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Pediatrician is changing the way we think about teens with 'lighthouse parenting' tips

Dr. Ken Ginsburg’s advice for parents is like a hug, TED talk and Masterclass rolled into one.

parenting teens
Photo by Josh Hild on Unsplash

'Lighthouse parenting' can help make raising teens less rocky.

As a parent of teens, I often wonder: Why didn’t anyone tell me it would be like this? I don’t mean the warnings and complaints about how challenging the teen years are. I don’t mean all of the “just you wait” admonitions. I don’t mean the cliches and memes. What I want to know is why no one told me how awesome raising teens can be.

Don’t get me wrong, raising teens is not without its challenges. But for the most part, the teen years are portrayed as something to survive, not something to enjoy—and Dr. Ken Ginsburg is on a mission to change that.

A pediatrician specializing in adolescent medicine, a professor of pediatrics at the University of Pennsylvania School of Medicine, and co-founder and director of programs at the Center for Parent and Teen Communication, Dr. Ginsburg has focused his career on changing how we think about, treat and raise teenagers.

His message of optimism is a welcome respite from the constant doomsday messages we hear about teenagers. The cliches, warnings and complaints about teens start early and continue often. Parents need to vent—and there is a lot to vent about—but the narratives we tell about teens are so one-sided and predominantly negative that I’ve been legit shocked at how fulfilling, rewarding and—dare I say—fun raising teens can be. Why didn’t anyone tell me about this?

Ginsburg told Upworthy he suspects that part of the reason for the success of his latest book—"Congrats, You’re Having a Teen"—is that people are hungry for a book about teens that doesn’t focus on survival.

Raising teens isn’t all sunshine and roses. It is nerve-wracking, terrifying and emotional. But Ginsburg has made it his life’s work to dispel common myths about teens. Some key culprits: the misconception that teens don’t care what their parents think, that teens are inherently risk-prone and that teens don’t act rationally. To counteract the damaging impact of these myths, Dr. Ginsburg promotes “lighthouse parenting.”

“Parents,” Dr. Ginsburg advises, “you should be like a lighthouse for your child—a stable force on the shoreline from which they should measure themselves against. You should look down at the rocks and make sure they don’t crash against them. Look into the waves and trust that they will learn to ride them, and it’s your job to prepare them to do so.”

Unlike other talked-about parenting styles, like helicopter parenting and free-range parenting, lighthouse parenting—or balanced parenting—is grounded in science. Decades of research shows that not only does lighthouse parenting yield better academic, social, mental/emotional health and behavior outcomes, but (perhaps most importantly) it also leads to better relationships between parents and their children.

How do we tell the difference between rocks and waves? Is graduating from high school a rock or a wave? What about getting into college? Is underage drinking a choppy wave or a sharp rock?

Ginsburg explains it like this: Waves are challenges that you can ride through with the right skill sets, but rocks are dangers you might not survive no matter how prepared you are. Didn’t study for an important test? A wave. Getting in the car with a driver who has been drinking? A rock, definitely a rock.

I’ll be honest, in today’s increasingly high-stakes and ultra-competitive world of college admissions, travel sports and prestigious schools, it can be hard to know when to step in and when to let your child lead the way—especially when you know a wave might crash on top of them, leaving them gasping for air. But Ginsburg has a navigational tool for that too: think about the 35-year-old you’re raising.

When we look at success narrowly in terms of accomplishments, Ginsburg says we’re focusing on what our children are doing rather than who they are being and becoming. But when parents shift their focus onto the 35-year-old version of their teen, we look at success very differently with a focus on who they really are.

“The starting point is to know your child,” he says. “For a child to be ultimately successful, it has to be success that matches who they really are, not your vision of who they might become.”

Another mind-blowing piece of advice? Raise teens for their second job, not their first. Their first job might be influenced by accomplishments like good grades and high SAT scores, but their second job is when character traits like compassion and perseverance have a chance to shine.

Being a lighthouse, raising the 35-year-old and preparing them for their second job can be easier said than done, especially when a teen is slamming a door in your face or telling you (once again) that you don’t know what you’re talking about. But our teens aren’t pushing us away, Ginsburg says, they are simply struggling with their own growing independence.

The frustration is real, he acknowledges, but it is rooted in misunderstandings about teen development. Research shows that young people actually do care deeply about what their parents think, and they want to have good relationships with their parents.

So stay calm, be the lighthouse, ride the waves.

“The most protective thing in a young person’s life is to be known, seen, and valued just as you are, with all of your strengths and all of your limitations,” he told Upworthy. “When you know that the person who knows you the most, knows your character strengths and those areas in need of improvement—and that person continues to adore you, that gives you strength to launch into adulthood truly secure in who you are. That’s what gives you the strength to navigate the waves of adolescence when other people are challenging who you are.”

Ginsburg’s book was released in early October and he's been doing television interviews that are resonating with many people. I’ll admit, I was on the verge of tears for nearly our entire interview. His advice feels like a hug, a TED talk and a Masterclass on parenting all rolled into one. In the words of Sheinelle Jones, who interviewed him on TODAY, “This was a sermon.”

Amen.

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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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