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Mom shares a beautiful positive parenting example when her 6-year-old was rude to her

Mom shares a beautiful positive parenting example when her 6-year-old was rude to her

No matter how great a parent you are and how well you teach your children how to behave, kids are occasionally going to be less-than-pleasurable to be around. They are human, after all. And they are engaged in an intense, years-long process of learning about being human, growing and change rapidly through various phases and stages.

As parents, it can be hard to figure out how to help them through all of that. Especially when they're pushing our own emotional buttons.

Mom and educator Dr. Chawanna B. Chambers— or "Dr. Chae," as she goes by on her website—shared a parenting tale from her own life that offers us all a beautiful example of how to teach a child who is seemingly acting disrespectful how to manage their responses. For many parents, a child talking back or being rude is met with immediate anger or sternness—perhaps an instinctual response from their own upbringing or beliefs about respecting our elders.

But for Chambers, her 6-year-old speaking rudely was an opportunity to teach a lesson about our brains and how we can head off a problematic interaction before it starts.

"I noticed that my 6-yo was being a lil rude/curt w/me, so I asked her what was up," Chambers wrote. "At first, she just looked at me, so I reiterated that I can't help her if I don't know what's wrong.


"Then I asked, 'Why are you being unkind to me? What happened?'

"She looked at me and said, 'I don't know,' and started crying. I told her, 'It's okay. Sometimes mommy just doesn't feel happy too. You're not in trouble. I just needed to know how to help.'"

Gold from the get-go. Even just asking the question, "Why are you being unkind to me?" invites a child to think through their thoughts and emotions in a way that doesn't put them in a space of fear or defensiveness. And having mom reiterate that she understands how it feels to not know why you're unhappy and share that she wants to help gives her daughter room to do this important work.

"She said, 'My brain tells me to be rude,'" Chambers went on. "I told her that's sort of how it happens for lots of people. When our emotions aren't happy, sometimes we take it out on others even when they don't deserve it.

"She asked, 'Wait. Your brain does it too?!' I told her yes, and then I asked her if I could teach her something that might help. She said yes, so I told her, 'When you aren't quite feeling right but don't want to be mean, you can say, "I'm not feeling my best self; I need a min."'"

Empathy. Compassion. Education. Concrete ideas for what to do instead of what they're doing. It's like a master class in positive, supportive parenting techniques.

Chambers continued:

"So, we practiced saying that over and over again until she felt better. She gave me a hug and stopped crying. I think about all the ways I *could've* responded, particularly a power trip bc 'I'm the adult,' but she needed to process something not even about me."

That right there is such a key thing that's easy to miss as a parent. So many times when our kids are expressing frustrations in our direction, they have nothing to do with us personally. We are merely a safe space for them to vent, and they may not even know why. That doesn't mean we should let them speak to us any old way they feel like it in the moment, but it does mean we can utilize that space to help them work through whatever they're feeling and figure out a different way of expressing themselves.

"Trying to be slower to projection or anger has really given me an opportunity to coach my children on emotional maturity," Chambers reflected. "Even at 6, she can learn how to challenge her own thoughts. She can learn how her brain works and the best ways to engage w/others."

Yes. Children are far better at this kind of emotional work than we give them credit for. It takes time and patience, but it pays off in the long run.

With a background in education, Chambers may have a leg up on many of us in terms of understanding child psychology and explaining it on a child's level, but that doesn't mean we can't all do our best to focus on empathy and education in our own parenting.

Not only does this kind of approach help kids learn how to manage their behavior, but it also strengthens bonds between parent and child. When your kiddo knows they can trust you to help them and not hurt them, when they get the message that their feelings are normal and they can learn to manage them, when they see that their mom or dad also have the same struggles they do sometimes and can help them through it, they know they've got support.

Our job is to teach them as the humans they are, not train them like animals at obedience school. And most importantly, we teach respect by exhibiting ourselves. When a child behaves in a way that's contrary to what we expect and what we've taught them, it usually means they're struggling with something. And nothing is more respectful than listening, acknowledging, empathizing, and helping when someone is clearly struggling.

Children learn what they live, as the saying goes. Thank you, Dr. Chae, for offering a beautiful example of what that looks like in action.

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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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