8 months since onset & mornings still my hardest.Waking up to not working & not the life I lived still throws me.Hugs to all who feel same.
ErikaS
Member From Pennsylvania, USAProfile posts Postings About
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In ears still vibrating when laying down. Night and morning. Worse when I put my head down/blood rush to head. Any input appreciated.
I dove into DNRS, neural reprocessing/retraining, & limbic system impairment this weekend & my eyes have been opened…
Did the intratympanic dexamethasone help
When I lay down for bed I hear vibration in ear. When I wake up its not there, but when I move around (get blood moving) it comes back.
With my T, I don't just hear sound(s) where my HL is. It's like all neural sound flood gates opened & I can hear it all in a quiet room.
I normally have 3-4 consistent sounds & a known level of sensitivity. Now, sensitivity is up w/ changing sounds. Is this normal w/ a spike?
In my worst spike/setback since onset. I think bad reaction to muscle relaxer. Hopefully it calms down in a few days ;(
Would even a little wax up against an eardrum cause T to be more sensitive and/or louder?
Just had a fleeting T that temp. knocked out my reactive high crap in R ear & only sound was the soft fleeting T. Pick that pathway, brain!
ACRN beeps with freq. set between 10.5-12k hz notably turn down my reactive high freq. tone(s) while listening...
Does anyone with fluctuating T / T that changes find that the acoustics of a room alone can affect how you hear it? Weird I know, thus is T.
Exhausted and depressed. I would do anything/take anything to lessen my ultra high frequency reactive shit.
Hi @ErikaS , I just wanted to come by to officially say hello :) I've also been dealing with multi-tonal, reactive tinnitus for over six months (not to mention hyperacusis...) & can completely relate to feeling worn out & depressed after all this time!
Even though T & R are still their crappy selves, since getting back from Cancun, my distortions are better/barely there. So odd.
Hi Erika,
You are still in the early days. I do hope everything improves for you and you are once again T free before any real treatments/cure come.
All I want to do is sit and watch TV without the reactive electric crap/tones turning up in my ears.
Almost home from our trip away. T is a bit irritated, need quiet but not looking forward to hard reality.
Hi all, day 5 in Cancun! Ears are much more tolerable here than home & I have been around so much more sound. Wearing protection off and on.
Have you noticed any improvements yet from your treatments Erika?
Thoughts plz.. Could .25mg of Ativan/daily not allow reactivity/overall improvement? I didn't think at low dose but maybe wrong.
I wish unilateral sudden loss equaled unilateral tinnitus. My left ear has no damage, yet it has the loudest tone and has up to 3 tones.
Tinnitus: A condition in which a thousand and one things can make it instantly worse, but not one thing makes it instantly better.
Two of my BFs from out of town surprised me with a weekend visit. Yesterday was the 1st day in so long that I didn't let T take priority..
6 1/2 months in and rain on my rooftop still aggravates my reactivity at 12k hz and up the same as it did 2-3 months in. Ugh ;(
If my ears can hear it, my T sounds will most likely change/react to it. Anyone else relate?
How are you today?
I will have 1-3 ok days where I push positivity, become hopeful, then mentally crash the following 1-3 days. This is so mentally taxing :'(
How are you doing
Did laundry, went to grocery store & Target, walked the pup, cleaned the shower, bathed the pup, now watching some TV. T did not win today! -
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