Here's the hilarious thought of the day: Most of the people watching this video have hearing loss (like me), and the guy talks really soft and monotone, while the music plays loud lol
I forget the name given to gradual trouble hearing voices against background sound whereby a person can still ace a hearing test. "Hidden hearing loss?"
I understand this is controversial, and many people in the deaf community don’t believe being deaf is a disability or something that needs fixing. I just think it is truly amazing that this exists and gives people the option to hear. A lot of people say to not do this on kids and wait till they can decide themselves. But kids learn language so much faster than adults. Being able to have the option to hear and learn to speak as a child can be extremely valuable and eliminate a lot of hard work and frustration later on in life. It’s nice that they can choose to remove the implant and sign if they want, but also have that option to hear. There’s so many beautiful things to be heard in life and I think people deserve to have the opportunity to experience it. However, I understand why one would prefer to identify with the deaf community and not want to “cure” it, but rather respect and celebrate who they are as is. I know many people who have the implant actually prefer to not wear them most of the time and I can understand why. But I feel like parents shouldn’t get hate for doing this procedure because giving their kid the option is a blessing and will make it so much easier for them to adapt early on if they do choose to stick with the implants later in life.
It's crab mentality: if I can't have it, you shouldn't be able to have it either. Many in the deaf community don't have any options for hearing so they don't want others to have that option either. It's not enough that they have support communties, they need to convince themselves that not being able to hear isn't a disability (it absolutely is) and they need everyone else to believe it as well in order to maintain their delusion. Like one crab in a fisherman's bucket working their way up and just about to make it out of the bucket to freedom and a better life, the rest of the deaf community wants to pull them back down to their level because they can't stand seeing others have things that they don't. As the old saying goes: misery loves company, but that's just a toxic mentality that needs to be called out for what it is.
@@EisenbisonThis resonates with me. My kid lost hearing on both ears, but it’s a weird situation. We are still in process of tests. They want to install the inplant asap. I have nothing against the implants, but he needs to go through a lot more. So I asked the r/deafcommunity - big mistake. “it’s not a disability” most of them commented. Which was weird for me. Dunno if it’s perhaps an american thing.
@@Fatjuice You go right ahead and listen to the doctors. Don't be guilt-tripped for one second by the most toxic "disability community" whose crab mentality has been well documented for over two decades. Looking forward to further updates on our mutual little champ. Whoever he is, count me as part of his team moving forward! ^-^
So if its an electrode that's placed in the head what happens if someone builds an antenna the same length as the wire in your head and the wire inside your head gets energised by the transmitter someone's using. If my thinking is right it would be good to know the frequencies to avoid. If the wire is about 82mm 234/860*304.8=82.9mm so that's around 860mhz as a guess. This also means that anyone with a cochlear could potentially be a walking bug snooping device that people with the right equipment could listen in on.
The only way to actually know this is to place a cochlear onto someone who had hearing all their life and suddenly lost hearing in one ear, Like ME! I lost the ear drum and bone.
@@SCREAMgoodTV I have lived with someone who wears a cochlear for years it supposed to sound robotic and your brain adjusts to it, they also have issues with device going off if the volume gets too loud say for instance i started up a leaf blower or chainsaw or angle grinder, I am also a Radio ham my radio drives her nuts and i am also and Electronics Engineer with two degrees. So i am aware about causing interference to these devices so far its been ok my transmitters hasn't managed to wipe her out but i am about to start using 23cm's for EME moonbounce so that's a concern as its 600 watts.
Hi, I love your video I live in Ethiopia Est Africa my son hearing loss both side at the age of 3 he is to day 5 years old. I am very worried about the future of my boy. pleas helping me if you have any way. thanks.
If deafness or blindness was a birth defect and not genetic it, may be possible for stems cells to read the genetic code of the area and produce a healthy organ if the defective organ is replaced strategically.
They might even be able to grow a cochlea with the patients cells and then transplant it. But I think they are making way too much money off of hearing loss so I doubt they'd do that.
Hi. I just want to help you so you can learn to speak English better. We say “my niece has hearing loss. We want to decide if a cochlear implant is ok. Is it a dangerous or safe surgery?” Just to help you on how our sentence structure works. I understand how hard it is to learn a new language. I grew up speaking Russian and English. However my grandparents are Czech. Not Russian. They only spoke Russian though. So as you can imagine, Russian was spoken to me. Now I’m trying to learn German to get my German passport (in the Us we can hold two passports from two countries if our mother was still a legal citizen in both countries, my mother was a German citizen when I was born) so I’m Learning German as we speak. My mom can speak it- but was never spoken to me. So I understand how hard it is to learn a new language. Keep practicing and good luck!
HEARING OR COCHLEAR HEARING . WE ALL USE OUR BRAINNS AND THOUNGS EVEN IF YOU STOP HEARING YOUR BRAIN CAN DEVELOP SPEECH BECAUSE YOUR BRAIN AND THOUNG ALREADY REMENBER THE MOVEMENTS
How about umbilical cord stem cell harvesting locations, if it is possible to connect a line through the mothers stomach and attach it to the umbilical cord and take small amounts of stem cells during a safe time of the pregnancy. Then people that are deaf or blind, surgical removal of part of the defect causing the person to be deaf, with a steady injection of stem cells to the location, then removal of the other part of the birth defect and a steady injection of stem cells to that location. Also, same process with the eyes. That's if the defect was a birth defect during the growth process and not genetic.
Why would they play music in the background when they are discussing how Cochlear Implants Work. They should know that this background noise interferes with our ability to hear this video. This video is from Yale Medicine, you'd think they would know. SMH
I imagine they hear the same thing as normal hearing people; the only missing component in patients with damaged inner ears is the translation of vibrations to electrical signals picked up by the brain stem. As such, the cochlear implants replace that missing component by translating the vibrations into electrical signals via the electrodes in the cochlear. Therefore, the nerve still gets stimulated via the electrodes in the cochlea by way of the implants.
It’s mostly the same, although for simplicity’s sake they don’t capture frequencies towards the upper and lower limits of our normal range because it would be very difficult and doesn’t matter for crucial things like hearing speech
not necessarily reversible, but as the implants inside of the head are attached via magnets and aren't visible, technically just taking the outer portion off would reverse it.
How about umbilical cord stem cell harvesting locations, if it is possible to connect a line through the mothers stomach and attach it to the umbilical cord and take small amounts of stem cells during a safe time of the pregnancy.*
IMPLANTS CAN BE BENEFIT BUT SOME PEOPLE DONT WANT TO WEAR IT ALL THE TIME SOME SCHOOLS INVADE PARENTS PRIVACY AND EVEN THE OWN STUDENT PRIVACY AS A PRENT I HAVE GOTTEN INVADED AND MISSTREATED BY SCHOOL STUFF WHICH SHOULD BE COMPLETELY ILEGAL
After all the years of having Menieres diseases and constant ear ringing , it is nice to sit in a quiet restaurant without anything bothering me. Even the fullness in the bad ear is hardly noticeable. And the constant ear ringing is gone..Took 4weeks thanks Dr Liam Ogbebor Herbal centre TH-cam channel for the tinnitus program and herbal ear drop treatment and I hope it stops for everyone else sooner.-;;:
Tell me about your health condition now what do u feel I m also suffering from mennier disease but sadly there is no cure for mennier disease tell me about your health do u feel any improvement in your health???
I wish I could know what will be medically possible in the far off future. We already do face transplants, lung transplant, eye transplant, bionic limbs, brain chips, grow new penises off people's arms and transplant them, etc.
Here's the hilarious thought of the day: Most of the people watching this video have hearing loss (like me), and the guy talks really soft and monotone, while the music plays loud lol
Hi Dave, all of our videos are fully captioned so that everyone can watch and understand the content. Hope that helps.
@@YaleMedicine I didn't even realize there was a cc option on TH-cam; I'm an idiot lol. Thank you so much
@@decoydavesmith you arent an idiot be happy for who you are
What is the purpose of the music, why do so many TH-cam people add music in this way. It’s a difficult distraction to content matters
I forget the name given to gradual trouble hearing voices against background sound whereby a person can still ace a hearing test. "Hidden hearing loss?"
I understand this is controversial, and many people in the deaf community don’t believe being deaf is a disability or something that needs fixing. I just think it is truly amazing that this exists and gives people the option to hear. A lot of people say to not do this on kids and wait till they can decide themselves. But kids learn language so much faster than adults. Being able to have the option to hear and learn to speak as a child can be extremely valuable and eliminate a lot of hard work and frustration later on in life. It’s nice that they can choose to remove the implant and sign if they want, but also have that option to hear. There’s so many beautiful things to be heard in life and I think people deserve to have the opportunity to experience it. However, I understand why one would prefer to identify with the deaf community and not want to “cure” it, but rather respect and celebrate who they are as is. I know many people who have the implant actually prefer to not wear them most of the time and I can understand why. But I feel like parents shouldn’t get hate for doing this procedure because giving their kid the option is a blessing and will make it so much easier for them to adapt early on if they do choose to stick with the implants later in life.
It's crab mentality: if I can't have it, you shouldn't be able to have it either.
Many in the deaf community don't have any options for hearing so they don't want others to have that option either. It's not enough that they have support communties, they need to convince themselves that not being able to hear isn't a disability (it absolutely is) and they need everyone else to believe it as well in order to maintain their delusion. Like one crab in a fisherman's bucket working their way up and just about to make it out of the bucket to freedom and a better life, the rest of the deaf community wants to pull them back down to their level because they can't stand seeing others have things that they don't.
As the old saying goes: misery loves company, but that's just a toxic mentality that needs to be called out for what it is.
@@EisenbisonThis resonates with me. My kid lost hearing on both ears, but it’s a weird situation. We are still in process of tests. They want to install the inplant asap. I have nothing against the implants, but he needs to go through a lot more.
So I asked the r/deafcommunity - big mistake. “it’s not a disability” most of them commented. Which was weird for me. Dunno if it’s perhaps an american thing.
@@Eisenbisonforgot to mention kod lost hearing on both ears at 1yo.
@@Fatjuice You go right ahead and listen to the doctors. Don't be guilt-tripped for one second by the most toxic "disability community" whose crab mentality has been well documented for over two decades.
Looking forward to further updates on our mutual little champ. Whoever he is, count me as part of his team moving forward! ^-^
Fucking sign language
So if its an electrode that's placed in the head what happens if someone builds an antenna the same length as the wire in your head and the wire inside your head gets energised by the transmitter someone's using.
If my thinking is right it would be good to know the frequencies to avoid.
If the wire is about 82mm 234/860*304.8=82.9mm so that's around 860mhz as a guess.
This also means that anyone with a cochlear could potentially be a walking bug snooping device that people with the right equipment could listen in on.
do they hear 1:1 the same as someone without hearing loss or does it sound differently?
No
The only way to actually know this is to place a cochlear onto someone who had hearing all their life and suddenly lost hearing in one ear, Like ME! I lost the ear drum and bone.
@@MarcmilitiaGNRand what do you say?
@@SCREAMgoodTV I have lived with someone who wears a cochlear for years it supposed to sound robotic and your brain adjusts to it, they also have issues with device going off if the volume gets too loud say for instance i started up a leaf blower or chainsaw or angle grinder, I am also a Radio ham my radio drives her nuts and i am also and Electronics Engineer with two degrees. So i am aware about causing interference to these devices so far its been ok my transmitters hasn't managed to wipe her out but i am about to start using 23cm's for EME moonbounce so that's a concern as its 600 watts.
Hi, I love your video I live in Ethiopia Est Africa my son hearing loss both side at the age of 3 he is to day 5 years old. I am very worried about the future of my boy. pleas helping me if you have any way. thanks.
If deafness or blindness was a birth defect and not genetic it, may be possible for stems cells to read the genetic code of the area and produce a healthy organ if the defective organ is replaced strategically.
i dont understand
They might even be able to grow a cochlea with the patients cells and then transplant it.
But I think they are making way too much money off of hearing loss so I doubt they'd do that.
Dear Dr. My niece have loss hear we want to decide for my niece cochlear implant is it dangerous or safe surgery sor
Hi. I just want to help you so you can learn to speak English better.
We say “my niece has hearing loss. We want to decide if a cochlear implant is ok. Is it a dangerous or safe surgery?”
Just to help you on how our sentence structure works. I understand how hard it is to learn a new language. I grew up speaking Russian and English. However my grandparents are Czech. Not Russian. They only spoke Russian though. So as you can imagine, Russian was spoken to me. Now I’m trying to learn German to get my German passport (in the Us we can hold two passports from two countries if our mother was still a legal citizen in both countries, my mother was a German citizen when I was born) so I’m
Learning German as we speak. My mom can speak it- but was never spoken to me. So I understand how hard it is to learn a new language. Keep practicing and good luck!
HEARING OR COCHLEAR HEARING . WE ALL USE OUR BRAINNS AND THOUNGS EVEN IF YOU STOP HEARING YOUR BRAIN CAN DEVELOP SPEECH BECAUSE YOUR BRAIN AND THOUNG ALREADY REMENBER THE MOVEMENTS
Has anyone ever had hearing, lost it, and then had an implant? Does it sound the same?
no but it sounds different for sure
it sounds just like normal sound ,i had it done after 60 years of hearing aids and its better. hearing aids only amplify sound
@@ronbeardon1918 oh wow I’ve had an implant since I was 1.5 years old. Because i was born too early.
According to the inventor, Professor Graeme Clark, it depends on the individual and the degree of hearing loss.
How about umbilical cord stem cell harvesting locations, if it is possible to connect a line through the mothers stomach and attach it to the umbilical cord and take small amounts of stem cells during a safe time of the pregnancy. Then people that are deaf or blind, surgical removal of part of the defect causing the person to be deaf, with a steady injection of stem cells to the location, then removal of the other part of the birth defect and a steady injection of stem cells to that location. Also, same process with the eyes. That's if the defect was a birth defect during the growth process and not genetic.
Why would they play music in the background when they are discussing how Cochlear Implants Work. They should know that this background noise interferes with our ability to hear this video. This video is from Yale Medicine, you'd think they would know. SMH
What do they hear though? Do they hear the same as hearing people or does what they hear sound robotic? Like Alexa in your head?
I imagine they hear the same thing as normal hearing people; the only missing component in patients with damaged inner ears is the translation of vibrations to electrical signals picked up by the brain stem. As such, the cochlear implants replace that missing component by translating the vibrations into electrical signals via the electrodes in the cochlear. Therefore, the nerve still gets stimulated via the electrodes in the cochlea by way of the implants.
@@cyanideisfun hope so!
your answer is correct thats is how it works
It’s mostly the same, although for simplicity’s sake they don’t capture frequencies towards the upper and lower limits of our normal range because it would be very difficult and doesn’t matter for crucial things like hearing speech
Are you put completely to sleep?
I assumed it was brain surgery for damage to the receiving end of sound stimuli.
amazing!!!!
Amazing
We have just knew that my two granddaughters twins of 15 months old have severe deaf !
Is it reversible or not
The future of gene therapy is very interesting, but for now something like this might suit.
not necessarily reversible, but as the implants inside of the head are attached via magnets and aren't visible, technically just taking the outer portion off would reverse it.
@@UHFStation1 way to answer the question
How about umbilical cord stem cell harvesting locations, if it is possible to connect a line through the mothers stomach and attach it to the umbilical cord and take small amounts of stem cells during a safe time of the pregnancy.*
CUT. THE. BACKGROUND. MUSIC.
IMPLANTS CAN BE BENEFIT BUT SOME PEOPLE DONT WANT TO WEAR IT ALL THE TIME SOME SCHOOLS INVADE PARENTS PRIVACY AND EVEN THE OWN STUDENT PRIVACY AS A PRENT I HAVE GOTTEN INVADED AND MISSTREATED BY SCHOOL STUFF WHICH SHOULD BE COMPLETELY ILEGAL
wat.?
@@GregorianMGI think he is a deaf community
After all the years of having Menieres diseases and constant ear ringing , it is nice to sit in a quiet restaurant without anything bothering me. Even the fullness in the bad ear is hardly noticeable. And the constant ear ringing is gone..Took 4weeks thanks Dr Liam Ogbebor Herbal centre TH-cam channel for the tinnitus program and herbal ear drop treatment and I hope it stops for everyone else sooner.-;;:
Tell me about your health condition now what do u feel
I m also suffering from mennier disease but sadly there is no cure for mennier disease tell me about your health do u feel any improvement in your health???
@@ayanmisra1694 yes , all my symptoms of Ménière’s disease is gone completely
I wish I could know what will be medically possible in the far off future. We already do face transplants, lung transplant, eye transplant, bionic limbs, brain chips, grow new penises off people's arms and transplant them, etc.
😊😊
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