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The Spooners are a definite example of 'relationship goals' — and the power of love.

Silhouetted couple forms heart with sunset sky.
Photo by Dev Asangbam on Unsplash

Silhouette romance against a fiery sunset sky.

True
Muscular Dystrophy Association

To be around 56-year-old Ray and Rae Spooner is to be in the presence of a not-so-ordinary couple.

Then again, that's exactly who and what they've always been.


Rae and Ray in their garden.

Long before his successful career; before her job as his full-time caregiver; before the epic, unbelievable cross-country bike ride that would go on to raise thousands of dollars for the Muscular Dystrophy Association and ALS, they were simply Ray and Rae.

Two madly-in-love 23-year-olds who decided they wanted to travel the world together.

Their motto? "Never buy a return ticket."

The adventurers got married for one primary reason: Ray, a native Brit, needed a green card. Their plan was to divorce after one year because both had seen their parents endure painful divorces, and despite their love for one another, each was a bit skeptical of this marriage thing.

That was 1983.

Rae helps Ray get dressed.

They are now 33 years into what Ray playfully calls their "failed divorce" — a marriage happily settled in Urbana, Illinois.

The past three decades have seen Ray bring over 2,000 babies into the world as a beloved male midwife, a rarity in his field. Together he and Rae have three accomplished children, one beautiful grandchild, and a global community of people connecting with them through Ray's blog and the work they have done to raise awareness for ALS, the neurodegenerative disease that affects nerve cells in the brain and spinal cord, causing weakness and eventually paralysis of all voluntary muscles.

Their marriage is proof, in more ways than one, that life doesn't always go as planned.

"People always ask us, 'How do you stay married to someone for that long?' We say we're not married to the same person. We have let each other grow individually and grown together. We have never been planners. We go with the flow and deal with whatever life sends our way."

In 2014, that life philosophy was put to the test.

Ray leans against the wall and hold Rae's hand to get downstairs safely.

While sitting in the hospital as their daughter labored with their soon-to-be-born first grandchild, their son-in-law Cory was tagged in the ALS Ice Bucket Challenge, the viral video phenomenon that asked people to donate money to help find a cure for the disease or pour ice water over their head. Most people did both.

For kicks and to pass the time during a long labor, Cory decided to accept the challenge right then and there. As his wife continued laboring, Ray and Rae poured ice water over Cory at the hospital.

None of them knew much about ALS, but challenged in turn by Cory, days later Ray too had Rae dump a bucket of ice water over his own head — continuing the viral chain to raise awareness for the rare but aggressive disease.

Little did they know that two months later, Ray would be diagnosed with the debilitating disease himself.

When Ray heard the news, he immediately knew what he wanted to do with the rest of his life.

"We're all dying. As much as we're living, we're all going to die. Now I can't say 'When we retire...' Whatever we want to do, we've got to do it now." He calls those must-do's a "f*ck it list" (not a "bucket list" because you don't have to be dying to do what you want to do). And at the top of that list was a cross-country bike trip.

A decorative bicycle hanging in their home.

Ray, an avid rider, had always wanted to do it. But that desire was no longer just about him. Now it had to have a purpose.

Despite the fact that he already had diminished use of one of his arms, he decided that it was the right time for the trip. And he would do it to raise awareness for ALS and the work of MDA, whose local care center (at the same hospital where Ray worked as a midwife) had given them the kind of medical care and support that Rae said "all care should be like."

On Oct. 18, 2015, a small group of friends, neighbors, and of course Rae, began the awareness-building cross-country bike trip with him. They called it "Ray's Little Ride."

The exciting ups and harrowing downs of that ride — three trips to emergency rooms, an accident that left Ray with several broken bones and blood clots, and an outpouring of public support — garnered quite a bit of press and, in turn, a lot of money for MDA. Videos of support from all over poured in, including from children who Ray had helped deliver over his 20-year career.

On Nov. 19, 2015, Ray finished his ride — nonfunctional arm, injuries, and all. And to date, he and the ride have helped raised over $80,000.

Ray out on a bike ride.

Today, Ray can no longer speak and has even less use of his limbs and other muscles.

He communicates now only via text to Rae. She is his primary mouthpiece. To watch them together is to see love in action. No fanfare, no false humility. Just two people who know each other intimately living life together. She can read his every chuckle, eye roll, yawn, and head nod. She intermittently leans over and wipes saliva from his mouth during conversation. The laughter is nonstop.

Rae gives Ray some water.

Rae calls Ray an amateur documentarian. The walls of their home are filled with pictures of their family and memories of their life together thus far. Now, they have graciously allowed photographer Justine Bursoni to come into their life and capture this phase of their journey together. According to Ray:

"It's funny really. To see your life through the eyes of someone else. Initially there were things I didn't want to be documented. But our life isn't a fairy tale. To be true to the whole narrative you have to include the hard to deal with moments. And there are many."

The hardest to deal with part of it all has been thinking about their children.

"I have had 34 years with him." Rae says. "They have not. They are all handling it differently, in their own way."

Ray and his son, Manu, programming what they called "Rayism" into an eye-gaze-operated communication program.

The second hardest part for Rae has been watching the physical deterioration of Ray's body, despite the unchanging brilliance and alertness of his mind.

"'Ray is an incredibly creative person. He's a jeweler by trade. He built a lot of things in our home and he always loved working with his hands. Now he just can't. This beautiful hand, he can't do anything with.' Rae picks up his hand as she says this and gently waves it in the air. 'Each day it deteriorates more and more. That's been the hardest part. I think in my mind, I thought maybe we wouldn't get to this point.'"

Ray wears his wedding ring on his right hand now that his left is completely paralyzed.

"When he was first diagnosed," she says, they looked for the "'Ray Spooner kind of ALS' — the one where you live another 30 years and what has happened to everyone else doesn't happen to you." But it is happening. And they, like their children, are dealing with it in their own unique way. Rae explains:

"On one visit to the clinic they hand me this huge ass book and they say 'Here, this is for the caretaker.' I'm like nooo, that's not for me. We do things the Ray and Rae way. Were we going to follow this guide? No. We were going to do what works for us. For example, our bathroom is still upstairs and we still live in a split-level home. Or, instead of hauling a wheelchair into a van, pushing Ray around and driving to our doctor's appointment, this morning Ray got on his tricycle, and I walked beside him the entire way."

Rae helps Ray onto his trike for an evening bike ride to Meadowbrook Park.

That isn't to say they don't need help. The importance of accepting and asking for help has been one of their greatest lessons. Nowadays, their house is often full of friends and visitors — everyone willing to pick up a rag or a cup or do whatever they can to help. And that has been their greatest surprise of the journey: just how much people care and are willing to help. Ray reflects on this:

"Initially I think there is a tendency on both the part of the person with the disease and their caregiver to think 'OK, we got this.' But time will come when you will have exhausted all your physical and psychological faculties. Take names. Take numbers. Don't be afraid to pick up the phone. It takes a tribe."

Their daughter, Sophia, wipes the saliva from Ray's mouth as they all enjoy the company of former co-workers on their patio.

But at the core of their tribe is each other.

"This isn't about one partner or family member putting their life on hold to help care for the other. It's about a partnership moving into the next phase of life together," Ray says, speaking about what many see as his wife's "sacrifice."

"One day Rae asked me, 'How will I know you’re still with me?' While the question surprised me, I did have an answer. But when I tried to verbalize a response, I couldn’t get the words out. The thought that one of us would not be with the other had never really occurred to me. But if one of us is not there physically, the essence of that person remains embedded within the person whose life you shared. So, really, how can we ever not be together?"

Ray now wears a BiPAP to bed. Here, he works with Rae to calm down from a panic attack.

He continues,
"I’ve been making movies as gifts for various birthdays in the future for Rae when I’m not around. Rae says I’m her memory so each mini movie is about a certain time or event in our life. I'm up to her 64th birthday. I've also made wedding/housewarming gifts for each of the kids. A book for Rae chronicling our 34 years together (its over 600 pages). A message for Jack on his bar mitzvah. You get the idea."


"Planning for the inevitable is my drug of choice. It may not work for everyone, but it's how I get through. When you're initially diagnosed everyone sends you info about therapy and miracle treatments. But as I said, preparation is my therapy. Fairly early on I decided not to spend my time chasing more time. I'm spending my time spending my time. Making sure that Rae knows I will always be with her."

Rae and Ray look in the mirror and embrace in a similar fashion, as they did for a photo taken years ago.

Ray jokes with Rae about her writing an advice book someday. It would be called, "Things You Need to Know Before You Have to Wipe Your Partner's Ass." They both laugh hysterically when she says this, but there's power in the underlying message. True love at its best requires service.

He continues to blog about his life at Ray's Little Ride.

There, he gives a raw, humorous, and poignant take on life as he knows it — not just living with ALS but the universally human experience of trying to live life as it's meant to be lived.

"Whether we have a disease or not, there is a number to our days. There is risk inherent in walking out the door in the morning. But ALS has given me an opportunity. To not leave things undone or unsaid. That is a gift."

And that's what both Ray and Rae are focused on appreciating. With their blog and their breathtaking photos, they have laid their life bare for the world to see. And he says confidently that he would do it all over again, just to know that he is helping someone.

Rae helps Ray out the back door of their home.

Pets

Dogs really do have favorite people, and here's how they decide who it will be

Sometimes their favorite people don't live in their house.

Dogs really do have favorite people. Here's how they decide

When my sister's dog, Junior, was on this side of the Rainbow Bridge, I was one of his favorite people. This dog would get full body wags every time I came around, and we'd spend most of the day cuddled up with each other. Now my dog, Cocolina, behaves in the same way whenever my sister comes to visit. But what goes into a dog deciding who their favorite person is? Spoiler, it's not always the person they live with.

Like humans, animals have their own personalities. You might rescue a dog thinking it will be the perfect companion, only to have the furry adoptee spend every waking moment following your partner around. You could spend hundreds of dollars on vet checkups, new harnesses, treats, and all the squeaky dog toys you can find, but that still won't be enough to convince a dog to love you. Instead of showering the giver of treats with kisses, they make goo-goo eyes at the pet sitter. It turns out they have their reasons.

dogs; dogs favorite; dog's best friend; pets; people and pets; rescue animals Corgi cuddles spreading joy and smiles!Photo credit: Canva

Since our canine friends can't talk, we have to rely on the experts to explain what the deal is with how dogs pick their favorite human. Carol Erickson, a Pennsylvania SPCA animal advocate, gave a brief interview with CBS News Philadelphia to explain her take on how dogs determine their bestest, most favorite person.

"What it comes down to for all dogs is they decide their very favorite family member by who gives the most consistent, high-quality attention, play, and physical affection: ear rubs, scratches, that sort of thing. Dogs get positive associations from being around people who consistently provide positive experiences, including treats, meals, play that they enjoy, and remember also that early association in those first six months can influence who a dog may like better later on," she tells the outlet.

Rover backs up Erickson's claim that the first six months are crucial in determining who will become the dog's favorite person later in life. The website says, "Many dogs bond hardest to whoever cares for them during their key socialization period, which occurs between birth and six months." However, they later note that dogs can still be socialized appropriately even as adults.

The dog-sitting website also explains that it's not uncommon for people who are not the dog's primary caregiver to be their favorite person. Pointing out that physical affection is vital to dogs, if the mailman gives out head scratches daily but the owner doesn't, the mailman may become the dog's favorite person. While physical affection and treats go a long way for some pooches, those aren't the only things that get puppy eyes melting with love.

dogs; dogs favorite; dog's best friend; pets; people and pets; rescue animals Joyful moments with furry friends! 🐶❤️Photo credit: Canva

"While positive experiences play a big role, a dog’s favorite person isn’t always just the one holding the treat bag. Dogs also respond to emotional connection, tone of voice, and even body language. Their preferences are shaped by a mix of familiarity, trust, and how well a person understands their needs," explains Elle Vet Sciences. They later add, "Dogs also take emotional cues from us. If a person is stressed, loud, or inconsistent, a dog may be less likely to form a deep bond with them. On the other hand, someone who offers reassurance and stability often earns the title of 'favorite' without even realizing it."

In short, if you want to be your dog's bestie, being consistent with affection, actions, and even training and grooming will get you there a lot faster than treats alone. Dogs aren't trying to be persnickety; just like humans, they enjoy being around people who show them that they enjoy their company—and maybe some treats.

Netflix/YouTube

Mats Steen led a richer, fuller life than anyone new.

Tragically, Mats Steen was only 25 years old when he passed away, his body succumbing to the genetic disease that had slowly taken his mobility since childhood. He'd lived in a wheelchair since his early teens, and by his 20s, his physical abilities had deteriorated to the point of only being able to move his fingers. He could push buttons and use a mouse, and he spent nearly all of his waking hours playing video games in his parents' basement.

His family loved him and cared for him through it all, giving him as much of a normal life as they could. But they also lamented everything they knew he'd missed out on. "Our deepest sorrow lay in the fact that he would never experience friendships, love, or to make a difference in people's lives," Mats' father shares.

Mats left behind the password to a blog he kept. Not knowing if anyone would actually read it, his parents published the news of Mats' passing in a blog post, adding their email address in case anyone wanted to reach out.

Much to their surprise, messages began pouring in from around the world—not just with condolences, but with heartfelt stories from people who called Mats their friend.

The Steens soon discovered that their son had lived a much fuller life than they'd ever imagined—one that included all the things they always wished for him.

As his online life was revealed, the family learned that Mats began his days with a routine 30-minute sprint through the forest. He frequented cafes and pubs, chatting with strangers and flirting with women. He sat by campfires having heart-to-heart conversations. He made friends and enemies. He fought heroic battles. He supported people in times of need. He gave advice that people took. He experienced his first kiss.

And he did it all as "Ibelin," his handsome, muscular avatar in the online game World of Warcraft.

- YouTube youtu.be

Mats' life is showcased in the documentary The Remarkable Life of Ibelin, in which his parents share the story of how they discovered their son's group of friends they didn't know he had.

People who've never played an open world roleplay game like World of Warcraft may wonder how real community can be built through it, but Mats' story proves it's possible. The friends he made through the game have shared the real influence he'd had on their real lives, from helping them with problems they were facing to empowering them to make positive changes in their relationships.

Though he never met them face-to-face, Mats' online friends say he made a significant impact on them.

A young woman Ibelin had connected with as a teenager—the one with whom he'd shared that first virtual kiss—shared that her parents had taken away her computer when they feared gaming was interfering with her studies. When she logged on at a local library, Mats gave her a letter he had written to give to her parents, encouraging them to talk with her about her gaming hobby and to work out a solution together that didn't require her to give it up completely. She printed it and gave it to them. Miraculously, it worked.

Another woman had been having a hard time connecting with her autistic son as a young adult. When she talked with Ibelin about her struggles, he suggested that she and her son start gaming together and connect in that way first. Eventually, that connection via the virtual world led to warmer in-person interactions between them—and a life-changing shift in their relationship.

"I don't think he was aware of the impact that he had done to a lot of people," the mother shared.

Mats interacted with the same online friends as Ibelin for years, going through the kinds of ups and downs all friendships experience. He kept his physical condition a secret until close to the end of his life, when he finally opened up to another player who convinced him to share his reality with the others. Some traveled from other countries to attend his funeral, with one of them speaking on the group's behalf and a few of them serving as pallbearers. Those who knew Ibelin also held a memorial in-game at his virtual gravesite—a tradition that has spread beyond just his own guild.

Typically, we think of someone escaping the real world and spending hours a day playing video games as unhealthy, but for Mats, it was a lifeline. As Ibelin, Mats was able to have a level of independence and a rich social life that simply wasn't possible for him in the offline world—an uniquely modern phenomenon that technology and human creativity have made possible.

Mats' impact on his online community was real, and 10 years after his passing his impact is spreading even further.

Duchenne muscular dystrophy (DMD), the genetic disease that Mats lived with and ultimately died from, affects 300,000 boys worldwide. It only affects males and it has no cure. But CureDuchenne, a global nonprofit dedicated to funding and finding a cure, partnered with video game company Blizzard Entertainment's World of Warcraft in Mats' honor from the end of 2024 until January 7, 2025. During that window, World of Warcraft players could purchase a limited-edition pet fox named Reven ("fox" in Norwegian). The Reven Pack, which includes a transmog backpack and Reven’s Comfy Carrier, costs $20, with 100% of the purchase price being donated to CureDuchenne.

The Reven Pack on World of Warcraft—100% of purchase cost goes to the CureDuchenne foundation. World of Warcraft/CureDuchenne

“Mats Steen lived a life in World of Warcraft that he couldn’t in the real world as he fought Duchenne muscular dystrophy alongside his incredible family, who I’m proud to have met and fallen in love with,” said Holly Longdale, executive producer of World of Warcraft. “Working with CureDuchenne for our Charity Pet Program, in honor of Mats’ memory, allows us to harness the power of our phenomenal global community to bring meaningful impact to so many lives.”

In February 2025, CureDuchenne announced that The Reven Pack raised over two million dollars in support. Later in the month, Debra and Hawken Miller of Cure Duchenne spoke with ViceVice and shared how The Reven Pack helped raise valuable awareness about Duchenne in addition to funds. For those interested in updates, the site keeps donors and supporters current on all developments in Duchenne research news.

Mats life was truly impactful in many ways and to many people. His love, kindness, and friendship touched lives and his legacy continues to help those struggling with this rare disease. According to the site, since the inception of CureDuchenne, life expectancy for those with the disease has increased by a decade and over fifty million dollars have been raised for research, education, and care.

You can learn more about Mats' story in the award-winning documentary, The Remarkable Life of Ibelin on Netflix.

This article originally appeared last year. It has been updated.

Photo courtesy of Kerry Hyde
Do cat buttholes touch every surface they sit on? Science answers.

Cat owners are a special breed of people. Sometimes, in dealing with feline friends, they have unique questions that even Google doesn't always have the answer to. This is probably the sole reason cat forums exist, but one kid who needed a 6th grade science project decided to skip the cat forums for answers and instead use the scientific method. Kaeden Henry, a sixth grader living in Florida, bravely pondered a question few (if any one) has been brave enough to ask: do cat buttholes touch every surface they sit on?

Since cats do whatever the heck they want, training them not to jump on kitchen counters is a feat even Hercules struggles to complete. These fierce felines don't care if you're cooking dinner or trying to get comfy in bed. If they want to sit somewhere, they're going to do it. The thought of cat butts on that expensive Serta pillow designed to feel like you're sleeping on a cloud can gross people out, but thanks to Kaeden, you no longer have to wonder if the butthole itself is also making contact.

cats; pets; cat lovers; cat parents; cats on counters; cat butts, pets, animals, humor, funny, science The scientific method as it was meant to be used.Courtesy of Kerry Hyde

The curious sixth grader is homeschooled and well-versed in the scientific method thanks to her mother's PhD in animal behavior with a concentration in feline behavior. And, since they own cats, the science experiment was pretty straightforward (and directly impactful).

To complete the experiment, Henry and his mom, Kerry Hyde, bought non-toxic lipstick and applied it to each of their cat's anuses. Then, the cats were given commands. (Commands... hilarious, right?)

cats; pets; cat lovers; cat parents; cats on counters; cat butts, pets, animals, humor, funny, science What are you planning on doing with that lipstick?Courtesy of Kerry Hyde

"Non-toxic lipstick was applied to their bum-bums, they were then given a series of commands (sit, wait, lie down, and jump up. Side note: Both cats have been trained since kittenhood with a variety of commands, they also know how to high-five, spin around, and speak.), they were compensated with lots of praise, pets, and their favorite treats, and the lipstick was removed with a baby wipe once we collected our data in just under 10 minutes," Hyde wrote in a Facebook post.

The results? Turns out that, no, cat buttholes do not touch every surface cats sit on.

Now, let's all take a collective sigh of relief while we go over the details. Kaeden's experiment covered long-haired, short-haired, and medium-haired cats (if your cat is hairless, you better stock up on Clorox wipes just in case).



"His results and general findings: Long and medium haired cat’s buttholes made NO contact with soft or hard surfaces at all. Short haired cats made NO contact on hard surfaces. But we did see evidence of a slight smear on the soft bedding surface. Conclusion, if you have a short haired cat and they may be lying on a pile of laundry, an unmade bed, or other soft uneven surface, then their butthole MAY touch those surfaces!" Hyde shares.

Now every curious cat owner can rest easy knowing that as long as their cat has hair, their bare bottom balloon knot is not touching the majority of surfaces in their home.

cats; pets; cat lovers; cat parents; cats on counters; cat butts, pets, animals, humor, funny, science You want me to sit on that?Courtesy of Kerry Hyde

The amusing experiment caught the Internet's attention. People laughed and commented, with one person writing, "This is probably the most useful information I’ve learned from a science fair project."

"Good to know!...I can now eat my sandwich left on the counter with confidence!" another writes.

cats; pets; cat lovers; cat parents; cats on counters; cat butts, pets, animals, humor, funny, science High five for an A+! Courtesy of Kerry Hyde

"A+++!!! Whew!! I am very grateful for your sciencing on this subject. My fears from walking in on my cat sitting on my laptop keyboard and subsequently being grossed out and cleaning furiously in a hyper-ocd manner have been somewhat allayed and now maybe I won’t have to use QUIIITE so many wipes." someone chimes in.

"Finally.. Someone answers the important questions!!"

The best part of the story? Kaeden's mom has a Ph.D. in animal behavior, specializing in feline behavior, and even she learned something new. The power of science!

This article originally appeared in April. It has been updated.

Jane Goodall leaves behind hope and survival guide for trying times

Jane Goodall was a wildlife conservationist, zoologist, and anthropologist. Her incredible career spanned multiple decades, resulting in the scientific community and animal lovers alike having a deeper, more thorough understanding of chimpanzees. The conservationist is most famous for living amongst the Gombe National Park (previously Gombe Stream Game Reserve) in Tanzania.

The anthropologist's approach to wildlife conservation was solidified when she founded the Jane Goodall Institute, where she expanded her work to include global advocacy "for human rights, animal welfare, species and environmental protection, and many other crucial issues," according to the institute's website. In their long tribute to Dr. Goodall, the institute reveals that the scientist dreamed about writing books about her work with animals since she was a child. A dream that came true, as the now late conservationist authored over 25 books.

Jane Goodall; hope; surviving trying times; survival guide; chimpanzees; Jane Goodall Institute Smiling woman with grey hair and blue shirt.Nikeush/Wikimedia

Goodall passed away from natural causes in October 2025 while on a speaking tour. She was 91 years old and still extremely involved in the work that has defined her life. While the humanist wrote books for children and adults, her final book, written in 2021 with Douglas Abrams and Gail Hudson, was left behind as a reminder of hope in hard times. The Book of Hope: A Survival Guide for Trying Times just might be one of the most treasured gifts one human can leave for humanity. It's fitting that Goodall helped author it.

Within the pages of the book, Goodall lists four reasons for hope: human intellect, the resilience of nature, the power of young people, and the indomitable human spirit. In the book, Goodall drives home the point that even in the most trying times, hope isn't something that happens blindly.

Jane Goodall; hope; surviving trying times; survival guide; chimpanzees; Jane Goodall Institute Discussion of chimpanzee behavior with an iconic photograph backdrop.World Economic Forum/Flickr

“Hope is often misunderstood. People tend to think that it is simply passive wishful thinking: I hope something will happen but I’m not going to do anything about it. This is indeed the opposite of real hope, which requires action and engagement,” she says.

In response to the back-and-forth dialogue between Goodall and Abrams in the book, Abrams explains the zoologist's approach to hope by adding, "She says that people who wonder how you can have hope in seemingly hopeless situations, like a death camp, confuse hope with idealism. Idealism expects everything to be fair or easy or good. She says it's a defense mechanism not unlike denial or delusion. Hope, she says, does not deny the evil but is a response to it. I was beginning to see that hope was not just wishful thinking. It did take the facts and the obstacles into account, but it did not let them overwhelm or stop us. Certainly, this was true in many seemingly hopeless situations.”

Hope is a theme throughout a lot of Goodall's writings and interviews. When speaking to Democracy Now in 2016, she was asked how one person can make a difference, and her response may help others who feel as if they've been working towards change without reward or results.

"Well, the thing is, it's not about one person. Can they make a difference? Everybody, every day, does make a difference. And if we think about the consequences of the choices we make, what we buy, what we eat, what we wear, and we start making the right ethical choices, then when that's multiplied by a thousand, a million, a billion, several billion times, and we see the world moving towards change. So the most important thing is to give people hope."

Image via Canva/Zinkevych

People share their absolute favorite words.

Without words, communicating with each other would be a lot more difficult. According to Merriam Webster, there are estimated to be about one million words in the English language (although there is no official count).

Some words are simply pure joy to say, like onomatopoeia—words that are a vocal imitation of the sound they are associated with it, such as "buzz" or "hiss." While other words hold special meaning or a silly backstory, some words can make you physically cringe.

Over on Reddit, linguistics lovers and grammar enthusiasts created a rich conversation delving into words that just hit. Here are 43 words that they absolutely adore:

- YouTube www.youtube.com

"Everybody has a favorite word. I have 2. Falafel & wicker. Just because they're fun to say." - AngelicDaemon420

"Onomatopoeia because of it's cadence and the idea of a word sounding like the thing it describes. It's like poetry in my ears." - MuckleRucker3

"I could never pick just one. There's like a top 10 or top 20. Some of them are starling, decanted, apoplectic, crestfallen, hubris." - rgtgd

"Scallywag and crocodilian are two of my favorite words. Also, the name Talleyrand is also great." - Hoppy_Croaklightly

"Cahoots." - looking4truffle

"Spleen and squeegee. They're both just fun." - scipio0421

"Indubitably and brouhaha." - lucidwrld4

"Mellifluous. Mellifluous means flowing like honey, Latin origin." AshevilleRen, Pristine-Pen-9885

- YouTube www.youtube.com

"Petrichor. I just find it so niche and precise." - dreamrock

"Facetious and abstemious because they both have all the vowels, in order. But I also like discombobulated, just because." - Horror_Bake4106

"When I was a teenager, my favorite word was spaghettification (what they believe happens inside a black hole). Now I lean towards onomatopoeia." - illizzilly

"Murmuration and defenestrate, for both the way they sound and their meanings." - jeekle

"Plethora. It means a lot to me." - Fosad

"Entendre, it just flows nicely. Also a fan of juxtaposition for the same reasons. No meaning, simply phonetic." - duh_nom_yar

"Tomfoolery. It's just so old-timey, as in 'what manner of tomfoolery is this?' And it has never become trendy again..." - AuNaturellee

"Skedaddle makes me laugh when I say it. Schadenfreude.... I love German words." - Royal_Ad_6026

skedaddle, skedaddle gif, you better skedaddle, skedaddling, skedaddle funny skedaddle gif Giphy

"Defenestration! Because of course we need a specific term for being shoved out a window. Also sphygmomanometer, but medical terms seem like cheating." - aequorea-victoria

"Vapid, it just sounds vicious when used. Cacophony is another fun one to say. My all-time favorite to say is French for butterfly- papillon." - Familiar-Year-3454

"Serendipity and tranquil/tranquility. They both sound like exactly what they mean." - nutcracker_78

"Overmorrow. The day after tomorrow." - isobel-foulplay

"Rancor. It always sounds so badass when people say it." User Unknown

"Phosphorescent. It’s a shame you can’t work it into many conversations." - jnadols1

"I like how awkward 'awkward' looks." - Etherbeard

awkward, awkward gif, awkward word, awkward word, awk, awks Awkward Ed Helms GIF by The Office Giphy

"Luxuriate is a great verb with a great vibe :D." - LittleNanaJ

"I love the word 'dialectic'—both pronunciation and meaning." - Jedi_Temple

"Tintinnabulation. I remember learning this in junior high when we read Poe’s The Bells. It’s a great descriptor. His use of words to so clearly describe each type of bell fascinated young me. Tintinnabulation was a word I had never seen before. And since back in the dark ages we had to read aloud in class and memorize poems this word fascinated me. I fell in love with poetry because of this word." - ReadNapRepeat