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WWI vets got the short end of the stick in the Great Depression. This was their answer.

Veterans risk their lives in the name of their country. But they often end up vulnerable when they return home.

On some occasions throughout our history, treatment of veterans has gotten so bad that it has led to major political change.

That's what happened on July 28, 1932, in Washington, D.C., when a confrontation between homeless vets and U.S. military personnel so outraged the public that it swayed a presidential election and had major repercussions.


The aftermath of the military action against the vets and their families is eerie at the Anacostia Flats with the Washington Monument in the background. Image via "Bonus Army"/PBS.

President Herbert Hoover, a Republican, was faced with an unsightly controversy: Thousands of destitute veterans had been camped out in the capital, forming one of several "Hooverville" encampments around the country. Hoover ordered the nation's military to march on the veterans, torch their makeshift homes, and run them out of town.

His opponent in the coming election, Democrat Franklin Delano Roosevelt, knew the move would incense the public. Upon hearing the news, he is said to have remarked, "Well, this will elect me."

The clash was one of the darkest chapters in the history of American veterans and still resonates today.

The unrest began when veterans demanded their lost wages be paid sooner than Congress wanted to.

When veterans of World War I returned home in the early 1920s, they petitioned Congress to offer some sort of compensation for lost wages; military pay was far below what they could have earned at home in the factories. Congress passed a law to compensate them, but the certificates issued to the veterans were not payable until 1945.

Meanwhile, in 1932, the Great Depression was in full swing, and those veterans became part of the destitute masses who had no money, no food, no jobs, and, in some cases, no homes.

Veterans eventually took to the streets. Here's a flier for the march. Image via Library of Congress.

Unemployment nationwide reached nearly 24% that year, so prospects were dim for everyone.

Feeling like they'd been rather chewed up and spit out by their country after doing what they felt was their duty, 15,000 to 20,000 veterans made their way to Washington to set up camp and make their case. They were known as the Bonus Expeditionary Force, later shortened to the Bonus Army.

They occupied abandoned structures along Pennsylvania Avenue between the Capitol and the White House and set up camp in nearby parks and the Anacostia Flats, a swampland east of the Capitol that had been converted into a park in the early 1900s. Those areas swam with tent cities and even some shacks erected from nearby scrap piles. Such encampments were known as "shantytowns" or "Hoovervilles" after the president who would not meet with them, talk to them, nor hear their stories.

These makeshift homes were filled with veterans from The Great War, both black and white, along with their families.

One of the shantytowns in the Anacostia Flats in 1932. Image via Library of Congress.

Protesters in Hooverville camps wanted to convince the public to support their cause.

Conditions of the camps were as shipshape as they could muster, and the veterans were highly disciplined, with their own post office, library, and newspaper. It was thought that if they did not keep things clean and organized, the public might go against them.

Another view of Hooverville shantytowns in the Anacostia Flats. Image via Library of Congress.

In fact, there was a risk of this; the infamous tactic of the Red Scare was used against them by Hoover and his military commanders. Basically, they were called Communists and agitators. It was to no avail, however; these tens of thousands of citizens remained within a stone's throw of the White House — sometimes on the lawn itself — and they continued pushing for relief.

"I never saw such fine Americanism as is exhibited by you people. You have just as much right to have a lobby here as any steel corporation. Makes me so damn mad, a whole lot of people speak of you as tramps. By God, they didn't speak of you as tramps in 1917 and '18." — Retired Marine Corps Gen. Smedley Butler, speaking to the veterans.


On June 15, 1932, with pressure mounting, the House of Representatives passed the Patman Bonus Bill, which would have taken care of the bonus payments in cash immediately. But in what sounds like something out of today's headlines of partisan politics, the Senate shot it down two days later, by a vote of 62-18.

More veterans head to Washington via rail car. Image via Wikimedia Commons.

Thousands of veterans headed to Washington in response to the defeat of the legislation to compensate them.

Initially, the local police were cooperative and even sympathetic; their chief, Pelham Glassford, had been a World War I veteran himself.

The Bonus Army camps out on the Capitol lawn, July 1932. Image via Library of Congress.

But by the end of July, some of the officialdom in D.C. had grown weary of these veterans. On July 28, Secretary of War Patrick Hurley ordered police to evacuate the buildings that the veterans occupied. In the skirmish that ensued, two veterans were killed.

The police begin their "removal" of the veterans. Image via National Archives.

Hoover then made the fateful order: The Army would rout them from the city entirely.

It was none other than Gen. Douglas MacArthur, with the help of Maj. Dwight Eisenhower, that removed the 1932 Bonus Army from the city, with an assist from Maj. George Patton, who was in charge of the cavalry brigade that headed the action.

They first cleared the abandoned buildings, then MacArthur made a decision to follow the veterans into the Anacostia Flats.

Hoover, sensing the political catastrophe this entire episode might create, twice sent word to MacArthur not to cross the 11th Street Bridge that led to the flats.

MacArthur ignored Hoover's suggestions and moved his troops ahead.

One of the Hooverville shantytowns burns in the Anacostia Flats with the Capitol dome in the distance. Image via National Archives.

The soldiers marched on the veterans and their tent homes, setting them ablaze.

Tear gas canisters flew ahead of them, bayonets flashed in the sun, a machine-gun brigade brandished its terrifying weapons, and a half dozen tanks lined up behind them for visual reinforcement.

The cavalry on its way to rout the veterans and begin the inferno. Image from "Bonus Army"/PBS.

When it was over, at least one baby died from the tear gas, and one veteran's wife miscarried from the same. Added to this toll were the two veterans killed by police a few days earlier, and 54 injuries from both skirmishes.

Almost immediately, MacArthur held a press conference where he tried to perform impromptu damage control, claiming the Bonus Army was composed of revolutionaries and Communists and that they had threatened the very institution of government.

Hoover's statement the next morning called into question the patriotism and loyalty of the veterans.

It didn't work; the general public held it against Hoover during the presidential elections that year. In newsreels at movie theaters nationwide, a chorus of boos would erupt when news of the military action against veterans took place.

Roosevelt was elected by a massive margin later that year. In addition, the Democrats won significant majorities in both houses of Congress.

While FDR himself did not support the Bonus Army, he did not forget the political cost that actions such as those perpetrated by Hoover exacted. Soon after his election in 1932, FDR established the Civilian Conservation Corps, which created jobs for 25,000 veterans and other Americans. Similarly, when a smaller Bonus Army went to D.C. a year later, rather than send troops, he sent Eleanor to meet with them.

A 1932 Bonus Army "cinderella stamp." Image via Steve Strummer/Wikimedia Commons.

In 1936, Congress passed legislation to honor all bonus payments — nine years early.

Ultimately, the plight of veterans led to the Servicemen's Readjustment Act of 1944 — known as the G.I. Bill of Rights — which offered multiple benefits, including college education for veterans, though it was rife with racial bias against African-Americans.

Here's a short video explaining the Bonus Army demonstrations, including testimony from eyewitnesses. The original 30-minute version is by PBS.

Politicians risk a lot when they treat veterans with callousness — and worse.

When unemployment benefits, food stamps, or other programs that help veterans are slashed, there are ramifications. And when deplorable conditions at VA hospitals are brought to light, it casts a shadow on whatever administration is in power at the time.

The story of the Bonus Army should make politicians more cautious when it comes to veterans' issues, but it shouldn't have to come to that. Veterans — like the rest of us — have a right to a good home and a good job in the United States of America.

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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

1/11

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.

Island School Class, circa 1970s.

Parents, do you think your child would be able to survive if they were transported back to the '70s or '80s? Could they live at a time before the digital revolution put a huge chunk of our lives online?

These days, everyone has a phone in their pocket, but before then, if you were in public and needed to call someone, you used a pay phone. Can you remember the last time you stuck 50 cents into one and grabbed the grubby handset?

According to the U.S. Federal Communications Commission, roughly 100,000 pay phones remain in the U.S., down from 2 million in 1999.

Do you think a 10-year-old kid would have any idea how to use a payphone in 2022? Would they be able to use a Thomas Guide map to find out how to get somewhere? If they stepped into a time warp and wound up in 1975, could they throw a Led Zeppelin album on the record player at a party?

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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.

via Pexels

People living to work, not working to live.

If we looked 60 years into the past, there are a lot of things that were accepted as “normal” that today most people find abhorrent. For example, people used to smoke cigarettes everywhere. They’d light up in hospitals, schools and even churches.

People also used to litter like crazy. It’s socially unacceptable now, but if you lived in the ’70s and finished your meal at McDonald’s, you’d chuck your empty styrofoam container (remember those?) and soda cup right out of the window of your car and onto the street.

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Mom has comical response to commenters who complained she was too old for her outfit choices

She made the cardinal offense of being 37 and daring to not dress like a grandma.

Mom responds to critics in the most comical way.

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Jessica Buwick, a mom on TikTok, found out fairly quickly that people still have interesting ideas about how "old people" should dress when going out in public. The 37-year-old mom ordered a plethora of outfits to try on to wear for her son's graduation, prompted by her seeing other moms on social media dressing much more fancy for graduations than parents did when she graduated.

It was a silly, lighthearted video showing her trying on all of the outfits that did not make the cut for various reasons. One was too short and didn't zip. Another was ill-fitting and confusing. They were obvious catastrophes that just didn't work, so she made the misfortune into funny content. And people had a lot to say.

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Pency Lucero taking in the Northern Lights

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Traveler and content creator Pency Lucero was willing to take that gamble. After thorough research, she stumbled upon an Airbnb in Rörbäck, Sweden with an actual picture of the northern lights shining above the cabin in the listing. With that kind of photo evidence, she felt good about her odds.

However, as soon as she landed, snow began falling so hard that the entire sky was “barely visible,” she told Upworthy. Martin, the Airbnb host, was nonetheless determined to do everything he could to ensure his guests got to see the spectacle, even offering to wake Lucero up in the middle of the night if he saw anything.

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Man makes an extra $10,000 a year renting out his driveway

If you've got the space, why not rent it out?

The Brighton Pier in England

With the cost of living skyrocketing, people are looking for clever ways to make an additional buck. The good news is there are many ways to make extra money, whether driving for Lyft, freelancing on Fiverr, babysitting through Care.com, running errands with Task Rabbit or renting your pool out with Swimply.

Joe Gorham, 54, of Brighton, England, told The Mirror that renting out the three parking spaces in front of his home was a low-key way to rake in some passive income with little effort.

He said that renting out the spaces brings in an additional £8,000 ($10,000) annually. The money comes in extra handy because he is a full-time caregiver for his partner.

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Can't really blame her.

Invisible work,” aka “invisible labor,” was a term coined in 1987 by socialist Arlene Kaplan Daniels to describe unseen, unacknowledged and unpaid work most often performed by women—though in an academic sense, it pertains to all marginalized groups.

The unpaid aspect, Daniels noted, has been a particularly important factor, since in Western society we have come to believe that it isn’t work unless there’s monetary pay involved. This philosophy has a two fold effect. One, even things that are enjoyable and easy are considered work if you receive an income from them. And two, domestic duties like childcare and house cleaning, no matter how arduous they are, are not recognized as work simply because they don’t result in a paycheck.

It’s easy to see how this widely accepted concept falls short of reality, especially for women performing said domestic duties with little to no recompense. What’s more, many women now have to balance out these tasks, which require time and effort, with a “real” job just to make ends meet.

That’s why more and more women are making their invisible labor impossible to ignore, be it in lighthearted or more serious ways.
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