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Shailene Woodley's Columbus Day arrest reminds us how Native Americans still need support.

Columbus Day has always been a bit ... contentious in the U.S.

In elementary school, most of us learned about Columbus as the man who discovered America. By middle school, we learned that he actually went to South America and the Caribbean. And also there were already people living there.

Then in high school, we might have learned the truth: Columbus had nothing to do with the United States at all ... and also he raped and pillaged lots of indigenous peoples.


Our country's relationship with its native inhabitants has been complicated from the beginning.

In fact, you could call it downright awful. Inhumane. Genocidal. To this day, Native American communities continue to suffer from poverty and police brutality at alarming rates.

And this year, on Columbus Day, three things happened that proved how complicated all of this continues to be.

Photo by Nicholas Kamm/AFP/Getty Images.

1. 524 years after Columbus "discovered" the "New World," actress Shailene Woodley and a bunch of other activists were arrested in North Dakota for protesting to protect Native American rights.

The situation began earlier this year, when Energy Transfer Partners began construction on the Dakota Access Pipeline, a $3.7-billion project that would threaten the water supply that serves more than 9,000 Native Americans.

The Standing Rock Sioux and other tribes appealed to numerous government departments and courts to halt the project. But despite a few temporary rulings, the conflict continued.

The company behind the pipeline bullied their way through thousands of Native American protesters and clandestinely destroyed the same sacred lands and burial sites that the tribes had hoped to protect.

Photo by Robyn Beck/AFP/Getty Images.

Over the weekend, Energy Transfer Partners denied another request from the U.S. Justice Department to voluntarily stop construction.

Once again, the tribes gathered in protest, leading to the arrests of more than two dozen people on Oct. 10, including actress Shailene Woodley.

Woodley broadcast her arrest over Facebook Live, and while that publicity didn't keep her out of jail, it did help to raise awareness about the unfair ways which Native Americans continue to suffer.

Native American communities have been largely ignored, which has only made it easier for the U.S. government and corporations alike to get away with egregious mistreatments, like what's happening in North Dakota.

Photo by Alex Wong/Getty Images.

2. Meanwhile, 26 U.S. cities and two entire states replaced Columbus Day with "Indigenous Peoples' Day."

Less than half of the country actually recognizes Columbus Day to begin with, which is a good step forward.

Over the last 25 years, communities across the country have started to use the holiday to celebrate the oft-ignored heritage of the country's indigenous inhabitants, instead of a man who did them harm. South Dakota was the first full state to replace the holiday with Native Americans Day back in 1990, with Vermont joining the charge just this past year.

"Indigenous Peoples Day represents a shift in consciousness," said Leo Killsback, a citizen of the Northern Cheyenne Nation and assistant professor of American Indian studies at Arizona State University, in an interview with CNN. "It acknowledges that indigenous peoples and their voices are important in today's conversations."

Photo by Robyn Beck/AFP/Getty Images.

3. The U.S. government also recently paid out nearly $500 million to 17 native tribes in a long-overdue settlement over property rights.

While European settlers took a lot of North American territories by force, the U.S. Department of Interior did enter into legal treaties with native tribes for the use of almost 56 million acres of land. Rather than selling the property outright, however, the tribes freely gave up the land, agreeing instead to take "just compensation" for whatever profits were made from the businesses and tenants that made use of it, including housing, timber harvesting, farming, livestock grazing, and oil and gas extractions.

Unfortunately, the U.S. government didn't do a very good job of managing the land resources or the money that was made from them. (And this is hardly the only example of U.S. interests ignoring legally-binding contracts with Native Americans.)

Since President Obama took office, though, nearly 100 lawsuits and billions of dollars have been settled between the government and Native American tribes — some of which dated back more than a century and had gone ignored all that time.

This might sound like some generous progress, but it's also something that the tribes have been legally owed for a long, long time. It's a tiny step forward.

Photo by Jim Watson/AFP/Getty Images.

This year, Columbus Day reminded me of just how far we've come in terms of respecting our indigenous brethren — and how far we still need to go.

We've taken two steps forward recently by paying back the Native Americans and beginning to abolish a problematic holiday. But we've also taken one giant step back by allowing corporations to destroy sacred Native American land, just to build an oil pipeline.

The good news is that social media is a powerful tool for change. Now that people are paying attention to their plight and the celebration of their culture is spreading, we might start to see some actual change.

We can't undo the damage we've already done nor can we change the fact that we've refused to make up for our mistakes so far.

But if we want to do what's right and build a brighter future for all the people who live in the United States, there's no better time to start than now.

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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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