Those seem similar to ordinary Peltor Optime III earmuffs and those earmuffs will not fully block the noise at an airport platform, if you have hyperacusis. I can tell from personal experience
I know, but if they endure 150 dB daily, they must be good. I think it's custom made for military, but I will research more.Those seem similar to ordinary Peltor Optime III earmuffs and those earmuffs will not fully block the noise at an airport platform, if you have hyperacusis. I can tell from personal experience
To me it does not seem possible they can block 150 dB, since the sound would go through by bone conduction anyway.I know, but if they endure 150 dB daily, they must be good. I think it's custom made for military, but I will research more.
It seems that the helmets (not necessarily the one in my photo) protect from bone conduction. That's why they are helmets and not just earmuffs.To me it does not seem possible they can block 150 dB, since the sound would go through by bone conduction anyway.
I had a lot of relief when I first had TRT 27 years ago. My tinnitus reduced to a level that I could hardly hear most of the time. I had very severe hyperacusis with pain, which was completely cured after two years of wearing white noise generators. It has remained this way to this day.CBT and TRT for tinnitus/hyperacusis treatment is the same as sending a patient with root canal infection to a psychiatrist instead, or advising him to bite down on a peanut for a few hours daily with that painful tooth.
This thread is about hyperacusis. Please read the paper. If OHCs (the amplifier) have nociceptors, then these can cause an uncomfortable feeling and pain. Mrs. Megan Wood told me there is other research claiming IHCs get more ribbons with age, so you get a double-whammy effect. This research isn't in the books of today's ENTs.I had a lot of relief when I first had TRT 27 years ago. My tinnitus reduced to a level that I could hardly hear most of the time. I had very severe hyperacusis with pain, which was completely cured after two years of wearing white noise generators. It has remained this way to this day.
Unfortunately, I had a second noise trauma in 2008, which resulted in my tinnitus changing to variable tinnitus. I had another 2 years of TRT with counseling and wearing white noise generators. It took 4 years in total to habituate for the second time. My tinnitus is still variable, from complete silence to mild, moderate, severe, and very severe.
I have explained this at length in my thread: My Experience with Tinnitus. I used tiex tinnitus machine for 11 years and it helped a lot. It stopped working a year ago. My tinnitus has remained variable and manageable. When required, I take Clonazepam to calm it down for 1 on 2 days.
My tinnitus began to increase in February 2024. Since I have had tinnitus a long time, I know it extremely well. Everything I tried wouldn't calm it down, so I had to take Clonazepam, which reduced the severity temporarily. Because the tiex machine stopped working, I ordered the Cleanhearing Sono device - this is the updated version of the tiex machine. I will be writing my experience with it at a later date.
Michael
Sorry to hear this.My tinnitus began to increase in February 2024. Since I have had tinnitus a long time, I know it extremely well. Everything I tried wouldn't calm it down,
Indeed, my experience living with severe hyperacusis enabled me to start this thread.This thread is about hyperacusis. Please read the paper. If OHCs (the amplifier) have nociceptors, then these can cause an uncomfortable feeling and pain. Mrs. Megan Wood told me there is other research claiming IHCs get more ribbons with age, so you get a double-whammy effect. This research isn't in the books of today's ENTs.
Thank you for your kind words @Jupiterman.Sorry to hear this.
Do you know what caused this?
Is it perhaps a spike?
Two years of pain hyperacusis (noxacusis)?! Cured with noise generators. Funny, people with noxacusis say you can't cure it with sound therapy. Makes people worse, in fact.I had a lot of relief when I first had TRT 27 years ago. My tinnitus reduced to a level that I could hardly hear most of the time. I had very severe hyperacusis with pain, which was completely cured after two years of wearing white noise generators. It has remained this way to this day.
Unfortunately, I had a second noise trauma in 2008, which resulted in my tinnitus changing to variable tinnitus. I had another 2 years of TRT with counseling and wearing white noise generators. It took 4 years in total to habituate for the second time. My tinnitus is still variable, from complete silence to mild, moderate, severe, and very severe.
I have explained this at length in my thread: My Experience with Tinnitus. I used tiex tinnitus machine for 11 years and it helped a lot. It stopped working a year ago. My tinnitus has remained variable and manageable. When required, I take Clonazepam to calm it down for 1 on 2 days.
My tinnitus began to increase in February 2024. Since I have had tinnitus a long time, I know it extremely well. Everything I tried wouldn't calm it down, so I had to take Clonazepam, which reduced the severity temporarily. Because the tiex machine stopped working, I ordered the Cleanhearing Sono device - this is the updated version of the tiex machine. I will be writing my experience with it at a later date.
Michael
Whether one wants to call it noxacusis, hyperacusis, reactive tinnitus or pain hyperacusis, in my opinion it all amounts to the same thing. Most people that are affected with these conditions have noise-induced tinnitus.Two years of pain hyperacusis (noxacusis)?! Cured with noise generators. Funny, people with noxacusis say you can't cure it with sound therapy. Makes people worse, in fact.
These aren't all the same. In fact, I have hyperacusis that makes something like ruffling a chip bag sound very loud from internal amplification, but I've never had noxacusis, pain, or reactive tinnitus.Whether one wants to call it noxacusis, hyperacusis, reactive tinnitus or pain hyperacusis, in my opinion it all amounts to the same thing.
With respect, I am not here to duel with you. I have said my piece and wish you well.These aren't all the same. In fact, I have hyperacusis that makes something like ruffling a chip bag sound very loud from internal amplification, but I've never had noxacusis, pain, or reactive tinnitus.
The best thing is to protect your ears from loud noise and be patient, and it might get better in a couple years. Some people have reported white noise generators / TRT making their tinnitus worse.
Thank you for your kind words @Hardwell.Hi @Michael Leigh, sorry to hear of your tinnitus becoming a little more troublesome! I hope this is temporary and reverts back to your normality at the very least.
I no longer experience hyperacusis, nor does my tinnitus spike. As I have mentioned many times, tinnitus spikes usually affect people who have noise-induced tinnitus. The underlying problem is having an oversensitive auditory system often caused by noise trauma. This oversensitivity to sound can manifest itself in a variety of ways much like tinnitus. It can be mild, moderate, severe, and can be extremely debilitating for some people. I once helped to counsel a woman whose hyperacusis was so severe that rain falling on her conservatory roof, which was made of glass, brought her to tears. Fortunately, with time, she did improve with the help of wearing sound generators and having counselling with an audiologist who specialized in tinnitus and hyperacusis management.I see you mentioned a few times about your hyperacusis causing pain, but I've not yet seen you describe the type of pain you felt, duration and triggers, etc. Is that something you'd be willing to share?
It sounds as if you had an amazing experience randomly finding the right medical people. I wish we all had such success.Thank you for your kind words @Hardwell.
As you know, I have variable tinnitus. It can be pretty severe at times but I have habituated to this for many years. In February, it increased to levels that I last experienced in 2008 when my noise-induced tinnitus changed to variable tinnitus after a second noise trauma. It took four years to habituate. Please read my thread: My Experience with Tinnitus.
I am using the Cleanhearing Sono device and hope to give an update on my experience with it by late May or June.
I no longer experience hyperacusis, nor does my tinnitus spike. As I have mentioned many times, tinnitus spikes usually affect people who have noise-induced tinnitus. The underlying problem is having an oversensitive auditory system often caused by noise trauma. This oversensitivity to sound can manifest itself in a variety of ways much like tinnitus. It can be mild, moderate, severe, and can be extremely debilitating for some people. I once helped to counsel a woman whose hyperacusis was so severe that rain falling on her conservatory roof, which was made of glass, brought her to tears. Fortunately, with time, she did improve with the help of wearing sound generators and having counselling with an audiologist who specialized in tinnitus and hyperacusis management.
The severe hyperacusis that I experienced 27 years ago is something that I hope I never have to endure again. Coupled with severe unrelenting tinnitus, I believe this experience helped make me become a stronger, more positive-thinking person and enabled me to help people who are suffering from tinnitus and hyperacusis.
My hyperacusis would often feel like thousands of sharp needles being stabbed into my ears. It would go right through my head and down into my face, which felt aflame with a burning sensation. It would cause my tinnitus to spike for days. I regularly had to ask people to please lower their voices as my ears were in so much pain when they spoke. I had to run out of the kitchen whenever plates and cutlery were being washed in the sink.
Everywhere that I went, I wore foam earplugs because my ears were so sensitive to sound. Back then, I didn't know this probably wasn't the best thing to do. My noise trauma was so severe that my whole head felt completely numb. I could hear, but it felt like my head was deep underwater. It was so incredibly frightening that I never told any member of my family what I was going through. They knew about the tinnitus and my hypersensitivity to sound (hyperacusis) but not about the numbness in my head.
I met a herbalist who knew about noise-induced tinnitus. I explained about my use of headphones. Told her about the severe hyperacusis, tinnitus, and numbness throughout the whole of my head. She said I had suffered a huge noise trauma and mentioned it had been coming on for some time. Looking back she was one hundred percent correct. I remember in bed at night, when it was very quiet; I could hear ringing but thought nothing of it; by the morning, it was gone because it was being masked by daily sounds in the environment.
The herbalist said the auditory system consists mainly of nerves, and I had effectively blown a fuse! She said this also caused the numbness in my head. Her advice was to start taking magnesium tablets, which would help to repair the nerves in the auditory system over time - these are not the same nerves or hairs that are attached to the cochlea. I was also advised to take Ginkgo biloba.
When I was seen at ENT, the doctor said the herbalist's advice was very good. He also advises all his tinnitus patients to take magnesium tablets and Ginkgo biloba.
Take care,
Michael
Thank you for your kind words @DeanD. My tinnitus is problematic at the moment, but I am able to cope, as long as it's not too severe, as it was in February when it reached excruciating levels. I am taking things easy and using the Cleanhearing Sono device, and I hope to provide information on my experience with it at a later date. I had been using the tiex device continuously for 11 years, but it stopped working last year. I believe it helped to keep my tinnitus under control. That is all I want to say at the moment.Sorry to hear of your worsening. No one deserves to have that happen.
You make a valid point @DeanD, for it does help to have the right people to turn to when one is in distress with tinnitus and hyperacusis. My audiologist was born with tinnitus and found her to be a very understanding and considerate person. I felt totally at ease having regular counselling with her for two years as part of TRT. Sadly some people are not as fortunate to find the right medical people. However, it should be noted that ENT doctors treat underlying medical problems within the auditory system that cause tinnitus, but they do not treat tinnitus.It sounds as if you had an amazing experience randomly finding the right medical people. I wish we all had such success.
I have been through the NHS system twice. My experience is different. ENTs hear 'tinnitus' and are not particularly caring. They simply carry out tests to look for an underlying condition, which, of course, is all they can do.Thank you for your kind words @DeanD. My tinnitus is problematic at the moment, but I am able to cope, as long as it's not too severe, as it was in February when it reached excruciating levels. I am taking things easy and using the Cleanhearing Sono device, and I hope to provide information on my experience with it at a later date. I had been using the tiex device continuously for 11 years, but it stopped working last year. I believe it helped to keep my tinnitus under control. That is all I want to say at the moment.
You make a valid point @DeanD, for it does help to have the right people to turn to when one is in distress with tinnitus and hyperacusis. My audiologist was born with tinnitus and found her to be a very understanding and considerate person. I felt totally at ease having regular counselling with her for two years as part of TRT. Sadly some people are not as fortunate to find the right medical people. However, it should be noted that ENT doctors treat underlying medical problems within the auditory system that cause tinnitus, but they do not treat tinnitus.
I believe most ENT doctors care about their tinnitus patients. They play an important role in helping to diagnose what the underlying cause of tinnitus is in the auditory system, and there are many. When no medical cause is found, as in noise-induced tinnitus, the patient should be referred to Audiology, as this is the usual practice in the UK.
I see no merits in this personally, but I can perhaps understand why some people are reluctant. This is partly due to what you say about 99% of medical professionals being useless regarding our conditions.It would be interesting, though, for everyone to discuss the merits of keeping medical consultants' names hidden.
The merit is sharing information that may provide help to the sufferers on here.I see no merits in this personally, but I can perhaps understand why some people are reluctant. This is partly due to what you say about 99% of medical professionals being useless regarding our conditions.
If somebody has found the luxury of a physician who takes them seriously and provides them relief and mental respite, and after posting the name here, members suddenly drag that name through the mud, the original poster loses their faith in said physician. That is the only reason I can think of why some people would gatekeep.
I don't get what people are hoping for. There is no cure, so what can a doctor do?The merit is sharing information that may provide help to the sufferers on here.
Aren't other sufferers on here entitled to the best shot with a recommended consultant rather than the typical gaslighting and lack of awareness with consultants many of us experience?
No, sorry. I meant that I see no merit in gatekeeping the information personally. I was just trying to summarise why I think others might.The merit is sharing information that may provide help to the sufferers on here.
I correspond with many people across the UK that have tinnitus. A lot of them have been referred to Audiology for tinnitus treatment and management. The NHS isn't perfect and does have its problems, but I have always received good treatment, and not just for tinnitus. Help does vary between Trusts.I have been through the NHS system twice. My experience is different. ENTs hear 'tinnitus' and are not particularly caring. They simply carry out tests to look for an underlying condition, which, of course, is all they can do.
Never was I then referred to audiology. Times have changed.
What happened in February to increase the tinnitus, if you don't mind me asking?My tinnitus began to increase in February 2024.
I don't mind you asking about the increase in my tinnitus since February @Stayinghopeful. In fact, I thank you for inquiring. As mentioned in previous posts on this thread, I ordered the Cleanhearing Sono device because the increase in my tinnitus was so severe.What happened in February to increase the tinnitus, if you don't mind me asking?
Hi Michael.I have corresponded with a few audiologists that work with tinnitus and hyperacusis patients. One in particular, said all her patients that follow her treatment programme have been cured of hyperacusis.
She is an NHS audiologist @Elho. I corresponded with her over a year ago but no longer keep in contact. Even if I did, I was asked not to divulge her name or the NHS Trust where she works.May I ask who is the audiologist with 100% success treating hyperacusis that you corresponded with?