Hi,
As I am writing this the high pitched whine in my ears seems worse than ever. Anything I do to research this problem seems to make it worse. Makes me understand that stress is just making it worse.
I have heard the high pitched noise in my ears before at much lower levels for at least a couple of years but lately (last few months) it has gotten a lot worse. It's keeping me up a night, not just the noise but thinking about how I'm going to deal with it especially if it gets worse.
I'm a 53 year old male living in Connecticut. I went to the ENT just after Thanksgiving and he gave me a little hope after the exam. They tested my ears and said my hearing was "perfect". If they only knew how hard it was to pick out the low level high freq tones (4 and 8kHz I think) below the higher frequency piercing tone in my head. I had a bunch of wax plugging up my left ear (the Dr cleared this before the hearing test). He said that because the noise got worse when I clenched my teeth , there was a chance that the muscle in the ear that protects it from damage by loud sounds was having spasms causing the problem. He told me to stop chewing gum ( I have chewed quite a but ( about 1.5 hours/day for about 3 - 4 days / week for a couple years) take 600 mg of Advil a few times a day, avoid chewing (eat soft foods / liquid diets) and put hot compresses on my ears and jaw for about 2 weeks. He also said maybe try TinniFree which he said might be slightly more effective than placebo.
Well I've stuck with it for almost a month now and still no better. I'm not sure if it just takes a long time to work or if I'm barking up the wrong tree. It's hard to apply heat during the day but I've been sleeping with a heating pad on my pillow and rolling from side to side throughout the night. (This isn't too hard since the ringing often keeps me awake).
Any suggestions.
Just a note - I'm a stage 4 Melanoma survivor who used a similar forum when I was battling that problem. In some ways that was easier since it was a lot easier to put out of my mind than this noise. From what I've seen so far this forum is very similar to the Melanoma Research Foundation Information Page Forum, and I am looking forward to learning and sharing with you all.
Thanks
Ed
As I am writing this the high pitched whine in my ears seems worse than ever. Anything I do to research this problem seems to make it worse. Makes me understand that stress is just making it worse.
I have heard the high pitched noise in my ears before at much lower levels for at least a couple of years but lately (last few months) it has gotten a lot worse. It's keeping me up a night, not just the noise but thinking about how I'm going to deal with it especially if it gets worse.
I'm a 53 year old male living in Connecticut. I went to the ENT just after Thanksgiving and he gave me a little hope after the exam. They tested my ears and said my hearing was "perfect". If they only knew how hard it was to pick out the low level high freq tones (4 and 8kHz I think) below the higher frequency piercing tone in my head. I had a bunch of wax plugging up my left ear (the Dr cleared this before the hearing test). He said that because the noise got worse when I clenched my teeth , there was a chance that the muscle in the ear that protects it from damage by loud sounds was having spasms causing the problem. He told me to stop chewing gum ( I have chewed quite a but ( about 1.5 hours/day for about 3 - 4 days / week for a couple years) take 600 mg of Advil a few times a day, avoid chewing (eat soft foods / liquid diets) and put hot compresses on my ears and jaw for about 2 weeks. He also said maybe try TinniFree which he said might be slightly more effective than placebo.
Well I've stuck with it for almost a month now and still no better. I'm not sure if it just takes a long time to work or if I'm barking up the wrong tree. It's hard to apply heat during the day but I've been sleeping with a heating pad on my pillow and rolling from side to side throughout the night. (This isn't too hard since the ringing often keeps me awake).
Any suggestions.
Just a note - I'm a stage 4 Melanoma survivor who used a similar forum when I was battling that problem. In some ways that was easier since it was a lot easier to put out of my mind than this noise. From what I've seen so far this forum is very similar to the Melanoma Research Foundation Information Page Forum, and I am looking forward to learning and sharing with you all.
Thanks
Ed