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A side-by-side comparison of the Dakota pipeline protest and Oregon militant verdicts.

The concurrent events of the Dakota Access Pipeline protest and Malheur National Wildlife Refuge verdict on Oct. 27, 2016, shed light on our country's history of scrappy rebel underdogs, land disputes, and inequality.

On the same day Native American protesters in North Dakota were attacked by police armed with LRAD sound cannons for standing up to a private oil corporation, a group of insurgent ranchers calling themselves Citizens for Constitutional Freedom (C4CF) were acquitted on federal charges after taking up arms and occupying government property in Oregon.

These two different groups of people each fought back against some incarnation of The Man, but with very different results.


To understand the irony of this, let's take a step-by-step look at the motivations for, and responses to, each occupation.

Ron His Horse Is Thunder (left), a spokesman for the Standing Rock Sioux; George Stanek, a member of the Malheur militants. Photos by Robyn Beck/AFP/Getty Images and Joe Raedle/Getty Images.

The inciting incident of both occupations was a dispute over land rights — each with its own unique and complicated history.

The occupation of Malheur National Wildlife Refuge was a retaliation for what the ranchers saw as unfair charges in an arson case — not a contestation of guilt, but a protest that the government shouldn't have re-jailed the arsonists because of its own minimum-sentencing error. (The arsonists, however, rejected the Malheur occupation.)

The conflict with the Standing Rock Sioux of North Dakota has to do with an in-progress oil pipeline that could threaten the water supply for thousands of people. It also risks desecrating sacred tribal sites that they argued should have been protected by an oft-ignored treaty from 1851.

Citizens for Constitutional Freedom leader Ammon Bundy. Photo by Justin Sullivan/Getty Images.

Religious freedom is a tenet of American culture, and the actions of both groups were certainly influenced by their religious affiliations.

C4CF is led by Ammon Bundy, a Mormon whose family has a history of insurrection against the federal government. He claimed to be acting under divine orders.

The Standing Rock Sioux and other Native American tribes that joined in their protest also engaged in religious practices, such as prayer circles and ceremonial pipes. Unfortunately, authorities allegedly interpreted these rituals as threats on more than one occasion.

Photo by Tom Stromme/The Bismarck Tribune via AP.

The tribes in North Dakota employed various means of nonviolent protest. C4CF, on the other hand, didn't hesitate to escalate the situation with firearms — and, sadly, they were treated more civilly than the tribes.

Oregon authorities even offered to protect C4CF if they left the wildlife refuge.

Bundy met on numerous occasions with both local sheriffs and FBI agents looking to negotiate a cease-fire or a peaceful transfer of power. During the occupation, militants were allowed to come and go from the refuge and even held a press conference on the premises.

It was several weeks before federal agents put a plan into action to arrest any of the C4CF occupiers. No shots were fired, and no force was used from Jan. 4 through Jan. 26, 2016, when LaVoy Finicum was shot and killed (the circumstances of which are still unclear).

LaVoy Finicum disabling a security camera at the Malheur National Wildlife Refuge during the occupation. Photo by Rob Kerr/AFP/Getty Images.

The Native American protesters, on the other hand, endured repeated assaults from public and private police forces as they pursued legal action.

While some members of the tribes tried to settle the dispute in court, others attempted to stand their ground at the actual site where the company behind the pipeline, Energy Transfer Partners, continued demolition and construction despite the requests from several federal organizations to stop. Several sacred sites were destroyed in the process.

North Dakota state authorities stripped the tribes of water and other emergency relief aids. On numerous occasions, tribal members were pepper-sprayed and threatened with assault by private security armed with attack dogs. Horses were killed, people were injured and shot with rubber bullets, and hundreds were arrested — including several journalists, one of whom is facing felony charges and up to 45 years in prison.

Photo by Robyn Beck/AFP/Getty Images.

C4CF was in direct conflict with the government. The Standing Rock Sioux, a sovereign nation, was fighting a private corporation and the public authorities who took its side.

Whether one agrees with the Bundy clan or not, there is certainly an established history of people battling government tyranny. And whether they win or lose, the consequences tend to be significant.

The situation in North Dakota, however, is a harrowing example of special interests taking precedence, where state authorities are used as the enforcers of a private company against the people.

If that scares you, well, it should. A group of armed rebels rising up against the state is very different from marginalized people trying to stop a for-profit company from further hurting them.

Photo by Robyn Beck/AFP/Getty Images.

The Native Americans took a stand when diplomacy failed and were bullied just as they've been throughout history. But the white guys who aimed guns at the government walked away scot-free.

In his testimony, Bundy invoked some familiar rhetoric. "It’s for my children, grandchildren," he said. "Everything comes from the Earth, and if [the government] can get control of the resources, they can get control of the people."

That's not so different from the language Native Americans have used time and time again to assert and defend their ancestral homes.

Native Americans protesting the Bundy militants. Photo by Matt Mills McKnight/Getty Images.

Whatever claims might be valid in their grievances, Bundy and his fellow Malheur mutineers still enjoy the perks of white privilege.

Meanwhile, Native Americans continue to suffer, fighting the exact same fight that they've been fighting for hundreds of years against a system that still won't bestow the same freedoms on them.

That's not the same at all.

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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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