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People like to feel special in some regard. When we're kids, it's about having the latest and most popular toy. When we're teenagers, we want to be popular or stand out from the crowd by being different from everyone else. Listening to and gatekeeping pretentious, obscure bands was my thing, personally, but there's no judgment among Pandas, right?
In a couple of threads online, people started sharing what makes them different from everybody else. The answers to the question "What are you in the 1% of?" varied: people covered everything from genetics, unique experiences, and, of course, some morbid stuff.
But what exclusive club do you belong to, dear Pandas? Don't forget to share with us in the comments and let us know what makes you special!
This post may include affiliate links.
#1
I had pancreatic cancer last year. Out of 10,000 patients they normally find 100 who have another form of this cancer who kill a little slower, like in 2 years instead of months.
I was one of the hundred. Out of those, normally 15 can have surgery. I was one of them.
Out of those 15, some die and some come back to basically normal life.
That's about a 0.07% chance in all.
I am still one of them. I should be dead by now. 🙂.
RELATED:
#2
Mine's pretty godawful. I have 2 uteruses.
Edit: lot of people asking why I put up with it till I was around 33. *I* *didn't* *know* . Because doctors don't listen to women complaining of menstrual issues, is why. The endless pain and bleeding? Suck it up, take 3 Advil not two (holla). Starting at age 12. Till I lucked into a rare empathetic gynecologist who, since I'd always known I was uninterested in parenting, offered me a minimally invasive (just removes the top of the uterus, the rest of me stayed there) hysterectomy to stop the pain and hemorrhaging. And in doing the surgery, he discovered what no other doctor had cared enough to find.
I love that guy!
N.B. in the States, it is rare and usually extraordinarily difficult for a young woman who has not borne children to get a voluntary hysterectomy. Criminal.
Fishpanda (fish/panda/it) 2 months ago (edited)
US needs better women's rights. A lot of surgeries that have to do with the uterus are refused for one stupid reason or another.
Roni Stone 2 months ago
At 68 years old, I had a 55+ pound ovarian cyst removed. I thought I was gaining weight - even the doctor thought that's what it was. During the pandemic it ballooned, and I could barely walk. Still didn't know what it was and was honestly afraid to go to the doctor because of the virus. Eventually had an unrelated chest CT that showed the cyst protruding into my abdominal and chest area. Fast forward and I was in surgery within three weeks. My surgeon was stunned but walked out of the hospital almost 60 lbs lighter. Only about 1% of women will experience a cyst that size in their lifetime.
MoMcB 2 months ago
Terrible. I have a friend who experienced similar in the UK, but yours is about twice the size. Hope you are on the mend x
Load More Replies... Disgruntled Panda 2 months ago
I'm now 37 and have never wanted children, not wavered once. Still I'm not allowed a hysterectomy because "I'm a fertile woman and might change my mind". This is in the Netherlands btw
MoMcB 2 months ago
When I was married to my ex (UK), I wasn't allowed unless he said yes. Has one at 57. The relief was palpable.
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Alia Hood 2 months ago
I went through hell before they found I had 2 (bicorneat uterus I believe is the name, I'm sure I spelled it wrong). Even after finding out, it took another 8 years before I found a gynecologist that would give me a hysterectomy.
Clown fish 2 months ago (edited)
It's called Uterine didelphys my friend has the same thing they knew before she was born that she has two as they could see them both on scans. She had 4 successful pregnancy and had a hysterectomy last year with they were doing the C-section for her last baby. A bicornate uterus is one that's the wrong shape they tend to end up love heart shape.
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Jane 2 months ago
Wouldn't they have seen that on an ultrasound? My first ultrasound was when I was 12... I had PCOS. The doctor wanted me to go on the pill to help with the symptoms. I wish he hadn't called it that, because my mother said we were Catholic and therefore couldn't take birth control. So I had to suffer until I was 21. Had I known PCOS contributed to infertility, I would have had a surgery to stop the madness. After adopting, my doctor still refused to do a surgery, because he said I might want to have more kids down the road (???) even though I explained my husband had a vasectomy (he said I might remarry?????). I never went back to him again. He should absolutely not be an gynaecologist!
Ansi 2 months ago
I don't know how it is for other people, but when I did a ultrasound in week 11 with my second child, and they knew what they were looking for, they had a hard time seeing my second uterus because it was like a deflated ballon pressed against the one. Later in the pregnancy they couldn't see it at all. Same with my second cervix, I had taken tests for cervixcancer and they never seen it. (It's smalland a bit deformed) I think my doctor said it best: when you see it (the thing they are about to examine) you don't keep looking.
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Lupita Nyong'heaux 2 months ago
i, too, had 2 uteruses, and my menstrual cramps were agonizing. i'd be incapacitated the first 2 days. when we were in college, we discovered that smoking a joint was the only thing that helped. so, every month when it started, my sister would go out and find a joint from somebody and bring it back to the room. best. sister. EVER!
Jenny Mason 2 months ago
It's not just the US. Here in the UK they can be pretty adamant about this stuff. My daughter has 6 children (hyperfertility) and was begging to get her tubes tied after number 3. They refused point-blank. She had 5 sons and then a daughter, only after the daughter was born 2 years ago did they finally agree to the surgery.
Ansi 2 months ago
I refuse to think this puts you in a 1%. I have two functional uteruses. I have different periods, one gives me mostly spottings and no pain, the other one is like a sharkweek. They discovered this after 24h in labour with my first child, my two birth canales are twisted with each other so I can't give birth. With my second child I was scheduled for a c-section but my placenta detached and we almost died. I was sterilised after that because the placenta could detach earlier with a third pregnancy so the baby would die, and with my second one he/we lived because we already was at a hospital..... and yes, they both work and my two kids didn't even want to share uteruses so they used one each. (It would be cool to have siblings like this and it has happened that a woman had siblings due with a few months apart. THAT is definitely 1%)
Mylo 2 months ago (edited)
It's actually closer to 0.5%. Although it often goes undetected due to reasons similar to OP's, so it's likely to be higher, but not by much.
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MrsFettesVette 2 months ago
Only 3 Advil?? I normally take four at a time and that barely touches my pain.
Agat 2 months ago
4 of which dose of ibuprofen? I was just wondering, why not switch to stronger meds? Or better yet, some antispasmodics?
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Deb Dedon 2 months ago
Most of us with excess pain are dismissed even now and at no point do we learn that having more than one uterus is even possible. However, many years ago a prominent magazine in the US (can't recall the name) produced a story of a woman who was told that the child she just bore wasn't hers because the genes didn't match! She ultimately learned she had two uteruses which didn't match genetically and she recovered her child. The cause of the double organs was thought to be that she started out as a pair of fraternal female twins and during the early stages of development, one twin (her) enveloped the other. All that was left of twin #2 was the uterus.
Hiram's Friend 2 months ago (edited)
Knew a girl with the same problem, but with two sets of ovaries and a vagina with a septum. Or so she told me.
Hiram's Friend 2 months ago
Saw this on the news the other day and just remembered it: https://edition.cnn.com/2023/12/24/health/woman-two-uteruses-birth-twins/index.html
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JessieJ&LilyLovebug 2 months ago
It would help if all the women were on the same side of the issues.
Roan The Demon Kitty 2 months ago
In the UK it's hard to get a hysterectomy too. I have a gynaecological cancer, and was supposed to have it removed as part of debulking surgery, but it didn't happen (because they said they saw no reason it should be removed, as there was no cancerous cells on it, as it had spread elsewhere (in my case, to the peritoneum and some lymph nodes etc) so I suppose in a way I should be glad... but still. gotta deal with my godawful periods for longer now, despite the fact I can't carry a child should i want to get pregnant anyway.
UncleJohn3000 2 months ago
If I sat in that position, it would take a team of paramedics, physical therapists, and a few pro wrestlers to get me back to standing.
NennyRoh 2 months ago
"Invisible women" from Caroline Criado Perez is a very good read on that topic, but caution! Your blood pressure will definitely go up
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Philly Bob Squires 2 months ago (edited)
The US needs an overhaul. Don't you know that politicians and judges know more about medicine than say... oh... over a million fully educated and studied doctors?? And on top of that, some kid in a suit fresh out of business scool gets to determine if your possibly terminal but curable issue is "elective" or "unnecessary" so is therefore not covered? And 14K a year for insurance that you can't use until you pay a 6 to 7K deductible? And our poor women. Yeah, we're not doing so well in the healthcare department.
Scott Rackley 2 months ago
My sister is the same. Didn't find out until she was pregnant with fraternal twins. Complications galore. They were born on their grandmothers bday, premature but came through strong.
Sara Frazer 2 months ago
I wish I could have a hysterectomy. I've been trying for a few years.
Jelena Kovacevic 2 months ago
A family friend of ours had 2, and never knew until she got pregnant 2x within 2 weeks....when she went for the scan for what she assumed was one baby, they saw the other one.......which measured smaller.....so even though they are born at the same time, and technically twins...they are 2weeks-ish apart as far as gestation goes, and not twins at all
#3
I have a double gene mutation that makes me highly resistant or even immune to the HIV virus.
Fishpanda (fish/panda/it) 2 months ago
I've been reading a lot of books on HIV for an essay recently. This is an amazing trait to have.
#4
I fell off a 100 foot cliff and landed head first on rocks.
Broke my neck and back. Smashed up a lot of my body. Had to travel about a mile to find help immediately after the fall. Doctor said I caused more damage by trying to walk for help, but would have bled out if I stayed where I fell. 15 months later, I am power lifting and ran a half marathon. Should not be alive, much less be able to walk.
EDIT:
How: Camping on a mountain. Found a spot to lay down and observe the stars. Had to pee, stepped into woods, lost my footing. Geronimo.
Injuries: Head was scalped. Huge piece of flesh was just hanging off my head. Must have been a sight to the folks who's door I knocked on in the middle of the night for help. Neck was broken and had to wear an immobilizing neck brace for many months 24/7, as they were concerned surgery may cause more damage. Initially a had a loss of sensation in my hands. Multiple vertebrae were broken, one had broken into over a dozen pieces. The neurosurgeon figures at impact my body folded in half causing that one to essentially explode. I had to have spinal fusion and relearn how to walk after. Multiple ribs broken.
Recovery: At first I essentially lived in one of those geriatric chairs that lift you up to stand. I could barely get around with a walker. Sitting on the toilet was the most excruciating thing. At some point it turned into laxative use and stand in the shower. I couldn't bend or care for myself much in any way. Some of my friends think that being a Marine made me tough enough to survive this, but I credit an inherent stubbornness to never give up. I constantly pushed through the pain to get myself to the next level. From walker, to cane, to walking sticks. The neurosurgeon told me the best thing I could do for physical therapy was walk, so boy did I. At first I could barely make it to the end of the block and back, then a quarter mile, then on and on. Every hard effort day required a day or two of sitting in the chair and suffering through the pain. Got off meds the moment that I could stand to. 5 months after the accident I got on a treadmill and tried to run. The impacts were excruciating, but I kept coming back for more and more. At 10 months I was able to race in a 5K on memorial day in honor of a fallen veteran. I raced my heart out and was able to run it in less than 30 minutes. I immediately began half marathon training and at 14 months was able to finish at about 2 hours and 40 minutes. Started back to lifting serious weights at about 11 months and here I am in month 16 about to become a member of the 1000 pound club. (Bench press, deadlift, and squat all totaling 1000 pounds.) I still deal with pain regularly and I have a lot of discomfort that makes sleep challenging. I've still got a couple of months until the bones reached 100% of their healing potential.
It's been quite a journey. Never give up my friends!
#6
I’m one of only @200 deaf pilots in the world and one of only four (that are commonly known of) in the world with Commercial & Instrument training.
I’m also one of the only deaf people who hold both a pilots license and a commercial drivers license.
FoxEcoLimaIndiaCharlieIndiAlfa 2 months ago
So I just learned something new because of this post. I was under the impression that in order to hold a commercial driver's license CDL, one has to pass a hearing exam, but in 2013 a law was passed allowing deaf people to apply for a hearing waiver which includes other documents. This is awesome for all those in the non hearing community.
#7
Only 2% of pregnant women experience 2 miscarriages in a row. Only 1% of women experience 3 miscarriages is a row. I have had 5 miscarriages in a row and I fully hate any type of statistics now. Statistics used to make me feel safe. Now I just know how easy it is to be on the wrong side of them.
Edit: Thank you for sharing your support and your stories. I feel for so many of you that also make up the 1% (or less than 1% I guess). Sending all the love and healing your way if you’re in this same sucky boat as me.
BeesEelsAndPups 2 months ago
This is so awful. I know from experience how dismissive doctors can be of women who've just experienced a miscarriage. In general, as a male person, I feel like women got the sh*t end of the stick in most things in our society. I don't know why people as educated as doctors have to pile onto the trauma (speaking from personal experience of two miscarriages)
#8
Survival. I fell 25 feet out of a window when I was about 2 years old. I’ve also been hit by a car that was traveling over 50mph/80.4kmh. I’ve had two near drownings. I was also held hostage at gun point for over three hours. All if these things happened before my 14th birthday.
#9
Genetics. A red head with ab- blood and hazel eyes. I’m a walking recessive gene.
Sinclair13 2 months ago (edited)
I have blonde hair, ab- blood, and green eyes. My second toe is also longer than my first toe.
#10
I’ve been in 2 helicopter crashes and 1 plane crash. There is only a small group of people who have survived that many crashes. I’m also not a pilot.
Nathaniel He/Him Cis-Het 2 months ago
Don't take this the wrong way, but I am not getting on a flight with you.
#11
I suffer from a relatively harmless “phenomenon” called “Aphantasia”.
I am incapable of conjuring images inside my head. I “know” what object or thing I’m supposed to think about but all I see is nothing.
When I dream, I know what’s happening and what I’m supposed to see but it’s just a whole lot of nothingness. I guess you could say I’m “blind” in my mind.
Apparently around 1% of the population suffer from this weird condition.
Must be nice having a screen in your head that shows anything you can imagine :/.
#12
I can make my eyes shake (voluntary nystagmus) and I can wiggle my ears.
It was a lot more impressive when I was 7.
Traveling Lady Railfan 2 months ago
Hey, me too! My brothers as well! It was fun as a kid to tell others "hey, look at my eyes" ....then they vibrate back and forth like a paint mixer and freak people out! Lol!! I don't bother with it anymore.
#13
Cancer survivor. Think that’s 5%. I had it 3 f*****g times.
#14
Far less than 1% of people make their living creating crossword puzzles. I've also written five novels, three of which were published.
#15
According to my step counter, walking.
Not even kidding, I manage a warehouse and walk 10-15 miles a day at work. Apparently this is more than 99.3% of users.
Turns out the one thing I'm exceptional at is the one thing almost everyone can do. Yay.
#16
Not me but my dad.
He was born with a backwards heart and didn’t find out till his heart attack a few years ago and it actually saved his life.
His doctor later told him that after being a doctor for over 30 years he’d never seen someone with a backwards heart and that apparently 1% of people on the planet have it.
Stephanie Did It 2 months ago
Does that mean the heart is on the opposite side of the body than normal, or that the heart is in the usual place but facing towards his back?
#17
I’m naturally ambidextrous. Apparently that’s something only 1% of people naturally are. I can use both right and left hands ably for any task. For example, I often switch which hand I write with based on how I’m sitting.
(It’s worth noting _natural_ ambidexterity is not the same as _learned_ or _acquired_ ambidexterity. For example, left handed people often have to use things designed for right handed people but otherwise are left handed.).
#18
Typing in my PC.. I can type up to 170 WPM sometimes, and in the human benchmark site that's 1%.
#19
Surviving a crossbow to the head. Directly between the eyes. Only one other person has been documented in surviving a crossbow head impact, and they became brain dead. Not only did I survive, but I still have enough brain function to type this out and even go to work on a daily basis. I'm very blessed to be here, and I do my best to not take it for granted.
Edit: apparently more people have survived this than I originally knew, and that's kinda cool to know!!
Edit 2: holy crap I did not expect this to blow up so much!!! Thank you all so much for the kind words and awards!!! I'm not going to reply to everyone just because there's so many comments, but if you have a question feel free to ask and I'll do my best to respond!!
#20
Mirror writing:
writing the same exact thing with my left hand, except backwards and to the left, while I write it normally and with my right hand.
#21
I’m an American of North Korean descent
#22
My actual name. My last name is one of the rarest in the country and I am the only person with my name out of the entire population.
MrsFettesVette 2 months ago
This is also true for me! I actually didn't think it was that rare. If you have an unusual last name it's gotta be pretty common to be the only "you".
#24
So apparently my left eye is 32mm. The average size is 21-27mm. My eye doctor said it was neat.
#25
I am a super recogniser. Super recogniser is a term coined in 2009 by Harvard researchers for people with significantly better-than-average face recognition ability. I am not in 1 percent to be precise actually, it is around 2% but wanted to share anyways.
There is a free online test for you to check if you are one as well.
#26
If you make 40k a year and have no debt... Wealth, globally speaking.
#27
Eyesight. I have 20/10 vision, turns out only about 1% of people have better than normal 20/20 vision.
BrunoVI 2 months ago
My Dad was a big Ted Williams fan. The best hitting non-Yankee in baseball history, and it was largely due to having freakishly sharp vision. The guy could read the stitches on the ball coming at him (which would tell him which way the pitch was going to bend or not bend). Never topped many career milestones because he served as a bomber in WW2 for three years, and went right back and served another two in Korea.... he thought he owed it to his country to put his eyesight to the best service possible.
#28
I'm a totally in the 0.2% of something. People who have a rather nasty reaction to the blood thinner, Heparin. Lost half my toes because of how lucky I am.
#29
Grandmaster in league of legends (0.02%) 😎, this results in not having a social life or girlfriend so don’t recommend.
_-DungeonKeeper-_ 2 months ago
It's OK I don't have a social life or any romantic interest in anyone whatsoever anyway
#30
Degrees. I have a BA, MA, JD and two PhD's. If I'm not mistaken, less than 1% of the world has that many (and neither should I).
Nathaniel He/Him Cis-Het 2 months ago
Did you hear about the man with 360 degrees? His education went full circle.
#31
I can stop my hiccups on command.
RaisedByCats 2 months ago
My husband can too and cannot fathom why other people can't control it ("you just tighten the muscle at the top of your stomach")
#32
Birth control. 99% effective right? I'm living proof of the 1% XD.
(It's cool though, my parents never acted like they didn't want me.).
#33
According to Amazon, I'm in the top 1% of kindle readers. They keep track of these things and within the last couple years started sharing the info with users as seasonal "Achievements."
At the end of the Spring season, they sent out emails with the final data: from April 1st to June 31st I read:
74 days
For a total
193 hours.
I don't really have a social life. As though that wasn't clear enough from the stats
#34
I’m of the .002% of people with osteopoikilosis. This freaked the s**t out of me because when I was diagnosed the first thing the doctor said was “wow I’ve never seen this in anything but textbooks before”...
RaisedByCats 2 months ago
Osteopoikilosis is a benign, autosomal dominant, sclerosing (hardening) dysplasia of bone characterized by the presence of numerous bone islands in the skeleton. (Wikipedia)
#35
I'm one of around 1% of people directly related to Swedens great king Gustav Vasa, still living. I'm one of 100k people.
#36
I have AB- bloodtype. Less than 1% of the worlds population have it.
LynzCatastrophe 2 months ago
Welcome the rare population! My sister and I have it. Nobody else in our family does.
#38
Hyperhidrosis. Excessively sweaty arm pits for no reason. I could be sitting there completely at ease and sweat rolls down my sides from my pits. I have found a product to fix the issue however I know no one else who has the same issue personally.
#39
Not as interesting or cool as others but im in the 1% of the population that has no immunity to Rubella even though ive been vaccinated for it several time. Apparently some peoples bodies dont take to some vaccinations. Fine with everything else like mumps measels etc its just the rubella.
Ive also got type 2 duanes symdrone in my right eye. Duanes being a uncommon eye condition anyway, right eye being least common to have it in an type 2 the least common of its type out of the 3 types. Won the duanes lottery with that one.
FoxEcoLimaIndiaCharlieIndiAlfa 2 months ago (edited)
So I recently had to make sure all my vaccinations were current since I'm back in college and I'm in the medical field and will be starting our internship for our clinical hours, so these are mandatory requirements for most hospitals. After getting blood drawn to prove that I've already had many of these vaccines required, which would show the antibodies. Well I somehow was no longer immune to the measles but the mumps and rubella part of the MMR vaccine both came back as reactive for those antibodies, meaning I was immune to them still. I did have to get another MMR vaccine though, anyway. So I'm fully immune once again but I'm a little curious now just how long I'll stay immune this time.
#40
I held a 2nd place world record for the Mushroom Gorge time trial in mariokart Wii for 15 minutes.
Edit: thanks for all the replies! Didn’t know this would touch the hearts of many!
#41
I am diagnosed with Visual snow syndrome. Basically seeing through static. It may not be rare as thought but I am one of very few people to be formally diagnosed.
EDIT:
1) no this isn’t normal and sorry to all the people who found out they had VVS through my stupid Reddit comment lol
2) lots of ppl asked how I was diagnosed- I was at an eye specialist for an unrelated reason and he asked if I had any other concerns. I described my sight to him and he said that’s probably VVS. He referred me to a neurologist and she diagnosed me.
3) I don’t remember not seeing flickering dots. I’ve never done psychedelics. I was unaware d***s could worsen or cause it. Thanks for the warnings though! Definitely won’t be doing psychedelics now haha.
penguino (they/them) 2 months ago
lol makes ur bedroom looks like an analog tv horror show at night
#42
Infertile people. The people who can’t have children after a year of trying, for whom no treatment works, have no diagnosis to explain why, and end up the 1% of the 1% and move on to surrogacy/gestational carrier.
YakFactory 2 months ago
It took me and my husband nine years of trying to have our first child. He died at 5 weeks, and it took another 4 years until our second child was born. No, we didn't try again!
#43
As a Lithuanian I belong to a nationality that makes up 0.03% of the world population.
WindySwede 2 months ago
With 8.2 billions today, it's not that difficult to be under 1% of something. Beeing a Swede is something like 0,1%..
#44
Everyone is born with a space in the base of your skull, I have an enlarged space. The Dr called it an Enlarged *Cisterna Magna*.
Having it isn’t what makes me part of the 1%, it’s the fact that it hasn’t caused me any trouble or neurological issues that puts me there. It was only found when I had an MRI for migraines.
Edit: totally got the wrong wording. I’m sorry for misleading anyone, that came on the back of flu meds and little sleep.
I have stress induced migraines and hormonal ones too. Nothing to do with the lack of brain function, that just makes me a little dull 😁.
#45
Being deaf.
Only 0.22% (roughly 600k people) across all age groups in the US are deaf. More than half are over the age of 65. I've been profoundly deaf since birth, so I'm in an even smaller percent than 0.22%. Lmao
[Source](https://www.gallaudet.edu/office-of-international-affairs/demographics/deaf-employment-reports/).
The Starsong Princess 2 months ago
There’s significantly fewer deaf and blind people now that children are vaccinated against measles.
#46
Distance runners. My marathon PR is faster than 99% of marathon finishers world wide. That said, the distance from my time to the world record is about the same as from the 70th percentile to me.
#47
According to the census, my town is 1% black. So that means it's just me.
Edit: Woodstock, CT POP: 8221 The racial makeup of the town was 97.2% White, 0.4% African American, 0.3% Native American, 0.7% Asian, 0.000001% Pacific Islander, 0.4% from other races, and 1.0% from two or more races.
Steve Sharpe 2 months ago
In a town with 8,221 people, one person is not one percent of the population... and I'm also curious about the Pacific Islander resident, because unless they're an amoeba something has gone spectacularly wrong!
#48
Technically this is 2% but I have curly blonde hair I don’t really have a trait that’s 1%.
tabitha donnelly 2 months ago
My sister has that? I don't think it's that rare. I have curly ginger hair and green eyes I don't know how rare that is.
#50
Fewer than 1% of Americans have completed a full marathon, I have completed 10.
Nathaniel He/Him Cis-Het 2 months ago
This statistic is getting smaller every year, ever since they renamed the marathon chocolate bar to snickers.
What do you think ?
WindySwede 2 months ago
Approximately 0,0000000121951219512195% according to Excel
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"Disembodied voice" 2 months ago
I've survived cpr outside of the hospital, also in the hospital but that's not as remarkable.
Sky Render 2 months ago
I've mentioned my biggest rarity before often, but... I was born with XX/XY chimerism, and also with a double genital tubercle. Both are very rare, but both simultaneously is so rare that there's no records of it ever happening. As an unusual side-effect of the chimerism, the two sets are different sexes, and both are fully functional. The doctors tried to seal away the female parts with a skin graft, likely believing that the parts would just "go away" somehow; they did not and that skin graft just gives me zero direct access to my female anatomy plus regular issues during periods.
Isaac Harvey 2 months ago
My name was misspelled on my first AAA insurance card as "IAFAC HARVEY."
ॐBoyGanesh 2 months ago
I’m a homosexual with heterochromia, have a form of synesthesia called “chromesthesia” and am fully ambidextrous. I’m one of the few Americans with duel citizenship and less than 1000 people worldwide have my specific job. None of these things enhance or highlight my flippant character or irreverent personality.
Justin Tyme 2 months ago
My me it is the combination of unusual events. I completed eight college degrees. I have been trapped in two malfunctioning elevators. I have been on five volcanoes while they were erupting. I have been bitten by two rattlesnakes, stuck in quicksand, struck by lightning, run over by a van, and had an anaphylactic allergic reaction to a bee sting. I have been in five car crashes, two motorcycle crashes, and one helicopter crash. I got shot once and stabbed twice. I have broken nine bones, one at a time. I have had 32 jobs.
Roan The Demon Kitty 2 months ago
me too, though my all time rank out of all users is 125,... but i guess when you consider the site probably has thousands, is still a bit impressive xD
Load More Replies... T 2 months ago
It's more like 2-4% of the population, but I'm pretty sure I have lexical-gustatory (LG) synesthesia, which is a long way of saying I taste words.
CanadianDimes 2 months ago
Oh that’s really cool! What do your favourite words taste like?
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Bouche and Audi and Shyla, Oh My! 2 months ago
My feet swear so badly I can't wear flip flops or any kind of rubber or plastic sandal without socks.
Auntriarch 2 months ago
I know it's just a typo, but it made me laugh to imagine your feet effing and blinding so much that you have to muffle the sound with socks....
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Anthorn 2 months ago
Ooo, this is where I shine. I have minor piebaldism (some white hair, blue eyes, vitiligo), I can wiggle my ears and my eyes, and I also have Stahl's! So I'm an elf! :)
Anthorn 2 months ago
Who the heck downvoted these...I'm not an elf, that was a joke...bc Stahl's gives you pointy ears...geez
Load More Replies... Carrie de Luka 2 months ago
I have camptodactyly in both hands... meant to be less than one percent of the population. Affected more than just my little finger so that's also a bit more unusual.
Barry 2 months ago (edited)
I have voluntary pulsatile tinnitus. That means I can hear my blood rushing through in my ears, but only voluntarily, i.e. by flexing a muscle in my head in a way I can't possibly explain. It's not even a good party trick because I'm the only one that can hear it.
Evagating Beewolf (she/they) 2 months ago
I'm in the well under 1 percent of women/girls diagnosed with autism! Hopefully that'll change as female autism is underdiagnosed.
Roan The Demon Kitty 2 months ago
ditto, though I never realised how few girls/women are actually diagnosed with autism, given a heck of a lot of (at least biologically) female people online say they are autistic or "neuro-divergent" as the new term apparently is.
Load More Replies... Dancing Armadillo 2 months ago
I am one of 1.2 % people of the world that have bear tracks in my eyes. Eye doctors get really excited when they see it. I don’t find it extremely exciting but I guess in the world of Optometry it is.. lol.
Lace Neil 2 months ago
I can lucid dream. I taught myself how from a book. I also have two coloured eyes; my eyes are blue with a golden ring around the iris.
Tempest 2 months ago (edited)
I have a rare heart disease. The disease is already rare (0.2% - 0.7% worldwide) but it has further subtypes and I have a less common one. So I just Googled the stats for the specific subtype and realised that it’s super rare. - “1 to 3 out of every 100,000 babies are born with the condition”. Was born with it but never had issues and it was only detected incidentally when I had to do a scan for a normal check-up in my early 20s. I’m mostly asymptomatic except for occasional palpitations & 1 episode of difficulty breathing at a very high altitude during the dead winter. I had the opportunity to get surgery at a leading hospital but opted out because I don’t want a midline chest scar at my age, lol. Being a med student I realised that even most doctors don’t know the condition (unless they’re in cardiology or cardiac surgery) cause it’s rarely studied about. I don’t really care much about it but I do love telling those closest to me that I have a broken heart 😆 (Scimitar syndrome is the name)
August 2 months ago
Did 9-12 grade work in reading in 5th grade, and was reading at a 5th grade level in kindergarten.(Really gifted in reading! I'm super happy about it!!! :D)
August 1 month ago
I also have double jointed thumbs, so thats another thing, although not that rare.
Load More Replies...
Big Chungus 2 months ago
My parents are kind 1% people...My dad survived three out of hospital heart attacks, two being widow makers and my mom survived sudden cardiac death syndrome and is now the proud owner of a new heart
Kaeda 2 months ago (edited)
I have natural auburn hair and blue eyes. It is supposedly a rarity to have both. 🥳 I also have talocalcaneal coalition, which affects about 3% to 5% of the world population, but mine occurs in both feet, which is only half of that 3-5%. EDIT: Added "of the" before "population".
Pablo Ramos 2 months ago
The percentage of people in the world with my IQ or higher is about 1.3%
Marti J 2 months ago
I have a couple. 1) I have AB- blood type which is very rare and the workers at the blood bank get very excited when they see this. Yes, I do try to donate, but my iron is usually to low. 2) when I was 3 I stumbled across a large wasps nest that was in some tall grass. I couldn't move as I was in shock as hundreds of wasps started swarming and stinging me. My mom can running and grabbed me and ran to the car to get me to the hospital. She was stung multiple times on her arms. The closest hospital was almost an hour away. I was covered in wasp stingers and this would have been the first time I'd ever gotten stung. I did swell up, but I didn't go into anaphylactic shock. They kept me and had to scrape all the stingers off. I later in life actually developed a severe allergic reaction to bees and wasp' stings and I have to carry an epi-pen just in case I get stung again. Very thankful I didn't react that first time
Kombatbunni 2 months ago (edited)
I was one of only 40 adults in the world that were diagnosed in 2016, with an arterio-venous malformation that wasn’t in the brain or internally in the body but in my left hand. Apparently it’s not very common in adults and certainly not that common to occur in an extremity like mine was. It’s where the arteries and veins get tangled up somehow and can either cause delayed circulation or increased circulation (mine was increased) so I had to have it removed. I now have a skin graft and a scar that runs from the base of my left thumb, to 3/4 of the way up my forearm. Friend of mine calls it my shark bite 😁
SkippityBoppityBoo 2 months ago
Medically? I'm a bit of an anomaly! 😄 I've a rare capsicum allergy, as in highly allergic. I've had TB, Covid, diagnosed with Lupus... I'm now disabled. I've had more things happen to me than you could shake a stick at!!! And yet I'm still somehow surviving! Although... My life expectancy is now maybe 10yrs after numerous tests, blood tests, MRIs etc... There's something wrong with my body but they don't know what it is. Whether it's genetic or whatever... It was hard to deal with with that when I got the news, that and when I was told I'm never going to walk freely again because of spinal bruising... But? I'm the goddamn person who they also first told that I was going to possibly be in a wheelchair for the rest of my life. I learnt to walk again, albeit with crutches and calipers but I bloody well did it. Don't ever tell me that I'll never achieve or accomplish something because I'll turn around and do it. Just... To... Pish... You... Off! Including living forever!!! 😁😜😁
V 2 months ago
I had to take a spacial awareness test as part of a job interview a few years back run by a third company. According to the company I was applying for a job at I scored in the top 1% of anyone who has taken that test. But if I have no hand/eye coordination so it's very much wasted on me, lol.
Roan The Demon Kitty 2 months ago
Green Eyes makes me one of 2%. Ginger hair? (well, before it came back blonde from chemo) 1-2%... Schizophrenia? 1%, DID? 1-1.5% my surname? Porphyria? idk exactly but I hear its rare. e_e Fibromyalgia? 2-4% of the population... Peritoneal cancer? Fewer than 7 per 1 million people are diagnosed per year. and lastly i can think of... absense siezures, which normally effect kids at around 1-4 people per 100 thousand. Yet are much less common in adults like me. I'm rare af, but maybe not in a good way lmao
Evagating Beewolf (she/they) 2 months ago
0.2 percent! But we're mostly in the US (2 percent of American population) and Israel (majority of the Israeli population) so we might have a skewed view. Or we might worry about saying we're Jewish.
Load More Replies...
Upstaged75 2 months ago
I'm in the top 1% on Bored Panda! :) (According to the stats at the top of my page) So I guess I'm really good at wasting time here when I should be doing other things?
Justin Tyme 2 months ago
It says that for everybody. Somehow all Bored Panda users are in the top one percent.
Load More Replies... CanadianDimes 2 months ago
I have music anhedonia, which about 5% of people have. The reward centres of my brain aren’t activated by music the way most people’s are. It’s a spectrum, not an either-or condition though I’m two standard deviations below the mean. You can take a great online test from the scientists who originally defined music anhedonia by googling it. Knowing this made my life so much better because I understood why music would made me tense and stressed. And before anyone offers me their sympathies - as far as I’m concerned, I’m not missing anything. I can’t love music, so I’ve not lost something I used to have. To me, it would be like mourning the fact that I don’t speak Spanish, even though I’ve never been able to speak Spanish.
Zoe's Mom 2 months ago
I have 7 different experiences that could have ended my life starting at 2 up until I was 27. I figure I'm here for a reason. I just hope when my time comes, it's an easy death. Don't we all?
Lyoness 2 months ago
Our son has an extremely rare chromosome disorder. There are 12 other known cases in the world, making him 1 in about 500,000,000. His Mum also has central heterochromia (rings of different colours around the iris in your eyes). There's a ring of gold around my iris, then a ring of green, then of blue. And the two conditions are not related. 😁
michael reid 2 months ago
I have an iq in the top 1% and I also have double y chromosome which is also about 1%
WindySwede 2 months ago
Approximately 0,0000000121951219512195% according to Excel
Load More Replies... "Disembodied voice" 2 months ago
I've survived cpr outside of the hospital, also in the hospital but that's not as remarkable.
Sky Render 2 months ago
I've mentioned my biggest rarity before often, but... I was born with XX/XY chimerism, and also with a double genital tubercle. Both are very rare, but both simultaneously is so rare that there's no records of it ever happening. As an unusual side-effect of the chimerism, the two sets are different sexes, and both are fully functional. The doctors tried to seal away the female parts with a skin graft, likely believing that the parts would just "go away" somehow; they did not and that skin graft just gives me zero direct access to my female anatomy plus regular issues during periods.
Isaac Harvey 2 months ago
My name was misspelled on my first AAA insurance card as "IAFAC HARVEY."
ॐBoyGanesh 2 months ago
I’m a homosexual with heterochromia, have a form of synesthesia called “chromesthesia” and am fully ambidextrous. I’m one of the few Americans with duel citizenship and less than 1000 people worldwide have my specific job. None of these things enhance or highlight my flippant character or irreverent personality.
Justin Tyme 2 months ago
My me it is the combination of unusual events. I completed eight college degrees. I have been trapped in two malfunctioning elevators. I have been on five volcanoes while they were erupting. I have been bitten by two rattlesnakes, stuck in quicksand, struck by lightning, run over by a van, and had an anaphylactic allergic reaction to a bee sting. I have been in five car crashes, two motorcycle crashes, and one helicopter crash. I got shot once and stabbed twice. I have broken nine bones, one at a time. I have had 32 jobs.
Roan The Demon Kitty 2 months ago
me too, though my all time rank out of all users is 125,... but i guess when you consider the site probably has thousands, is still a bit impressive xD
Load More Replies... T 2 months ago
It's more like 2-4% of the population, but I'm pretty sure I have lexical-gustatory (LG) synesthesia, which is a long way of saying I taste words.
CanadianDimes 2 months ago
Oh that’s really cool! What do your favourite words taste like?
Load More Replies... Bouche and Audi and Shyla, Oh My! 2 months ago
My feet swear so badly I can't wear flip flops or any kind of rubber or plastic sandal without socks.
Auntriarch 2 months ago
I know it's just a typo, but it made me laugh to imagine your feet effing and blinding so much that you have to muffle the sound with socks....
Load More Replies... Anthorn 2 months ago
Ooo, this is where I shine. I have minor piebaldism (some white hair, blue eyes, vitiligo), I can wiggle my ears and my eyes, and I also have Stahl's! So I'm an elf! :)
Anthorn 2 months ago
Who the heck downvoted these...I'm not an elf, that was a joke...bc Stahl's gives you pointy ears...geez
Load More Replies... Carrie de Luka 2 months ago
I have camptodactyly in both hands... meant to be less than one percent of the population. Affected more than just my little finger so that's also a bit more unusual.
Barry 2 months ago (edited)
I have voluntary pulsatile tinnitus. That means I can hear my blood rushing through in my ears, but only voluntarily, i.e. by flexing a muscle in my head in a way I can't possibly explain. It's not even a good party trick because I'm the only one that can hear it.
Evagating Beewolf (she/they) 2 months ago
I'm in the well under 1 percent of women/girls diagnosed with autism! Hopefully that'll change as female autism is underdiagnosed.
Roan The Demon Kitty 2 months ago
ditto, though I never realised how few girls/women are actually diagnosed with autism, given a heck of a lot of (at least biologically) female people online say they are autistic or "neuro-divergent" as the new term apparently is.
Load More Replies... Dancing Armadillo 2 months ago
I am one of 1.2 % people of the world that have bear tracks in my eyes. Eye doctors get really excited when they see it. I don’t find it extremely exciting but I guess in the world of Optometry it is.. lol.
Lace Neil 2 months ago
I can lucid dream. I taught myself how from a book. I also have two coloured eyes; my eyes are blue with a golden ring around the iris.
Tempest 2 months ago (edited)
I have a rare heart disease. The disease is already rare (0.2% - 0.7% worldwide) but it has further subtypes and I have a less common one. So I just Googled the stats for the specific subtype and realised that it’s super rare. - “1 to 3 out of every 100,000 babies are born with the condition”. Was born with it but never had issues and it was only detected incidentally when I had to do a scan for a normal check-up in my early 20s. I’m mostly asymptomatic except for occasional palpitations & 1 episode of difficulty breathing at a very high altitude during the dead winter. I had the opportunity to get surgery at a leading hospital but opted out because I don’t want a midline chest scar at my age, lol. Being a med student I realised that even most doctors don’t know the condition (unless they’re in cardiology or cardiac surgery) cause it’s rarely studied about. I don’t really care much about it but I do love telling those closest to me that I have a broken heart 😆 (Scimitar syndrome is the name)
August 2 months ago
Did 9-12 grade work in reading in 5th grade, and was reading at a 5th grade level in kindergarten.(Really gifted in reading! I'm super happy about it!!! :D)
August 1 month ago
I also have double jointed thumbs, so thats another thing, although not that rare.
Load More Replies... Big Chungus 2 months ago
My parents are kind 1% people...My dad survived three out of hospital heart attacks, two being widow makers and my mom survived sudden cardiac death syndrome and is now the proud owner of a new heart
Kaeda 2 months ago (edited)
I have natural auburn hair and blue eyes. It is supposedly a rarity to have both. 🥳 I also have talocalcaneal coalition, which affects about 3% to 5% of the world population, but mine occurs in both feet, which is only half of that 3-5%. EDIT: Added "of the" before "population".
Pablo Ramos 2 months ago
The percentage of people in the world with my IQ or higher is about 1.3%
Marti J 2 months ago
I have a couple. 1) I have AB- blood type which is very rare and the workers at the blood bank get very excited when they see this. Yes, I do try to donate, but my iron is usually to low. 2) when I was 3 I stumbled across a large wasps nest that was in some tall grass. I couldn't move as I was in shock as hundreds of wasps started swarming and stinging me. My mom can running and grabbed me and ran to the car to get me to the hospital. She was stung multiple times on her arms. The closest hospital was almost an hour away. I was covered in wasp stingers and this would have been the first time I'd ever gotten stung. I did swell up, but I didn't go into anaphylactic shock. They kept me and had to scrape all the stingers off. I later in life actually developed a severe allergic reaction to bees and wasp' stings and I have to carry an epi-pen just in case I get stung again. Very thankful I didn't react that first time
Kombatbunni 2 months ago (edited)
I was one of only 40 adults in the world that were diagnosed in 2016, with an arterio-venous malformation that wasn’t in the brain or internally in the body but in my left hand. Apparently it’s not very common in adults and certainly not that common to occur in an extremity like mine was. It’s where the arteries and veins get tangled up somehow and can either cause delayed circulation or increased circulation (mine was increased) so I had to have it removed. I now have a skin graft and a scar that runs from the base of my left thumb, to 3/4 of the way up my forearm. Friend of mine calls it my shark bite 😁
SkippityBoppityBoo 2 months ago
Medically? I'm a bit of an anomaly! 😄 I've a rare capsicum allergy, as in highly allergic. I've had TB, Covid, diagnosed with Lupus... I'm now disabled. I've had more things happen to me than you could shake a stick at!!! And yet I'm still somehow surviving! Although... My life expectancy is now maybe 10yrs after numerous tests, blood tests, MRIs etc... There's something wrong with my body but they don't know what it is. Whether it's genetic or whatever... It was hard to deal with with that when I got the news, that and when I was told I'm never going to walk freely again because of spinal bruising... But? I'm the goddamn person who they also first told that I was going to possibly be in a wheelchair for the rest of my life. I learnt to walk again, albeit with crutches and calipers but I bloody well did it. Don't ever tell me that I'll never achieve or accomplish something because I'll turn around and do it. Just... To... Pish... You... Off! Including living forever!!! 😁😜😁
V 2 months ago
I had to take a spacial awareness test as part of a job interview a few years back run by a third company. According to the company I was applying for a job at I scored in the top 1% of anyone who has taken that test. But if I have no hand/eye coordination so it's very much wasted on me, lol.
Roan The Demon Kitty 2 months ago
Green Eyes makes me one of 2%. Ginger hair? (well, before it came back blonde from chemo) 1-2%... Schizophrenia? 1%, DID? 1-1.5% my surname? Porphyria? idk exactly but I hear its rare. e_e Fibromyalgia? 2-4% of the population... Peritoneal cancer? Fewer than 7 per 1 million people are diagnosed per year. and lastly i can think of... absense siezures, which normally effect kids at around 1-4 people per 100 thousand. Yet are much less common in adults like me. I'm rare af, but maybe not in a good way lmao
Evagating Beewolf (she/they) 2 months ago
0.2 percent! But we're mostly in the US (2 percent of American population) and Israel (majority of the Israeli population) so we might have a skewed view. Or we might worry about saying we're Jewish.
Load More Replies... Upstaged75 2 months ago
I'm in the top 1% on Bored Panda! :) (According to the stats at the top of my page) So I guess I'm really good at wasting time here when I should be doing other things?
Justin Tyme 2 months ago
It says that for everybody. Somehow all Bored Panda users are in the top one percent.
Load More Replies... CanadianDimes 2 months ago
I have music anhedonia, which about 5% of people have. The reward centres of my brain aren’t activated by music the way most people’s are. It’s a spectrum, not an either-or condition though I’m two standard deviations below the mean. You can take a great online test from the scientists who originally defined music anhedonia by googling it. Knowing this made my life so much better because I understood why music would made me tense and stressed. And before anyone offers me their sympathies - as far as I’m concerned, I’m not missing anything. I can’t love music, so I’ve not lost something I used to have. To me, it would be like mourning the fact that I don’t speak Spanish, even though I’ve never been able to speak Spanish.
Zoe's Mom 2 months ago
I have 7 different experiences that could have ended my life starting at 2 up until I was 27. I figure I'm here for a reason. I just hope when my time comes, it's an easy death. Don't we all?
Lyoness 2 months ago
Our son has an extremely rare chromosome disorder. There are 12 other known cases in the world, making him 1 in about 500,000,000. His Mum also has central heterochromia (rings of different colours around the iris in your eyes). There's a ring of gold around my iris, then a ring of green, then of blue. And the two conditions are not related. 😁
michael reid 2 months ago
I have an iq in the top 1% and I also have double y chromosome which is also about 1%
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