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Parents of kids mid-meltdown get support instead of judgment, and it's so dang beautiful

Parents of kids mid-meltdown get support instead of judgment, and it's so dang beautiful

Practically everyone who has had kids knows that meltdowns happen. Whether it's a two-year-old who doesn't know how to express themselves or an older kid who is having a particularly rough life moment, children sometimes lose control of their emotions. Unfortunately, meltdowns that happen in public can bring the Judgey McJudgertons out of the woodwork—which is why a Twitter thread of parents receiving kindness and support instead of side-eye and judgment has parents breathing a sigh of relief.


Writer Joy McCullough shared a brief but beautiful story on Twitter that got thousands of shares and prompted parents to share their own stories of strangers' kindness in their darkest parenting moments.


"Toddler is melting down in the library," McCullough wrote. "The mom is mortified. A stern old lady approaches & I hold my breath. 'It's okay,' she tells the mom. 'I've been there. You're doing great.' And then to the toddler, 'You're doing great, too. You're doing your best.'

Now THAT is what every parent—and toddler, for that matter—needs to hear in the midst of a meltdown moment.

Other parents chimed in with stories of their own, and they're the balm all parents of young kids need.


One mom shared how her son was having a public meltdown a few years ago and she was on the verge of tears herself trying to calm him down, when and older woman came over and asked if she could walk with them for a bit.

"She pushed my cart with my son in it while I grabbed our groceries (and monitored) and just talked quietly to my son for a few minutes. He was quiet and listened to her. Once he was calm she patted my arm, said 'it takes a village, right?' and went on her way. She was my angel."

Seriously, unless you've been there at your wit's end as a parent, you can't imagine how helpful someone's kindness and understanding can be.


And other times just a few words of encouragement while you're trying to wrangle an unruly, overtired kiddo can make a world of difference. A simple shout out like "Be strong, mama!" can be just the boost you need to not completely melt down your self.

The thread includes a few "yOuR ToDdelR iS mAnipUlatTinG yOU!" comments from the get-off-my-lawn crowd, but they are far outweighed by stories of support and understanding.


"7yo melted down in hardware store," wrote Melissa Harris. "I did my best to keep calm and calm him. Get to checkout & woman came up to me. She wanted me to know that she thought I had done an amazing job and even in a meltdown my son was cute. Made my month."


"Those moments mean so much to a parent," added Alexa Winton. "My 4yo daughter had literal Roid rage on a flight (steroids for asthma) and the lady next to us only said to me "I forgot how hard it is to travel with young children" And I will never forget that act of kindness."

RELATED: 10 ways kids appear to be acting naughty but actually aren't.



You just never know what a child or parent is dealing with. Even in the absence of special needs, occasional meltdowns are a developmentally normal behavior. With gentle guidance and consistent parenting, kids do eventually move beyond that phase and gradually gain more control over their emotional regulation, but it takes time. And once the tantrum train has left the station, it's usually just a matter of waiting it out until they can actually be reasoned with.


Indeed. It's not like parents teach their kids to throw fits in public. I can't count how many times I heard people say, "If you don't give in to tantrums, they'll stop," when my kids were little. Yeah, no. I never gave my kids something they demanded during a tantrum, but that didn't stop them from occasionally melting down because they were overtired, overstimulated, or simply taxed beyond what their tiny human psyche could handle in the moment.

The whole thread is worth a read. It will restore your faith in humans and remind you of the importance of everyday heroes.


Parents need support, and going out of your way to be kind is far more helpful than going out of your way to judge. Let's hear it for kind old ladies trying to save the world, one little pep talk at a time.

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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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