Does anybody else suffer with Tinnitu... - Fibromyalgia Acti...
Does anybody else suffer with Tinnitus? I started with it about 3 years ago. It always seems worse when I have a fibro flare.
i have for as long as i can remember, its always worse the more tired or stressed i am xxx
Thanks for a quick reply you two,
it took my doc ages to diagnose tinnitus because it wasn't a ringing noise he said it couldn't be. I went to see an audio specialist and he said it was he said any continual noise can be tinnitus even hearing voices. So that pleased me the voices have a name, so do the bells, buzzing whooshes and whistles.
Hi I too have had this for years and yes when I am ill it goes into overdrive drives me nuts so I tend to put on music to try and reduce the noises.
Hugs Ruby xx
P.S Mine is whistling as we speak lol
Me too, had it for years, definitelty worse when I flare but flaming annoying the rest of the time too. Its 24/7 for me so I have learnt to ignore it to an extent but I hate never having silence
yes bacaolca it drives me potty i find going to bed is worse i cant tune it out so i put on audio books ( harry potter) of course this helps me get to relax going to sleep is hard enough.
Me too. I've either got a dirty big chinook helicopter in my head or a lorry with it's engine running in my head.