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A photographer asked these kids what they hoped to become. Here's what happened.

This is Kadijatu Mamane Zeinan and she wants to be a teacher.

She may seem familiar, like your child, little sister, or even like you when you were younger. Her eyes sparkle with a carefree joy and wonder most of us tend to lose as we grow old.

But Kadijatu has it in spades. Happy and full of life.


All photos by Vincent Tremeau, used with permission.

Her sweet spirit is especially impressive considering Kadijatu is growing up in country prone to crisis.

She's living in Niger, a west African country plagued by external threats. Attacks from terrorist group Boko Haram have killed thousands and driven families from their homes. And new threats from Libya make it tough to secure her country, which is about twice the size of Texas.

But despite the uncertainty, Kadijatu remains optimistic about her future.

"I want to be a teacher like my father," she said.

Photographer Vincent Tremeau captured Kadijatu, and dozens of other children living in western and central Africa for his latest project, "One day, I will."

The series features portraits and stories of the children dressed up as the people they want to become.

Like Salifa Adamou, who wants to protect forests in Niger.

Tremeau, a former aid worker turned photographer, began the project while completing an assignment on the humanitarian crisis in the Central African Republic (CAR). He decided to get to know the children at the refugee camp and came up with the idea for portraits.

"It is a game to come dressed up as what you want to become," he told Upworthy. "So it is always a fun activity to do, especially for the kids..."

Now in between assignments, Tremeau travels to schools throughout the region and chats with the teachers about participating in the project. In the small villages he travels to, many of the kids don't have access to cell phones or computers, so many are excited to be photographed.

The kids at this school were so excited to dress up and share their big dreams with Tremeau.

The career goals and kid-made costumes are as creative and inspiring as the kids themselves.

This young lady in Niger wants to be a journalist.

Georgine, 13, from the Democratic Republic of Congo (DRC) wants to be on the radio.

And then there are electricians, like this little guy in the CAR.

Sakima, 10, from Niger hopes to be an educator.

Yakouba Senou, 11, from Kolondieba, Mali wants to be a science teacher.

And check out this fabulous future pilot from the CAR.

Healthcare professions are popular too. Like this future nurse in the CAR.

And Sekou, an aspiring doctor from Mali.

Some of the kids hope to work with their hands, like Rajikou Ibrahima of Niger who wants to be a mechanic.

Or Issouf Konaté of the Fakola Village in Mali who wants to become a chicken farmer.

And get your first look at David Kamaté , age 9, who is just a few decades away from becoming the president of Mali.

But even after photographing dozens of children, some of their responses still catch Tremeau off guard.

"I think about this young girl who said she wanted to be a basket makers, so she can sell baskets and take care of her future children if she has to get married with a drunkard or a irresponsible husband," he told Upworthy.

"When you are still a kid, it is surprising to have such a maturity. But unfortunately this is the reality she lives in too, and she already knew she had to take care of herself, even at this young age," he said.

And for every aspiring teacher, nurse, or president, there are soldiers and diamond collectors.

Their countries are plagued by war and conflict, and many of the young boys in the Democratic Republic of the Congo and the Central African Republic hope to become soldiers, not to pillage and destroy, but in the hopes of protecting their families.

12-year-old Patrick of DRC is one of them.

Children also look forward to working in the diamond industry, which employs many people in western and central Africa, but is incredibly dangerous and unforgiving.

Many use makeshift boats to find diamonds in the riverbeds.

This young girl in the CAR even made a paper boat as part of her costume.

But with education and opportunity, these creative, talented kids can turn their dreams and ambitions into reality.


Ibrahim, a young boy in the CAR who wants to be a soldier.

"It is something I deeply believe in," said Tremau, whose parents were both teachers. "Education should be at the center of every priority, even in time of turmoil, so it can change mentalities, and hopefully bring a better future for the next generation."

For years, many children in the region didn't have access to primary education. In the Democratic Republic of Congo alone, millions of children remain out of school, as the region struggles to come back after war and continued violence.

But things are turning around. Just ask Francoise, a teenage girl with an infant son, who's determined to become a nurse through hard work in school. She shared her story of resilience with Tremeau.

“My name is Francoise, I am 15 years old, I have a child named Chance. He is 1 year and 4 months old. As soon as I wake up in the morning, I wash my baby’s clothes before I go to school. While I am away, my grand-mother looks after him.
When I go to school, I am not ashamed of anything. But others cannot understand why I am a student while I already have a child.
I tell them that if I study, it is exactly because I want to help my child. Even though others make fun of me, I let them talk and go to school anyway."

Tremeau is continuing his project in other African nations and hopes to expand the series to other continents as well.

"I would be curious to do it in developed countries like in Europe, the U.S. or in Canada and see what comes out of it. We will see if I have the opportunity to," he told Upworthy.

Tremeau is also sharing a picture from his series every day on his Instagram page, where you can find even more pictures and personal stories. And he hopes to put the photographs on exhibit sometime in the next year.

Driver Hassan poses dressed up as a driver, in Carnot, Central African Republic. "I want to go to school so I can learn traffic regulations so I can be a good driver". Photo by @vtremeau Carnot is an isolated city, in Western CAR. Most of the car you can see belongs either to humanitarian organizations or the UN soldiers. It can take days to reach the capital Bangui by road. In 2014, there wasn’t any gas stations in the country anymore, except in the capital. Play the game! Join us on @1day1will and use #1day1will to participate in this project and show that #youngmindsmatter #Africa #CARCrisis #CentralAfricanRepublic #everydayafrica #photojournalism #documentaryphotography #portrait #dressupasthefuture #driver
A photo posted by One Day I Will (@1day1will) on

Here's to these bright, hopeful young people.

They're on the path to amazing things. And thanks to photographer Vincent Tremeau, we can see and share their stories and work together to encourage their education and push for greater opportunities.

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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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