons of love.

"Bullying is bullshit," summed up World Cup champion Ali Krieger. "We need to start coming together, supporting each other and most importantly, standing up for beautiful kids in this world like Keaton."

Similarly, the music world had words of encouragement and support for Jones.

Demi Lovato predicted that Jones would come out of this experience much stronger than he entered it. Enrique Iglesias called the video "heartbreaking."

"This extremely raw and real moment has brought hope and truth to so many people," wrote Kevin Jonas. Nickelback called Jones "a brave young man," asking if there was anything the band could do for them.

Justin Bieber and Snoop Dogg posted words of support on Instagram. "The fact that he still has the sympathy and compassion for other people when he's going through it himself is a testament to who he is," said Bieber.

Anti-bullying activists, models, and YouTube sensations all got in on the act as well.

Monica Lewinsky offered a few kind words, saying that she's sorry Jones is being treated this way, saying that other kids "would be lucky to be friends with [Jones]."

Model Mia Kang said Jones is her "absolute hero," offering to fly out and visit him at school for lunch.

Logan Paul offered to chat with Jones on FaceTime and send some gear his way.

Politicians across the political spectrum offered words of kindness and courage.

Senator Bob Corker (R-Tennessee) thanked the young man for his courage, and Representative Joe Kennedy III (D-Massachusetts) asked others to look to Jones as a positive example.

Responding to an offer from UFC head Dana White to visit the organization's headquarters, Donald Trump Jr. offered the Jones family a place to stay. Jane O'Meara Sanders of the Sanders Institute urged action over platitudes, calling on the country to "stand up to bullies — in our schools and communities, on social media and in politics and the White House."

Media personalities joined the chorus with offers of support and workplace tours.

Jemele Hill and Sean Hannity offered Jones and his family tours of ESPN and Fox News, respectively. NBC's Stephanie Ruhle pointed to Jones as a motivation for a more honest, brave, and kind world.

HLN's S.E. Cupp shared a story about being bullied as a child, saying, "It's got nothing to do with you and everything to do with them." Sunny Hostin, from "The View," ended with a reminder that "being different makes you special."

It's wonderful to see so many people, from so many backgrounds, come together in support of this one boy.

It's worth remembering, however, that he's not the only child in the world being bullied.

According to StopBullying.gov, 28% of U.S. students in grades 6 through12 have experienced bullying. 30% of students have admitted to being a bully to others. School bullying creates a hostile environment not conducive to learning and puts students' physical, emotional, and mental health at risk.

If Keaton Jones' story inspired you to take action, check out the StopBullying prevention toolkits for students, parents, teachers, and community members.

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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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