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17 assumptions modern newlyweds are sick of people making about their marriages.

17 assumptions modern newlyweds are sick of people making about their marriages.

This article originally appeared on 11.06.15


If you just got married, chances are lots of people think they know what your life is like.

These people are totally well-meaning! And also, mostly wrong.

Being married isn't exactly like it used to be. Which is great, as there are so many different, amazing ways to be newlyweds than ever before. But it's also occasionally frustrating, as we newlyweds are frequently forced to dispel a lot of myths about our relationships.

So let's get them out of the way in one fell swoop.

Here are the most common (but mistaken) assumptions strangers make when you're a newlywed couple, and what our lives are really like.


Assumption #1: We went on our honeymoon already, and we left right after the wedding.

Just like we imagined it. Because we did imagine it.

Photo via iStock.

Reality: In our dreams, we definitely did — and we had a great time!

In real life, however, most of us can't just take a week (or more) off work at will. The office is hella busy, and on top of that, we live in the only wealthy country in the world that doesn't mandate any paid vacation. Many of us were barely able to get the day of our actual wedding off (ultimately, we compromised with our manager and took a half-day).

We're planning to get to it ... eventually. But it might be a while. We promise we'll send pictures!

Assumption #2: We're going to have babies ASAP.

Yay?

Photo via iStock.

Reality: We love being married! But, you know, we actually haven't decided? About babies? We're just enjoying being married right now. But we'll let you know when it happens. We promise.

Assumption #3: We're going to move out of "the city" one day.

So many cheap noodles, so little time.

Photo by Anthony Quintano/Flickr.

Reality: It makes sense to assume that, like so many newly married couples in generations past, we're already planning our escape from our local metropolis to a less population-dense area TBD. But many of us who live in the city really, really like it! The city is great. There are good schools here. We can get nachos delivered at 3 a.m.! From either the good nacho place or the OK-but-cheap nacho place.

Sure, some of us are planning to one day move to the 'burbs for more space (and many already are), but many of us aren't. And still others of us who already live in the suburbs are making the suburbs more like the city.

Having a yard is really nice, but so is not having car insurance payments.

Assumption #4: We feel superior to our second-cousin Frieda whose boyfriend of 19 years still hasn't proposed.

Look! They seem happy!

Photo via iStock.

Reality: Even though we're feeling pretty good about being married, Frieda and Richard are adults and get to make their own decisions — no matter what Aunt Cindy thinks. Maybe they have financial reasons. Maybe they decided a long time ago they don't want to be married. Maybe they believe marriage is an oppressive, archaic, patriarchal institution that they don't want to participate in, and also they're vegan now.

In any case, leave Frieda and Richard alone.

Assumption #5: We're going to have babies soonish.

Aw?

Photo via iStock.

Reality: So, yeah. Like I said. Really haven't decided about babies. Keeping our options open. But probably not soon? You know?

Assumption #6: One of us changed our last name.

Uncanny, really.

Image by Mary Rose Pickett/Sketchport.


Reality: There's totally nothing wrong with couples who decide that one partner will take the other's last name, of course. But not all of us do. At least 1 in every 5 women decide to keep their maiden names, according to a New York Times survey. And if you haven't taken your partner's last name, it's kind of frustrating to constantly hear yourself referred to as Mr./Mrs. Someone Else (for opposite-gender couples, this pretty much applies exclusively to women).

If you're not sure what last name to use, just ask! We'll tell you what the deal is.

Assumption #7: We're having Guinness Book of World Records amounts of sex.

Photo via iStock.

Reality: For those of us who waited to have sex until marriage — which is, of course, totally cool — you might need a supercomputer to tabulate. But lots of us have been together for a long time already and may even have been living together already, so we're probably having whatever amount of sex is normal for us. It's just a regular part of our lives that throwing a wedding doesn't really have a magical impact on.

After many years in a relationship, most of us take "Netflix and chill" quite literally. And seriously.

Assumption #8: We've finished all our thank-you notes.

It. Just. Doesn't. Get. Easier.

Photo by happy_serendipity/Flickr.

Reality: Never. We'll be writing these until the end of time.

Assumption #9: Hanging out with one of us means hanging out with both of us.

You will listen to us talk about our trip to Block Island and you will enjoy it.

Photo via iStock.

Reality: We're still different people. Each of us is a self-sufficient being with free will. And we're probably totally down to hang out with you, even if our spouse isn't available.

Except you, Greg. We're totally avoiding you.

Assumption #10: We're going to have babies ever.

Bujjy bujjy boo?

Photo via iStock.

Reality: So um, like I said, there's actually a chance we might never have babies? We might decide we don't want them after all. We might find out we can't — in which case, these questions might become extremely invasive and painful. We might adopt a child ... who's not a baby. We haven't figured it out yet.

At the end of the day, It's kinda up to us, you know?

Assumption #11: We never use the garlic press you got us.

Such a great gift.

Photo by Lee Kindness/Wikimedia Commons.

Reality: We use it all the time! Thank you so much!

Assumption #12: One of us is going to stay home and take care of the house from here on in.

We will still make the hell out of some lemonade, though.

Photo via iStock.


Reality: Some of us might want to be a housewife or husband. Others of us shudder at the thought of giving up our careers, or urging our spouse to give up theirs. Still others of us might want to, but might not be able to forfeit the second income. There's really no right — or standard — way to do it anymore.

Assumption #13: We both have all the same likes, dislikes, preferences, outlooks, and opinions now.

Missy and I have been getting really into '80s ice dancing.

Photo via iStock.

Reality: My wife will never convince me to like jazz. And I will probably never convince her to like "Captain Phillips" fan fiction. And you know what? We're OK with that.

For the things that matter, we're committed to presenting a united front. But we're still individuals with different thoughts, feelings, and opinions about what Tom Hanks was up to two weeks before the Somali pirates attacked, 'cause honestly, that's where the real drama of the story probably is.

Assumption #14: We wear wedding rings.

Help. Someone glued our hands together. Please call the cops.

Photo by TanyaVdB/Pixabay.

Reality: Some of us like wearing a physical symbol of our connection and duty to our spouse. Some of us don't as much. So we don't wear them. But don't worry! We're still extreme double married 5000.

Assumption #15: Making us a pink cake that says "baby" on it is going to change our mind about babies.

Mmmmmmmm. Nope.

Photo by Frosted with Emotion/Flickr.

Reality: It won't. But we will definitely eat that cake.

Assumption #16: Our lives are a lot different now.

Married or not, we still have three more seasons of "Justified" to get through.

Photo via iStock.

Reality: Beginning roughly seven seconds after we say, "I do," lots and lots and lots of well-intentioned people ask: "How does it feel?!" seemingly expecting to hear: "So much has changed! We got matching ponies! Being married really is a whole new world!" It feels like we're disappointing them when we answer, "Pretty much the way we did the day before the wedding." Which is silly, since there's no shame in that.

For some couples, life is a lot different after marriage, and that's great. But if stuff is kinda sorta the same, that's OK too! Life was great before. That's why we decided to get married.

Assumption #17: If we're not going to lay out a precise plan for having babies, at least we'll probably get a pet.

Blah.

Photo by Madalena Provo, used with permission.


Reality: OK. This one is true.










Sponsored

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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