+
Most Shared

They'd never seen a computer. Now they're training to be the tech experts of tomorrow.

True
Johnson & Johnson Caring Crowd

Over 247 million children in Sub-Saharan African countries have no school supplies. Not even a backpack.

[rebelmouse-image 19397746 dam="1" original_size="3456x2304" caption="Photo courtesy of CodeToHope." expand=1]Photo courtesy of CodeToHope.

Sub-Saharan Africa has one of the highest poverty rates in the world. And with all money going toward food, shelter, and tuition fees (many schools aren't free), parents are often unable to afford the supplies their children need to succeed. That's why it's not uncommon for kids to show up to school empty-handed.


But that's just one of the factors that puts Sub-Saharan Africa at the top of the list for education exclusion. According to the United Nations Educational, Scientific and Cultural organization (UNESCO), more than one-fifth of children between the ages of 6 and 11 aren't in school. That number increases to one-third among children between the ages of 12 and 14. And by the time they're 15, over 60 percent of children are no longer attending school.

Thankfully, there is an organization working to bridge the education gap. It's called CodeToHope.

[rebelmouse-image 19397747 dam="1" original_size="735x750" caption="Philemon Padonou distributing laptops to a teacher. Photo courtesy of CodeToHope." expand=1]Philemon Padonou distributing laptops to a teacher. Photo courtesy of CodeToHope.

CodeToHope is a non-profit dedicated to bringing technological skills training to youth who may have never experienced it otherwise due to lack of access. The organization was founded by Philemon Padonou, an engineer who grew up in the Benin Republic of West Africa and then moved to The United States to work and learn English.

When he enrolled in computer science classes in the US, though, Padonou made an important discovery: His lack of early computer literacy was holding him back.

"One of the biggest setbacks for him was that he couldn't type as fast as his peers," says Jacqueline Gaston, a Technology Services Analyst with the organization.

"His assignments were taking so much longer, even though he understood the material in the same way his peers did. These basic computer literacy skills, which he had to pick up on the spot, would have given him more opportunities."

So Padonou decided that he had to find a way to give those skills to the kids in his community. He was going to offer them an education in digital literacy so they could have opportunities that he didn't.

CodeToHope's goal is to fight poverty by giving future leaders the tools they need to empower their communities. That meant starting with the bare necessities.

[rebelmouse-image 19397748 dam="1" original_size="750x500" caption="Photo courtesy of CodeToHope." expand=1]Photo courtesy of CodeToHope.

Since its launch in 2016, CodeToHope has provided over 1000 children with backpacks full of supplies.

"The backpacks have notebooks, pens, pencils and a ruler," says Gaston. "Things that we would consider as being basic necessities. For some students, even buying this is unattainable." The kits also contain mosquito nets to help students prevent the spread of malaria. 90% of all malaria cases occur in Sub Saharan Africa, and two-thirds of those who succumb to the disease are children under the age of five. Even giving kids this seemingly meager protection can help keep them in school, and may even save their lives.

And these supplies are only one part of CodeToHope's campaign against poverty. The second part is all about technology.

[rebelmouse-image 19397749 dam="1" original_size="750x750" caption="Photo courtesy of CodetoHope." expand=1]Photo courtesy of CodetoHope.

The organization's main thrust is to provide children living in Sub Saharan Africa with access to computers and the education they need to become experts in the field of technology. Such access, the people at CodeToHope believe, will not only provide more opportunities, but allow communities to create better links to healthcare, knowledge and economic growth.

To date, CodeToHope has donated more than 400 computers to schools in Benin, which has, in turn, allowed the non-profit to serve nearly 3,000 students in the short time they've been an active organization. CodeToHope also arranges for expert mentors to teach children how to use the new devices — something that's incredibly important in a place where there's no oversight on digital education.

And this is just the beginning of CodeToHope's initiatives.

In 2019, CodeToHope plans to harness solar power to help the remote villages of Ganvie and So-Ava gain access to reliable electricity for the first time. The hope is that electricity allows for major improvements to occur, which may help bring the community together.

"Our model isn't to go in and provide help and leave. We're trying to create a sustainable model where we can help communities and make sure that we're having a positive impact."

The idea is that the education provided by this project will help prepare these children for the ever-changing world around them, which will, in turn, go miles to improve the overall health of their village, as there is a known correlation between education and health conditions of an area.

"We're not trying to fix their problems. We're trying to enable them to fix their own problems."

CodeToHope is only growing, and that's largely thanks to Johnson & Johnson's initiative, CaringCrowd®.

[rebelmouse-image 19397750 dam="1" original_size="750x503" caption="Photo courtesy of CodeToHope." expand=1]Photo courtesy of CodeToHope.

Philemon Panodou works at Johnson & Johnson. The company's credo  — to put the needs and well-being of those the company serves first — is actually what inspired him to create CodeToHope. It's also where he was first introduced to the logistics of creating a non-profit and where he secured initial funding. When Panodou began looking for gently used computers to bring to Benin, his J&J colleagues donated some along with funds.

Today, two of CodeToHope's major projects have been funded via CaringCrowd — a new type of fundraising platform that utilizes the power of social sharing to do good and improve wellbeing on a global scale.

CaringCrowd allows people like you to make the goals of non-profits around the globe a reality. Each project is independently reviewed by a team of outside experts so you know the money you pledge is going to a reputable place.

Best of all, Johnson & Johnson will match up to $250 per person per project as long as funds last. So the more we share the projects we're passionate about, the more monetary momentum they gain.

That means more backpacks, more computers, and more education for children in Benin and beyond.

The fight against poverty is long and arduous. But every notebook, pencil, mosquito netand computer brings CodeToHope one step closer to transforming the lives of the children who need it most — widening their futures to a dazzling array of opportunities they may have never had otherwise.

With organizations like this and people like Panodou constantly fighting for a better world, those brighter futures are entirely possible.

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.

Ring doorbell video captures what it's like to be the default parent.

Kids, man. I'm not sure of the scientific way audacity is distributed, but kids have a lot of it and somehow make it cute. That audacity overload is especially interesting when you're the default parent—you know, the parent kids go to for literally everything as if there's not another fully capable adult in the house. Chances are if your children haven't sought you out while you were taking a shower so you could open up a pack of fruit snacks, then you're not the default parental unit.

One parent captured exactly what it's like to be the default parent and shared it to TikTok, where the video has over 4 million views. Toniann Marchese went on a quick grocery run and *gasp* did not inform her children. Don't you fret, they're modern kids who know how to use modern means to get much-needed answers when mom is nowhere to be found. They went outside and rang the doorbell.

Back when we were children, this would've done nothing but make the dogs bark, but for Marchese's kids, who are 3 and 6 years old, it's as good as a phone call.

Keep ReadingShow less

Little girl shocks her mom by pulling out a pocket full of worms

Kids will absolutely test all parts of your personality. Not out of malicious intent, but simply because kids are innocent and don't don't understand unspoken social rules, especially when they're very little. One of those seemingly common sense unspoken social rules is that you don't go to the nail salon with worms in your pockets.

Scratch that, you don't walk around with worms in your pocket, period. That is unless you're on a fishing boat and you're in charge of bait and you run out of room in the canister filled with worms. I mean, there are a lot of things that would have to come into play to make having worms in your pocket socially acceptable. But kids don't know that, and one little girl, Kylee Grace, gave her mom a shock after they left the nail salon one day.

In the video posted to TikTok, which has now gone mega-viral with over 11.5 million views, Kylee and her mom are walking down the sidewalk after getting their nails done. Jenae, the little girl's mom, asks her daughter if she has a worm in her pocket. Then things quickly get hilariously weird.

Keep ReadingShow less
@geaux75/TikTok

Molly was found tied to a tree by the new owners of the house.

Molly, an adorable, affectionate 10-year-old pit bull, found herself tied to a tree after her owners had abandoned her.

According to The Dodo, Molly had “always been a loyal dog, but, unfortunately, her first family couldn’t reciprocate that same love back,” and so when the house was sold, neither Molly nor the family’s cat was chosen to move with them. While the cat was allowed to free roam outside, all Molly could do was sit and wait. Alone.

Luckily, the young couple that bought the house agreed to take the animals in as part of their closing agreement, and as soon as the papers were signed, they rushed over to check in.
Keep ReadingShow less

A Golden Retriever taking a break on the floor.

If you’re having trouble meeting a romantic partner, research shows you could improve your chances by getting a dog. A 2020 YouGov study found that 50% of Americans would be more willing to date someone if they had a dog, while only 9% would be less willing to do so.

Women are more interested in meeting someone with a dog (54%) compared to 46% of men.

People are more attracted to dog lovers for a pretty simple reason. They assume that those who have dogs are better at having long-term relationships. “People might infer that a dog-walking man knows how to form lasting attachments, has the resources to care for someone else (dog ownership is expensive!), and is reliable enough to do the daily work involved with dog ownership,” Theresa E. DiDonato Ph.D. writes in Psychology Today.

Keep ReadingShow less
Family

Mom calls out 'weaponized incompetence' by flipping the script on parental expectations

Hearing a woman say these things is ridiculous, and that's the whole point.

@clarabellecwb/TikTok

Too real. Tooooo Real.

While marriages are by far much more egalitarian than they have been in decades past, many women will tell you that when it comes to emotional and domestic labor, they still take on the lion’s share of responsibility.

Many women are using TikTok to call out this imbalance, even going so far as to share how it led to them filing for divorce. As for Clare Brown, she’s opting to illuminate the issue in a more satirical way.

Brown has amassed over 400,000 followers on her TikTok account, where a major part of her schtick includes what she calls “flipping the script” on social issues. And as of late, it’s her focus on parenting expectations that has people—particularly fed up moms—nodding in agreement.

In a series titled “flipping the script on weaponized incompetence,” Brown pokes fun at fathers who remain willfully ignorant by asking their partners for help on even the most basic tasks, thus escaping the responsibility of pulling their weight.

Keep ReadingShow less

Redefining comfort: Your guide to seamless athletic leggings for women

Experience the perfect balance of comfort and style with women's seamless athletic leggings.

Editor's Note: Upworthy earns a percentage of revenue from the sale of items mentioned in this article.


In athletic wear, a good pair of leggings can make or break your workout experience. Comfort, flexibility, and style are key factors contributing to the perfect pair, and finding ones that marry these elements seamlessly can be challenging. Whether you're a yoga enthusiast, a gym-goer, or someone who values comfort in their everyday attire, these seamless leggings offer something for everyone. Dive in to discover the perfect pair that will elevate your athletic wardrobe and enhance your workout routine.

Keep ReadingShow less