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Colin Kaepernick just snagged a top honor also given to Malala and U2. He deserves it too.

Sometimes the smallest actions can have the biggest impact.

All former San Francisco 49ers quarterback Colin Kaepernick did was sit down. He didn’t shout, he didn’t stomp, he didn’t set anything on fire — he simply didn’t stand up during the national anthem.

Photo by Mike Ehrmann/Getty Images.


That one small act sparked conversations about racial injustice and police use of force — in addition to the meaning of the national anthem and American flag — and ignited a social media controversy the likes of which I have rarely seen.

But Kaepernick didn’t continue to sit. After consulting with veteran and fellow football player Nate Boyer, Kaepernick switched to kneeling instead of sitting, to show respect for veterans while still protesting racial injustice in America’s law enforcement and justice system. Throughout the 2016-2017 football season, despite the controversy swirling around him, Kaepernick quietly knelt on the sidelines at every game.

Photo by Ezra Shaw/Getty Images.

Some people hated him for it. Some people loved him for it. Amnesty International just awarded him their highest honor for it.

Global human rights group Amnesty International named Kaepernick their 2018 Ambassador of Conscience — the top human rights award given by the organization. Previous winners include Malala Yousafzai, Nelson Mandela, and U2.

Many Americans celebrated the honor, while others rolled their eyes. But whether or not you agree with Kaepernick’s message or methods, there’s no doubt he earned and deserves this award.

As Salil Shetty, secretary general of Amnesty International, said:

“The Ambassador of Conscience award celebrates the spirit of activism and exceptional courage, as embodied by Colin Kaepernick. He is an athlete who is now widely recognized for his activism because of his refusal to ignore or accept racial discrimination. Just like the Ambassadors of Conscience before him, Colin Kaepernick chooses to speak out and inspire others despite the professional and personal risks. When high profile people choose to take a stand for human rights, it emboldens many others in their struggles against injustice. Colin Kaepernick’s commitment is all the more remarkable because of the alarming levels of vitriol it has attracted from those in power.”

Kaepernick sacrificed his football career for a cause. And he’s done much more than that.

Some people have focused so much on Kaepernick’s anthem protests that they’ve missed the work he’s been doing off the field.

He started the Colin Kaepernick Foundation, with a mission "to fight oppression of all kinds globally, through education and social activism." Through his foundation, he has donated a million dollars of his own money to various organization working for justice and police reform. He’s created a camp for kids to learn about their civil rights. And he has inspired others in the NFL, and throughout the entertainment world, to donate to similar causes.

When I started the #10for10 #Encore as part of my #MillionDollarPledge it was because after I ended the Pledge I still had an amazing show of support from friends that wanted to be involved, so I decided on one more day to continue to support the organizations on the ground. Well that one day, turned into two days after an outpour of support from friends wanting to join to giveback to the community who are fighting hard for us on the ground everyday. 10 people in my original #10for10 turned into 20 people adding on at the end of these two days! Amazing! · Of course, I couldn’t end the #10for10 without hearing from this amazing singer, philanthropist, mother, wife, actress and activist, @aliciakeys. She messaged me instantly as the #10for10 was going to show her support and Pledge $15k to Silicon Valley De-Bug! @sv_debug is an organization that has initiated and lead successful social justice campaigns to advance the rights of youth, workers, immigrants and those impacted by the criminal justice system. · Thank you, Alicia for all the work you do in the community to help our brothers and sisters globally. And thanks to everyone that was involved with the #MillionDollarPledge! Together we are strong. See everyone involved as well as all the organizations we donated to that are on the frontlines everyday fighting for social justice on Kaepernick7.com! #PowerToThePeople

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All of this in addition to serving as a catalyst for conversation, a powerful symbol of peaceful protest for some, and a highly controversial figure in the social and political landscape for others.

You don’t have to agree with Kaepernick’s philosophical — or physical — stance to agree that he's met the criteria for the Ambassador of Conscience Award.

Standing — or sitting, or kneeling — for what you believe in takes courage, especially in the face of great resistance. After many teams had the opportunity to pick him up, Kaepernick still remains jobless with the NFL. He has been the target of the president of the United States, who referred to protesting players as a “son of a bitch” and encouraged people to boycott games when players kneel or sit during the anthem. There’s no question he made enormous sacrifices in his career — and in the court of public opinion in a “spirit of activism.”

In doing so, he joins an elite group of activists around the world who have been recognized with Amnesty International. And no matter what people think of his method of protest, he has rightfully earned his place among them through his uncompromising stand, and unwavering dedication to fighting injustice.

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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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