SayWhatYouSee
Central Defender
Any sufferers on here and if so do you have any good tips for managing it? Well, coping with it because I know there’s no cure. Mine seems to have worsened recently.
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That’s a good way to describe it. Mine is like that but multi level, like TV interference. I’ve just found a site where you can identify your sound as everyone hears differently. It’s so annoying and I’m trying to not focus on it.My dad suffered terrible and also had menniers (sp) and vertigo and was crippled at times.
I think I'm starting to develop it, ATM its only certain times like when I yawn or put pressure around my ears I get the ringing.
Could never get my head round when my dad tried to explain it, but for me now, it's like when you run your finger round a crystal glass, that type of ring.
There are tracks now that you can play to mask it, choosing one that fits your own personal noise. I find listening to rain sounds or running water helps.I've had it on and off for about 15 years - used to get it terrible when i used to DJ when i was younger. Now it comes on worse when i get a cold - only thing that used to help me sleep was a tv tuned into static - that helped a lot as i used to be surviving on about 3 hours kip a night.
That’s a good way to describe it. Mine is like that but multi level, like TV interference. I’ve just found a site where you can identify your sound as everyone hears differently. It’s so annoying and I’m trying to not focus on it.
I've had it about a year n a half. I think its manageable but I hate to say it but a lad local I got to know via a facebook page committed suicide recently because of his roaring T.
I have downloaded about 15 mp3's of various masking sounds which help reduce spikes and help me to sleep.
i'm seriously considering lenire.ie which has had some success in lowering the symptoms. (although my suicidal friend it didn't help)
Seems to have crept in last 6 months or so.Any sufferers on here and if so do you have any good tips for managing it? Well, coping with it because I know there’s no cure. Mine seems to have worsened recently.
I can associate with what you’re saying, I’ve had hearing tests and been told that my hearing loss is minimal, so yes my tinnitus does affect being able to hear conversations in a crowded room etc. I also have difficulty holding a telephone conversation if there is background noise (tv etc)I’m 49 now, and for the last ten years the tinnitus is starting to degrade the level at which I can pick up what people are saying. Cannot pick out conversations in a noisy room.
This is where mine's at. I was given high doses of IV antibiotics as a young un then a near death experience made it worse.Mentioned this on another thread, I was born with the condition. i always thought it was normal to hear constant sound all the time.
About 38 years before I discovered that it wasn’t normal, I was watching a telly show and it was all about Tinnitus. Went to a hearing clinic, and discovered that as I was a premature birth, Tinnitus was a side effect of this.
Later on I was sitting talking to my Mam, told her about the tinnitus and also what the hearing clinic had said, she went off it! She said she knew from when I was quite young that my hearing wasn’t right, but doctors kept telling her that there wasn’t anything wrong. She was proper pissed off about it.
I’m 49 now, and for the last ten years the tinnitus is starting to degrade the level at which I can pick up what people are saying. Cannot pick out conversations in a noisy room.
Some days are better than others, but as it’s a condition I’ve had all my life, I have ways to cope with it.
Are you dehydrated or have you had a cold?Any sufferers on here and if so do you have any good tips for managing it? Well, coping with it because I know there’s no cure. Mine seems to have worsened recently.