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'13th' wasn't around to watch in your history class. 13 reasons to watch it now.

If you see only one Oscar-nominated film this year, make it "13th."

Directed by Ava DuVernay, the stirring documentary explores America's long history of overpolicing and imprisoning black and brown people since the passing of the 13th Amendment. DuVernay sat down with scholars, educators, elected leaders, authors, and activists to tell this troubling but necessary story.

DuVernay (left) interviews scholar and activist Angela Davis for "13th." Image via Netflix.


While these issues are difficult, we need to talk about them and, better yet, do something about them. "13th" truly couldn't have come at a better time.

Here are 13 lessons everyone should learn from this from powerful must-see film.

1. The 13th Amendment had so much promise ... almost.

Section 1 of the 13th Amendment reads:

"Neither slavery nor involuntary servitude, except as a punishment for crime whereof the party shall have been duly convicted, shall exist within the United States, or any place subject to their jurisdiction."

The clause, "except as a punishment for crime whereof the party shall have been duly convicted,"was included so farmers and landowners could essentially continue a form of slavery to support their businesses — so long as the black men and women were deemed criminals. There's no such thing as a throwaway clause in the Constitution. This is an intentional legal loophole.

A political cartoon from 1865 featuring President Lincoln and an amended U.S. constitution. Photo by Hulton Archive/Getty Images.

2. The legal loophole in the 13th Amendment led to mass arrests and incarceration during the late 19th century.

It was the United States' first prison boom.

Black people were arrested en masse for petty crimes, like loitering or vagrancy, and incarcerated. Once labeled criminals, landowners and farmers could "lease" convicts from the state in exchange for full control of their lives.

These convicts were leased to harvest timber. Photo circa 1915, via World Digital Library/State Library and Archives of Florida.

3. While black men filled prisons, popular culture stoked fears.

Black men were portrayed in films as menacing, evil, and in relentless pursuit of white women.

In the 1915 film, "Birth of a Nation," which is essentially three hours of racist propaganda masking as a historical film, a white woman throws herself off a rocky cliff to save herself from being assaulted by a black man. Critics raved, drowning out mounting protests.

As a result of the popular film, membership in the Ku Klux Klan boomed.

Still image from "Birth of a Nation," (1915). Image via "Birth of a Nation"/Wikimedia Commons.

4. As the KKK grew, black people were terrorized and murdered.

Lynchings were used to reinforce white supremacy while traumatizing and terrorizing black people. There was a disgusting entertainment aspect to it, as mobs of white people — including elected officials and community leaders — gathered to watch victims get beaten, shot, and tortured. Picture postcards were made of the swinging, mutilated bodies.

More than 4,000 lynchings occurred between 1877 and 1950 across Texas and the American South.

A large crowd watches the lynching of 18-year-old Jesse Washington in Waco, Texas. Photo via Library of Congress.

5. The murder of Emmett Till kickstarted the Civil Rights movement.

14-year-old Emmett Till was brutally beaten and murdered by a group of white men for allegedly whistling at and flirting with a white woman in 1955. (The woman recently admitted she fabricated at least part of her testimony.) Photos from his open casket funeral and the face of Till's weeping mother sent shockwaves around the country, galvanizing black people and their allies in the fight for equality.

6. But then the War on Drugs started an unrelenting wave of mass incarceration.

Crime started to increase in the early 1960s, and many in power quickly blamed the uptick on the end of segregation. Before long, the word "crime" was a stand-in for the word "race."

Nixon appealed to southern Democrats with thinly-veiled racism and promises to clean up the streets. His rhetorical "War on Drugs" became very real in the 1980s under President Reagan, who threw money, resources, and the full weight of the executive branch behind the issue. A wide swath of an entire generation was essentially removed from the narrative.

President Ronald Reagan and his wife Nancy wave to supporters in November 1984. Photo by Don Rypka/AFP/Getty Images.

7. The numbers are astonishing. Full stop.

In 1970, there were 196,429 sentenced prisoners in state and federal prisons. In 1980, there were 329,821 people in state and federal prisons, and by 1990, that number more than doubled to 771,243.

Today, the American criminal justice system holds 2.3 million people. This is not normal. It is not OK.

8. Republicans are not solely to blame for this crisis. President Clinton did his part too.

In the wake of President Reagan and President George H.W. Bush, appearing "soft on crime" wasn't an option for President Bill Clinton. In 1994, he signed the Violent Crime Control and Law Enforcement Act. It expanded the list of death penalty eligible offenses and included a "three strikes" provision, which meant mandatory life sentences for people convicted of their third felony. It also funded new prisons and provided the budget for 100,000 police officers.

President Bill Clinton. Photo by Paul Richards/AFP/Getty Images.

9. Sadly, there's a lot of money to be made off mass incarceration.

Private correctional facilities made a reported $629 million in profits in 2014, and that's just scratching the surface. From the corporations building and maintaining prison facilities, to the food vendors, health care providers, and equipment and textile manufacturers who keep them running, many companies have a lot to gain from maintaining the status quo.

An inmate stands with handcuffs in San Quentin State Prison. Photo by Justin Sullivan/Getty Images.

10. As mass incarceration starts to get a bad rap, the winds are shifting — and not necessarily for the better.

As mass incarceration and America's prison problem take center stage, legislators and businesses are looking for new ways to redefine the narrative while still making money. What does that look like? For starters, monetizing bail, probation, parole, and house arrest.

Photo by iStock.

11. We can't forget the people and families caught in the struggle.

In 2010, 16-year-old Kalief Browder was arrested for a robbery he insisted he did not commit. Browder was thrown into an adult correctional facility where he would spend nearly three years awaiting trial and almost two years in solitary confinement. In 2013, the district attorney dismissed the case against Browder, and he went home a free — but forever changed — young man.

After many attempts, Browder died by suicide in May 2015.

Browder's story is far too common. Many poor people, especially poor people of color, are locked up for years either awaiting trial or because they cannot afford bail.

ABC News' Juju Chang, Venida Browder, mother of Kalief Browder, and civil rights attorney Paul V. Prestia discuss Kalief Browder's life and death. Photo by Slaven Vlasic/Getty Images.

12. American prisons are intended to punish, but former felons continue to suffer after they have served their time.

Former felons are stripped of voting rights, have difficulty securing employment, applying for aid, and finding housing.

"Ban the box" campaigns that seek to end asking about felony convictions on job and aid applications are popping up across the country, and for many, these initiatives can't come soon enough.

Outreach materials at a press conference for a Ban the Box Petition Delivery to The White House in 2015. Photo by Larry French/Getty Images for ColorOfChange.org.

13. As President Trump settles into office, many are worried about his next moves — and rightfully so.

He repeatedly refers to parts of Chicago as lawless, dangerous, and worse than parts of the war-torn Middle East. He's threatened the city with federal intervention to get the "carnage" under control. His repeated calls to arrest and deport undocumented immigrants tend to include gross mischaracterizations of immigrants as gang members, rapists, or drug dealers.

His "law and order" catchphrase is the same dog whistle Nixon used to kickstart the War on Drugs. His comments about Chicago and other inner cities are stoking fears and playing to the imaginations of his base, much like the horrifying scenes in "Birth of a Nation."

Photo by Mario Tama/Getty Images.

These facts are alarming, but here's what you can do about it.

Use your privilege for good. Pass the mic to voices that may go unheard. Help others register to vote. Support Ban the Box initiatives and organizations that help people with criminal records land on their feet.

Ask to see the numbers. Plenty of police data is publicly available. Check out the numbers in your community. Look at the demographics of people being stopped, arrested, or convicted. Numbers don't lie. Hold your leaders accountable and make them answer for racial disparities.

Stay active in schools. Overpolicing and the criminalization of black people doesn't begin and end with police officers. Black children are nearly four times as likely to be suspended as white children. Ask tough questions of your child's teachers and administrators. Attend school board meetings.

Photo by iStock.

This is no ordinary crisis and it will require extraordinary solutions.

Watch the film, do your part. Let's get to work.

Sponsored

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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