Every DEADLIEST Disease Explained in 16 Minutes
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- Опубліковано 18 чер 2024
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00:00 - Porphyria
01:15 - Necrotizing Fasciitis
02:25 - Progeria
03:34 - Toxic Epidermal Necrolysis
04:54 - Fatal Familial Insomnia (FFI)
06:04 - Alzheimer's
07:20 - Hemophilia
08:27 - Guillain-Barré Syndrome
09:39 - Fibrodysplasia Ossificans Progressiva
10:57 - Ehlers-Danlos Syndromes
11:53 - Myasthenia Gravis
13:36 - Familial Hypercholesterolemia
14:34 - Staphylococcal Infections
We cover interesting topics that you might not know about!
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i remembered you when you were at 19k subs 😭
Love the narrator 🎉
Hey dude hemophilia doesn't mean your royal. It can mutate spontaneously in a woman at birth and become a carrier for the disease. The version your thinking of in Russian royals is type B hemophilia. Missing platelets that repairs joint and muscle damage.
Cancer:
Holy crap, I had no idea necrotizing fasciitis was so dangerous and rare. When I was around 11, my grandfather got it. They kept telling us it was "flesh eating virus" and that we had to be careful not to touch him near his wound. It was so difficult because I wanted to help with his wound care, but he had to do it all himself. Now I am amazed at his strength, he never showed us any pain or fear.
Amazing video, as always!
did he survive?
@@Luis-kl6nx"he had to" yeah sorry but no.
May he fly high.
@@vladsoloshchenko5551 im sorry, rest in peace
I laughed as a heard fasciitis because of the history of ww2, but when I heard this I became silent.
With fatal familial insomnia it’s not insomnia itself that causes death. The cause of death is brain degeneration which causes the insomnia. Additionally all the cases have come from one family.
Thank you so much. I love learning but have high anxiety so I get worried that things may happen to me. This puts me at ease
It’s also a prion disease which adds to the brain degeneration
Not just one family but it's extremely rare 50 to 70 families in the whole world . like someone else said it's a prion disease causing protein in the ( I think hypothalamus) to misfold .
It causes holes in the brain and makes it impossible to function normally not being able to sleep isn't the only thing. The pupils in the eyes can't adjust anymore and you also sweat al the time your body just goes in overdrive .
It's absolutely terrifying though .
Thank FUCK
prions
I am a survivor of MRSA. I was infected by a staph infection on my forehead, then I took a regiment of antibiotics, and it laid dormant in my joints. I twisted my ankle and got osteomyelitis, because the MRSA infected my joint from the inside out, from the bone out. I was one of the first people to try zyvox as an experimental drug, and that is one of the main medicines that they now give. I am crippled, I will forever limp like I have a twisted ankle. But, I'm alive and I'm very thankful to everyone who helped me from the surgeons to the nurses and my family . I was according to the doctors 48 hours away from dying from sepsis . But I'm here now, and that was 15 years ago. If you read this, thank you
That so sad 😔
Glad you're still here :)
Me when I lie on the internet
@@fakeaccount6319 nice!
@@fakeaccount6319Shut up.
This is truly the best channel I've come across, consistent upload schedule, simple animation, good voice over and very informative
And not a 10 hour intro telling people to like and subscribe if they love they’re mom and if they dont like and sub they are automatically worshippers of satan💀
glad you like it
Yes very good channel
This is the mainly facts guy speaking in the video
Totally agree
I have EDS, and have also had MRSA- in fact, I had a period over a year where I suffered repeated cases of MRSA due to the school making us sit on the gym floors as part of PE.
I also have another condition that is a "sunlight allergy," though it isn't Poryphiria. It doesn’t have as severe of a response, but still means that I have to avoid sunlight. Polymorphic Light Eruptions, or PMLE is what it is called.
I also have several other 'rare' issues, so I am overall a genetic catastrophe.
I had to apply for disability at 17, and have been legally disabled since I was 22.
I would not wish this existence on anyone.
Damn. I know it ain't much but...I hope you find peace in your day to day someday.
@@CrowCodedI mean, I am at peace with my day to day existence, at least as much as one can be. That just doesn't exclude me being able to acknowledge that I have a low quality of life.
My doctor told me to be really careful and told me not to do any sports in school at all because I have Ehlers-Danos, and my friends make fun of me and call me weak and tell me to go to the gym and go on a bulk, but my doctor told me I will dislocate my joints if I do that. :(
aw man, what type do you have? I have the hypermobility type and I'm able to do sports. (with the occasional hyperextension in arms)
Damn that's tough :(
@@SnowySalenski I think I also have hypermobility, but I am not completely sure because the doctors are still trying to figure things out.
nah those aint friends
Drop those friends.. whatt..
As someone with Ehlers-Danlos Syndrome (or just EDS) my experience from it goes as follows:
Pros:
1. Cool party trick to be able to extend my arms and legs and being able to literally pull my eye lids off my eyes and make a popping sound, become a human pretzel, etc.
2. sexy times goes hard ngl.
Cons:
1. If I take my sleeping meds (I take a skeletal muscle relaxer which basically loosens your bones and muscles around joints) then the next day I walk around like the jangly man from scary stories to tell in the dark and gotta wait a few hours till I can pop everything back in place.
2. Mild pain and numbness can happen but only if I *really* push myself too hard, can last the whole day.
As also someone diagnosed with EDS I’d totally add dislocations by just walking also
As someone with EDS I use a wheelchair everyday because my tissue is so messed up I risk severe injury and I’m only a preteen so hopefully it won’t get worse when I’m older but it is a very interesting condition that has taught me so much and gave me a different perspective on life that most people don’t have. It’s also very interesting how much of a spectrum the condition is. I’ve seen people who needed assistance breathing and others who obviously still have challenges but have not had any severe consequences.
Wait it's not normal to be able to pull your eyelids away with the popping sound?? (adds that to my list)
@@WARRIORLUNA37 Yeah I'm kinda in the middle road. Lucky since I mostly just have all the fun quirky aspects of it other than some joint pain every once n awhile. When I pull stuff out of socket it's mostly on purpose rather than on accident, It can hurt when its on accident but either way it normally just feels like a slight numbness/disconnect. I am sorry about your condition though, hope the best for you ❤
@@MazCat Yeah lmao, I normally do it to gross out my friends, along with just extending my arm and putting my hand on their shoulder from an extra 5-6 inches away. Check it out, maybe you have it :P
Hypermobile EDS: because you totally wanted to know what it feels like for your collarbone to dislocate during a meeting.
Real
I once dislocated my shoulder doing nothing but carrying a small bucket of ice to a trough when I worked in fast food. It was a very small bucket, and I did not fill it all the way, and it wasn’t particularly heavy, but when I lifted my arm to pour the ice, my entire shoulder made a loud “CLUNK” sound and I just kinda
Dropped to the floor
That was a workman’s comp case I almost had to sue for
And I was 19
@@krystalreverb Jeez! I'm sorry to hear that. Worker's comp stuff is always a fight, and it's like, I'd rather get crappy care from my own providers than battle to get crappy care from whatever bottom feeding suction eel they assign me.
(I've had a couple of VERY bad experiences with worker's comp.)
I didn't know you could dislocate a rib. Apparently in normal people, it only happens from an impact to the ribs. It happens to me weekly just walking around. Gotta love EDS.
@sircrumpets_ wait dislocating ribs isn't normal? Another thing to add to "list of hEDS symptoms to bring up at the doctor's
Fun fact about Fatal Familial Insomnia (4:54) there’s another condition exactly like it called Sporadic Fatal Insomnia (sFI). This does the exact same thing to you as FFI, except it’s not hereditary. It just…happens. The mutation just appears. Your prion just mutates spontaneously for unknown reasons.
Gotta love those prions. They can screw you up hereditarily, sporadically, or caught
Oh my god, that’s terrifying. New fear: unlocked
@@ShinyRedStar-dn2yf whenever my insomnia gets bad, I think “is this sFI?“ even though there’s only been 25 recorded cases worldwide since 2018
CJD works the same way. There is a variant form Sporadic and inherited
@@grobanite4ever85 eeyup, they're both prion diseases
For me my biggest fear is Alzheimer’s because you keep forgetting everything until your just a shell
My grandfather passed 3-4 years ago, from Alzheimer's. Now I know what he had to suffer through, forgetting everything
I think my mom has been getting it.
I hope she's fine..
@@jakeg3126 i wish the best for you and your mom
@@wu_SER1 thanks. I think she’s got a bit to go, but answering the same question that she asks once in a while 3 times in 5 minutes is a bit annoying sometimes.
FINALLY! EHLERS DANLOS MENTIONED IN ONE OF THESE VIDEOS!
I'm on tv!
This was exactly my reaction too!
I begged for it to be mentioned, finally recognition: D
I want to see your fantastic plush fingers Mr GoofGoober
MY EXACT RESPONSE
not a good video to be mentioned on deadly diseases that seems like a good thing i have eds too but i was shocked to see it in this video
*new fears unlocked*
Me 😭
*ULTRA KILL!*
Totally
bfdi pfp spotted
r/suddenlybfdi
@@thalal.uh oh wheres the pfp now
As someone who had GBS, yes it also hurt af if you try to move, also have like life long problems cause of it, mainly damaged lungs and nerves dying after going to a shop and back, luckily im not paralyzed and im really grateful for that.
i had guillain-barré syndrome back in 2019, mind you i was 10 when it happened and even tho its been 5 years i still havent recovered and i had one of the most severe cases
I know it's weird to say, but I hope it was caused by an infection and not a vaccine.
It'd be a shame if something that is supposed to help and protect you caused damage like that.
@@ceneblockIts from viruses.
I had Guillain Barre and it resolved itself within 48 hours. It was the start of my natural healing journey from all the damage that lifelong medication caused. Look after your liver health and the rest will take care of itself. Big Harma use chemicals to suppress your liver, the harm to which causes all the symptoms of so called diseases.
Hey, i got this syndrome 12 years ago when i was 10 too, i don't remember how bad it was but it really changed the structure of my life a bit, I'm here today with vary minor side effects, i hope things will get easier on you and wish you best with your recovery, lots of love 💖
@@ceneblock actually it wasnt but that is a very common reason people get gbs!
Hey, these are super informative. I've been going through all of your videos and have been enjoying them.
Just wanted to let you know, your hard work and effort is being appreciated!
can you do a video with scoliosis? It would make me happy :) I also learn a lot from your channel, i’m glad I found your channel.
happy EDS awareness month! thanks for making this video :)
I had MRSA from 15-18. When it did flare up I was in immense pain, but at the same time I was always quarantined at the hospital so it was super cool to not be near anyone. This was pre-Covid so being quarantined felt like I was special! I got rid of it with antibacterial ointment up my nose for 3 years.
11:45 "Oh no, i sneezed too hard while sitting too vigorously and it appears my skeleton has gotten the IKEA treatment" why is this so funny 😂
As someone with EDS, it caught me off guard seeing it here, lol. The way you described it is hilarious.
Same here .
Your channel is amazing. Keeep it up
One of my friends has Guillain-Barré! They struggle a lot, but recently got a custom wheelchair that’s helped them out in daily life!
I LOVE THESE VIDEOS OMG FIRST THING I WATCH WHEN STUDYING I CANNOT EXPRESS MY LOVE FOR CHANNELS LIKE THESE ESPECIALLY THIS ONE OMG RAHHHHHHHH
This videos are very underrated. Great content.
Thanks!
@@TheEvaluat0ryour welcome
You should touch on the different EDS types! The vascular type would have done well here as an example. I have the classical type (lovely), but hearing about the vascular type makes me shiver.
I’m worried that I could die because of this
because of what?
@@TheEvaluat0r literally anything
Ikr
@@TheEvaluat0r Dracula thing
EDS won’t kill you, im alive :)
ive got ehlers-danlos and i was 100% not expecting to see it in this vid 😭
(its mostly just really annoying, lots of joint pain and easy dislocations, plus i bruise/break skin super easily)
Im about to binge all your vids. Not sure if you included in an ither video. But steven johnson sybdrome is probably one of the most terrifying in my opinion
Ehlers-Danlos Syndrome patient: (Sneezes)
Their body: *(lego breaking sound effect)*
This channel grew so quickly. I watched the channel when it had 3-4 vids!!!
His hardwork was paid
BRO THANK YOU FOR COVERING GBS, I CANT BELIEVE SOMEONE ACTUALLY TALKED ABOUT IT 😭😭😭 I had this at age six!
I was wondering when you would go over Ehler Danlos, I was recently diagnosed 😅
How do you make so much good videos in a short amount to time within a short time frame
Two years ago, my mom had Guillain Barre and she nearly died. She went to the hospital on Christmas Day but had gone to the ER a couple weeks ago before. They had just thought she was hungover because she had trouble walking and focusing, so they rejected her. She finally called my aunt and her cousin and they brought her to the hospital, the nurses said she was only a day or two away from passing. She was there for ten days and is still, two plus years later, having troubles with focusing and remembering things. She had a carpentry business for about a year and a half before she got sick, and she still hasn’t started it again because she is still recovering.
Do you mind doing a video on every type of radiation?
isnt there only 3 types?
@@adamsime630 that just means he could go more in-depth which would be nice to see
@@thegenderofkel yeah, that would be cool because there is surprisingly a lot to comment on about the radiation occurs
That would be soooo cool!
@@adamsime630 4 actually, alpha, beta, gamma and neutron radiation
You make some of the Most Witty and Clever Illustrations and Hilarious Wording and sayings!
This is Why I Love your Videos!
These bone diseases are so interesting! More of those please!
both me and my sibling had MRSA when we were younger that was passed down from our dad’s father. it was so horrible and painful to experience at such a young age
ayyyyy, my boy with another fire video
yupppp!!
FFI has been my greatest fear for the longest time
My entire family has EDS, (the rubber one) most of us are just extra hypermobile but my mom has to go to the chiropractor ever week to keep from falling apart. It's actually really common, my mom thought for 30 years that everyone could dislocate their jaw at will. Most hyper-mobile have some form of it. But it is funny when I pull my skin like an "old rubber band" and everyone freaks out.
I love allowing my hip joints to partially dislocate and fall to the ground like woody from toy story. It's hilarious to me and terrifying to others
Brilliant Explanation 👏. I've watched all your videos in loop. I would love to collaborate with you. Do you need any help with scriptwriting and research?
I survived gbs with almost no permanent side effects, it's always nice to see people speaking about this syndrome
I have hypermobile Ehler’s-Danlos and it has been passed down maternally through my family. As the generations have progressed the symptoms have gotten worse. It started with very thin skin and rickety joints and devolved into me needing a wheelchair due to barometric pressure changes. As awful as it is, I’m lucky to have the hypermobile version and not the vascular version.
Edit: dislocations and subluxations from mundane tasks is a very real thing. I once squatted and dislocated my hip so aggressively that the muscles couldn’t force it back into place. So for 3 months my hip joint was teetering on the edge of being in and out of its socket.
I had MRSA before, I don’t remember much about it, but the cleaning was BRUTAL.
I had mrsa in second grade but I had no idea how bad it could get till I was older
MRSA also can start as just a cut or scrape that doesn’t heal right and progressively becomes redder. Both my grandfather and mother got MRSA and started with those symptoms. It was in the same home, meaning the bacteria are always present and can strike at any time with a fall or a scrape.
We got countryballs, we got spaceballs, and may I present to you: diseaseballs
Lmao
One of my clients had porphyria and so did both her parents. She was miserable. Her father had the cutaneous type, her mother and she had the intestinal type.
I had the very beginnings of Stevens-Johnson Syndrome, which can end up as TEN sometimes. I developed blisters on mucous membranes and the next would have been my skin sloughing off. I can never take that medication off again or I could die. Thankfully there are other epilepsy medications that I'm not allergic to that work on me.
you should include serotonin syndrome, or neuroleptic malignant syndrome (which i had gotten from being given Reglan for projectile vomiting! 😊)
Damn, I’m kinda scared. I hope the people that have these diseases are ok. Tbh, this is probs one of the best channels ever! And also I didn’t even know that some of these diseases even exist! Well…you learn something new everyday, don’t you?
My EDS isn’t so bad that I need a wheelchair (yet) but it’s definitely possible that I may need it eventually. I have the hypermobile version and the only other thing besides pain and frequent dislocations is crippling fatigue. Some days my fatigue is so bad I can barely reach over to my bedside table to put on my glasses. Other days I just stay in bed and lay there, and sometimes I’m so fatigued it makes it hard to move and breathe.
I also have some extra chromosomes that contribute a lot to my health issues as well.
My grandfather (my mom's adoptive dad) died of myasthenia gravis. He went to jail and they didn't give him his medication like they were supposed to. I was too young at the time to have any memories of the whole ordeal.
story time
my aunt had necrotizing Fasciitis from her trip to Asia. She was riding a motorcycle in the streets of a country in Asia (can't remember which one) and fell over she thought nothing of it until her leg started to turn black like a dead body. she had to be rushed to a hospital she would have died if she had not been treated. she is ok now but it was scary for me and her kids. so be safe out there
I knew a kid at my elementary school who's older sister suffered from FFI. She was only 12 when she died. She would have been turning 25 this year. I wish her family the best.
Is it ok if I ask what ffi
yeah i have a condition similar to hemophilia (vomwillibrands i think is how its spelled) and it surprised me to see that on the list
Oh hey I have Ehlers Danlos syndrome! The way you describe the body just being like "hey, screw you, *falls apart*" is hilariously accurate
5:36 - Ooh. I actually had heard of Fatal Familial Insomnia. Oddly enough, it appeared in an episode of Law and Order: Special Victims Unit.
I forget the intricate details, however, I do remember the person who had it had actually witnessed a crime during one of his nightly walks.
The psychologist who was a regular character at the time, had noticed the oddities of the witness and then proceeded to explain what he had. It was stated that it was very, very rare and according to the episode it was most common among people who were from a certain village in Italy (if my memory is correct).
The witness had not been able to fall asleep despite taking over the counter meds, prescribed sleep aids, drinking tea, watching tv, reading a book… you get the picture.
I suffer from insomnia and have been for decades, it does truly suck so I cannot imagine being unable to sleep but not only that, it was shown in the episode that he had trouble remembering the days because it had gone on for so long, time and dates meant nothing to him.
I have EDS, it causes me lots of pain in my knees and legs especially when walking far distances and also effects my bowels by making them very lazy
EDS MENTION!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! one thing about EDS or at least some versions is that the skin is thin and sometimes almost velvet-like. For me it can often manifest as stretchmarks in unusal places, easy bruising, petechia (very small bruises) from scratching something, and so on.
Yeah, I asked for it to be mentioned because no one ever does, it’s a lot of pain on your body too, and bruising is so easy I almost have 5 bruises per day 😔😔
I was honestly shocked to see EDS on here. I was diagnosed a year ago, but I've been suffering with symptoms for years. Unintentional hip and shoulder dislocations, having bruises that don't go away for weeks, and being in constant pain. But on the bright side, I never have to use lotion because my skin is disturbingly smooth 😌
There was a famous politician (can't remember who he was, but he was one of the good guys) had Guillain Barre Syndrome and made a pretty good recovery, although it made his trademark lisp a bit worse.
OH MY GOSH?? GBS MENTIONED?? gbs usually if treated in time will go away completely, but there is a chronic life long version called cidp, which i have.
I’ve noticed quite a few of these start off with a perfectly happy and healthy person going about their day..
Now that I think about I have all of the symptoms of fatal familial insomnia except for the insomnia and shutting down parts
Im not sure how MRSA infections differ between skin and lung infections but all these stories in the comments make me happy that i recovered from an MRSA lung infection relatively unscathed besides having to be in the hospital for a few weeks a few years ago
Do gut flora next!
porphyria has a cousin disorder called solar urticaria, an allergy UV; the rays the sun emits. my mum has this disorder and it is genuine agony for her
I don’t want’s to watch this anymore because there’s someone in my life downstairs who is dying to Alzheimer’s
Same. But they’re upstairs😥😢
As someone with EDS, the sneeze on the couch thing was too accurate
Another bad thing about staph infections is that S. aureus can mutate very easily and it is also one of the only bacteria that can penetrate the skin. Mostly through hair follicles causing folliculitis or inflammation of the follicle.
Didn’t expect to see myasthenia gravis on this list. My mom has it. It sucks
I remember when I subscribed! One of the first few hundred!! Awesome channel !!
Yeeeeees! thank you for your support
Ofc!! Your channel has always put out awesome content :)
I also had a video idea for you :)
“every parasitic infection” like pork tapeworm, lung fluke, entamoeba histolytica, cryptosporidium, Naegleria fowleri. Just to name a couple :)
15:04
I did this, I ended up in the ICU with Pnemonia completely taking over my right lung and pulmonary embolisms and this was about a year ago and i still have issues with breathing, finish your whole dose of antibiotics folks, dont end up like me
you know you have something horrible when one of these things happen
1 - You can barely pronounce the name
2 - It has "Necro" on the name
3 - You're told to name the disease
I have porphyria, but luckily I have cutaneous porphyria which isn’t as severe and doesn’t come with the internal issues.
me too! we think i have accute intermitent, but we arent entirely sure. theres a chance i could have this one mutation that like 200-ish people have? i cant remember what its called but i know my symptoms line up a little TOO well ykwim LOL
The video was good
bro
thanks!!
@@TheEvaluat0rit was tho
@@TheEvaluat0r 🤣 it was meant to confuse people because the video just came out a few seconds ago and I said that the video was good (as if I had watched the whole video in just a few seconds)
BTW THANKS FOR THE SHOUTOUT
that's only the skin porphyria's that have sensitivity to light, there are Acute porphyria's too! It depends on what part of the haem synthesis pathway is affected :)
i love seeing my issues represented!! eds survivor :)
I have just now come to the realisation that his name is The Evaluator
I thought it was The Elevator
Lolll
What happens to someone with FOP if they get a concussion? That sounds terrifying.
My neighbors have hemophilia, they usually take shots everyday, with a tube and stuff, they are pretty young, but they are going strong!
Ehlers-Danlos Syndromes, also known as Gomu Gomu no Mi.
Why?
3:33 I had this. Thank you Carbamezapine
Bro are you ok?
@@1_hate_mys3lf_rn I was 6 when I got this from Carbamezapine overdose for treating neurocysticercosis and it took me approx 6 months to recover so yeah I am fine. I am 22 now
same! for me it was cefdinir. SJS/TEN is no joke but i’m sure we both know that lmao
no talk about rabies the deadliest of them all?
I believe he has already spoken about it
@@hyuncut6187 yeah just saw the video
Good job my guy
@@barry7331 This channel is amazing, I love to have it on my bg when doing something different
it has a vaccine and a relatively low infection rate from exposure even without it, but if you do get it you're cooked
@@iexist_nt actually the manifestation from rabies can happen in years so as long the patient goes to the hospital and gets proper washing on the injure, vaccine and, if needed, a specific treatment they should be good
whenever i watch videos like these i always think that i have every disease talked about
I have hemophilia!! people are always shook when i tell them but to me it’s just everyday life
11:14 oh hey my stepmom has this, doctor say she will be wheelchair bound by her 50s. She used to dislocate her body all the time before moving to get medical treatment n such. Has a helper. Wears KT body tape to keep things in places better. Wears knee, wrist, and shoulder braces. Kinda sad. She can’t work anymore and solely replies on disability checks.
Goated videos
I have one of the conditions here. Neat
Nice video
Very informative❤❤❤
So basically i have an mrsa right now?? _😭_
And yes there are painfully itchy red bumps on my hands, they got bigger over time (hopefully ill be okay or maybe its hopefully just bug bites)
Watching this at night :)
I used to get staff infections on my skin all the time when I was little, but instead of taking me to the doctor, my mom just sterilized and needle and poked them to let the pus out. And I don’t have any scarring, but like what the fuck. I had no idea it was that bad and that I could’ve died. It was just like mildly inconvenient.
Fatal familial insomnia is a prion disease, the insomnia is a symptom of the neuro degeneration, and there are cases of it that don't always include insomnia.
I have insomnia, its not that big like ffi, but i still cant sleep in some cases bc of anxiety and shit. But now im scared im gonna get ffi.
Now give them all to one person and watch what happends.
Can you do a video covering Urban legends from around the world, in 13 minutes? Asian countries have some good ones!
Hi, EDSer here. Basically my parents got my structural collagen from Wish 😂. Most folks with EDS have the less-intense hypermobile type, which doesn't have the hyperextensable skin. Still, it's basically like having muscular dystrophy but for your ligaments and tendons. I've had osteoarthritis since the tender age of 14 and chronic debilitating fatigue and pain. So much more than your joints are affected by collagen: horrible menstrual cramps, tinnitus due to instability in the inner ear, migraines, heart issues like prolapsed valves, aortic dilatation, and tachycardia, reflexes that are ridiculously strong, poor vision, weak gums, IBS, the list goes on and on.