So have you found anything that helps for tinnitus?
I'm asking because I have it all the time and gets worse right before my vertigo kicks in. I have vestbular migraines (migraines w/vertigo) & now have recently found out I most likely have Menier's. I've had vestbular migraines for over 15 yrs, my vertigo can come on at any time & in seconds super strong (so not good) or I can have it where it's managable & I can semi-function and can eat. When it hits really bad I'm done, stuck in one position & sick for hours. This last year started getting these other symptoms associated with Meniere's. I have to say I thought my vertigo was bad before, it was mild compared to now. Doc says I can have both .. just the news I wanted to hear. I wouldn't wish this on anyone!
I’m sorry....I haven’t. I got this from a MRI test of all things.
Anyway, at night I use a “lectrofan” sound device which helps sleep a tiny bit, but I can still hear my T everywhere, even outside. In the morning it is like a fire alarm in my head, then it usually calms down to a dentist drill for the day...sigh.
Hang in there....I’m sorry you are going through this. They can get a fake vaccine in less than a year, yet no solutions for tinnitus in the last 4 decades.
I know right? Well it's not important enough to scientist. They don't realize how loud it can be and can drive you crazy. With Meniere's my ear gets a "full" feeling and the more full it gets I loose more hearing and the ringing gets much louder, that's when I know any day the vertigo will hit. Just had an episode this past week, and still my head feels slightly dizzy. After the vertigo hits bad, the fullness slowly goes away, but not totally away, like a hint of it always stays. Eventually I will loose my hearing, have no idea how long that will be, and there's no cure and from what I have read not much in way of treatment, I already have the meds they use for them, don't work at all when it's bad. Surgery for it will take my hearing away, so I think doctors don't like that option unless your hearing is already impaired.
It doesn’t for me, I was up to 2500mg/day for a while....my urine glowed yellow. I do appreciate the kind suggestion though. :-)
So have you found anything that helps for tinnitus?
I'm asking because I have it all the time and gets worse right before my vertigo kicks in. I have vestbular migraines (migraines w/vertigo) & now have recently found out I most likely have Menier's. I've had vestbular migraines for over 15 yrs, my vertigo can come on at any time & in seconds super strong (so not good) or I can have it where it's managable & I can semi-function and can eat. When it hits really bad I'm done, stuck in one position & sick for hours. This last year started getting these other symptoms associated with Meniere's. I have to say I thought my vertigo was bad before, it was mild compared to now. Doc says I can have both .. just the news I wanted to hear. I wouldn't wish this on anyone!
I’m sorry....I haven’t. I got this from a MRI test of all things. Anyway, at night I use a “lectrofan” sound device which helps sleep a tiny bit, but I can still hear my T everywhere, even outside. In the morning it is like a fire alarm in my head, then it usually calms down to a dentist drill for the day...sigh.
Hang in there....I’m sorry you are going through this. They can get a fake vaccine in less than a year, yet no solutions for tinnitus in the last 4 decades.
I know right? Well it's not important enough to scientist. They don't realize how loud it can be and can drive you crazy. With Meniere's my ear gets a "full" feeling and the more full it gets I loose more hearing and the ringing gets much louder, that's when I know any day the vertigo will hit. Just had an episode this past week, and still my head feels slightly dizzy. After the vertigo hits bad, the fullness slowly goes away, but not totally away, like a hint of it always stays. Eventually I will loose my hearing, have no idea how long that will be, and there's no cure and from what I have read not much in way of treatment, I already have the meds they use for them, don't work at all when it's bad. Surgery for it will take my hearing away, so I think doctors don't like that option unless your hearing is already impaired.
Sorry this is not Q related, mods feel free to delete if too far off-topic...
That doesn't make my opinion invalid.
I'll feel the same way in a year or 10
That is true....with the amount of three-letter infiltrators here, I always check history’s....again, no offense.