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A dad's viral shower door photo comes with a sweet recognition of his wife's work

Kudos to stay-at-home moms.

A dad's viral shower door photo comes with a sweet recognition of his wife's work

Anyone who has been a stay-at-home mom knows that it's not easy. But many people who haven't been one assume that it can't be that hard. I mean, what's so hard about taking care of a baby or a toddler or two? Don't babies basically just lie there? Don't you have all kinds of free time while they nap?

It's hard to describe what it's like to those who haven't experienced the near-constant demands of hands-on, full-time mothering. I've had multiple jobs in my life, from flipping fast food burgers to teaching in public schools, and nothing compares to being a mom. Don't get me wrong, it's wonderful in a million ways, but it's friggin' hard. My kids are all in the double digits now, but I remember those early years of staying home with my wee ones and feeling totally and completely spent by the end of the day.

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Many moms I know lament that their husbands don't seem to understand why they are so exhausted when "all they do" is "just stay home" with the kids all day. That's probably why this dad's photo of a steamy shower door has resonated with so many.


The Facebook page His View from Home shared the photo and story credited to Zack Williams of The Tattooed Sales Guy, and it's been shared thousands of times.

It reads:

"I came home yesterday evening after working 12 hours. I went into the bathroom to get cleaned up and ready for dinner. I noticed my daughter's bassinet in the bathroom.

I asked my wife if she had put her in there, and how she did in it. She said she put her in it as she had showered during the day. We continued to talk about how good she had been and how much she's growing up and so forth.

This morning I came home from the gym and turned the shower on to get cleaned up for work. I turned to the door and saw where my wife wiped away the steam from the glass, so she could see our baby girl in the bassinet.

I literally just sat there and stared at the glass and smiled. I could see it, I imagined it, it was like I was there in the room with them. I could see Heather just looking through the glass and making faces at Lottie as she smiled and played in her bassinet! I just melted!

It's so crazy to me, how the smallest things can make me so appreciative of my wife. It's the little sacrifices my wife makes for this family, that would normally go unnoticed. From caring for our daughter 24/7, to caring for me, cooking, cleaning, taking care of the animals, and taking care of herself (yeah right, there's no time for that.)
It just makes me stop and think.

I work hard. I work long 10-12 hours days, I get tired, I have stressful days and that's my right, as the working member in the household. I have the right to be catered to hand and foot when I get off?!?
All she does is have to take care of a baby.

So, it should be that she cooks, and keeps the house clean, dishes washed, laundry clean and put up, animals tended to... and I'm a man, have I mentioned my needs yet?!?

I mean seriously, she's at home all day after all!

Mannnnn... I can't tell you how much this fogged up glass means to me!

The fact that my wife can't even shower without caring for someone else; tending to someone else's needs. She doesn't get a second to herself to relax.

My wife doesn't get to clock out, my wife doesn't get the satisfaction of seeing a check deposited in the bank in return for her hard work, my wife doesn't get to eat lunch with coworkers, my wife doesn't get to just walk outside and just take a deep breath.

This may be just a fogged-up piece of glass to some, but to me it means so much more. It's the little things like this that don't go unnoticed. it's the little things like this that constantly remind me how badass she is. it's the little things like this that make me fall in love with her all over again, Heather Williams!

Thank you for being the amazing woman you are... it doesn't go unnoticed!

I love you My Queen." 👑 ❤️

The fact that he saw in this smeared glass the sacrifices his wife makes being home with their baby is wonderful. I know some will say this dad doesn't deserve a cookie simply for seeing his wife, but so many stay-at-moms would love to receive this kind of acknowledgement from their partners.

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The reality is when you are taking care of a baby, you are "on" all the time. When the baby is asleep, you might get a chance to do some housework. Or you maybe get to close your eyes for a few moments to try to make up for the lack of sleep you got the night before from the baby waking you up to eat. Sometimes the kiddo won't stop crying and your nerves get fried by noon. Sometimes it's 2:00 in the afternoon, you're covered in breastmilk and spit up, you haven't showered, and you can't figure out where the time has gone. Once your baby is crawling or toddling, you can't take your eyes off them or they might literally die. There's pee and poop and every other bodily fluid you can think of, all day, every day. It's non-stop attention, non-stop need-meeting, non-stop love, but also non-stop work.

And then people ask you what you do all day.

More shower door recognition please, partners. Trust me, the mother of your children will appreciate it.

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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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