Thanks Pete. Good luck with your appeal.I get Magnesium Bisglycinate. Any brand. I don't know if it helps but I figure, it can't hurt.
Thanks Pete. Good luck with your appeal.I get Magnesium Bisglycinate. Any brand. I don't know if it helps but I figure, it can't hurt.
All I know is without a psychiatrist in your arsenal it is like playing chess with 1 Rook.The problem is lots of people have a physician who will refer a psychiatrist but what if one of those people who has a doctor WHO WON'T?
From my experience, doctors in general are horrible people - some of the most cold-hearted and callous people around (up there along with cops and politicians) - which is ironic considering their chosen profession.
As some people said, it seems easier or an easier process in various American states. But, what if your family physician is not accommodating and not supportive? What if you don't have a psychiatrist in your corner?
I'm nervous about an impending appeal - my last chance. I don't want to repeat this entire process again - it has taken about 3 years?
Are you on disability?All I know is without a psychiatrist in your arsenal it is like playing chess with 1 Rook.
I don't know what to tell ya buddy. You def need a family doctor sympathetic to your cause because that's the backbone of your claim. I wish you success.
Did you qualify?
Agree with this. From what it seems, they are not in it because of a profession for helping people, but rather family expectations or money. You need to have an analytical and logical mind to be a doctor, which leaves bedside manner--and nuanced thinking for patients who happen to be outliers--a lot to be desired.The problem is lots of people have a physician who will refer a psychiatrist but what if one of those people who has a doctor WHO WON'T?
From my experience, doctors in general are horrible people - some of the most cold-hearted and callous people around (up there along with cops and politicians) - which is ironic considering their chosen profession.
As some people said, it seems easier or an easier process in various American states. But, what if your family physician is not accommodating and not supportive? What if you don't have a psychiatrist in your corner?
I'm nervous about an impending appeal - my last chance. I don't want to repeat this entire process again - it has taken about 3 years?
Fuck! Not looking forward to 4th of July.
TRT is such a scam, you fell for it.Tinnitus loud and whistling. Can hear someone opening a beer bottle in the kitchen from my bedroom. Thanks TRT, you sure are helpful.
I told my audiologist I was getting worse and she said it was a positive. Why?
I spoke to another person who did recover from TRT and they claimed it only helped them, never made them more sensitive. And that hearing protection made it worse. Well, it's the opposite for me. And many others. Why won't the people who get worse with noise and better with quiet be believed?
Can't get a straight answer either. I asked, why is me getting worse 'a good thing'? But nothing. I hate this goddamn industry, and I'm sick of living in the Twilight Zone where everyone thinks I'm crazy. Do I need to make my already sub 40 dB LDLs even worse for 6+ months only for people to be satisfied, for me to write it off and give them the "told ya so"?
I didn't fall for it. I was always skeptical but I have no other options. And trying this treatment is the only way to tell disability that I've at least tried everything and that I can't get better. I have severe loudness hyperacusis so my chances were a bit better than pain hyperacusis cases. But I just clarified with the audiologist today and she said that if they are making me worse, I should stop.TRT is such a scam, you fell for it.
Sorry you're getting worse. I had to do the lowest possible sound and maybe 10-15 minutes at a time in the ears and maybe an hour on phone. Tinnitus was worsening for a bit, then started to improve quite a bit. Then COVID-19 struck and well, we will see, it's squealy again now.Tinnitus loud and whistling. Can hear someone opening a beer bottle in the kitchen from my bedroom. Thanks TRT, you sure are helpful.
I told my audiologist I was getting worse and she said it was a positive. Why?
I spoke to another person who did recover from TRT and they claimed it only helped them, never made them more sensitive. And that hearing protection made it worse. Well, it's the opposite for me. And many others. Why won't the people who get worse with noise and better with quiet be believed?
Can't get a straight answer either. I asked, why is me getting worse 'a good thing'? But nothing. I hate this goddamn industry, and I'm sick of living in the Twilight Zone where everyone thinks I'm crazy. Do I need to make my already sub 40 dB LDLs even worse for 6+ months only for people to be satisfied, for me to write it off and give them the "told ya so"?
I haven't checked your thread in a bit, I'm glad your tinnitus is improving but I'm sorry you got COVID-19 and hope there's no lasting bad effects. I know it can be killer on the ears. I really want to learn about more 'getting worse before getting better' cases and believe, but at the same time it's so hard to hold onto this when my heart beat is so loud in my ears now and I'm losing more tolerances every day.Sorry you're getting worse. I had to do the lowest possible sound and maybe 10-15 minutes at a time in the ears and maybe an hour on phone. Tinnitus was worsening for a bit, then started to improve quite a bit. Then COVID-19 struck and well, we will see, it's squealy again now.
I do believe everyone is different.
I don't know about no hope, but it's hard as hell to find what helps you while you get worse while attempting different methods. I understand how discouraging it is. That and life does not let up.I didn't fall for it. I was always skeptical but I have no other options. And trying this treatment is the only way to tell disability that I've at least tried everything and that I can't get better. I have severe loudness hyperacusis so my chances were a bit better than pain hyperacusis cases. But I just clarified with the audiologist today and she said that if they are making me worse, I should stop.
I lost no money, they were fully covered by insurance.
I believe sound therapies, not always just TRT, can help some cases of hyperacusis. I don't know if I will try other approaches, because it seems my brain just does not like sound period. I want to believe in central gain models, I want to believe this "overprotection" myth, but all evidence regarding my own case stacks against it. There is no hope.
I understand, it's good to hold off for now.I haven't checked your thread in a bit, I'm glad your tinnitus is improving but I'm sorry you got COVID-19 and hope there's no lasting bad effects. I know it can be killer on the ears. I really want to learn about more 'getting worse before getting better' cases and believe, but at the same time it's so hard to hold onto this when my heart beat is so loud in my ears now and I'm losing more tolerances every day.
Indeed. My audiologist also thinks I should look into other underlying medical causes, but it's so difficult to do so when I have to wait for so long, drag my ass to appointments while getting worse from setbacks, and doctors just shrugging their shoulders in the end due to being unfamiliar with hyperacusis or still thinking this is all in my head. It's maddening. Still no full analysis of my nervous system, and without an MRI, who knows what is possible?I don't know about no hope, but it's hard as hell to find what helps you while you get worse while attempting different methods. I understand how discouraging it is. That and life does not let up.
You're not doing wrong at all, you're trying. Just because things aren't helping now, it doesn't mean it won't help later ya know? Just need to keep pushing forward and somehow hope things don't worsen at the same time. I'm in the same boat.Indeed. My audiologist also thinks I should look into other underlying medical causes, but it's so difficult to do so when I have to wait for so long, drag my ass to appointments while getting worse from setbacks, and doctors just shrugging their shoulders in the end due to being unfamiliar with hyperacusis or still thinking this is all in my head. It's maddening. Still no full analysis of my nervous system, and without an MRI, who knows what is possible?
And I hate being stuck in the middle between teams "you aren't thinking positively enough" vs "you fell for the TRT scam" too, both online and offline. These comments hurt from both sides. What else can I do? If there was no loss here, I wouldn't care, the risk of going through the trials just to come out worse in the end is terrifying. But me not trying at all just convinces others I'm a faker who wants to remain miserable and uncured.
I've had it for over a year now, I just keep getting worse. Currently can't leave my house, and have to have earmuffs 24/7. I can't drive, and I can only have conversations for no more than 20 minutes. There are people in even worse situations.How long does noxacusis take to improve? Years?
Jesus.I've had it for over a year now, I just keep getting worse. Currently can't leave my house, and have to have earmuffs 24/7. I can't drive, and I can only have conversations for no more than 20 minutes. There are people in even worse situations.
Oh my noxacusis is bad. I have 2 dogs, the big one barely ever barks. The little one barks a lot but I never let him in my room. When I hang out with my dogs they almost never bark, and when they do, it's because they are outside chasing squirrels and I'm inside the house. I also have delayed pain, a dog can bark and I could be good at the moment, but later on the day I'll be paying for it. Usually with excruciating stabbing pain.Jesus.
I just read you have a barking dog and that you get potentially exposed to barks. Your noxacusis can't be that bad if a dog bark at close range doesn't kill you.
Not to minimize your pain but if you can stand a dog bark outside your door and not be worse immediately, your noxacusis is about moderate level. Having said that, if you want to get better, get rid of your dogs. I'm saying that because noxacusis is cumulative.Oh my noxacusis is bad. I have 2 dogs, the big one barely ever barks. The little one barks a lot but I never let him in my room. When I hang out with my dogs they almost never bark, and when they do, it's because they are outside chasing squirrels and I'm inside the house. I also have delayed pain, a dog can bark and I could be good at the moment, but later on the day I'll be paying for it. Usually with excruciating stabbing pain.
I wear double hearing protection inside my house, I am completely housebound. I literally just told you I have delayed pain, so if they have to bark anywhere near me, even with double protection I get a nasty spike. I have constant stabbing pain all day, and being housebound is literally the definition of severe. Like I said, the dogs barely come in the room, and when they bark, they aren't in the house and bark from a distance, we have a huge yard. Again I wear double hearing protection inside my house.Not to minimize your pain but if you can stand a dog bark outside your door and not be worse immediately, your noxacusis is about moderate level. Having said that, if you want to get better, get rid of your dogs. I'm saying that because noxacusis is cumulative.
Oh I didn't know you wore double hearing protection in the house, sorry.I wear double hearing protection inside my house, I am completely housebound. I literally just told you I have delayed pain, so if they have to bark anywhere near me, even with double protection I get a nasty spike. I have constant stabbing pain all day, and being housebound is literally the definition of severe. Like I said, the dogs barely come in the room, and when they bark, they aren't in the house and bark from a distance, we have a huge yard. Again I wear double hearing protection inside my house.
I know it's cumulative, I've had it for over a year now.
Do you have any pets? I think I have both hyperacusis and noxacusis. My dog used to bark occasionally - usually outside, at other dogs if they got too close or if they were hyper and approached too energetically. Dog barks can hurt my ear or ears - even my own dog's bark. My dog also used to have, what I call anxiety attacks - she would do a sudden howl that would turn into a few barks. At least, she rarely does that now.Not to minimize your pain but if you can stand a dog bark outside your door and not be worse immediately, your noxacusis is about moderate level. Having said that, if you want to get better, get rid of your dogs. I'm saying that because noxacusis is cumulative.
Yes yes I know exactly what you mean brother. I'm thinking getting a cat.I want to avoid problems from not wearing hearing protection but when I wear it, it's another form of torture - maybe you know what I mean?
I was thinking of a cat too. I wonder if they make noise at night?Yes yes I know exactly what you mean brother. I'm thinking getting a cat.
They hiss when pissed, they meow when hungry or when seeing food. Sometimes they cry out kinda loud for no reason. They make clicking noises when seeing birds outside... but that's not loud, just funny lol. They get wild hairs and randomly run into stuff and knock it down. Still quieter than dogs.I was thinking of a cat too. I wonder if they make noise at night?
Although better then barking, the thing with cats is they purr A LOT, and often they get in your face and do that and also while you sleep they'll snuggle up in your face and purr. I actually got a kitten in my early days of tinnitus and hyperacusis (when my hyperacusis wasn't even as bad as now) but the purring was really uncomfortable in my ears and made my eardrum vibrate/flutter too. I found myself showing the kitten away from me, and it broke my heart because it deserved better than that, so I gave it another home.I was thinking of a cat too. I wonder if they make noise at night?