Request : Every Great Fire Explained -Great Fire of Rome -Temple of Diana -Library of Alexandria -Great Fire of London -Great Fire of Chicago -Great Fire of Boston -Triangle Factory -Reichstag -Luna Park -Brazil's National Museum -Australia's 2019 Bushfire Season -Notre Dame -Kyoto Animations
I bro I can’t imagine what it feels like to have any of these diseases. Thank goodness I don’t have any of them but I feel bad for the people that need to deal with this daily
Sometimes pancreatitis can be cured depending on the cause. For me it caused by lose gallstones causing a blockage so removing my gallbladder and the lose stones fixed the problem. I wasn’t even allowed to drink water for a few days because they wanted my pancreas to calm down before surgery
my younger sister has sickle cells. it’s something that’s been bothering her since birth and takes pain killers and drinks water as a means of ridding the pain. she’s grown up and her pain attacks have become a rare occurrence. but it’s still something painful she has to deal with it. thank you the evaluator for covering the disease
@Real_ame Hot water helps but if its heat triggered pain stay away from hot water get some snacks to eat if your appetite is small if not try to eat nutritional meals but get food and water and tell doctors when you feel sick if you need more info. Feel free to reply!
I am one of the "lucky" 30-40 million with interstitial cystitis. I started showing symptoms as young as 6 years old with frequent trips to the restroom. Any flare ups (times when my bladder was in agonizing pain for days) that I had were always treated as UTIs. When I was 11 my Mom was diagnosed with IC after nearly a year of being bed bound by the debilitating pain. She was put on amitriptyline and changed her diet to bland foods (no spices or acidic foods). That allowed her to finish her schooling and become a nurse. 5 years later I am in her position. My flare ups are so bad I can barely go to school and have severe anxiety and depression. Before I was diagnosed I would take my Mom's pain meds to relieve the pain. I was taken to a specialist once my panic attacks prevented me from attending school. I was put on a restrictive diet, prescribed meds, and had multiple bladder installation treatments over the course of a year. Now at 22 I can say I live a normal life. My diet is still restrictive and I am still on medications but I am now symptom free and know what to do in case of future flare ups. Being hydrated and not holding in urine helps. There is hope if you have or think you have IC!
I have interstitial cystitis it is hell. It’s more of a never ending feeling of having to pee. But when you try to go there is absolutely nothing. Every once in a while there’s some relief but not very often. I will say I am lucky compared to other people with IC. I don’t experience the pain. I just experience ALOT of discomfort. I also have ibs which is a common comorbidity that goes along with IC
My grandpa had throat cancer, it's gone now so he's fine but he lost his voice and it's really hard to understand him when he talks but we got over with it )
I wonder if you can do a video that includes idiopathic intracranial hypertension, or IIH? I have it, and it’s a condition that does need a bit of explaining, and I would love to see your take on it.
let's give honourable mentions to: endometriosis (women), testicular torsion (men) and kidney stones (unisex).....i'm a man but have known women with endometriosis; i don't think you can understand the pain until you've been through it and being a helpless bystander makes you feel really useless when you're with someone going through it.
My father has trigeminal neuralgia and it was cm aused by when he was in Afghanistan in a war and the shower water was so potent and gross that somehow it effected him 17 years later.
I'm surprised that bronchitis wasn't mentioned, as it was a nightmare for me, I couldn't even eat chocolate pretzels without puking. The only good thing about it was that I was able to drink apple juice
i injured my tailbone in my sleep somehow (i sleep in the worst positions you could ever imagine lol) and it made sitting down and getting up from my seat incredibly painful for weeks, and for almost a year after that i still had pain there but it wasn't severe anymore
I have IC and I experience relief with drinking lots of water so it’s very possible. Keep in mind IC can look very different for each person, different triggers, different severities, different relief methods etc
Well this was a weird thumbnail to see on my homepage during my pancreatitis recovery... Oh, btw, it doesn't just last a few days. My doctor said it could be up to six WEEKS. I'm just about two weeks into my recovery and I'm really hoping things calm down soon... EDIT: I've never had ischemic colitis, but I DID have ulcerative colitis (which Google says is essentially the same thing but more chronic and with a different cause) and it got so bad that my intestine was going to BURST so they took the whole thing out. That wasn't fun either.
God I hate having IC. I’m 23 and unfortunately one of the small demographics who has not only severe symptoms, but also bladder polyps that I had to have removed via a TURBT. I’ve been in remission since December. But your description was SO vindicating because I have been struggling to get disability, since it makes it near impossible to hold a steady job as a student
I had ulcers around 2-3 weeks ago and it was torture. If I were to ask what is the most pain I’ve endured. It would have been that. For the last 3 days I have been in pain.
Oof, Gout. I had Gout on my right big toe back in April and it hurt enough to go to the hospital for it. The bus I sat on hit the tiniest divit in the road that made my foot bump the side and it felt like Shaq slam dunked a bowling ball on my foot. Naproxen is a godsend.
I'll never forget the 8th grade field trip to the roller rink the day before Christmas break. My first time roller skating, and I was using the "walker" things provided for people learning to skate. I was having a great time until I fell on my butt while using the walker. I was a bit sore as expected right after. However much time later it's time to put our shoes back on and board the bus back to school. I was struggling a bit because it hurt to sit and bend over to change shoes. After the ride back I was hurting quite a bit more, it was becoming difficult to walk. I wake up the next day in immense pain. Unable to walk for a couple days, and limping around the entirety of my 2 week Christmas break I had been looking forward to. I had bruised my tail bone, and it hurt like a motherfucker. As an adult now with your typical knee and back pain in my mid 20's, I would not wish coccyx injuries on my worst enemy. I didn't even break mine, I just bruised it pretty good. If I was in that much pain as child, I don't want to imagine going through it again now.
Idk if it’s related to coccydynia, but when I was anywhere from 7 to 8 and a half I was with my church’s singing group and my parents for rehearsal and one lady moved a chair, for a reason I can’t remember, and my ADHD brain forgot she moved it and muscle memory took over and I sat on a ghost chair and fell flat on my butt. Then ever since at random times my tailbone hurts a little bit or agonizingly bad. My mom told me a little bit after that I bruised it and that I wasn’t alone as she bruised hers at some point too.
Idk why but he on day I was looking at my chest and realized a had a big purple mark that looked like a Bruce and it get bigger and doesn’t stop spreading
as someone who is day 1 in being pain-free from a sickle cell crisis, how the pain was described was absolutely accurate! i still need a walking stick to get out of bed and go down the stairs and a wheelchair in mediocre-sized malls. sickle cell pain is no joke, but it doesn’t sound as bad as the pain described for the other diseases 😅 the worst part is, is that if it isn’t caught early even pain medication like morphine won’t work. (i was put on 40mg of morphine in the hospital for 2 of 3 crisises.. in a row but panadol and mybulen worked perfectly fine at home for a small arm crisis spike) edit: yes, they even gave me liquid morphine. i was shook when i heard that, where are you keeping the cameras, hm? not to mention that blood transfusions are useless since the blood gets destroyed, i was given nearly 10 and was still at a haemoglobin of around 4, highest 6 over the course of two weeks.
I don't have IC but after that description, I sometimes feel like it 😭 like I'll piss, then a few minutes after I feel like going again, but nothing comes out and it burns. Then it's done. Happens very rarely but it does happen 😭
Me too, it was like in 2019/2020, it was like hell and now years later im scared to even eat and eat very little or just eat vegetables most of the time, very rarely i treat myself to very little junk food:(
12:41 additional fun fact 1 365 BLACK people have it and 1 in 13 for the trait. I did a project on this and teacher thought we made the slides black to represent this, thats when we learned. The slides were black because i liked it but i guess it meant something additional. 14:29 helen keller had this and scarlet fever
I have a gene that causes pancreatitis every few months on and off and this year I’ve got it 5 times but most times they were minor luckily but the few times I’ve got full attacks off them he’s not wrong you don’t eat or drink for days constantly vomit and are in constant pain it’s truly something you don’t want
Ive gotten pancraatitis in 2020 :/ it was horrible. Trust me, it was not fun, and its anything you dont want to expirience, i was in the hospital for 10 WEEKS!!! so please be careful❤ this usually happens when you eat too much junk food
ok, i’m gonna throw my painful disease out there; chron’s disease. it’s a chronic disease that affects the bowel region creation ulcers and horrific pain. it feels like belly flopping on shards of glass. oh, i also didn’t mention that it’s an auto-immune disease. yeah, chron’s, it’s painful and has no know cause other than genetics.
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Alright
Request : Every Great Fire Explained
-Great Fire of Rome
-Temple of Diana
-Library of Alexandria
-Great Fire of London
-Great Fire of Chicago
-Great Fire of Boston
-Triangle Factory
-Reichstag
-Luna Park
-Brazil's National Museum
-Australia's 2019 Bushfire Season
-Notre Dame
-Kyoto Animations
Who else randomly found The Evaluator one day and can’t stop watching him 😭
Rn 😢😢
So true lol
Me😅
Me
Agreed
I bro I can’t imagine what it feels like to have any of these diseases. Thank goodness I don’t have any of them but I feel bad for the people that need to deal with this daily
I do have these but these happen like once a every 5 months for me they hurts like hell
Tail bone is different I fell at a skate park and I fell on my tail bone... it hurt
@Magicspeed13.offical Oh so you have all of these? Damn
@SHAITfam not all of them but I do have the tale bone one and the stomach pain one
Sometimes pancreatitis can be cured depending on the cause. For me it caused by lose gallstones causing a blockage so removing my gallbladder and the lose stones fixed the problem. I wasn’t even allowed to drink water for a few days because they wanted my pancreas to calm down before surgery
I always think I’ll start having unbelievable pain when I when I watch these.
my younger sister has sickle cells. it’s something that’s been bothering her since birth and takes pain killers and drinks water as a means of ridding the pain. she’s grown up and her pain attacks have become a rare occurrence. but it’s still something painful she has to deal with it. thank you the evaluator for covering the disease
same
I have sickle cell what did she do to ease the pain
@Real_ame Hot water helps but if its heat triggered pain stay away from hot water get some snacks to eat if your appetite is small if not try to eat nutritional meals but get food and water and tell doctors when you feel sick if you need more info. Feel free to reply!
@@Real_ame she takes medication. prescribed medication that she gets refilled
@@rapid_onions thx
poor stickman he just got every disease😢
He suffred unendurable pain. ever since the very start...
@@PrincePalisa fr
Miserable
he’s been through all of it 😪 he’ll never get a break
@@unknown.fishyy😔
I am one of the "lucky" 30-40 million with interstitial cystitis. I started showing symptoms as young as 6 years old with frequent trips to the restroom. Any flare ups (times when my bladder was in agonizing pain for days) that I had were always treated as UTIs. When I was 11 my Mom was diagnosed with IC after nearly a year of being bed bound by the debilitating pain. She was put on amitriptyline and changed her diet to bland foods (no spices or acidic foods). That allowed her to finish her schooling and become a nurse.
5 years later I am in her position. My flare ups are so bad I can barely go to school and have severe anxiety and depression. Before I was diagnosed I would take my Mom's pain meds to relieve the pain. I was taken to a specialist once my panic attacks prevented me from attending school. I was put on a restrictive diet, prescribed meds, and had multiple bladder installation treatments over the course of a year. Now at 22 I can say I live a normal life. My diet is still restrictive and I am still on medications but I am now symptom free and know what to do in case of future flare ups. Being hydrated and not holding in urine helps. There is hope if you have or think you have IC!
Smoke some weed lol
🫂❤️
@@JohnLemon-xq4pd tf wrong with you
Womp Womp 💀
@@dylanmercergo7853 Pretty sure weed is a goated pain relief tf wrong with you?
As a person with sickle cell anemia, this is such a perfect description
Don’t know why but I got trauma from some of the icons for the diseases
Me too
Me three
I relate
Ive had coxxydynia since 3rd grade. Lemme tell you, the pain of standing up after sitting for a while is excruciating.
I have interstitial cystitis it is hell. It’s more of a never ending feeling of having to pee. But when you try to go there is absolutely nothing. Every once in a while there’s some relief but not very often. I will say I am lucky compared to other people with IC. I don’t experience the pain. I just experience ALOT of discomfort. I also have ibs which is a common comorbidity that goes along with IC
This was my reminder not to hold in my piss all night just because I’m comfy under my covers.
now im scared to sit down
My grandpa had throat cancer, it's gone now so he's fine but he lost his voice and it's really hard to understand him when he talks but we got over with it )
My body steady making crystals that I can't sell for cash😒 damn body.
Have you tried?
@@lordpumpkinhead265you wanna buy?
I wonder if you can do a video that includes idiopathic intracranial hypertension, or IIH? I have it, and it’s a condition that does need a bit of explaining, and I would love to see your take on it.
A friend I had in primary school.
His mum had survived Meningitis and because of the disease and how severe she got it, she went permanently blind.
4:40 anime jumpscare
put chronic cholecystitis on there, shit is awful
I have sickle cell anemia, SS hemoglobin. My doctors say I have a severe case and this explained it really well, thanks for the coverage!! :)
let's give honourable mentions to: endometriosis (women), testicular torsion (men) and kidney stones (unisex).....i'm a man but have known women with endometriosis; i don't think you can understand the pain until you've been through it and being a helpless bystander makes you feel really useless when you're with someone going through it.
My father has trigeminal neuralgia and it was cm aused by when he was in Afghanistan in a war and the shower water was so potent and gross that somehow it effected him 17 years later.
I'm surprised that bronchitis wasn't mentioned, as it was a nightmare for me, I couldn't even eat chocolate pretzels without puking.
The only good thing about it was that I was able to drink apple juice
Apple juice is fire
Bronchitis DOL or NRS isn't that high right
Bronchitis DOL or NRS isn't that high right
@@rlalbiaksangi4528 nah, but it does suck.
@@l3ilani333 agreed
i injured my tailbone in my sleep somehow (i sleep in the worst positions you could ever imagine lol) and it made sitting down and getting up from my seat incredibly painful for weeks, and for almost a year after that i still had pain there but it wasn't severe anymore
i think i have interstitial cystitis but when i drink water it goes away or is it not it
I have IC and I experience relief with drinking lots of water so it’s very possible. Keep in mind IC can look very different for each person, different triggers, different severities, different relief methods etc
@@brookeleden it happens to me rarely sometimes 5 times a year its really rare i dont really know if its interstitial cystitis
5:15 GOUT
The evaluator the most educational and funny youtuber who agrees
thanks, now i can study Pathology in 16 minutes for my exam.
The most underrated and hardworking content creator
One time I broke my coccyx and got coccydynia. This was 5 years ago and it still feels like there’s a horrible bruise.
Well this was a weird thumbnail to see on my homepage during my pancreatitis recovery...
Oh, btw, it doesn't just last a few days. My doctor said it could be up to six WEEKS. I'm just about two weeks into my recovery and I'm really hoping things calm down soon...
EDIT: I've never had ischemic colitis, but I DID have ulcerative colitis (which Google says is essentially the same thing but more chronic and with a different cause) and it got so bad that my intestine was going to BURST so they took the whole thing out. That wasn't fun either.
Doctor: you have interstitial cystitis...
Me: I c... (i see)
19 likes!?!?!?! thank you so much
Really bro 😒
@@bloonbrawler9872 He said it too at the start. hes my inspiration 😯
Bro why explain the joke within, ruins a nice lil joke
@@__-tp4tm because some people wont get it (holy cow 19 likes!!?!?!!)
i thought i made this comment then i realized i hadn’t watched this video before
God I hate having IC. I’m 23 and unfortunately one of the small demographics who has not only severe symptoms, but also bladder polyps that I had to have removed via a TURBT. I’ve been in remission since December. But your description was SO vindicating because I have been struggling to get disability, since it makes it near impossible to hold a steady job as a student
My mother had pancreatitis it was so awful she was in the hospital
I had IC and it feels like my bladder is a balloon about to explode
Anyone else have phantom pains now too?
I had ulcers around 2-3 weeks ago and it was torture. If I were to ask what is the most pain I’ve endured. It would have been that. For the last 3 days I have been in pain.
Oof, Gout.
I had Gout on my right big toe back in April and it hurt enough to go to the hospital for it.
The bus I sat on hit the tiniest divit in the road that made my foot bump the side and it felt like Shaq slam dunked a bowling ball on my foot.
Naproxen is a godsend.
I worked with someone with trigeminal neuralgia. She had to take a lot or time off, as the attacks went on for 2-3 days, 😢
If you haven't yet, can you do one on kidney infections
I remember when I had gotten a tailbone cyst, worst back pain of my life.
i've had trigeminal neuralgia it really feels like getting stabbed in the face
i had tail bone pain once. It sucks, it's manageable but it sucks.
My dad has tail bone pain but has been trying to treat it but he has said “it’s not that bad”
I have a weird pressure feeling that occurs in my lower back right around my kidneys occasionally. Does anyone know what that could be?
Blind people: 😃
Deaf people: ☠
Deaf people use subtitles
I have sickle cell anemia
I'll never forget the 8th grade field trip to the roller rink the day before Christmas break. My first time roller skating, and I was using the "walker" things provided for people learning to skate. I was having a great time until I fell on my butt while using the walker. I was a bit sore as expected right after. However much time later it's time to put our shoes back on and board the bus back to school. I was struggling a bit because it hurt to sit and bend over to change shoes. After the ride back I was hurting quite a bit more, it was becoming difficult to walk. I wake up the next day in immense pain. Unable to walk for a couple days, and limping around the entirety of my 2 week Christmas break I had been looking forward to. I had bruised my tail bone, and it hurt like a motherfucker. As an adult now with your typical knee and back pain in my mid 20's, I would not wish coccyx injuries on my worst enemy. I didn't even break mine, I just bruised it pretty good. If I was in that much pain as child, I don't want to imagine going through it again now.
Idk if it’s related to coccydynia, but when I was anywhere from 7 to 8 and a half I was with my church’s singing group and my parents for rehearsal and one lady moved a chair, for a reason I can’t remember, and my ADHD brain forgot she moved it and muscle memory took over and I sat on a ghost chair and fell flat on my butt. Then ever since at random times my tailbone hurts a little bit or agonizingly bad. My mom told me a little bit after that I bruised it and that I wasn’t alone as she bruised hers at some point too.
Drinking morphine doesn't help with sickle cell anemia, oh my gosh im so glad I don't have that
Does it count for breathing in smoke when you are not smoking
Treatment plan should be be told also with illnesses
Idk why but he on day I was looking at my chest and realized a had a big purple mark that looked like a Bruce and it get bigger and doesn’t stop spreading
I have Trigeminal Neuralgia, and it's a torture even trying to chew on one side!
as someone who is day 1 in being pain-free from a sickle cell crisis, how the pain was described was absolutely accurate! i still need a walking stick to get out of bed and go down the stairs and a wheelchair in mediocre-sized malls. sickle cell pain is no joke, but it doesn’t sound as bad as the pain described for the other diseases 😅 the worst part is, is that if it isn’t caught early even pain medication like morphine won’t work. (i was put on 40mg of morphine in the hospital for 2 of 3 crisises.. in a row but panadol and mybulen worked perfectly fine at home for a small arm crisis spike)
edit: yes, they even gave me liquid morphine. i was shook when i heard that, where are you keeping the cameras, hm?
not to mention that blood transfusions are useless since the blood gets destroyed, i was given nearly 10 and was still at a haemoglobin of around 4, highest 6 over the course of two weeks.
Day 3 of commenting until the evaluator responds
Can you talk about Laryngitis
I don't have IC but after that description, I sometimes feel like it 😭 like I'll piss, then a few minutes after I feel like going again, but nothing comes out and it burns. Then it's done. Happens very rarely but it does happen 😭
I had pancratis once. It was painful. You really don't want to experience it
Me too, it was like in 2019/2020, it was like hell and now years later im scared to even eat and eat very little or just eat vegetables most of the time, very rarely i treat myself to very little junk food:(
I have sickle cell anemia
My brother had pancratis he described as a drill in his abdomen
12:41 additional fun fact 1 365 BLACK people have it and 1 in 13 for the trait. I did a project on this and teacher thought we made the slides black to represent this, thats when we learned. The slides were black because i liked it but i guess it meant something additional.
14:29 helen keller had this and scarlet fever
Evaluator:every painful disease explained in ...minutes/me:Life
You should do rashes
I have a gene that causes pancreatitis every few months on and off and this year I’ve got it 5 times but most times they were minor luckily but the few times I’ve got full attacks off them he’s not wrong you don’t eat or drink for days constantly vomit and are in constant pain it’s truly something you don’t want
I’m literally scared to do anything now 😭😭 even if I only drink water
I fell on my tailbone once as a kid when I slipped on a wet wooden deck. The pain described is not an exaggeration 💀
my dad had gout last month(on his foot)
I have sickle cell, and im currently at home because of it 😢
That happened to me, but it ended quickly ask at least one day
My grandfather has Gout
I have meningitis,sickle cell,interstitial Cystitis,and Gout..
Ive gotten pancraatitis in 2020 :/ it was horrible. Trust me, it was not fun, and its anything you dont want to expirience, i was in the hospital for 10 WEEKS!!! so please be careful❤ this usually happens when you eat too much junk food
9:53 Vertebruh
Thank God i don't have any of these diseases
I think i have the first illness...it's not that bad.
The only problem is that it's hard to sleep.
I had bacterial meningitis edit: I was 3 month old
Why isnt his guy being mentioned by millions for explaining these 😅😅😅
My dad had Spinal Meningitis when he was younger.
Is he ok?
Not the goofy music at the end 🚪🚪🚪🚪🚪🚪🚪🚪🚪🚪🚪🚪
Why does bro sound like T.T.S? ☠️
pls say these diseases are rare
I have Gout lol
9:36
Poor stickman
My dad has gout 😔
I might have the first one
He has gout
I had acute pancreatitis caused by lose gallstones causing a blockage 🥲 *IT HURT!!*
ok, i’m gonna throw my painful disease out there; chron’s disease. it’s a chronic disease that affects the bowel region creation ulcers and horrific pain. it feels like belly flopping on shards of glass. oh, i also didn’t mention that it’s an auto-immune disease. yeah, chron’s, it’s painful and has no know cause other than genetics.
it’s crohn’s btw
@@slayomgkonifers wdym?
@@hendrixglazer4733 it’s crohn’s disease not chron’s disease lol, also i hope ur doing well cuz the disease must suck
ik i spelt it wrong, i was half asleep while writing this
@@hendrixglazer4733 ohh lol
Under a day gang
I
V
GYATT
What
You're missing a lot of diseases, some of which would make your toes curl. maybe call it "Some Painful Diseases"
Had the first one, would not recomend.
endometriosis ;_;
bro where is chronic prostatitis ? ı am %100 sure it is much worse than all of them
My Mother has Trigeminal Neuralgia.......😢
I hope she's okay
@Itz_Chaotic_YT sometimes yes, but other times the pain is too much. Thank you for your comment though. I definitely appreciate it
@@crazymulatto8981 I'm always here If you need someone to talk to
My mom has it too 😞 sending all the love 🙏 its hard
@@nathalie8941 thank you
W a new video
awseomesauce
Uh
Hey 👋
haha pale virus go brrr ( changed 2024 trailer real)
IC sucks so much