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Meet 4 moms who created the one toy they wish they had as kids.

Being told that girls are weak and soft and that boys are aggressive and unemotional is about as played out as the Macarena and Harlem Shake. Yet, it still happens often in our society.

We've all witnessed gender stereotyping in our daily lives, but what impact does it have on our children?

A big one.


Studies show that stereotypes can significantly limit a child's full potential and happiness by ignoring who they truly are in order to "fit in" to what society expects of them.

The world can be a confusing place for our children at times. Image via iStock.

But there is some good news, and it comes in the form of toys, which are scientifically proven to help kids learn.

Here's the story behind four cool toy companies you may not have heard of that are shattering stereotypes and helping kids believe they can be anything they want to be.

1. For mom and psychotherapist Laurel Wider, it all started when she heard her son say boys aren't supposed to cry.

The market is full of toys that encourage little girls to express empathy and emotions, but what about the boys? Wider felt she had to do her part to help little boys embrace their sensitive sides.

Enter Wonder Crew. Each 15-inch doll combines the adventure of an action figure with the emotional connection of a stuffed animal. Guess what? Little boys love them.

Boys can be nurturing, too. Photo from Wonder Crew, used with permission.

"Wonder Crew is a part of a new conversation about boys' potential and how feelings and connection are a valued piece of their identity," Wider told Upworthy. "I wanted to create a play experience that empowers them to go anywhere and be anything."

Even if that means being a chef or a superhero.

2. When Alice Brooks was 8 years old, she asked her dad for a doll for Christmas and received a saw instead.

She used that saw to build her own doll out of wood and nails — and 10 years later, she went on to study mechanical engineering at MIT and Stanford.

That's what led Brooks to create Roominate, a line of building sets designed for girls in order to bridge the gender gap in science, technology, engineering, and math (STEM) fields. Once her company received funding on the hit TV show "Shark Tank," the rest was history.

News flash: Girls like to build stuff, too. Photo from Roominate, used with permission.

"I was lucky that I found my passion at such a young age, but so many girls never think about engineering as an option for them," Brooks told Upworthy. "I believe we need to give girls more options so they can find what truly interests them."

3. Julie Kerwin is a woman who loves superheroes, but she wasn't digging what was out there — especially for little girls.

"Many female action figures tend to be more hooters than heroine," Kerwin told Upworthy.

Her company IAmElemental aims to reinvent the superhero game by creating female action figures that are focused more on powers than looks. She believes that opens up a whole new form of play for little girls.

Meet the badass female superheroes from IAmElemental. Photo from IAmElemental, used with permission.

"By making females the protagonists of their own empowering stories, you can change the way they think about themselves and the world around them," Kerwin told Upworthy.

As a mom of two sons, Kerwin is also quick to point out that IAmElemental is "girl targeted, boy inclusive." That's because she understands the value of teaching boys to see (and play with) strong female action figures.

"We cannot move towards gender equality if we don't teach boys what it means to be a powerful woman," she said.

4. Jodi Norgaard never wanted to go into the toy business, but she took matters into her own hands for the sake of her young daughter.

That's when she created a line of plush sports-themed dolls for girls called Go! Go! Sports Girls to help encourage healthy and active play.

That's not to say that there's anything wrong with fashion and princesses, of course. It's just that Norgaard wanted to give girls more options than what was available.

Girls really dig these dolls. Photo from Go! Go! Sports Girls, used with permission.

"Girls are strong, smart, and adventurous — but instead, many toys geared towards them are focused on how they should look," Norgaard told Upworthy. "Girls love sports and we need more representation of that."

Because in today's world, the word "beautiful" has many definitions.

In order to truly make the world a happier place, we should teach our kids that they can be whatever they want to be — without limitations.

Thankfully, many of the larger companies are getting the memo as well. For example, Lego, usually known as a toy for boys, recently introduced Lego Friends, and little girls love them.

Even though more work needs to be done to change gender stereotypes, it's nice to know that we're heading in the right direction.

So when little Susie says she wants to be a computer programmer when she grows up while little Johnny says he wants to be a nurse, we should just smile and say, "Go for it."

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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.

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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