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Field trips cost money. So they came up with a brilliant plan to bring the fun straight to kids.

Instead of bringing the kids to the world, this nonprofit is bringing the world to kids.

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TOMS One for One

At my middle school, the “cultural education" element of Spanish class consisted of reading about Spanish-speaking countries in a textbook ... and an annual potluck day.

Don't get me wrong — I love a good tamale as much as the next person! But eating culturally inspired meals can only get you so far in terms of cross-cultural understanding.

Teachers and schools understand this, too, which is why field trips and visits to museums are built in to most schools' curricula. But that can be expensive, and many schools don't have the funds to take their students off-campus to learn about other cultures very often.


The Connecting Cultures Mobile Museum is a great solution to small field trip budgets. GIFs via ConnectingCulturesMM/YouTube.

One nonprofit saw this problem in their own backyard, so they devised an ingenious solution to provide cultural education to under-resourced schools.

Instead of bringing the kids to a museum, they would bring the museum to the kids.

Los Angeles' Connecting Cultures museum on wheels is now 20 years old, and thousands of kids (most of whom attend low-income schools) have gotten to see the world each year, all without leaving their own campuses.

The mobile museum has three main exhibits.

There's the commercial collection, which focuses on resources, trade, and colonization. The spiritual exhibit teaches kids about world religions, rituals, and music.

But my favorite is the "Everyday Connections" exhibit. It shows kids the stuff that other cultures considered parts of their day-to-day lives — boring details that we probably wouldn't think to share but are actually super-interesting to learn about. Students get to try on clothes that people from other countries wear, see what games they play, and learn about what other cultures cook and eat.

Image provided by Connecting Cultures.

Remember how awesome it was when the Scholastic Book Fair set up shop at your school for a week?

The whole idea of the museum-on-wheels is kind of similar … except instead of buying books, students get to learn about other countries' ways of life.

Students can grind and taste their own spices at the museum.

The museum staff drive to different schools each week to set up a collection of artifacts in a big room inside the school, like the library. Kids get an opportunity to explore the museum during their social studies class. They learn about the artifacts — but unlike some museums, they also get to pick up and touch some of the things on display.

That means there isn't a glass case between you and the thing you're supposed to be learning about — it's right there in front of you.

Image via Connecting Cultures.

This is especially important because we all learn in different ways. Some students may be able to absorb lots of information about, say, what goes on in a Moroccan marketplace by seeing a market on a video and hearing the market's ambient sounds. Other students might learn better by handling a 50 dirham note or touching the fabric that a vendor might sell.

The point here is that there's a huge difference between looking at a picture in your world geography textbook and actually holding a piece of culture in your hands.

Kim Moreno, a teacher at a school that hosted the mobile museum, said the exhibit allowed her students — a group of kids with diverse, international backgrounds and families — to understand each other better. Rather than relying on stereotypes, the mobile museum gave them a way to see other cultures as three-dimensional and real.

This is the type of learning that I can really get behind.

The Connecting Cultures Mobile Museum leaves a lasting impression on students, and we need more programs like it

In the words of the mobile museum's founder, Valerie Lezin, “I can take kids from bewilderment to understanding, and from shock to acceptance."

Check out this video of students getting the full mobile museum experience 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.

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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.

Should babysitters be expected to clean?

When it comes to babysitting, you can hit the jackpot with someone who not only enjoys hanging out with your kiddos but also cleans out of boredom. The only babysitter I've had that experience with is my mom, but I do hear they do exist. While walking into a spotless house after a much-needed night out would be amazing, it's not really part of a standard babysitting package.

Typically, whoever babysits for you is solely there to focus on the well-being of your children. They feed them snacks, play games with them, and follow their bedtime routine to the letter. Then they hang out on your couch reminding Netflix that they're still watching and wait for you to return. Sure, they clean up dishes from dinner and whatever toys were pulled out during their time with your kids, but they don't typically clean your house.

But in a private parenting group I belong to, a long debate was started when a mom asked a group of 260k of her closest friends if it would be appropriate for a parent to ask a babysitter to clean their home.

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Pop Culture

Guy with 90s-style radio show on TikTok is actually changing lives for aspiring musicians

"The Bun 91.3" is giving unknown artists massive followings and even record label deals.

This guy rocks.

TikTok is a place where obscure music is celebrated, retro comedy is king and lives can be changed overnight. But it’s a rare feat for all three of those corners to intersect on the platform.

As is the way with many TikTok sensations, faux radio show “The Bun 91.3” started off as a fun hobby. The DJ, known only to listeners as “The Bun,” highlights songs by up-and-coming artists all while sporting aviator sunglasses and mastering that cheesy, old-school radio voice.

Much to his surprise, The Bun’s passion project has actually been bringing major attention to aspiring musicians who might otherwise go unnoticed, just like real radio shows did back in the day.

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@thehalfdeaddad/TikTok

Dad on TikTok shared how he addressed his son's bullying.

What do you do when you find out your kid bullied someone? For many parents, the first step is forcing an apology. While this response is of course warranted, is it really effective? Some might argue that there are more constructive ways of handling the situation that teach a kid not only what they did wrong, but how to make things right again.

Single dadPatrick Forseth recently shared how he made a truly teachable moment out of his son, Lincoln, getting into trouble for bullying. Rather than forcing an apology, Forseth made sure his son was actively part of a solution.


The thought process behind his decision, which he explained in a now-viral TikTok video, is both simple and somewhat racial compared to how many parents have been encouraged to handle similar situations.
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Woman proves social media is fake by using filters.

Social media has made it very easy to alter your appearance using filters. They may come in handy when you need to record a video but look a bit under the weather—just turn on a soft glow or a makeup filter, and boom, you're camera-ready in less than two seconds. But there has been a lot of talk around the use of filters and teen girls' self-esteem and unrealistic expectations seemingly placed on women.

One woman has taken it upon herself to strip away the filters to prove that, while she is beautiful, her face doesn't actually look the way it does with the filter on. The most interesting thing about these filters is that they're so good, you can't tell they're filters. Gone are the days of filters that made everyone look like a Glamour Shot from the 90s. These filters move with you and even have pores so no one can tell it isn't actually your face.

Well, it is your face—kinda.

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Barack Obama speaking at the World Travel & Tourism Council, 2019

If you’re looking for career advice, there are few better people to ask than former President Barack Obama. After all, he got the most prestigious job in the world after only spending four years in the U.S. Senate and seven in the Illinois State Senate.

Obama clearly knows how to work his way up in the world.

Now, he’s investigating what it means to have “good” work in his new Netflix show, “Working: What We Do All Day.” According to Netflix, the show explores compelling ideas and issues about labor and work, while focusing on the lives of individuals in various professions.

Obama sat down with LinkedIn Editor-in-Chief Daniel Roth to talk about employment-related topics, including the role of work in our lives, disruptions in the workplace in the new Millenium, and the coming AI revolution. During the 15-minute conversation, Obama shared his most important career advice for young people, and it was simple, especially for such a thoughtful, well-spoken man. The former president said, “Get stuff done. Just learn how to get stuff done.”

He then unpacked what he meant by his simple motto.

“I've seen at every level people who are very good at describing problems, people who are very sophisticated in explaining why something went wrong or why something can't get fixed, but what I'm always looking for is, no matter how small the problem or how big it is, somebody who says, 'Let me take care of that,'” Obama said. “If you project an attitude of, whatever it is that's needed, I can handle it and I can do it, then whoever is running that organization will notice. I promise.”

Obama is spot-on with his analysis. You can talk about things all day, but what really matters is taking action and making things happen. Maybe that’s why his campaign slogan in 2008 was a simple three-word phrase about taking care of business, “Yes, we can.”

"The best way to get attention is, whatever is assigned to you, you are just nailing. You're killing it. Because people will notice, that's someone who can get something done," Obama continued.

As someone who has managed people at the top levels of government, Obama has a rare understanding of the importance of relying on people to carry out essential orders and knowing who to trust to get it done efficiently and correctly. When you’re president of the United States, you must have complete trust in the people you delegate work to because thousands or even millions of lives could be at risk.

Obama also added that young people shouldn’t focus on a specific job title but on things that interest them. "The people that I find are the most successful are the people who say, 'I'm really interested in computers and figuring this stuff out,' and they end up being a Bill Gates," he said.

People will be happier with careers that are rooted in their interests because they’re doing what they love. We only get 24 hours in a day. Most people sleep eight, work eight and enjoy eight for themselves. Everyone loves sleeping and time off, but you can be happy 24 hours a day when you love your job.

Photo by Andrew Gaines on Unsplash

Firefighter Jeff Ohs resuscitated Xavier Dimples as a toddler.

We all know that Upworthy loves a good hero story. Suddenly humanity seems a little less dark after hearing about students coming to their teacher’s rescue, moms taking on entire swarms of bees to keep their kids safe or entire bank heists being thwarted by a single hug.

However, we rarely get a glimpse of what happens after those feel-good stories take place. It’s not often that we get to witness firsthand the lasting impact made from one good deed. That’s what makes this story so special.

Xavier Dimples was only 2 years old when his house caught fire, leaving him trapped inside. Without a firefighter named Jeff Ohs bravely entering the burning building to pull the toddler out of the wreckage and resuscitating him, Dimples would have perished.

Twenty-three years after the incident, Dimples was able to reunite with Ohs, introducing him to his son who was the exact same age as Dimples when Ohs rescued him.

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