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Parents are empowering their kids to imagine exciting new careers in STEM

FIRST robotics, stem robotics challenge, stem education

via FIRST

FIRST students learn real-world career skills through robotics competitions.

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In today’s rapidly changing world, most parents are concerned about what the future looks like for their children. Whether concerning technology, culture, or values, young people today are expected to navigate—and attempt to thrive in—a society that’s far more complicated than that of their parents. It’s one of the reasons why parents are keen to involve their kids in activities that will help them become more resilient, well-rounded and better prepared for life when they enter adulthood.

One such activity is FIRST^®, a volunteer-based global robotics community that helps young people discover a passion for science, technology, engineering and mathematics (STEM) through exciting, multifaceted challenges. FIRST helps kids ages 4 to 18 to build confidence, resilience, cooperation and empathy as they compete and collaborate with one another.

You may have seen the transformative power of FIRST programs featured in the new 2022 Disney+ documentary “More Than Robots.”

More Than Robots | Official Trailer | Disney+www.youtube.com

Through FIRST, students develop skills to help them thrive in changing times while connecting them with skilled mentors from as many as 200 Fortune 500 companies. These connections often lead to job placements in high-paying and rewarding STEM careers.

“If you want your child to be ready for the real world in ways that school and classroom experiences won’t necessarily fully prepare them for, FIRST is the program for you,” Erica Fessia, vice president of global field operations at FIRST, told Upworthy.

A wonderful example of the impact FIRST has on students is Aaron, who lives in Watts, an underserved neighborhood in south Los Angeles. Aaron was a reserved kid until he joined FIRST, where he developed a passion for robotics that pushed him to become a leader of his team, the aptly named TeraWatts.

Fatima Iqbal-Zubair, a schoolteacher and TeraWatts mentor, has seen Aaron make tremendous strides over the past two years. “He’s one of the most technologically competent students on our entire team. But I am 500% more proud of his growth as an individual in his confidence and his leadership,” she said, noting it’s the type of growth she rarely sees through traditional educational settings.

Aaron believes he has learned resilience through the program due to its fail-forward approach to engineering. “Normally, I get really frustrated when I can’t solve a problem,” he told Upworthy. “Robotics helped me to calm down instead of getting angry. If you don’t get it right the first time, you just keep trying, trying until you do.”

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Problem-solving is an important goal of engineering and FIRST inspires students to stretch the limits of their innovation and imagination to reach their goals. When each annual FIRST season begins, student teams are assigned a sport-like challenge, typically themed around a critical global issue like recycling, transportation or energy, and are asked to build a robot that can compete in that challenge. They are given a kit of materials with limited instructions. It encourages them to experiment and attempt new iterations until the robot works.

When the students hit a roadblock, they can get help from adult mentors with either educational or professional experience in STEM fields. This provides the invaluable experience of working with positive role models who’ve made STEM their life’s work. It’s a big reason why FIRST students are better prepared for STEM careers than those who’ve only studied the subject in school (that is, if they even have access to STEM education in their school).

Afzaa Rahman has been a FIRST student for seven years as a member of the Durham, North Carolina-based Zebracorns. After high school, she hopes to pursue a degree in biomedical engineering.

“The Zebracorns have a special place in my heart as they have provided me with a community of individuals who stood by my side, willing to assist, support, encourage and motivate me in my endeavors,” she told Upworthy.

She hopes that being part of FIRST will inspire other girls to do the same. “It’s important that we leave our mark and continue to make meaningful contributions to STEM fields,” she said. “By participating in STEM, today’s girls and women will inspire future generations to do the same until we are no longer a minority.”

Afzaa’s father, Mujib Jinnah, encourages other parents to involve their children in the program, too. “I think other parents should definitely consider having their child participate in FIRST. In addition to STEM learning, FIRST encourages the development of teamwork and soft skills, which are essential qualities to enhance from a young age,” he told Upworthy.

One of the most important goals of FIRST is to recruit women and students from underserved or underrepresented communities into the program to help bridge the gap in STEM participation. This can help uplift individuals and communities by putting their issues directly in the hands of a new generation of problem-solvers.

“When we talk about diversity in technology, we talk about bringing more voices into technology,” Fazlul “Fuzz” Zubair, systems engineering department manager at Raytheon Technologies and mentor of FIRST team The Vitruvian Bots, told Upworthy.

“When young people of all backgrounds learn they can get into technology, they bring the issues they see to the forefront and say, ‘I can solve this with technology.’ That way you don’t just get technology that’s developed for one class of people,” said Zubair. “We need more developers from underserved areas because they understand the issues.”

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FIRST robotics challenges inspire competition and cooperation—what it calls Coopertition^®. Two teams may be competing alongside one another in a challenge and then later compete against each other. To make this work requires another FIRST value: Gracious Professionalism^®, a term coined by the late Dr. Woodie Flowers, a distinguished MIT professor emeritus and a pioneer in hands-on STEM education, including many years spent tirelessly supporting FIRST.

“The ethos of Coopertition and Gracious Professionalism encourages all who participate in the FIRST community to emphasize and respect the value of others and their opinions, including those that might differ and differ strongly from yours,” Fessia said.

Iqbal-Zubair says that, win or lose, the unique nature of the competition builds practical empathy that students won’t learn elsewhere.

“You can be kind to a team and understand what they’re going through in one competition. Then, work against them in the next and be gracious in both situations. That takes a lot of empathy,” she said. “FIRST requires technical empathy, emotional empathy and strategic empathy,” she added.

Keys to thriving in a world where change is happening at a breakneck speed are resilience and flexibility as well as the 21st-century skills of cooperation and empathy. FIRST students are developing those skills while building some pretty amazing robots, too!

FIRST is open to students from the ages of 4 to 18. To learn more about FIRST programs in your area and how to become involved, go to firstinspires.org.

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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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best of humanity

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.

Jessica Buwick|TikTok

Mom responds to critics in the most comical way.

Once women reach a certain age, society does something weird. It starts sending messages that you're simply too old to dress as if you have a social life. In general, it seemed as if society had been moving away from those unrealistic expectations laid upon moms and women over the age of 35, but maybe not.

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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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 horse Gina 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 rowing Nathalie 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 dane Helga'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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