Imagine if she never asked to be transferred to another hospital. Why didn't the doctors do a research or seek help from other doctors out there? A lot of people die due to lack of research in some diagnosis.
some hospitals dont have the capability to diagnose some diseases and have to be referred to another hospital that specializes in what is ailing the patient
I’ve had PG for 23 years. The speed at which the wounds accelerate in size is frightening. I’ve had it double and grow centimetres deeper overnight. At its worst I had a wound 40cm x 20cm and 7cm deep on the back of my thigh. I’m treated with immunosuppressants and for most parts I’ve been ok. With God’s blessing, my amazing family and an awesome wife I lead a fairly life, work in education and this year had a beautiful daughter. Over the last two decades I’ve had several relapses which have nearly cost me my leg and life. The pain at times is indescribable. If you’re reading this and have PG I hope it’s going well, wounds are healing and life is getting back on track. You’re in my thoughts and prayers.
Hiya PearlJam. Yep. I have it too. Misdiagnosis almost led to right bka in 2021. Multiple ulcers. Arterial bleeding. The pain you know about. Last episode, all ulcers healed. Scarring below the knees and on the forearms is frightening. I hope you’re doing ok too. Cyclosporine for me
Ikr! A lot of people have left their partners because they were sick, or even if one of their children were sick. I guess some people just aren’t built as strong as others
My baby nephew was having the projectile vomiting and crying all day and night. Till I suggested they did a full check on him and they found out he had a hole in his heart. We flew him to India for the surgery and till today he has no problem. When you have a medical issue don't wait just visit as many hospitals as possible to get different options. Lord Jesus I thank you for your guidance.
@@y.n.7534 India's image is presented as a poor and underdeveloped country in the western media, but there are world class medical research and facilities here. These are costly for the average Indian but for the patients from the developed nations the costs are dirt cheap compared to costs in their country.
i was born in 1998... when i was 8 months i had same disease as this child... my mom told me i cannot breath, my eyes was same as this child, my hand moved automatically. even the doctor told that i cannot live no more years, i cannot play sports. i was diagnosed till 10 years.... but now i m 20 everythings gone, now i play sports, i live like other child.... thanks god and i hope this child also will be healthy
I hope now, going into 2019 that these types of rare disorders can be diagnosed faster. With the internet and fast access to scientific literature and medical journals online it seems hopeful.
th-cam.com/video/ypmsjqytMpA/w-d-xo.html please check out the series monsters inside me. So many people might be affected and misdiagnosed etc. Its scary asf. The more we knoe the more we can help eachother.
Well the internet is one of the last places where you would get the right diagnosis.. Ask any health care professional what they think of people self diagnosing trough google..
@Vyrex420 I'm not talking about a patient putting their symptoms into a search engine like google. I'm talking about healthcare professionals using online medical journals (Pubmed etc) to access papers / articles / reviews from around the world. As a person with a degree in Pharmacology, hands on experience with stem cells and heading into a masters in Regenerative Medicine I know all too well the importance of medical journals in research. So yes I do know what I'm talking about. I'm not saying the internet will solve all our medical mysteries but you can't deny it's benefit for doctors and researchers.
Leanne Carroll Thank you, it was so nice to read something positive in these videos, what people don't think about, is watching these videos it will help with diagnosis for other people. The blinking of the eye thing......don't they realise that is like a marker for the brain to remember what they watched, the eyes are meant to be the window to the soul, whether that's true or not, eyes talk!
Ever wondered why there are Sub-Sub-Specialties in the medical field?? You cannot imagine the mental stress that doctors go through, yet you wont find a doctor who's knowledge in medicine encompass everything.
exactly, there are sub specialties so they shouldn't give a diagnosis very fast without even considering other diseases. Wrong treatment and medication might harm the patient. I've encountered doctors like that, They told me it's just a fungal infection but ended up i have Psoriasis.
the first case is like a dr house episode. after treating the patient wrong again a surprising clue appears. house : give her steroids stat team: but if it is an infection the steroids will kill her house: i said do it house goes to cuddy. cuddy: you have to confirrm the diagnosis first house: there is no time, the diagnosis will be confirmed when she gets better patient gets better.
Lol, thats why I LOVE house! I mean, why do hospitals have so many different doctors when house and his team can do everything from MRI scans to in utero baby heart surgery
Thank goodness that these great doctor is there and actually performing their job and passion for people who needed it. Life is saved by these great people.
It is not normal for a baby to constantly vomit for weeks on end. In Germany they wouldn't let her go home until they found out what was wrong and it would be a top specialist.
My mum had pyoderma gangrenosum! She developed it after I was born and was on steroids (prednisone) for over 20 years. This is the first time I've heard of it outside of my mother's case!
It's more common than you think. I got pyroderma gangrenosum that took a year to heal but I still have all the scars. I had to inject medicine into my stomach due to having Crohns and my major veins were clotted due to issues having my nutrients through my veins.
@Nova Lynn You were lucky. Took them 6 years to figure out that I have PG. No underlying conditions, the first 6 years I had 1 or 2 small ones a year, treated them as spider bites. This year I had over 40 since last Christmas they melded and became 3 large sites. The 1st one was debrided and went evil grew as big as my hand, the wound care nurse made me an emergency appointment at a Dermatologist who did the diagnosis. He didn't know how to treat it but called around to find out what to do. We are in August now and I'm still mending only 2 sites left. Very rare, I had to move and need to find a new Dermatologist again and help them understand PG including the pain.
It's 1:100k, so quite rare yes. Doctors learn about it, yet it's hard to recognize. Biopsies or surgery are often the cause. Terrible symptom, you never want to see a patient go through that!
@@Ennello yeah it's a horrible disease. Simple knocks or scratches would turn into large gangrenous masses that were excruciating. Hopefully it's not genetic! That's not the lottery I wanna win
When I was a baby I would projectile vomit every time I ate, and mum was told I had colic. I would cry loads and very loud too. It was awful for my family. It turns out that the valve in my stomach never formed properly so that’s why I had trouble feeding. Now I have bad acid reflux and must take a cocktail of pills to help it.
I have a dodgy valve too. I also had Oesophaeal cancer from the damage to the oesophagus (cured now) . I find that a handful of Pretzels can ease reflux if done early enough! Do watch out for the salt content though!.
This happened to my godfather's wife, she got it from the garden and had to have skin graphs and a skin suit for years. They didn't know what it was, however, a foreign doctor happened to walk past the hospital room and saw it and recognised what it was. I still remember the first time she ate normally again, my godfather sent the video of her eating a mango to everyone in celebration. She used to tell little kids who wondered that she was bitten by a shark jokingly.
The doctors probably had a lot of clues as to June's breast but none of the clues gelled together, they are human but professionals have to know when to say "We don't know. We are transferring you for a second opinion". I hope June lives every day to the fullest knowing that she is much loved and needed.
Ingrid Åkerblom I was thinking the same thing here. It took my 8 years to get some decent pain relief and I have EDS. I have up to 30 joint dislocations daily and they’re extremely painful. I live in the UK and they don’t hand out drugs like tic tacs here because of the addiction element.
@@tammyearrye1172 hi, i hope you are okay, i was wondering if you could shade some light about your condition, the dislocations, what did were you dignosed with. I have severe dislocations several times a day, my wrist, rip, hip, ankle and shoulders, my shoulders are so sore as if its broken, it hurts so bad and the dislocations happens abruptly that i scream out and scare people around me. I have been dignosed with hypermobility syndrome, however i believe its something more , because i feel like there is a virus eating my bones or muscles, i have asked that sample of my bone or muscles be take for test but they refused saying that can only be done if i have a mole growing on my skin. I need help please share ur experience if its similar and anything that might help me. Thank you Esther jaja
Wow, I understand why a young first time mum would not know about pyloric stenosis, but it’s not exactly unknowably rare. I’m aghast that it wasn’t on the list of possibilities for the doctors, and pretty high on the list at that.
@@firstname9845 if it wasn't something abnormally harmful for the body it wouldn't be the starting point of her disease. She lived her all life normally till she put her body in their hands. There's definitely something made her white blood cells reacts in this particular manner but of course it will take them other 10 victims to find out what they're doing wrong.
I do hope all in these films are now doing well. Especially that gorgeous lil girl Briana bless her. Drs really do have to keep up with their training right the way through their professional lives. So many new diseases and illnesses rearing their evil heads to even imagine! Love and best wishes to these people and their families x
1 in 10 will suffer atleast 1 siezure in their lifetime.. Is extremly exhausting on the whole body, on every function & system.. somone that has suffered one is very tired, completely exhausted, anf it can last for days after.. Is you see someone having a fit with spasms (not always), the best thing you can do is to hold the head to protect it & then stay eith the person when he / she is comming out of it bcs they are often quite dased & confused, besides the exhaustion.. try to time the fit & always call 911 if it lasts over 5min or comes back in waves! Remember, a person having a fit, can go completely limp to, just falling down & being completely still, it dosen't have to be violent convulsions.. NEVER put anything in the mouth of someone experiensing a fit the risk of choking on it is huge! They will NOT swallow their tounge & It's better to have a bitemark in your tounge, than being dead..
So you thank god instead of the extremely intelligent doctors? They were the ones who found the cure. I dont get why people thank god instead of thanking the doctors that saved their lives.
My husband has suffered with PG for over 12 years and has had his leg amputated due to it , he has also had a further 2 sites where PG appeared, his was caused by trauma too, very mysterious condition
I have been trying to find more info about a thing that happened when I was born but I have no clue what it can be called or how rare it is. My mom's body had made antibodies against Hyperthyroidism and when I was born those antibodies attacked me. My parent told me that I was brain dead and not breading at one moment but the doctor got me breading again and made my brain become active. There hade been only one chase before me that had a survived the same thing that happens to me. They looked up information from a Frace hospital on what they had done to save that child. They had to give me a blood transfusion to give me completely new blood. My parents told me that the doctor had said I had 1 in a million on surviving and if I was a boy I had even less than that of a chance to survive. But as I am sitting here in front of my computer. It is not hard to guess that I survived the ordeal.
It's sad to see how long people wait just assuming the Dr knows best. The Dr is working 9-5 and can't wait to get home like the rest of humanity and if they can palm off a problem they will. It's not their life. I was ill for over 7 years because I kept listening to my Dr, only when I took my health into my own hands and did the research, did I finally get rid of my symptoms. Be your own advocate when you know something is wrong.
If youre a hypochondriac you shouldnt be watching these, going on google or read medical books because you will, by the nature of your mental illness actually convince yourself that you have something wrong with uou. A little knowledge can be a dangerous thing in the wrong hands !
Would have been worst if ur in philippines, the diagnoses would be “ u disturbed some creatures that cannot be seen from the tree near ur house, That’s why they did that to u 😂.
keeponrockin in ph, any disease that are mysterious are always cause by some supernatural creatures. 😂 it’s probably because the sick person disturbed them and it’s some sort of revenge 😂 .
@@marjbernaldez6156 thanks for explaining. Well, that's bound to make you feel better - being really ill and then being told that it's your own fault xD
I guess people who aren't in a relationship or about to "start a family", don't keep fit and not climbing any career ladder with similar conditions don't get chosen to appear on this programme.
there is a disease called necrotizing fascitiies also known as the flesh eating disease that is a rare infection that can be fatal if not treated correctly and quickly how do i remember that and not a maths sum??? ps I wrote this before I knew what her diagnosis was
Chloe Guys, if you listen attentively, it's not a flesh eating bacteria! It's her wbc that's attacking her healthy flesh as the doctor said, she has a rare disease where wbc is overacting that causes death to healthy cells instead of just healing it. Wbc took a signal that they have to heal a portion of her that has been cut out after biopsy but because her wbc or white blood cells responsible for repair is problematic, instead of their action to heal, they already attack the body instead..
Joy Y. Z. I'm 12 and I'm pretty sure that's partially what Necrotizing faciities is and I'm almost certain I hear the man say she had it and if I'm wrong oh well I aint a doctor yet
@@Chloe_P_B No, necrotising fasciitis is not caused by white blood cells. It is caused by an antibiotic resistant bacteria and is a bacterial infection. Pyoderma gangrenosum is an inflammatory auto immune condition. They are completely different. (Nurse in plastics and dermatology)
Emily Rose k did I i know u know more than me but im still working on learning everything about different be bacterial infections cause i would love to work with them in the future (did i mention about blood cell) (also did i mention that im 12) but anyways thank for telling me something new about it so i can build up my knowledge
They said "the couple felt like they were living in a nightmare"... Well, I understand that, but what do you think the baby was thinking? Poor girl. So glad she's doing better now.
Fluffy a. k. a. Hibiscus Pap smears are offered once every 3 months for free where I live and we have the 2nd highest average life expectancy in the world so it’s not really as counter productive as you’ve made it seem
Really interesting and quite sad documentary but please for the love of god stop with the dramatic eye closing
Yeah it´s really annoying and stupid.
Abimations lol
Those dramatic eye closing might make you remember these awful conditions!!
Abimations yeah that dramatic eye closing seriously irritates
I know right! It’s so annoying!
It seems like being a doctor is a lot like being a mathematician- except if you get the answers wrong, someone dies.
Woah😁
Like how everything is either a potato or not a potato
That's why it takes a lot of years to finish studying medicine💓
Victor Hugo said, The doctor buries his mistakes.
Imagine if she never asked to be transferred to another hospital. Why didn't the doctors do a research or seek help from other doctors out there? A lot of people die due to lack of research in some diagnosis.
I've had NF, I also caught it from a hospital that had no clue what was going on, it's not as rare as people think.
some hospitals dont have the capability to diagnose some diseases and have to be referred to another hospital that specializes in what is ailing the patient
@@TheHawkBubble sorry
True
@@Elidandeb aaaa
9
how much he loves her makes me feel so warm
I’ve had PG for 23 years. The speed at which the wounds accelerate in size is frightening. I’ve had it double and grow centimetres deeper overnight. At its worst I had a wound 40cm x 20cm and 7cm deep on the back of my thigh. I’m treated with immunosuppressants and for most parts I’ve been ok. With God’s blessing, my amazing family and an awesome wife I lead a fairly life, work in education and this year had a beautiful daughter. Over the last two decades I’ve had several relapses which have nearly cost me my leg and life. The pain at times is indescribable. If you’re reading this and have PG I hope it’s going well, wounds are healing and life is getting back on track. You’re in my thoughts and prayers.
Hiya PearlJam. Yep. I have it too. Misdiagnosis almost led to right bka in 2021. Multiple ulcers. Arterial bleeding. The pain you know about. Last episode, all ulcers healed. Scarring below the knees and on the forearms is frightening.
I hope you’re doing ok too.
Cyclosporine for me
I really appreciate this man for saying I just want her to be healthy weather she has 3 boobs or one boob . It took my Heart . Hats off to such men
When you love someone you just want them to be alive and with you. Physical stuff is not nearly so important.
I have one, gone through it twice with me.
Ikr! A lot of people have left their partners because they were sick, or even if one of their children were sick. I guess some people just aren’t built as strong as others
The only thing i can think about are the medical bills...
Was thinking the same thing. 😂😂
Same here, they must have been horrendous!!
And THAT is why I love being an Aussie!! No need!
@@chelsea_belle Same here in Germany.
So glad I live where we don’t pay for medical treatment
My baby nephew was having the projectile vomiting and crying all day and night. Till I suggested they did a full check on him and they found out he had a hole in his heart. We flew him to India for the surgery and till today he has no problem. When you have a medical issue don't wait just visit as many hospitals as possible to get different options. Lord Jesus I thank you for your guidance.
So nice of you . May God bless the baby
Why India ?
@@y.n.7534 sorry I didn't understand ur question?
@@y.n.7534 bcz India has one of the best medical research and progress on cardiology
@@y.n.7534 India's image is presented as a poor and underdeveloped country in the western media, but there are world class medical research and facilities here. These are costly for the average Indian but for the patients from the developed nations the costs are dirt cheap compared to costs in their country.
i was born in 1998... when i was 8 months i had same disease as this child... my mom told me i cannot breath, my eyes was same as this child, my hand moved automatically. even the doctor told that i cannot live no more years, i cannot play sports. i was diagnosed till 10 years.... but now i m 20 everythings gone, now i play sports, i live like other child.... thanks god and i hope this child also will be healthy
Do you still have to take medication for it?
(It’s a silly question, I know, but I am curious if things get better, or if it will be lifelong)
"But now I'm 20" ..... "im like every other child" .... you are 20 mate that's not possible
Omg the zoom camera on eye thing is soooo f annoying!!
I thought i was the only person whom noticed
R
@@mrscat129 g
Lmao. It had me laughing. So mf dramatic. 😅
@@mrscat129 *whomst've
Honestly the eye zooming/ blinking thing doesn't bother me at all 😁 surprised to see so many comments about it
Yes me too 😂
me too
count me in
I think its cool as I like drama so yes I agree
Shan Serv same
I hope now, going into 2019 that these types of rare disorders can be diagnosed faster. With the internet and fast access to scientific literature and medical journals online it seems hopeful.
th-cam.com/video/ypmsjqytMpA/w-d-xo.html please check out the series monsters inside me. So many people might be affected and misdiagnosed etc. Its scary asf. The more we knoe the more we can help eachother.
Well the internet is one of the last places where you would get the right diagnosis..
Ask any health care professional what they think of people self diagnosing trough google..
@Vyrex420 I'm not talking about a patient putting their symptoms into a search engine like google. I'm talking about healthcare professionals using online medical journals (Pubmed etc) to access papers / articles / reviews from around the world. As a person with a degree in Pharmacology, hands on experience with stem cells and heading into a masters in Regenerative Medicine I know all too well the importance of medical journals in research. So yes I do know what I'm talking about. I'm not saying the internet will solve all our medical mysteries but you can't deny it's benefit for doctors and researchers.
Leanne Carroll Thank you, it was so nice to read something positive in these videos, what people don't think about, is watching these videos it will help with diagnosis for other people. The blinking of the eye thing......don't they realise that is like a marker for the brain to remember what they watched, the eyes are meant to be the window to the soul, whether that's true or not, eyes talk!
@@craftylittlerthings Thank you, that's so kind :)
the woman in 23:54 has pair of bright green eyes and its very beautiful. Thanks for coming to my tedtalk.
Indeed she does!
You can tell how much the first lady's husband loves her
I really love these shows. Interesting indeed. However,, the constant shots of eyes opening or closing for dramatic effect is bloody ANNOYING.
I agree with you
It’s creepy &wrong. There is no correlation with the type of show.
Yes, and it's not as if those illnesses weren't dramatic enough on their own.
jay bomb yes! Agree totally.
I like the dramatic blinking
STAHP WITH THE FRICKING ZOOM INS ON THE BLINKING OF THEIR EYES😵😵
SABBIBEE DA BUMBLEBEE finally someone said it
SABBIBEE DA BUMBLEBEE ik right the eye zomming parts are starting to give me a headache
It doesn't annoy me lol, stop focusing on that xd
What a lovely woman June is! Her smile really lifts me up. I wish her all the best!
wrong diagnosis like cases like this makes me want to be a doctor myself.
Ever wondered why there are Sub-Sub-Specialties in the medical field?? You cannot imagine the mental stress that doctors go through, yet you wont find a doctor who's knowledge in medicine encompass everything.
exactly, there are sub specialties so they shouldn't give a diagnosis very fast without even considering other diseases. Wrong treatment and medication might harm the patient. I've encountered doctors like that, They told me it's just a fungal infection but ended up i have Psoriasis.
I hope Briana is doing well to this day ❤️
0:25 America's editors choice. The drama... the eyeclosing galore...
5:46
the first case is like a dr house episode.
after treating the patient wrong again a surprising clue appears.
house : give her steroids stat
team: but if it is an infection the steroids will kill her
house: i said do it
house goes to cuddy.
cuddy: you have to confirrm the diagnosis first
house: there is no time, the diagnosis will be confirmed when she gets better
patient gets better.
Haha so true !!!
Iii im mmž cga
I was just thinking that XD
Lol, thats why I LOVE house! I mean, why do hospitals have so many different doctors when house and his team can do everything from MRI scans to in utero baby heart surgery
That's _often_ the dilemma with corticosteroidal drugs, especially when a definitive diagnosis can only be made _post-administration._
Thank goodness that these great doctor is there and actually performing their job and passion for people who needed it. Life is saved by these great people.
KUDOS to the 2 beautiful and intelligent doctors! hats off
“But nothing could have prepared them for what happens next”
It is not normal for a baby to constantly vomit for weeks on end. In Germany they wouldn't let her go home until they found out what was wrong and it would be a top specialist.
I believe anywhere in Europe.
Richtig
Denise G- Hill Yeah, there can be quite a few barely qualified doctors in murica depending where you are
Also in Denmark
Also in the UK 🇬🇧
My mum had pyoderma gangrenosum! She developed it after I was born and was on steroids (prednisone) for over 20 years. This is the first time I've heard of it outside of my mother's case!
It's more common than you think. I got pyroderma gangrenosum that took a year to heal but I still have all the scars. I had to inject medicine into my stomach due to having Crohns and my major veins were clotted due to issues having my nutrients through my veins.
@Nova Lynn You were lucky. Took them 6 years to figure out that I have PG. No underlying conditions, the first 6 years I had 1 or 2 small ones a year, treated them as spider bites. This year I had over 40 since last Christmas they melded and became 3 large sites. The 1st one was debrided and went evil grew as big as my hand, the wound care nurse made me an emergency appointment at a Dermatologist who did the diagnosis. He didn't know how to treat it but called around to find out what to do. We are in August now and I'm still mending only 2 sites left. Very rare, I had to move and need to find a new Dermatologist again and help them understand PG including the pain.
I have never heard of this condition, either. What a terrible disease😔
It's 1:100k, so quite rare yes. Doctors learn about it, yet it's hard to recognize. Biopsies or surgery are often the cause. Terrible symptom, you never want to see a patient go through that!
@@Ennello yeah it's a horrible disease. Simple knocks or scratches would turn into large gangrenous masses that were excruciating. Hopefully it's not genetic! That's not the lottery I wanna win
seriously
every
single
video
has
dramatic
blinking
Remove ''I think".
@@unknown-ig8hw SURE!
I
See
People
In
Every
Fcking
Video
Commenting
The same
Thing
Every
Time
😂♥♦
@@bangtanloverjinstan9022 😂😂😂
Sooooo annoying I swear 😂
Scary stuff. She lost some of her breast but she has her life. I wish June well. Xxx
This is insane how people have to move hospital to hospital and that's when they find out what they have danm this is just insane
It happens.Happens in India too
@@april110 danm that's just wish this happens across the whole world
that's normal.......some hospitals are more equiped and specializes in different fields of medicine
I had to search 2 months too until I found a Doktor how could give me a diagnosis. Germany.
Ikr! Would mean that you’d have to travel to get there as well
Well done to both couples for demanding a second opinion! Sometimes drs get so fixated on the puzzle they can't see the wood for the trees!
When I was a baby I would projectile vomit every time I ate, and mum was told I had colic. I would cry loads and very loud too. It was awful for my family. It turns out that the valve in my stomach never formed properly so that’s why I had trouble feeding. Now I have bad acid reflux and must take a cocktail of pills to help it.
There is an exam wich should be taken after bearth
I have a dodgy valve too. I also had Oesophaeal cancer from the damage to the oesophagus (cured now) . I find that a handful of Pretzels can ease reflux if done early enough! Do watch out for the salt content though!.
I feel so bad for that baby
Thanks to the new doctor
I think that the parent was so happy when she is fine
That made me cry
oh I forgot this is the show where they blink dramatically at the end of each segment! hahahaha!!
Best comment ever!
"It's just colic" Every paediatrician ever 🙄🙄🙄🙄🙄🙄
This happened to my godfather's wife, she got it from the garden and had to have skin graphs and a skin suit for years. They didn't know what it was, however, a foreign doctor happened to walk past the hospital room and saw it and recognised what it was. I still remember the first time she ate normally again, my godfather sent the video of her eating a mango to everyone in celebration. She used to tell little kids who wondered that she was bitten by a shark jokingly.
This video encourages me to keep studying 😊 peoples lives could be saved if I read that one extra book, who knows 🤷🏽♀️
I'm going to have a hard time trusting doctors after this 😭
I never did to start with
Doctors try their best but sometimes they don't know, some things are so rare you won't know they exist
What’s with the dramatic blinking???
Idk but what I do know is that Phil in your profile is getting onto the trend
It’s for dramatic effect
I have big respect for real doctors who knowing their jobs and seeing this I start to cry.
at 19:12 it's the same hospital lobby used in a scene in Bird Box .
Oh yeah yeah
Lynn Mekkawi Ye right
Probably a set
True
The doctors probably had a lot of clues as to June's breast but none of the clues gelled together, they are human but professionals have to know when to say "We don't know. We are transferring you for a second opinion".
I hope June lives every day to the fullest knowing that she is much loved and needed.
I'm so happy the baby is okay! ❤️
When I become a mom, I just wish my kid never has to go through all this... I feel so bad for all that the parents had to go through
Clever doctor at the second hospital!
Well done these doctors who saved her 💖💖
It's hotrible how easy it is to get really strong pain & anxiety medication in the US..
Ingrid Åkerblom I was thinking the same thing here. It took my 8 years to get some decent pain relief and I have EDS. I have up to 30 joint dislocations daily and they’re extremely painful. I live in the UK and they don’t hand out drugs like tic tacs here because of the addiction element.
@@tammyearrye1172 hi, i hope you are okay, i was wondering if you could shade some light about your condition, the dislocations, what did were you dignosed with. I have severe dislocations several times a day, my wrist, rip, hip, ankle and shoulders, my shoulders are so sore as if its broken, it hurts so bad and the dislocations happens abruptly that i scream out and scare people around me. I have been dignosed with hypermobility syndrome, however i believe its something more , because i feel like there is a virus eating my bones or muscles, i have asked that sample of my bone or muscles be take for test but they refused saying that can only be done if i have a mole growing on my skin. I need help please share ur experience if its similar and anything that might help me. Thank you
Esther jaja
Wow, I understand why a young first time mum would not know about pyloric stenosis, but it’s not exactly unknowably rare. I’m aghast that it wasn’t on the list of possibilities for the doctors, and pretty high on the list at that.
Dr. Yang's one eye is beautiful.
This is what is going on you can go to a hospital very healthy and come out with a disease.. now we don't know who to trust....🤔🤔🤔🤔
aminu aidara It was her autoimmune response. It was caused by her biopsy.
Still better than the many more things you can come out of the hospital with when unhealthy and obese.
Ikr like those people who did her first test weren't sterilized!!!
Lost Paradise it has nothing to do with sterilisation wbc are responsible for healing skin, the cutting of the skin caused it
@@firstname9845 if it wasn't something abnormally harmful for the body it wouldn't be the starting point of her disease. She lived her all life normally till she put her body in their hands. There's definitely something made her white blood cells reacts in this particular manner but of course it will take them other 10 victims to find out what they're doing wrong.
The mum in the second part has the most amazing blue green eyes
.... set in the most amazing gorgeous face!!! x
._. Why do they tell us the story of how the couple met and got married...
They could just say: these are a married couple
I guess to make it even saddef
I do hope all in these films are now doing well.
Especially that gorgeous lil girl Briana bless her.
Drs really do have to keep up with their training right the way through their professional lives. So many new diseases and illnesses rearing their evil heads to even imagine!
Love and best wishes to these people and their families x
Rihannah please get well. You make me cry.please get well baby girl.
Brianna* !!!
1 in 10 will suffer atleast 1 siezure in their lifetime..
Is extremly exhausting on the whole body, on every function & system.. somone that has suffered one is very tired, completely exhausted, anf it can last for days after..
Is you see someone having a fit with spasms (not always), the best thing you can do is to hold the head to protect it & then stay eith the person when he / she is comming out of it bcs they are often quite dased & confused, besides the exhaustion.. try to time the fit & always call 911 if it lasts over 5min or comes back in waves!
Remember, a person having a fit, can go completely limp to, just falling down & being completely still, it dosen't have to be violent convulsions.. NEVER put anything in the mouth of someone experiensing a fit the risk of choking on it is huge! They will NOT swallow their tounge & It's better to have a bitemark in your tounge, than being dead..
I've read the comments a bit before watching and now I laugh every single time one of these dramatic eye closing scenes pop up. Thanks!
Me too haha
Don’t watch while eating
ok they need to fire the editor or person who approved the close up blinking bc its getting real annoying and hard to take this docu seriously
Just one prayer can be miracle
Praised be the Lord God that both of them are finally healed esp.the baby. Thanks be to God!!!
god aint real
So you thank god instead of the extremely intelligent doctors? They were the ones who found the cure. I dont get why people thank god instead of thanking the doctors that saved their lives.
Incoming atheists
My husband has suffered with PG for over 12 years and has had his leg amputated due to it , he has also had a further 2 sites where PG appeared, his was caused by trauma too, very mysterious condition
the editor should really stop with their dramatic eye opening and closing
*Dramatic Blink*
Me: Stop It!
Wonderful documentary and all,but the dramatic blinking is really bugging me.I wish this couple the best of luck though.🤗
That editing...good lord.
Murican TV in a nutshell overly-dramatised..
You have to be so much in shock if you can't remember the number for 911
Sorry, I really wanted to see this but the directors eye fetish is a real turnoff! Please stop with eye close iOS.
I have been trying to find more info about a thing that happened when I was born but I have no clue what it can be called or how rare it is.
My mom's body had made antibodies against Hyperthyroidism and when I was born those antibodies attacked me. My parent told me that I was brain dead and not breading at one moment but the doctor got me breading again and made my brain become active. There hade been only one chase before me that had a survived the same thing that happens to me.
They looked up information from a Frace hospital on what they had done to save that child. They had to give me a blood transfusion to give me completely new blood. My parents told me that the doctor had said I had 1 in a million on surviving and if I was a boy I had even less than that of a chance to survive.
But as I am sitting here in front of my computer. It is not hard to guess that I survived the ordeal.
Glad you survived it
@@ΠανωραίαΓιαννούτσου Thank you! I am too glad that I did. I hope you have a wonderful life! :)
It's sad to see how long people wait just assuming the Dr knows best. The Dr is working 9-5 and can't wait to get home like the rest of humanity and if they can palm off a problem they will. It's not their life. I was ill for over 7 years because I kept listening to my Dr, only when I took my health into my own hands and did the research, did I finally get rid of my symptoms. Be your own advocate when you know something is wrong.
What was ur disease?
It feels scary with those eyes closing it made me nervous ...
These documentaries satisfies my hypochondria... And it feels really obsessive.. I feel like I'm feeling these illnesses in myself.
If youre a hypochondriac you shouldnt be watching these, going on google or read medical books because you will, by the nature of your mental illness actually convince yourself that you have something wrong with uou. A little knowledge can be a dangerous thing in the wrong hands !
I had pyroderma gangrenosum all over my stomach that took nearly a year to heal.
Would have been worst if ur in philippines, the diagnoses would be “ u disturbed some creatures that cannot be seen from the tree near ur house, That’s why they did that to u 😂.
Very true...
This diagnosis has a 79-89% chance in INDIA as well.... :P
Pamahiin hahaha
Could you explain further? I'm not familiar with the culture, I don't understand the reference
keeponrockin in ph, any disease that are mysterious are always cause by some supernatural creatures. 😂 it’s probably because the sick person disturbed them and it’s some sort of revenge 😂 .
@@marjbernaldez6156 thanks for explaining. Well, that's bound to make you feel better - being really ill and then being told that it's your own fault xD
Now I know why UK and USA are so dependent on Asian doctors 👍
The best Doctors are from Greece
Asian nurses here in New Zealand are unless and rude same goes to Indians
this is just a truth that not all doctors knows what they're doing
My heart ached for Brie n her parents... As makes me relive what I been thru with my younger son when he was 8 mths...
The dramatic blinking gets me everytime
Ikr its kinda funny i dont know why people are so pressed about it
Ok TH-cam, I am watching it, now please, stop recommending it to me. Lmao.
Love the dramatic eye zooming !! Thank you 😘
I hope you are joking
That hospital video wasn’t very comfortable
Yeah had to stop watching and just listened
Am I the only one who's hysterically laughing when they're doing the eye zooms?
This was after knowing that everyone is very mad about this eye zoom 😂
I guess people who aren't in a relationship or about to "start a family", don't keep fit and not climbing any career ladder with similar conditions don't get chosen to appear on this programme.
stop with the close up eye thing please!!!!
Stop that camera focus on their eyes. So annoying!!
there is a disease called necrotizing fascitiies also known as the flesh eating disease that is a rare infection that can be fatal if not treated correctly and quickly
how do i remember that and not a maths sum???
ps I wrote this before I knew what her diagnosis was
Chloe Guys, if you listen attentively, it's not a flesh eating bacteria! It's her wbc that's attacking her healthy flesh as the doctor said, she has a rare disease where wbc is overacting that causes death to healthy cells instead of just healing it. Wbc took a signal that they have to heal a portion of her that has been cut out after biopsy but because her wbc or white blood cells responsible for repair is problematic, instead of their action to heal, they already attack the body instead..
Joy Y. Z. I'm 12 and I'm pretty sure that's partially what Necrotizing faciities is and I'm almost certain I hear the man say she had it and if I'm wrong oh well I aint a doctor yet
@@Chloe_P_B No, necrotising fasciitis is not caused by white blood cells. It is caused by an antibiotic resistant bacteria and is a bacterial infection. Pyoderma gangrenosum is an inflammatory auto immune condition. They are completely different. (Nurse in plastics and dermatology)
Emily Rose k did I i know u know more than me but im still working on learning everything about different be bacterial infections cause i would love to work with them in the future
(did i mention about blood cell)
(also did i mention that im 12)
but anyways thank for telling me something new about it so i can build up my knowledge
It seems like it's eye closing episode as well 😂😂😂
Tbh I live for the dramatic eye closing
Congrats for the videos, hope that the doctors and future doctors will watch and learn!!!! 👏👏👏👏
"She might die"
*Dramatic blick*
PLEASE DON'T GET BABIES IN THIS! I CAN'T WATCH THOSE
eyes closing dramatically....i broke out laughing
They said "the couple felt like they were living in a nightmare"... Well, I understand that, but what do you think the baby was thinking? Poor girl. So glad she's doing better now.
I like when the screen gets dark !
It’s thrilling !
Ok the slow blinking eye thing has to stoppppp
Yall stay being mad at the dramatic eye closing while im here dying with laughter😂
Hahahaha. Same! 😂
The blinking makes it like a joke
Annual mammograms, annual papsmears. No wonder health care in the US is expensive. (we get it every 5 years and don't have higher rates of cancer)
Fluffy a. k. a. Hibiscus Pap smears are offered once every 3 months for free where I live and we have the 2nd highest average life expectancy in the world so it’s not really as counter productive as you’ve made it seem
*Time to queue the dramatic blinks*
Why would you wait overnight before going back to the hospital with a festering open wound? that is stupidity.
23:54 Her eyes are gorgeous
DRAMATIC BLINKING
👁👄👁 ----👄---- 👁👄👁