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23 facts to pull out the next time someone says, 'Actually, the wage gap is a myth.'

The wage gap is real, but we can put an end to it.

You've probably heard the stat about how for every dollar men make, women make just 80 cents — but there's a lot about the pay gap that might still surprise you.

April 4 marks Equal Pay Day, which represents the number of days this year women have essentially worked "for free" as the result of the wage gap. While the day is an excellent moment to raise awareness about society's inequalities, fighting for fair pay and equal rights is something you can do 365 days a year.

Students at Barnard College attend the school's 2016 commencement ceremony. Photo by Timothy A. Clary/AFP/Getty Images.


If you're in the mood to be surprised, angered, encouraged, or just plain informed, check out these 23 interesting facts about equal pay.

1. Even Batgirl had to fight for equal pay.

2. On average, it takes women 459 days to make as much as men do in a single year. (This is kind of the whole point of Equal Pay Day.)

The British-based National Women's Liberation Movement protests in London in 1971. Photo by Daily Express/Hulton Archive/Getty Images.

3. Even when women "lean in" and negotiate harder, they're less likely to get raises than men.

4. Women lose out on an estimated $419,000 over the course of a lifetime as the result of the pay gap. What?!

A Miami woman protests on International Women's Day. Photo by Joe Raedle/Getty Images.

5. What does a year’s worth of lost wages (an average of $10,470) add up to? For starters: 15 months of child care, 78 weeks of food for a family, 11 months of rent, nearly nine years of birth control, or 1.2 years’ tuition at a four-year public university.

6. Millennial women across the political spectrum say they’re more likely to support politicians who fight for equal pay, including 70% of Republicans, 83% of Independents, and 88% of Democrats.

7. There's some good news: The pay gap is closing. There’s also a bit of bad news: None of us will be alive to see it. One estimate suggests that we’ll be waiting until 2152 for paycheck equality. Ooof!

A cheeky lemonade stand highlights the pay gap. Photo by Molly Riley/AFP/Getty Images.

8. Yes, it’s illegal to pay women less than men for the same work (thanks, Equal Pay Act of 1963!) Unfortunately, it still happens. There's not exactly a whole lot of transparency when it comes to wages, and enforcing the law means an employee has to learn they're being discriminated against and then take their employer to court. Without additional steps to encourage transparency and reduce the possibility of retribution, the law doesn't quite cut it.

9. The first bill President Obama signed into law was the Lilly Ledbetter Fair Pay Act, which got rid of the 180-day statute of limitations on wage discrimination claims. In other words, it made it so that if you found out your employer had been discriminating against you for years, you’d be due damages on the whole time, not just the last six months.

Lilly Ledbetter watches as President Obama signs the law bearing her name. Photo by AP Photo/Susan Walsh.

10. Fun fact: If we eliminated the pay gap, poverty among working women would decline by more than half in 28 states!

11. From a “What can I get on my member of Congress’ case about?” point of view, the Paycheck Fairness Act is a good place to start. The bill would help make wages more transparent, would require your bosses to prove that any differences in pay are actually related to qualifications, and would block companies from retaliating against employees who raise concerns about discrimination. There's a whole list of things you can chat with your Congressperson about when it comes to pay equality.

President Obama signs an executive order banning federal contractors from retaliating against employees who raise concerns about pay discrimination in 2014. In March 2017, President Trump rescinded the order. Photo by Mark Wilson/Getty Images.

12. The pay gap isn’t a myth. It’s math. Even when you control for things like age, experience, race, location, and education, it’s still just as real as ever.

13. Not all states are equally unequal! For example, the pay gap in North Carolina (where women make 86% of what men do) is much smaller than in Wyoming (where women make just 64% of what men do).

Jensen Walcott (right) speaks at the 2016 Democratic National Convention. Walcott was fired from her job for asking for equal pay. Photo by Saul Loeb/AFP/Getty Images.

14. The most surefire way to score a box office hit in 2016 was to cast Scarlett Johansson, that year’s top-grossing actor (that is, her movies made more money than any other actor's). Even so, a quick look at the five highest-paid actors of the year is just a bunch of dudes. Really?

Scarlett Johansson. Photo by Jason Merritt/Getty Images.

15. In 2016, the women of Iceland protested the wage gap by going on strike. In response, lawmakers recently unveiled a five-year plan to get the country to paycheck equality.

16. Women in Australia are trying a similar tactic: walking off the job at 3:20 p.m., the time that women in the country basically start working for free because of the wage gap.

Child care workers march for higher wages on March 8, 2017, in Melbourne, Australia. Photo by Scott Barbour/Getty Images.

17. Despite now being America’s most educated group, black women are hit especially hard by the wage gap, making on average nearly $20,000 a year less than white men. What even?

18. Actress Emmy Rossum took a bold stand for pay equality, pushing to get paid the same as William H. Macy, her male counterpart on the set of Showtime’s “Shameless.” And guess what? It worked. She even got paid back wages for earlier seasons.

Emmy Rossum. Photo by Monica Schipper/Getty Images for Variety.

19. So did “Star Wars” actress Felicity Jones.

20. As did “X-Files” actress Gillian Anderson.

"X-Files" stars David Duchovny and Gillian Anderson. Photo by Frederick M. Brown/Getty Images.

21. One way companies can show they're taking the fight for wage equality seriously is by getting EDGE (Economic Dividends for Gender Equality) certified. If you're in a position to push the company you work for to get involved, give it a shot!

Image via iStock.

22. Another thing you can do is support companies that met President Obama's 2016 Equal Pay Pledge and encourage other companies to make similar public statements.

23. And if you're looking to hone your own negotiating skills, there's even a Facebook chat bot that'll help you navigate your way to a fair wage.

No matter your gender, equal pay is something worth fighting for — and yes, there are things you can do to help out.

The above list has a few suggestions, but you can learn about other ways to help out over at the American Association of University Women's website. Every week, they post a new action you can take to help build a better, more fair world for us, our children, grandchildren, and beyond.

A Fort Lauderdale, Florida, woman joins a March 14, 2017, protest calling for equal pay. Photo by Joe Raedle/Getty Images.

We all have an important role to play in fighting discrimination. Whether you're a man, a woman, a business owner, a legislator, or just someone who believes in equality, there are concrete steps people can take.

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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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Given that language evolves so rapidly, it’s hard to imagine what people sounded like 200 years ago, let alone 500 or a thousand. Even when we watch movies about ancient civilizations, the characters usually speak in a language similar to the audience, giving us a false sense of what people in those times were like.

The folks at Equator AI are giving people a realistic idea of what people in ancient civilizations sounded like by recreating the languages of 15 languages that haven't been heard in centuries. In the video, the languages are spoken by computer-generated recreations of people who lived in that era.

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We all love a romantic love story, but it's just as fulfilling to witness these platonic love stories play out.

Ted and Rebecca's friendship is one of the best things about the "Ted Lasso" series.

"Ted Lasso" has wrapped up its third and final season, leaving people analyzing and debating and feeling all kinds of feelings about the series and its characters.

Since watching the final episode, I've been thinking about what I've loved most about the show, because seriously, there's a lot to love. Ted himself, of course. The quirky cast of characters. The humor. The triumph and redemption. Roy Kent's grumbles. Sam Obisanya's everything.

Then there are the relationships, which is where the show really shines. Not so much the romantic relationships—those were somewhat meh in the end—but the way the show portrayed genuine platonic love in its various hues. Considering how many shows (over)utilize romance and sex for dramatic effect, it was refreshing to see multiple relationships develop and deepen over three seasons without any romance involved.

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"Imagine telling them that their free unlimited minutes only started after 9:00 and on the weekends."

Things Gen Z would be outraged by that were normal for millennials.

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Dwight Thomas uploaded a video to TikTok listing things that millennials grew up with that the generation below him would be outraged by. As someone who would be considered an elder millennial by some people, I'd have to agree. The man makes some valid points about things we experienced as teenagers that would likely make teens today aggressively send out Change.org petitions.

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Meet the 11 outstanding nonprofits that took home this year’s Classy Awards

Each organization has gone above and beyond to make our world a better place.

All images provided by the Classy Awards, used with permission

Give these organizations all the awards

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Since 2009, the Classy Awards have celebrated nonprofits for their unique approaches to making our world a better place for everyone. Winners are given a platform to amplify their cause and showcase the positive impact of their programs.

This year, we are proud to announce that the Classy Awards have partnered with Upworthy, and we are thrilled to shine a spotlight on the 2023 winners.

From championing gender equality, to massively reducing food waste, to providing trade-based skills training to the neurodivergent community, each organization has made an incredible contribution to the betterment of our world.

Collectively through their efforts, nearly 1.5 million people and animals were served across 34 countries worldwide last year alone. That’s a win in itself.

Check out the 11 winners for 2023 below:


​412 Food Rescue

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In an effort to address the growing concern of food waste, hunger, and environmental sustainability, 412 Food Rescue uses an innovative app to match volunteers, aka Food Heroes, with other organizations that might have a surplus of perfectly good but unsellable food that would otherwise be wasted and redirect it to people who need it.

Food Heroes has redirected 137 million pounds of edible food from landfills to the people who need it most.

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"It reminds me of Howard Stern's question to me. 'Tell me, governor, what happens to us when we die?' I said, 'Nothing. You're 6 feet under,'” he told DeVito.

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