The BIZARRE Treatment That Could Actually Reduce Tinnitus
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- Опубліковано 12 кві 2024
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Researchers from the University of California Irvine released new research about a tinnitus treatment approach they developed that generates a targeted electrical current into the inner ear. Today, let’s take a look at what the device is, how it works, and whether I think it can actually help your tinnitus.
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I click on the link but can't see how I get my free telephone consultation, am I eligible as I live in England?
If only, you were in the UK...
Sorry guys, currently the free consultation is only offered inside the United States
Me India Se hu
we NEED a CURE to reduce tinnitus (at least) by 90%
Susan shore is can be 75% after 6 weeks. And it likely keeps improving it over time.
I think we are close to a cure. People are starting to realize that this is a big issue in the world. love your videos btw
@@g.s.5868 have some faith the technology is going forward fast. You probably got your tinnitus in the 70s-80s. It is 2024 bro.
A very important thing to check when considering a therapy is: with how many people there are adverse effects of the therapy?
If it works in e.g. 70% but worsens the situation in e.g. 30% you should be careful.
Often the latter number is omitted in the information provided.
It seems promising, although the science regarding tinnitus seems to literally know absolutely nothing. Today I had a terrible spike without doing anything, then it went back to "normal". These treatments need to advance and not just remain in research. Hope that in the future it actually reaches people.
I’ll be glad to be a trial client for the new treatment for research!
My brother-n-law is a ENT in North Louisiana that could work with the trial. Just saying 😮
I was gonna have myself strapped to a metal table and put up on a roof during a thunderstorm, probably get a charge out of that but will probably wait until there is a science backed treatment that provably delivers real results that they aren’t gonna charge you some ridiculous amount to get access to.
Lol I’m sorry man but what !!!
So they built it without even knowing if it works? What are they waiting for?
Just as with any emerging technology, extensive studies are being conducted to assess the effectiveness of the product. These studies will guide the next steps forward.
Sir iam soilder of indian Army .sir my 15 years service in heavy sounds and gun shots. My both ears ringing connued .i treat by all best doctors of india but my both ringing continue d
Don't worry the Susan shore device really seems like the key to the problem. Tinnitus is neural hyperactivity in the auditory brain. The Susan shore device directly treats this hyperactivity. Its awaiting FDA approval now when released it will be served to America first. But will spread to the rest of the world over time.
It reduced Tinnitus by 60% to 75% over the course of 6 weeks to everyone who used it. And likely would further suppress Tinnitus though further use. Unfortunately all anyone with Tinnitus can do is wait for actual treatment right now.
Susan shore device should work based on what we know about tinnitus today. Aka its neural hyperactivity in the auditory brain.
Don't think it will help for peoplke with tinnitus from noise induced hearing loss.
@@shootalot523 That's the most common type of tinnitus. Almost all types of tinnitus is caused by neural hyperactivity in the brain. The hair cell theory of tinnitus is outdated. That only applies to actual hearing loss. It definitely will help that kind of tinnitus.
About the neural hyperactivity in the auditory brain would that be the auditory cortex or some other networks in the brain ? Thay may be the reason why some ppl with hearing loss dont experience tinitus like loss of tiny hair cells in the snail like cochlea or a lesion etc but t 0:00 He other factors are the common loud noises or continued exposures but thete other causes like viruses covid 19 one of them orher viruses or lyme disease sometimes or even sometimes heavy metal toxicity which is new to me medication otoxity certain head injuries or diabetes very mulfifactoral thats why its very difficult to treat too many factors to figure ot out so would the susan shores device help anyone regardless of their origin of chronic tinnitus?
TRT + sound therapy first! TRT + sound therapy first! TRT + sound therapy first! But hey, thanks for the interesting information 😊
what is TRT? and what sound therapy?
@@toshobg tinnitus retraining therapy; basically a form of CBT specific to people with bothersome tinnitus. Sound therapy is listening to crickets, for example, I’m order to help your brain filter tinnitus.
Hello! Could you tell me more about the correct use of sound therapy? Should I hear a sound that resembles my tinnitus frequently? How many hours a day? For how long? At what intensity? With speaker or headphones? And if you can, tell me how to do TRT correctly. Thank you very much.. Don't ignore my comment please! I need someone with experience. Unfortunately, doctors don't know much about tinnitus. 🙂
I thought it involved white noodles in your earhole...
I will volunteer..asap
Sir I have my tittinis past 5 years but no doctor has found out correct treatment its a God curse for us to suffer like 😢 this Ramesh Bangalore India.
We are a fully remote company and would be happy to speak with you over zoom. Schedule a complimentary consultation with one of our Audiologists: treble.health/international-consultation
I suffer last 05 years from tinnitus
From 1 it has increased to 10 after 3 years
I wish you good luck. I have lived with multi-toned tinnitus for 68 years. I was prescribed large doses of aspirin (a triple-compounded tablet 4x per day) as a child with an erroneous diagnosis of juvenile arthritis that was only corrected in my 40s to be polymyositis. My acoustic nerves are probably too damaged to heal since years ago. Sometimes my head is ringing so loudly I can’t believe no one else can hear it…😵💫😜. It doesn’t bother me as much when I am absorbed in books, or concentrating on a complicated task, but when I get tired or lose focus, it comes back with a roar!
I hope you find relief and release. Keep trying. Best of luck and best wishes for your health and happiness.
me last 8 years
@@vegetossgss1114 life is ruined
Sir iam from india.i want your treatment
Doctor says my disease named biletral senso neural hearing loss
There is a company in SPAIN calls Ototech doing this same type of treatment since many years...
What’s up with all the negative comments?
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Technology can treat tinnitus but large study required
Why did my reply to gentleman from India disappear?
Same here I'm probably banned
Yes i am sure it work but required more improvement
As a person who has had cholesteatomas, can you honestly guarantee a permanent solution to tinnitus? Tbh not a lot of medical folks even have a clue what cholesteatoma's even are. I lost everything in my middle ears because of this condition. Instead of advocating so much about tinnitus, let's advocate for better ear health such as cholesteatoma's and other ear conditions that destroy our everyday lives.
Appreciate your “heads-up” (no pun intended). My 1st cousin (female) has had cholesteatoma surgeries but very unusually, per her medic, had both ears develop “pearl”s that caused infections and eroded bone. Our shared grandfather had ear problems that would now probably be dx’d as cholesteatoma. Our shared grandmother also gradually lost hearing in one ear and lost her sense of smell (and consequently lost sense of taste). Our grandfather had had bouts of vertigo, what one doctor called over-abundance of earwax, and mild deafness; his father went deaf in one ear, and HIS father in his late teens had vertigo, then hearing loss, then in his 20s lost his sight (but remained farming per census).
Per studies in Sweden, approx 90% of cholesteatomas have a genetic component. Of course the research was based on all males in the subject population…
Our shared grandmother is the only female I have any medical history on relative to ears; on that side of the family, our great-x grandmothers mostly died young, before their children could remember any history to hand down. Data from stepmothers, wonderful as those ladies were, is not insightful in this case.
I agree this is a rare disorder that deserves be better known-affecting estimated 1 out of every 100,000 people. It took about 2 years for there to be a diagnosis for my cousin and that was only made when erosion and infection of the bone behind the right ear broke through the skin. The left ear pearls were noted by accident on a series of CT scans several years later when she had not cleared the infection and noted discharge from the left ear. A doctor assumed she did not know her left from her right, since a history of both ears involved was not documented.
I sympathise with you and your experience, and hope you are doing well. All best wishes and thank you for your important message.
Cifra
another 5000 usd snake oil promise from them/?I dont think this is the one doc but thx keeping us up with the news
There is plenty of treatment if you have lots of money
such as?
I knew that they sooner or later will think of a chip implant :D
Faith and prayer has helped me immensely
My tinnitus has almost fixed itself