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This queer teen made it through a terrible night — thanks to a text. Their story matters.

A couple years ago, Brendon Scholl was having a terrifying night.

They can't recall many of the details. "Most of it is just a big blur," says the now-17-year-old, who is transgender and non-binary, and uses they/them pronouns.

But they do remember crying hysterically, rattled by an inescapable sense of loneliness and an isolating anxiety that'd often accompany them to bed, when their friends were asleep and unreachable by text.

"I was in a really bad place," Scholl says. "I was kind of freaking out ... I was having a really hard time with [the idea that] people didn't want me around."



[rebelmouse-image 19346007 dam="1" original_size="589x617" caption="Brendon Scholl's aunt happens to be singer Jennifer Lopez, who bragged about Scholl's achievements on Instagram in July 2017. Photo via Jennifer Lopez/Instagram." expand=1]Brendon Scholl's aunt happens to be singer Jennifer Lopez, who bragged about Scholl's achievements on Instagram in July 2017. Photo via Jennifer Lopez/Instagram.


Scholl's scary night reflects a much larger issue at hand: a generation of young queer people whose mental health desperately needs to be addressed in serious, systemic ways.

According to a report published in May from the Human Rights Campaign and researchers at the University of Connecticut, an alarming 95% of LGBTQ teens said they, like Scholl, have trouble sleeping at night. 77% reported feeling depressed or "down" during the week. Only about one-fourth reported feeling safe in their schools, and a similarly sobering number claimed they could "definitely" be themselves at home.

Plenty of policy victories and improving media visibility have helped grow Americans' acceptance of LGBTQ people in recent decades.

So why do statistics like these remain staggeringly high among queer kids like Scholl?

"It's complex," answers Amit Paley, CEO of The Trevor Project — a suicide prevention and crisis intervention nonprofit for LGBTQ youth. "There are a lot of reasons that young people need help and are reaching out."

For starters, LGBTQ youth aren't insulated from America's larger, worsening suicide crisis, Paley says. Between 1999 and 2016, overall rates of suicide rose — and often dramatically — in almost every U.S. state, according to new data from the CDC. What's more, in its newly released "Youth Risk Behavior Survey," theCDC found 23% of high school students who identify as lesbian, gay, or bisexual have attempted suicide.

That's four-times the rate of their straight peers.

Other research suggests the figure is even higher among transgender and non-binary teens, like Scholl.

[rebelmouse-image 19346008 dam="1" original_size="750x479" caption="Chart via the CDC." expand=1]Chart via the CDC.

Entrenched anti-LGBTQ attitudes in schools, churches, and homes continue compounding issues associated with mental illness among queer teens too.

In Scholl's case, it's easy to see how. "I remember very vividly my grandma calling me and being like, 'I'll give you a $100 if you go back to being a girl,'" they recall. "I didn't even know what to say, really."

Those attitudes have been around for awhile, sure. But now, LGBTQ kids have Trump to worry about too.

Call volume to The Trevor Project more than doubled the day after the 2016 presidential election, according to Paley. LGBTQ kids were terrified by the rhetoric they'd heard from Trump on the campaign trail.

Photo by Chip Somodevilla/Getty Images.

The flow of calls coming in has remained relatively high ever since too, thanks in part to a divisive 24/7 news cycle with bigotry on full display.

When the fight over LGBTQ rights has gotten heated in the headlines — like the day the president tweeted that transgender people would be banned from serving in the military, or when Texas debated whether to implement a transphobic bathroom bill — The Trevor Project noticed spikes in need from the kids they're aiming to protect.

"We know that words have consequences," Paley says. "We know that hateful policies have consequences."

Across the various crisis lines young people can use to contact the nonprofit —along with its 24/7 phone hotline, The Trevor Project also operates a text service and online chat platform — Paley says the organization estimates it will make contact with young people in crisis about 75,000 times this year alone.

That's an increase from last year, and one reason the group is focused on expanding services and programs for youth across the country.

At a time when we seem to be moving ahead on LGBTQ issues in many ways, the need to take care of young queer kids has never been greater.

"Our ultimate goal is to put ourselves out of business," Paley notes. But that seems unlikely in the short-term. So The Trevor Project aims high.

The nonprofit wanted to raise a record-breaking $2 million to further its mission through Trevor Live — the group's annual, star-studded fundraising gala — on June 11. It exceeded that ambitious target, but it's a bittersweet benchmark to pass, knowing why those funds are so needed.

Trevor Live was hosted by openly gay Olympians Gus Kenworthy and Adam Rippon. Photo by Craig Barritt/Getty Images for The Trevor Project.

There are still too many kids who, in a moment of crisis, desperately need Trevor to be one call, text, or online chat away. Kids just like Scholl — who decided to use the group's text service that awful night a couple years ago for help.

"They got back to me immediately and helped me feel a lot less alone," Scholl explains. "Even if I get that bad again, [I know] I'm not going to be completely alone."

Now, Scholl is out and proud — and refusing to stay silent.

They're out to their family. And their friends have been "super great" about respecting their pronouns and identity as a non-binary person.

At Trevor Live, Scholl bravely shared their story to a room full of celebrities and supporters. The speech was met with cheers and a standing ovation.

A vicious political climate and lack of mental health resources may mean kids like Scholl live in an especially hostile environment. But LGBTQ teens — who are coming out earlier in life and reshaping how we see and respect gender and sexuality — are also totally badass.

Scholl walks the Trevor Live red carpet. Photo by Craig Barritt/Getty Images for The Trevor Project.

Scholl, a high school junior, now has their sights set on another big hurdle drawing nearer: college admissions.

They're determined to find the right school with a welcoming environment for LGBTQ students, equipped with gender-neutral housing. That's not a terribly easy feat, to be sure — "I'm excited, but also stressed," Scholl admits of the process — but it's one worth working for.

It's another mountain they're determined to climb.

"I know it's like the most cliche thing to say ever, but it does get better," Scholl says. "It's like, when you're going up a hill: You're tired, it feels like it's going on forever, and you're never going to get to the top. But once you do, you look back, and you're like ... 'I made it that whole way.'"  

Watch Scholl speak at Trevor Live below:

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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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