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'Marriage: A Story of Love in 28 Parts' has long-time couples rolling

'Marriage: A Story of Love in 28 Parts' has long-time couples rolling

As someone who's been married to the same human for 22 years, I can say with confidence that a big key to marital bliss is to come at it with a sense of humor. Living with and loving someone for life (hopefully) is a shared journey with ups and downs and unexpected detours. The story of that journey is filled with big life events and mundane daily details, and with moments both precious and perturbing.

If you've been married a while, this collection of funny tweets about marriage will hit home. Shared by Joshua Johnson on Facebook, this "Marriage: A Story of Love in 28 Parts" compilation includes universal sentiments, classic spouse conundrums, and pandemic-specific realities for people in long-term love

Here they are, linked to the original tweets so you can follow the creators if you wish, and written out in text for our friends with audio aids. Grab your partner and have a good chuckle at your own expense:



"DATING: can't wait to see you again

MARRIAGE: part of your knee was on my side of the bed again last night"

@TheCatWhisprer

(BTW, you also pulled the covers off me every time you rolled over. Thanks for that. Love you.)

"Marrying someone is easy. Staying married after going to IKEA on a Saturday with an empty stomach, is not." @maryfairybobrry

(Have done this. Can attest it's a mistake.)

"My wife and I play this fun game during quarantine, it's called "Why Are You Doing It That Way?" and there are no winners" –@ericspiegelman

(Pandemic togetherness is so fun, isn't it?)

"Before marrying someone, listen long and hard to the sounds of their chewing because that's the soundtrack to the rest of your life." @LizerReal

(This is legit advice, young people.)

"There are two kinds of people. The ones that pack six days before a trip, and the ones that wake up day-of and realize they need to do a load of laundry. And they marry each other." @dadmann_walking

(And the early packer spends six days panicked over the last-minute packer not being packed. Ain't love grand?)

"Marriage is having separate tubes of toothpaste because your spouse squeezes it wrong" @mom_tho

(Always from the bottom, rolling as you go. This is the way.)

"I told my husband I wanted to buy an expensive blender, he said we don't need an expensive blender. Long story short, how long should I wait before I tell him it arrives tomorrow?" @3sunzzz

(Pssst. Don't tell him at all. He might not even notice.)

"Wife: You're doing it wrong.

Me: What?

Wife: *motions vaguely in the direction of my entire life*"

@XplodingUnicorn

(Ouch.)

"My wife said she'd buy her own birthday cake this is a test right" @DadBroDad1

(Yes. Yes it is.)

"Listen: I just found out that my husband eats spaghetti with a spoon so I can't listen to your problems right now." –@thearibradford

(This is just psychopathic behavior, honestly.)

"In 34 years on this planet I've learned one very important lesson that I'm going to pass on to you fellas. She can eat your fries. You cannot eat her fries."–@CrockettForReal

(It's funny because it's true.)

"-commercial break-
Husband: *silent*
-fight scene-
Husband: *completely and utterly silent*
-quiet dialogue scene-
Husband: so let me tell you about the history of rockets"

–@Megatronic13

(SHUSSSHHHH.)

"Me:

My wife:

Me:

Wife:

Me:

Wife:

Me:

Wife:

Me: (stands up)

Wife: While you're up...."

–@simoncholland

(This one hits a little too close to home. I LIKE SITTING, OKAY?)

"My wife and I are both working from home.

She microwaved fish.

Time to alert HR."

- @Xploding Unicorn

(Or a divorce lawyer. Honestly, woman.)

"Me, giving my husband's eulogy: It's so hard

Husband, from coffin: ᵀʰᵃᵗ'ˢ ʷʰᵃᵗ ˢʰᵉ ˢᵃᶦᵈ."

–@mommajessiec

(Even when he's stiff. That's what she said.)

"I miss how my wife would say "he's a rescue" whenever I misbehaved at parties." –@SladeWentworth

(The pandemic has ruined everything.)

"This needs to be over soon because my husband is starting to realize I'm not out of his league." @RachelNoise

(Seriously. COVID ruins every darn thing.)

"MIL: You have to teach them really young to pick up after themselves

Me: *watching my husband take off his socks and leave them in the middle of the living room*"

–@mom_ontherocks

(Ahem. Thanks for the advice, "mom.")

"I have a cold and it's pretty bad but my wife has a husband with a cold and apparently that's way worse." –@simoncholland

(I believe the Latin term for this is spousus patheticus.)

"[my husband has the man flu. After 3 days]:

M: will you please just take medicine??
H: *pouts* fine, what flavor is it??
M: what flav...it's ADULT FLAVORED!"

@jaxwax04

(Case in point.)

"Welcome to marriage. Here's the new way you fold towels." @HenpeckedHal

(And you're pretty much guaranteed to never do it quite right, so don't bother trying.)

"Made it to that level of marriage where you get in trouble for being able to fall asleep so fast." @simoncholland

(Oh, but wait until you find out what you did to piss her off in her dream...)

"My husband: We were way over on groceries last month.
Me: How did THAT happen?
Him: Well we spent like $100 on ice cream sandwiches...
Me: ...
Him: ...babe, that's bad.
Me: I HATE THIS PLACE IT SUCKS HERE"

@thearibradford

(Seriously. I'm a grownup, I do what I want.)

"My wife managed to open a jar of pickles herself and I am now nonessential." thedadvocate01

(It's okay. If you keep on taking out the garbage that she could take out herself, she'll probably keep you around.)

"Husband, "I'm going to the store, do you need anything?"

Me, "A bottle of champagne."

Husband, "Oh, I got you one yesterday.

"Me, "I said what I said.""

@Parkerlawyer

(And I meant what I meant.)

"My wife asked me if she had any 'annoying' habits and then got all offended during the power point presentation." @BattyMclain

(Hey now. Two can play at this game, buddy.)

"Husband: Does it bother you when I —

Me: Yes."

@mommajessiec

(Ouch again.)

"Wife: Are you just going to walk around all day without a shirt on?

Me: Just giving you a show.

Wife: Can I change the channel?"

XplodingUnicorn

(And they lived happily ever after.)

If I've learned anything in two decades of marriage, it's that there are few things a good belly laugh together can't fix. Here's to taking care of one another and finding the humor in marital bliss.

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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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