The Most Painful Illness Known to Man
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- Опубліковано 19 тра 2024
- There are some illnesses that are so painful you wish you were dead! In today's video we are going to take a look at the most painful illness known to man. Trigeminal Neuralgia is an illness that affects the Trigeminal nerve, leaving you in excruciating pain, and making even some of the most simple tasks, like brushing your teeth, seem impossible.
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“The most painful illness known to man”
*Ad 1 of 2*
The purple diamond Stormtrooper don’t forget the 15 second un skippables
Lol
already cured that with my trusty adblocker,
The purple diamond Stormtrooper and they are non skippable political ads
@@younodavibes6342 I remember britta. That company that makes water filters did a four hour documentary about how some countries don't have clean water and used it as a UA-cam ad and I got it once and it was unskippable. I refreshed the page and got another ad I think for Call of duty world War 2 or something like that
As someone with trigeminal neuralgia, I greatly appreciate your uploading this video. The way I’ve always described it to people is: Imagine if someone took a fork, stuck it in your temple...and then attached that fork to an electric socket.
Right there with you brother. 👍 Hang in there and stay strong.
Bob Bobson I feel ya. Mine sometimes feels like a probe through the head down to my jaw. And needles I’m going through my inner ear and jaw line to teeth. I’m sorry you have to go through this too
Bob, I completely agree with your assessment.. Temple. nose, ear. Mine was brought on by head trauma that wasnt more than a roller coaster ride.
Bob Bobson - is it constant? as in, all day everyday?
or does it come in waves, every few days, and doesn't last long?
MO JO There’s two types of TN, and I have what’s called type 2. That means it comes in waves - it comes without warning, stays for a few minutes, and leaves without warning (usually). I do acupuncture for it, so the attacks are less severe than they’d be entirely untreated.
As someone who has this, I can attest to the fact that the attacks from this disorder will make you seriously want to take a dirt nap. As someone who has experienced the pain of childbirth, I can seriously say that I would rather give birth naturally every month for the rest of my life (yes, I know that not actually possible), than have TN.
Editing to add: I was already a fan of this channel, but I love them even more now, for this video, especially the message at the end about not judging others because you don't know what they may be experiencing.
Right there with you fellow warrior. Hang in there and stay strong! 👍
Really hope everything gets better
Have a nice day
Ashley Williams I hear you. Unmedicated childbirth was nothing compared to the pain I get from Rheumatoid Arthritis or when I had nerve pain from an extruded disc.
I hope you get better! No pain is fun to deal with
Ashley Williams my perineal nerve was badly damaged in a car crash & I can honestly sympathise! After four days of no sleep & vomiting with the pain I wanted to cut my leg off ❤️💕
Wrong, the most painful illness is getting *Wither III*
Lol
*Wither IV*
@James Smith nah, those are pests
*69th like*
F it *WITHER MCCL*
This thing is no joke cause my mother still has it and even tho she's a beast she almost cries when she gets it...
The fact that she doesn't cry is crazy
@@Noname-uk9mu It's hard to cry from pain when crying makes the pain even worse.
Try CBD
@@marisu9765 so edgy
@@Rocky-oq9cy Not really with this disorder
Another great video. I love the professionals in the background saying “blah, blah, blah, blah, blah, blah, blah..” when they are talking. It reminds me of the adults in the Charlie Brown cartoons.
The teacher goes like "Wonk wonk wonk wonk wonk wonk" XD
I love it too, infograpics show rules! 😌
i wouldn't wish this torture not even to my worst enemy
Still not as painful as stepping on a Lego though.
Lego on my eggo
that joke isn’t funny anymore
L.o.l XD Okay but, I think the illness is worse though
Oh hey. Will I have a mustache when I grow up too???
Just Some Guy without a Mustache word
I have had it for 7 years, after I had a TBI at the age of 19. Isolation along with the anxiety from anticipation of the pain alone is enough to scramble one’s brain. It would be impossible for the pre injury me, to begin to comprehend an affliction such as TN.
Mark Twain how bad did it hurt
Jordan Fakhoury the epitome of agony, surgery and meds help but not nearly enough.
Mark Twain so it’s that bad
I haven't been diagnosed with it (can't afford to go to the doctor all the time), but a few years ago I'd get an insanely sharp pain in the side of my face all along the jawline. I'd be trying not to wake my family up because I'd be screaming in pain.
Imagine someone shoving a screwdriver through your jaw. That's what it feels like. Thankfully I haven't had any episodes recently. In my experience, nothing really helps. You just have to kind of hope it goes away, and it does eventually. Only to come back again when you're trying to sleep.
I wish you luck
I literally felt the pain watching the video only. Can't believe what the patients must feel.
So many comments under these videos speak about being diagnosed within their 20's even. Can't lie, I'm really scared of my 20's now. I have so much empathy for these people... I feel like I have to cry I just wish treatment will get better...
Imagine a SEVERE earache, several toothaches, to the point where you can actually FEEL the roots and nerves in your gums, your lips go completely numb, coupled with the worst migraine headache you've ever had, multiply it by 100, and you get the idea...
Then imagine going to the the doctor but you're in so much pain that all you can do is point to your entire head...
Now imagine the doctor telling you that there isn't a cure, all they can do is set you up with pain management.....
I've only recently.been diagnosed with TN, and the attacks I've had have been debilitating to the point I couldn't even go into work.
Wouldn't wish this on my worst enemy...
This is the best, most all-around informative short I've seen on TN. I truly appreciate the time and effort put forth. From someone who's lived it, thank you for doing this right. Excellent job.
Got this, that title was a trigger for me, lol. Clicking on it I was like "did they get this one right?"
Luckily my severity wasn't as bad as others. Odd part is I am male and developed it in my teens. Mostly women in their 50s get this. It wasn't till about 32 that I needed to find help and then took over 10 years to figure it out (bad neurologist), lots of MRIs and crazy tests. The symptoms described in this video are nearly perfect, bugs me my neurologist couldn't figure it out. What was left out of the video is common triggers for pain is cold stuff like breezes, drinking ice water, ect. I feel for people living in a cold environment, I live in Tucson and love it.
The suicide rate is 50% in the first 2 years. This is likely higher due to misdiagnosis (cases that go unknown). My belief is, the people that make it are the ones that were able to find treatment. Without treatment the end result is inevitable. I was allergic to many of the medications and had a difficult time, my neurologist took me off medication to "try it without for a while" without bothering to tell me there were other medications that could help. Luckily I went to my family care doctor for anti-depressants and he told me it also stops Trigeminal Neuralgia, much better doctor. Thanks doc
I have MS, and I have friends with MS who suffer from trigeminal neuralgia, the suffering is no joke :’(
Same. I first had this before being diagnosed with MS. I thought I had a severe tooth issue but all my teeth were fine. I was so scared
@@xxviciousbeautyxx I’m sorry to hear that, I hope you get better soon 🙏🏼
Thank you, thank you, thank you for making this. It is so hard to explain to people who either don't see me on a bad day or just think I need a dentist.
I was in my early 20s when it started, luckily diagnosed with in a month. It felt like some thing was trying to pry loose my jaw by pulling out or pushing in my teeth ... or part of me thinks/ remembers that all I wanted to do was rip out my jaw.. at the same time it was more like I was trying to hold it in place? It’s hard to describe. It only happened when I would recline, even just a little and sometimes it was the act of falling asleep and it would last minutes to an hour every time. luckily if I stayed upright and awake it was minimal or gone... but after days and then weeks of trying to do that.. it was nearly impossible. I felt I was going insane and I basically was..
Anie Anton I’m in the my 20s as well. My doc thought it was TMJ which I took at face value. But the pain got so severe I went to my gp to get another opinion. My pain usually happens as I’m so going to bed or lying down. Feels like my jaw is locking up but it’s now. And my inner ear on right just makes these weird vibrating pain m. Hope you have found a way to manage
How did you go into remission?
Anie Anton - is it constant? as in, all day everyday?
or does it come in waves, every few days, and doesn't last long?
wow well that sounds BAD
My mother had it twice, once on each side of the face. She had to be hospitalized.
She took gabapentin.
I was diagnosed with this several years ago and was also prescribed Neurontin/Gabapentin for it, and although it's made it a bit less severe, it hasn't reduced the frequency of attacks I get. I still have attacks anywhere from 2-4 times a month, sometimes more. The Gabapentin just makes it where I don't want to literally die every single time it happens. Glad you mother hasn't had to suffer with it more than a couple times.
@@AshDub86 I had acupuncture done and it took my attacks down from 3 weeks to less than a week. That combined with gabapentin and steroids have brought my pain down considerably. If the accupuncture is a placebo, bring on more placebos.
Also I avoid my triggers like the plague
Cold wind,
Loud bass music
Swimming in cold water.
I also load up on l lycine because my TN is type 6 (post herpetic) from shingles and it acts up whenever I have a cold sore.
I hope the Gabapentin worked for her. Ive been on it for over ten years for my Fibromyalgia and I really haven't noticed a great deal of difference, even at 2400mg a day
You dont have it twice. You have it for the rest of your life. Its a progressive disease.
@Unbreakable Patches Im on 90mg of Duloxetine HCL a day already. Have been for nearly a year. Had been on Zoloft for years before that. Im also on maximum doses of Amitriptyline, Cyclobenzaprine, Fluticasone, Gabapentin, Montelukast, Meloxicam, Topiramate, and Tramadol. Just to be able to barely function. I am in constant full body pain all day long. Physical Therapy did not help. Chiropractic and Electro-stim made it worse. Sonogram therapy didn't have any lasting effect, minutes at best. Cortisone injections made the pain far worse for several hours then no change. I cant walk unaided and ive had this since I was at least 3, possibly before that. It was originally diagnosed as Juvenile Onset Rheumatoid Arthritis even though my Rheumatoid count was only slightly out of norm. I also have all the secondary symptoms of fibromyalgia, mental and digestive system difficulties, of the most severe cases.
I’ve just been diagnosed with trigeminal neuralgia. And they are right it’s no laughing matter. I haven’t been able to eat or sleep ( I get woken up at odd hours of the morning from severe pain and spasms) and while medication helps to manage it, I still have relapses and will have sudden attacks during the day (and at work). I’m currently waiting on an appointment with the neurologist. 🙋🏻♀️ thanks Infographics for creating this video. I’m sharing this with my family to give them more insight to my condition 🥰
Normally people wouldn’t really think of you guys as someone they could relate to because it looks so professional and there’s so many people that go into an episode. But your sense of humor, writing, and especially the fun challenges to the guinea pig make you feel like a real channel with real great people behind it
Dang, hopefully we bigfoots won't have to worry about getting these diseases out here in the forest
Just Some Bigfoot With Internet Access there’s a race of First Nations called Blackfoot in Canada you racist!
actually you'll die faster cause im hunting some bigfoots with a shotgun
Adults can be very dumb sometimes. Except for my mommy my daddy my uncle my brother my aunt my sis my doctor my teacher nice people and me. *Oh wait*-
Dragon_God26 Official but on steroids yo don't ya dare touch Bigfoot he my homie yo Bigfoot if ya need a gun call me up or ya can rip him off limb by limb like the people who get to close to you in the forest
I love seeing you around on YT. It makes my day.
My mom has this desease and still goes to work. She uses pain killers to try stoping the pain which still only works sometimes
the illness you “have” when you want to stay home from school
Hamburger
@@someonezx4622 i agree
I legit try to get sick so I don’t go to school
@@tcuty1059 i did that few hours ago
@Dr. sludge yes it did 😂
I had a cyst in my brain which also caused major brain swelling when it popped and I totally understand this pain you're talking about. When i was admitted, I screamed in pain until I passed out and woke up screaming. I was given high pain meds and steroids for my brain. I still have brain damage from when the cyst popped and it's going on two years now
I suffer from Trigeminal Neuralgia. I was diagnosed at 36. It's called the 'suicide disease' for a reason.
same here. Im now sure how much longer I can do this.
@@maddawgzzzz seek treatment. Carbamazepine and Gabapentin. I was on a cocktail mix with Lyrica. These meds well help. Just keep them on hand at all times. It only gets better with treatment.
Wowzers! !! Thank you... I don’t want to lose my brain. I don’t know what’s worse. Losing myself or the pain.
At first I thought this would be Cluster Headaches, which are similar and are also referred to as suicide headaches.
When they scream I can’t help but laugh, the animation is hilarious
;~;
As someone with Trigeminal Neuralgia, I appreciate you making this video as I now share this with people.
Thank you for posting this video. As someone who has TN, I appreciate the the awareness!
This is by far the best explanation I have watched on this monster known as trigeminal neuralgia! Thank you, thank you!
If any of you saw the "Scream " painting , it's considered the visual representation of this condition
Nah
A+ to the sound team on this one
I had a TN scare a month after I got my wisdom teeth removed. My face was getting the electric shock pains like every 10 minutes for days AND I had burning sensation as well. At first the doctors thought it was TN but after running test they ruled it as nerve sensory pain...like residual pain my wisdom teeth removal I guess. They gave me medicine for lamb and eventually the pain stopped after 2 months.
Anyways, I’m so glad that you guys made a video and bringing awareness on this! It is a pretty scary disorder!
Hello brother I need your help 😊
Please
@@hamzakhan9045 with what?
My mom had this disease and I am glad to see it covered by this channel.
I've had trigeminal neuralgia since I was 21, no known reason for having it, no cure, unexplainable torturous pain......
Oh my grandfather had that. My mom said when he was still alive that was one of the most extraordinary pain a person could ever feel.
He even tried to have surgery to cut off his nerves because he couldn’t stand living.
Yes it’s that bad. I have TN! Feels like burning and stabbing every hour every second of everyday. Thank you for spreading this information so people can start to understand this chronic pain condition. I’m in the process of trying to get microvascular decompression surgery with a neurosurgeon. Wish me luck. So much pain. I will pray for doctors to find a cure soon so all of us TN warriors can be set free from horrible pain.
it's so interesting how many uses gabapentin has as a medication
I take it for the neuropathy issues i got from chemotherapy
acb 1994 I used it for headaches lol
And now a word from our most painful sponsor "RAID SHADOW LEGENDS"
Thank you so much for bringing awareness to this ❤️!
I have had this disorder for 10 years. I describe the pain as a three week long brain freeze. Behind my eye. I fought the urge to scoop out my eye and asked dentists to pull my molars. Oddly enough, my son had pediatric SUNCT, and researching that is how I found out about TN.
You should do a “what if everyone on he planet jumped at the same time” video
Nick Tingle they have I think
Danielシ no I think
Lol
Nick Tingle nothing would happen
*whispers Vsauce
To me, it feels like an ice pick stabbing all over my face while being connected to a cattle prode on high. I have bilateral (Left AND Right sided) Trigeminal Neuralgia. I had my MVD (brain surgery) on my right side in Feb 2021. I still deal with it on that side, but much less. The left side is getting worse all the time. Will need to do that side in the next few years.
I love the background sound FX in these videos.
I too have TN and I can tell you it’s horrific. Last night I went through an entire night of these horrible shocks, and It’s totally debilitating. I would rather die than feel it. You can’t talk and don’t want to be touched. Going to the hospital is excruciating because they don’t get it. It’s pathetic because they think you want drugs. All I want is to be knocked out.. just put to sleep. The meds make you lethargic so your life is basically nothing while you’re going through it. I have a pretty high tolerance for pain, but this.. no one can tolerate. It’s like being electrocuted in your face over and over again, so if you’re loved one or friend has this, listen to the video and BE KIND!
I know someone whose son had this. It was hard watching them go through it. They ended up having brain surgery and it alleviated the symptoms
This is a lot like complex regional pain syndrome (CRPS) or RSD except the pain can be anywhere in your extremities (i.e. legs, arms, hands,feet, etc) although it is a lesser known disease commonly focused on the elderly it is in people of all age groups.
My little sister was diagnosed with trigeminal neuralgia at 18. For days before we figured out what was going on we watched her curling up in pain and had no idea how to help her. Now when people ask what she's going through she will be able to this to them. Because the social stigma is real and people don't understand.
@infographics you should do a show on crohn's disease I have it and was diagnosed when I was on the fire line last year and I would like to know more about this disease. I love this show and I would love to see more information on this painful inflammation of my intestines that I have
Throughout the video, I was wondering what actually causes this excruciating pain
Me: **Reads title**
Also Me: Love?
I felt that
Right in the feels
Try long term depression
Depression and suicidal tendencies?
That's a neurological problem as well.
My mother has trigeminal neuralgia. It’s a horrible, horrible condition and I hope that we find a cure during this decade. My mother had to leave her career as a nurse because the pain is so intense. It’s the kind of pain which immobilizes you, to the point at which you cannot move. It’s really sad 😥
I have TN bilaterally, they came on a year apart. The first flare up lasted TWO whole months and that's when I got my first diagnosis. I don't know how I got so lucky, and when either of them flare up I always debate with myself about playing in traffic. I take gabapentin because Tegretol effects my hearing pretty bad. My jobs do their best to accommodate me but it's hard working with it. Going to the hospital seems a waste of time and my neighbors can hear me screaming through the walls.
The ONLY illness I think is worse is Complex Regional Pain Syndrome, or CRPS.
Thanks for covering my illness.
Finally something I can relate to lol I've suffered for years with this, however I have found a helper with the condition Medical cannabis but as always doesn't work for everyone & yeah all true about the symptoms, my attacks happen at random I do get about a 20 second warning of a warm liquid or tingly feeling & as soon as that starts find a seat cause you gonna be a WHILE! However with mine when the rambo knife feels like it's halfway I normally lose my vision for 10mins at a time. It's a fun world we live in!
Depression/Friendzone:Allow me to introduce myself
Those are both mental. Nothing really painful if you chose to be happy.
Terrell Brumfield first of all its a joke. Second of all you can’t just CHOOSE to be happy.
@@scrub7457 you actually can Choose to be happy. Life is all about choices. You can chose to do things that make you happy instead of feeling sorry for yourself.
@@nuttbag6658 change locations
@@tejaybe_sensei I can't just open settings and set my location to Canada
I had to show my science teacher this for work and they even subbed and now we watch these videos almost everyday after science
man i love your show so much
Im so early, I love the Infographics show. My favorite videos are challenges and you vs. I hope that lab rat of yours is ok.
Infographics is very lucky to have their very own human guinnea pig
𝕍𝕆𝕃𝔸𝕀ℝ𝔼 YOU AGAIN!
Lol yeah
𝕍𝕆𝕃𝔸𝕀ℝ𝔼 you are the new Justin y
All these people saying she's everywere probably don't realize that it means they're also everywhere
@Arthur Waxton r/iam14andthisisdeep
It’s rare in itself but I had a very severe reaction when I started prep. I saw one article where another suffered the same.
Five years ago they didn’t believe the reaction I had but it’s real painful
As someone who suffers from this it is in fact the most painful illness. I also have fibromyalgia so I can compare the two and this is a bazillion times worse. I have a kid I'm pregnant and I'm not allowed to take any medication for it. And the medication I did take which was the gabapentin and the carbamazepine actually destroyed my memory and caused brain death in certain areas of my brain. So I no longer allowed to take any of those medications and on top of that the surgery didn't work. So I have turn to acupuncture which has finally given me some relief. But this is something many people don't understand and I often end up in my room alone crying because people don't get it but also because it makes me feel like a really bad mom. So it's not just the pain but also the anxiety and depression that comes with it.
my mom has this condition and is sometimes worried it is something I may develop since it can be hereditary
Thanks for tackling the social bit head-on. That's often an incredibly difficult part of any illness, physical and/or mental. For me with depression, I truly, TRULY believed that it was just a matter of "Stop being sad". Once I saw videos from groups like you, REPUTABLE groups that many people look up to, saying that suffering does not make you weak, it really has helped me open up to others. Mostly, I've found sympathy, but not pity. People willing to help me, without holding my hand.
Mostly, I've found other people like me. Us humans were never meant to live alone, I think.
My cousin got this after a really bad car accident. I don't know everything he has to take but I do know they talked about botox on top of all the other medication to try and dull it.
Ouch. Always grateful when in full health! Thank the creator!
Can you try “Who was the green river killer?”
I got so scared after I heard this who else did
K
yea you fortnite players get easily scared
@@ledianberishaa i want fortnite to be DELETED FROM EXISTENCE
@@blasphemyg2025 lol whi doesn't
Divine unfortunately it’s successful
Can you guys do a video on IBS? (Irritable bowel syndrome)
I also have this horrible affliction. Ashley, I have also said I would rather have a baby than this pain. I have also said I wouldn't wish this on anyone. No one on earth deserves to suffer this kind of pain. I am fortunate that my doctor understands this affliction. There are people who haven't heard of it, so I don't talk about it unless it becomes necessary. I do stay home when it flares up. Seeing this is something I am going to save. It describes the pain issue when peoples can understand it. Thanks for posting it.
I Studded the same toe twice in one hour. Nothing can beat this pain
Video: 82 comments
Me: Can I see them?
UA-cam: NO
Lol
Info you are the best :)👍
I am a doc and used to have a pain clinic. I agree that this is the worst in regards to pain. Worst i ever experienced was gout. It woke me out of a hard sleep and felt like i was shot in the foot.
My grandpa has this in his cheek and lower jaw he said it feels like lightning In his jaw we’ve researched this and it’s pretty bad it’s gotten better with some pills and surgery
Face reveal when?!?!???
My Grandma had this she went through surgery, she tried medicine and nothing really helped her. Some days she can even talk. I felt so bad for her.☹️💔
I have trigeminal neuralgia but thankfully it’s not as bad as this video portrays. It’s definitely debilitating though even at a mild form of the problem so I hope it never gets this bad!
I love the infographics show
Me too!
Me too!
Me too!
Me too too!
Me too Me too Me too Me too
Me too Me too Me too Me too
Me too Me too Me too Me too
Me too Me too Me too Me too
Me too Me too Me too Me too
0:43 I wish every video would skip the small talk.
Thank you for this video. My doctor diagnosed me quicklyʻ after I described an electric knife stabbing me in my ear thus couldnt open that eye. He said “ Im so sorry you have this.” Yikes! Gabapentin works for me though so Im lucky
I’ve had TN for about a year, and the term “suicide diseases” is absolutely true. In just a year, I lost count on how many occasions I thought I want to died.
I love the background sound of blah blah blah blah... it sounds so funny... 😂😂
Rage is one of the most painful illness
Video suggestion: chemicals/products to avoid exposure in large amounts if your male or female.
**Heard about the UK study that found male teens had a large amount of a chemical that was very similar to female hormones that came from water bottles. Don't know if it was the water itself of the bottle used.
Plus I heard a rumor that the Impossible Whopper had a lot of estrogen in it.
Please do a video on Complex Regional Pain Syndrome.
It’s called the Infographic show
Edit:
Because of nobody understanding the joke for a odd reason I MEANT the title not their name
blake yes
blake sorry but it’s not it’s infographics show and if you don’t believe me look at it
blake kinda dose to me but you can not care it’s none of my business
Dude I think they know the name of their own channel.
Doctor Thirteen I was meaning the title of the video of it being them let me fix the title so people can realize
stepping on lego hurts
so does stubbing your toe
🤔
*stubbing your toe on lego*
Yes all accurate. I have Trigeminal neuralgia. Diagnosed at 30
My family is traumatized from watching me in agony. Meds have fortunately helped!
This sounds like every single day for me, except throughout my entire body since I was 3 years old. I have Fibromyalgia. And ive been on all those medications you mentioned for over ten years just to be able to get out of bed every day.
The Most Painful Illness Known To Man:
12 year old fortnite players.
Gaymer Studios but there is a cure not playing fortnite at all it helped me
Ur right
COULD YOU PLEASE DO A VIDEO ON COMPLEX REGIONAL PAIN SYNDROME!!! CRPS IS SO BAD IT HAS PAIN IN THE NAME!!!
I suffered with a burning in the stomach line and went thru the worst pain known to man and lost 3stone or 39lb weight in a month from constantly being sick and in 24 hours pain it was so bad I wouldn't wish this on my worst enemy
Know a lady who has this, she does her best to work and function but can't imagine how difficult it must be
The most painful Illness: I'm here to hurt ya
Cerebral palsy: let me just fix that
Actually TN is the most painful according to the mcgill pain scale. Research it before you assume. Just bc it looks visually worse on the outside doesnt make more painful. Thats the entire point of the vid.
@@levitatewalker8166 true ok but idc
@@exostatics 'true but you dont care'? Lol WOW
@@levitatewalker8166 well I do care but I'm not gonna change my comment
The most painful illness is ligma cause ninja died to it
Feirce he still alive
Wow! That pain sounds horrible!
I've often heard that cluster headaches were the most painful "suicide disease".
I would hate to down play anybody's pain.
At least there is psilocybin and LSD for cluster headaches.
I had this twice. It happened when I was on a 5-hour flight and the plan was landing. Half of my face and body hurt extremely, like half of my teeth, jaw, eyes, brain, limbs hurt so much while the other half was normal. Like I could felt the pain in my muscle and nerve. I was in so much pain that when the plane landed, my friend had to help me get off as I could barely see or move.
*WHEN YOUR SCOOTER HITS YOU IN THE SHIN*
the schin is the bone that is at your foot
the lack of likes can be attributed to the small number of people who have experienced this
We know what a shin is, you don’t need to explain
@@Yasuuuuuuuu N o t a l l p e o p l e
@@Yasuuuuuuuu yeah i know but some kids watch this and their brain might not be fully developed to know what a schin is like some people know but others dont
I felt pain in my shins just reading this😖😖
"The most painful illness known to man"
Club Penguin: Am I a joke to you?
Club penguin was an illness???
now we need a video talking about conoravirus
While I don’t have this disease, I understand chronic pain and wish them the best to be able to deal with the pain and have understanding friends and family