Hi Dr. Nagler.
Welcome back and I hope you enjoyed your vacation!
I'm new to TT, and it has really been a blessing to be able to talk to people who also suffer from Tinnitus. In all the years that I have had it, almost 14, I could count on one hand the people I've met who have it and actually understand. So I'm very grateful to be here around Doctors and people who know what I'm going through.
My personal journey with T is a long one. I used to work in very loud environments, and sometimes when I went home my ears would be ringing. It never worried me too much because I used to go to the shooting range with my dad as a kid, so I knew it was natural for your ears to ring after exposure to loud noises. It would sometimes last into the night, but for the most part it would always be gone by morning. This was around 97-2000. In 2001 I was put on paxil to manage my depression and that was when it became constant. Soon it got so bad that it started throbbing and the volume would spike with each time it throbbed or pulsated. When I decided I wanted to get off the paxil because I believed there was a correlation it got even worse, the volume spiking got louder the throbbing seemed to get harder, and it became painful each time it throbbed, similar to an electric shock. After a while all the shocking and throbbing stopped, and it turned in to what it is today, a constant ring, about a 6 on a scale of one to 10, and for the last 2 years there have been two different pitches it rings at that can be heard over anything.
I've tried lots of different things to alleviate my tinnitus. Changes in my diet like no salt, no caffeine, and lots of exercise. That didn't work, in fact when I exercise I think it gets worse for some reason. I also tried Lippoflavinoids (sorry about the spelling) and that didn't help. I've been to an audiologist who was able to tell me that I have some very minor hearing loss in the high frequency range, and through a suggestion I got from someone here I checked out an ACRN website where I was able to duplicate my tinnitus to find out that it rings at about at about the 9500-10500 Hz range. ACRN is helpful but only provides relief while it is on. It is the only masking method that works. I have a sleepmate and an app on my phone that plays nature sounds, but I have to play them so loud to match my ringing that they end up getting on my nerves. I've also been to The House Ear Institute in LA where they told me there was no damage to my inner ears, and that it would be pointless to get an MRI because I've had it for so long that if it was something physiological in my head I would have been dead by now.
Anyway that's my story. Sorry about the length, but I wanted to make sure you had my info before asking you to make any suggestions. Also, I was told you could possibly help me find a TRT doctor in my area. I've been looking on the internet, and I talked to the audiologist, but I haven't had any luck. I live in San Luis Obispo county in California and my zip is 93422.
Thank you,
Kevin
Welcome back and I hope you enjoyed your vacation!
I'm new to TT, and it has really been a blessing to be able to talk to people who also suffer from Tinnitus. In all the years that I have had it, almost 14, I could count on one hand the people I've met who have it and actually understand. So I'm very grateful to be here around Doctors and people who know what I'm going through.
My personal journey with T is a long one. I used to work in very loud environments, and sometimes when I went home my ears would be ringing. It never worried me too much because I used to go to the shooting range with my dad as a kid, so I knew it was natural for your ears to ring after exposure to loud noises. It would sometimes last into the night, but for the most part it would always be gone by morning. This was around 97-2000. In 2001 I was put on paxil to manage my depression and that was when it became constant. Soon it got so bad that it started throbbing and the volume would spike with each time it throbbed or pulsated. When I decided I wanted to get off the paxil because I believed there was a correlation it got even worse, the volume spiking got louder the throbbing seemed to get harder, and it became painful each time it throbbed, similar to an electric shock. After a while all the shocking and throbbing stopped, and it turned in to what it is today, a constant ring, about a 6 on a scale of one to 10, and for the last 2 years there have been two different pitches it rings at that can be heard over anything.
I've tried lots of different things to alleviate my tinnitus. Changes in my diet like no salt, no caffeine, and lots of exercise. That didn't work, in fact when I exercise I think it gets worse for some reason. I also tried Lippoflavinoids (sorry about the spelling) and that didn't help. I've been to an audiologist who was able to tell me that I have some very minor hearing loss in the high frequency range, and through a suggestion I got from someone here I checked out an ACRN website where I was able to duplicate my tinnitus to find out that it rings at about at about the 9500-10500 Hz range. ACRN is helpful but only provides relief while it is on. It is the only masking method that works. I have a sleepmate and an app on my phone that plays nature sounds, but I have to play them so loud to match my ringing that they end up getting on my nerves. I've also been to The House Ear Institute in LA where they told me there was no damage to my inner ears, and that it would be pointless to get an MRI because I've had it for so long that if it was something physiological in my head I would have been dead by now.
Anyway that's my story. Sorry about the length, but I wanted to make sure you had my info before asking you to make any suggestions. Also, I was told you could possibly help me find a TRT doctor in my area. I've been looking on the internet, and I talked to the audiologist, but I haven't had any luck. I live in San Luis Obispo county in California and my zip is 93422.
Thank you,
Kevin