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Youth Collaboratory

Sex trafficking is happening in the U.S. — and young people need to know about it.

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MANY

Have you witnessed sex trafficking? Your first response is probably "no." But many of us have seen it — we just didn't realize it at the time.

Maybe you remember a friend that suddenly started coming to school with much nicer clothes and a new cellphone, which she said were "gifts" from someone older. Or you may recall that guy who seemed a little bit too old to be dating a classmate, even if she was "technically 18." Maybe you encountered someone's sketchy "older friend" at a party who had the hookup for drugs or alcohol, or a classmate who wanted to “introduce you" to an unfamiliar crowd.

It might have been the woman who hung around the bus stop for no clear reason, the man who was chatting up teens at rest stops, or a friend's "modeling manager" making promises that just seemed too good to be true.


The reality is that sex trafficking doesn't just happen in faraway places. In fact, young people are sexually exploited — forced to perform sexual acts for money or other resources like food, shelter, or support —in every state in the U.S.This even includes sex trafficking of youth under the age of 18.

The reality is, though, that we aren't always quick to recognize it.

[rebelmouse-image 19397870 dam="1" original_size="5184x3456" caption="Photo by Victor Van Welden/Unsplash." expand=1]Photo by Victor Van Welden/Unsplash.

Learning what sex trafficking looks like is the first step to ensuring it doesn't happen to us or someone we care about. These 15 facts about youth sex trafficking and exploitation in the U.S. are a great place to start.

1. Yes, sexual exploitation could happen to anyone — including you.

While some youth, like those who are homeless or transgender, are especially vulnerable, the reality is that victims do exist across every demographic. They could be the class valedictorian, the boy who lives across the street from you, or the captain of the cheer squad.

“The victims that I come in contact with come from all different walks of life," says Mirielle Milne, Youth Catalyst for MANY and Advocate for The Jonah Project. “But I do think people get it in their mind that it is a certain type of person."

Traffickers don't discriminate and they're experienced in manipulation. They're looking for a person's vulnerabilities, and if they're able to find them, virtually anyone can be a target.

2. Traffickers may take on a generous and caring persona as part of a tactic called "grooming."

“Grooming" follows a few predictable steps. First a victim is targeted, usually because they appear to be struggling emotionally, have lower self-esteem, or need resources like a job, money, or a place to live.

The trafficker then establishes trust by befriending the victim all while learning more about them, like where they live, who their family and friends are, and what their insecurities might be.

3. And at first, the behavior of a sexual trafficker might not seem threatening at all.

Traffickers know that before they can exploit someone, they first have to earn their trust.

For example, a victim might be led to believe that a person they've connected with online just wants to be a friend. They might even help them through a difficult time. According to Milne, this kind of behavior is designed to make victims feel cared for, special, and even protected.

But this “friend" will gradually become a little more than friendly, perhaps even making grand, romantic gestures and promises.

4. Trafficking can even begin with something that seems harmless, like a job opportunity, gift, or innocent “favor."

For example, a trafficker posing as a modeling manager might set up a careful ruse by taking a victim to photoshoots and gigs that seem perfectly legitimate. Other times, traffickers might offer to help a struggling teen by buying them clothes or lending them money. Sometimes, it's even a family member that will lure youth in with a “job," insisting they need help to make ends meet.

This is all in an effort to make the victim feel as if they “owe" something to the trafficker, which they'll use later on to pressure and control their victim.

Arash Ghafoori, Executive Director at the Nevada Partnership for Homeless Youth (NPHY), says it's that “need" that becomes the entry point into exploitation. “[Traffickers] lure youth into victimization — whether it be through love, or through drugs, or through support," he explains. “[Whatever youth] are desperately seeking."

Youth Survivor, Kristi House Project GOLD.

5. But sexual exploitation doesn't always happen overnight.

Part of why exploitation is so sinister is that it can happen gradually, making it more difficult to see at first. According to Lenore Jean-Baptiste, Project Coordinator at NPHY, some traffickers take a year or more to lure their victims and earn their trust before ever trying to sexually exploit them. Other times, an exploitative family member or peer might take advantage of the trust they've already earned to manipulate victims.

6. The trust they earn allows them to slowly escalate their abuse.

As a trafficker becomes a more central part of their victim's life, they begin to isolate them from family and friends. This can involve pitting them against their loved ones, or even controlling their phone and internet usage.

When the victim becomes completely dependent, the trafficker then demands sexual acts as repayment for the “debt" owed.

As Ghafoori explains, “As that dependency — whether it be from a relationship or a resource point of view — is developed, it turns into the sexual exploitation … these are used as tools for trade."

7. And traffickers are getting smarter about how they find and learn about their victims, too.

Social media is a tool often used by traffickers. Not only is it easy to find and contact victims through social media, it's easy to gather information about them, and keep track of their whereabouts and their support system.

“Youth are not [always] going through the person's page to see who they are," explains Jean-Baptiste.

“They introduce themselves via social media, and a lot of times, [they're] promising careers," she continues. At a time in which self-made stars are born online, the prospect of a modeling gig coming from Instagram doesn't seem so far-fetched.

8. And once they have information on their victims, traffickers can blackmail them.

Many traffickers use threats to keep victims under their control. They might threaten to harm a victim's family members or friends, or claim that they'll publish photos or videos of the abuse to shame and expose their victim.

Some traffickers coerce victims into having children as well, and will blackmail victims using their children as leverage, either by threatening to take them away or harm them.

9. Fear of law enforcement can make it difficult for victims to reach out for help, too.

Traffickers can also take advantage of an existing fear of law enforcement, making claims that victims won't be believed, or that they will be arrested for prostitution or drug use if they come forward.

People of color who might have an existing fear of police brutality struggle even more with this. “Now we're talking about historical trauma between communities [of color] and police officers," Jean-Baptiste says. “A lot of times traffickers can use those kinds of stories and experiences to make individuals feel fearful."

10. Self-blame can also make it difficult to leave even though it's never the victim's fault.

Many victims feel responsible for the abuse and exploitation they've endured, which can, in turn, make them believe they're not victims at all. Self-blame is often a big part of the trauma they experience. They feel that, by accepting money, gifts, or friendship, the abuse was their own fault.

But even if they feel that way, victims are never to blame. “It doesn't matter if you got money, it doesn't matter if you got to keep all the money," Jean-Baptiste says. “If you felt you had to engage in that activity for any survival or need … then it's exploitation."

Advocates like Milne agree, affirming that when we're talking about youth, sexual exploitation is never a job or a choice — and certainly never a victim's fault.

Traffickers use powerful abuse tactics to ensure that victims will give into their demands, and that manipulation is designed to be difficult to identify and resist. The only person responsible for abuse is the perpetrator of that abuse — no matter what a victim does or doesn't do.

11. Trauma can even be powerful enough to drive victims back to their traffickers after they've escaped their control.

If you've ever seen a victim of abuse and wondered why they didn't just leave or why they went back, it's a phenomenon known as “trauma-coerced bonding."

This is an emotional attachment that victims form with their abusers, and it's unfortunately very common. Traffickers' initial acts of kindness and generosity make a strong impression on their victims. As the exploitation worsens, the trafficker can keep up that image by switching back and forth between positive attention and abusive behavior to keep victims hooked.

[rebelmouse-image 19397872 dam="1" original_size="4650x3100" caption="Photo by Carlos Arthur/Unsplash." expand=1]Photo by Carlos Arthur/Unsplash.

“We're trying to tell [these youth] that this person is a trafficker… how do you say that to somebody about the person they've been having dinner with every single night for the last year?" says Jean-Baptiste. “It's hard because they've now had a relationship… [sometimes with] years involved."

12. But there is hope and support waiting for victims.

Despite these obstacles, help for victims does exist. “There is help and there are people that are looking for [you] and do care," Jean-Baptiste says.

If you believe that you or someone you know might be at risk or is being victimized, the National Human Trafficking Hotline can help. You can text 233733, use the chat feature on their website, or call them at 888-373-7888. They can connect you with local organizations and support to figure out your next steps.

If there's any possibility that an abusive person has access to your phone or internet history, clear your internet history, and consider using a payphone or borrowing someone else's phone instead.

[rebelmouse-image 19397873 dam="1" original_size="5184x3456" caption="Photo by Jenna Jacobs/Unsplash." expand=1]Photo by Jenna Jacobs/Unsplash.

13. Recognizing the red flags can make a big difference, too.

Knowing what to look for, and being aware of what healthy relationships do and don't look like, can be lifesaving for young people.

For example, Jean-Baptiste advises caution when someone offers you a gift. Before accepting anything, always ask if there's an expectation to pay that person back or reciprocate.

And if anyone tells you to do something with your body or pressures you, it's time to reach out for support. “You should have the full right to consent to what you do with your body," she says.

14. Don't allow a trafficker to be the first person to validate someone who's struggling.

If you're not a victim yourself, it's important to check in with your peers who may be having a tough time. If a trafficker is the first person to reach out to someone who's struggling, those individuals are much more likely to be exploited.

“We need to be more involved in our community," Milne says, noting that young people who feel supported by those around them are less likely to look to an abusive person for validation.

Jean-Baptiste says this is why young people whose families or communities have all but abandoned them, like homeless and LGBTQ+ youth, are frequent targets. “[Traffickers are] willing to have [a] conversation… that we're not having in our community."

If communities can fill the needs that traffickers try to exploit, those young people would be much safer.

15. And remember, your body is yours. Period.

Too often, it's suggested to young people — especially teens — that they should defer to the adults in their lives when making decisions. However, when it comes to our bodies, the only person in charge is you.

[rebelmouse-image 19397874 dam="1" original_size="2992x2000" caption="Photo by Oscar Obians/Unsplash." expand=1]Photo by Oscar Obians/Unsplash.

“No one should tell you that you have to do anything with your body… [they have] no right, no access, no privilege," Jean-Baptiste says. “You belong to you."

When we're educated and vigilant, we can make a difference in our communities! Learn more about how to get involved, and help us work towards a future where youth are no longer victimized.

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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.

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