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The actual history of these Confederate statues explains why they should come down.

Robert E. Lee, Jefferson Davis, and P.G.T. Beauregard were responsible for a war that killed more than 600,000 Americans to defend the right to keep millions more enslaved.

Years after the end of that war, the City of New Orleans honored each of the three men with a statue.

Recently, those statues finally came down.


A statue of Robert E. Lee is removed in New Orleans. Photo by Scott Threlkeld/AP.

Mayor Mitch Landrieu delivered an emotional speech commemorating the day Lee's statue was removed from its home in Lee Circle where it had stood for 133 years.

New Orleans Mayor Mitch Landrieu. Photo by Cliff Owen/AP.

Landrieu's speech is remarkable not for its full-throated condemnation of the Confederate figures memorialized in stone, but for addressing why the statues were put there in the first place.

Critics of the move to take the memorials down, which was approved by the city council, insist the statues represent New Orleans' "heritage," and their removal is tantamount to "denying history."

Landrieu's argument — one backed by a growing historical consensus — was that the monuments were not erected as sober tributes to fallen military leaders, but as a political act, decades after the Civil War, in a conscious attempt to whitewash the past.

"The historic record is clear: the Robert E. Lee, Jefferson Davis, and P.G.T. Beauregard statues were not erected just to honor these men, but as part of the movement which became known as The Cult of the Lost Cause. This ‘cult’ had one goal — through monuments and through other means — to rewrite history to hide the truth, which is that the Confederacy was on the wrong side of humanity."

With the end of Reconstruction, which abortively attempted to establish political equality for blacks throughout the South, lawmakers throughout the region began valorizing Confederate figures to assert white control while simultaneously playing down those figures' ties to slavery.

Photo by Kevin McGill/AP.

A 2016 study undertaken by the Southern Poverty Law Center found over 1,500 such public memorials spread across the United States. As Landrieu stated:

"After the Civil War, these statues were a part of that terrorism as much as a burning cross on someone’s lawn; they were erected purposefully to send a strong message to all who walked in their shadows about who was still in charge in this city."

A fourth statue that came down commemorated the Battle of Liberty Place, in which white supremacist vigilantes overran New Orleans, ousting the state's integrationist government for several days.

An inscription on the original Liberty Place monument read: "United States troops took over the state government and reinstated the usurpers but the national election November 1876 recognized white supremacy in the South and gave us our state."

In his speech, Landrieu acknowledged that many of his constituents are emotionally attached to the statues, though they might not be fully aware of the context surrounding their construction.

Protestors rally against removing Confederate monuments. Photo by Justin Sullivan/Getty Images.

The mayor, compassionately, refused to criticize those who support keeping the memorials in place, stressing the importance of learning and maturing:

"So I am not judging anybody, I am not judging people. We all take our own journey on race. I just hope people listen like I did when my dear friend Wynton Marsalis helped me see the truth. He asked me to think about all the people who have left New Orleans because of our exclusionary attitudes."

He continued by asking those protesting the monuments' removal to consider them from the perspective of others, particularly those whose families were affected by the evil legacy of slavery and segregation.

"Another friend asked me to consider these four monuments from the perspective of an African American mother or father trying to explain to their fifth grade daughter who Robert E. Lee is and why he stands atop of our beautiful city. Can you do it?"

There's no easy way to reconcile two versions of history.

The only way to do so is by, as Landrieu asserted, grappling with the past honestly and openly.

Often, the process is slow and painful. It involves acknowledging mistakes, empathizing with others, and letting go of deeply rooted beliefs.

[rebelmouse-image 19528085 dam="1" original_size="750x563" caption="The former site of Jefferson Davis' statue in New Orleans, where the word "love" has replaced the monument. Photo by Kevin McGill/AP." expand=1]The former site of Jefferson Davis' statue in New Orleans, where the word "love" has replaced the monument. Photo by Kevin McGill/AP.

Occasionally, if done meticulously and assiduously, it can lead to lasting reconciliation.

From 1861 to 1865, Confederate leaders, like Robert E. Lee, Jefferson Davis, and P.G.T. Beauregard, fought to keep human beings as property. The following century saw political leaders throughout the United States fighting to deny those same human beings full citizenship — a struggle memorialized by the statues that, until recently, loomed over the city of New Orleans.

Taking down the statues, Landrieu insists, is a necessary first step toward making his community — now inhabited by the descendants of both enslaved people and those who kept them in chains — whole.

"Centuries-old wounds are still raw because they never healed right in the first place," he said in the speech.

Here's hoping that starts now.

You can (and should) read the full speech here.

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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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