Tinnitus and Hyperacusis: Hello all, I am new... - Tinnitus UK

Tinnitus UK

10,732 members5,466 posts

Tinnitus and Hyperacusis

SyntaxError profile image
7 Replies

Hello all,

I am new to this forum and would like to share my experience to see if anybody has had anything similar.

Before the tinnitus and hyperacusis arrived I was having severe impacted wisdom tooth pain on my lower right part of my mouth. After taking penicillin and a bunch of ibuprofen for a week the pain had gone away.

I took various x-rays at different locations since my local dentist was closed and I was just trying to find answers as soon as possible.

One day after eating an extremely hot spicy dish of ramen I experienced some hearing loss on my left ear. Now, I didn't think much of it and went to sleep. This was on June 22nd of this year. June 23rd, a Saturday morning I woke up with an extremely loud seashell swooshing sound on my left ear. I freaked out and after 9 hours of it not going away I went to the ER. I was prescribed prednisone which is a steroid for 5 days 60mg daily. Within 8 - 10 days of hell, the swooshing sound had gone away. However, within the 4th day I was experiencing pressure and sensitivity on my right ear and then Hyperacusis came into play. That swooshing sound also changed into a variety of different rings and it ended up been a low ringing sound on my left ear.

At times, within the 12th day or so I would try and find that sound but it felt as if the ringing completely went away. The only thing bothering me was the H at the moment. Fast forward to July 16th, I woke up last week Monday morning with ringing in both ears and H. The H was just as bad as I initially got it and I didn't have ringing in both ears until now.

I'm scheduled to hopefully extract my two lower impacted wisdom teeth out this following Wednesday and I hope that shows some relief but so far I've gone to the ER and ENT specialist and haven't gotten a straight forward answer.

My nose is congested and I was told to do nasal rinse and spray and within two days of doing that my T and H came into play which was July 16th.

I'm not sure what's causing the T and H as I still have to go to a neurologists and need some more blood work but has anybody had T and H from impacted wisdom teeth problems?

I can provide more information if anyone wants to know about it.

Written by
SyntaxError profile image
SyntaxError
To view profiles and participate in discussions please or .
Read more about...
7 Replies

Hi - I have had both T and H for a few years. I did have all my impacted wisdom teeth out many years/ decades ago aged 19 but the T & H only started a few years ago so for me there’s unlikely to be a connection. I’ve recently had a full vestibular work up (ugh) for this and vertigo. Nothing at all was wrong with my ears or vestibular system apart from minor hearing loss and a structural abnormality on my jugular - discovered by ENT - which he feels explains the pulsatile tinnitus at least.

So very recently I’ve learnt that I have herniated discs in my neck and was reading up and learned that neck arthritis and degenerative disc disease can cause both T & H. I think this is the case for me and steroids for post viral asthma didn’t make any difference to mine.

I do have autoimmune disease though so I think these are partly to blame as well.

SyntaxError profile image
SyntaxError in reply to

Yes, I've read about discs being a cause on T & H as well. What kind of steroids did you take?

Also, what kind of autoimmune disease do you have?

in reply toSyntaxError

Sjögren’s Syndrome and Hashimoto’s.

SyntaxError profile image
SyntaxError in reply to

Sorry to hear that. I hope we all feel better soon. Do you know what test were done in order to diagnose you of those?

in reply toSyntaxError

Hashimoto’s is diagnosed by blood tests - antibodies and thyroid hormone levels. Sjögren’s is often very hard to diagnose and is either in your autoimmune antibodies or in your salivary glands - which have to be biopsied for diagnosis if it isn’t in your blood -along with very dry eyes, mouth, IBS, joint and nerve pain and chronic fatigue.

NicTinnitus profile image
NicTinnitus

Hello and welcome to the British Tinnitus Association forum SyntaxError. Do feel free to ask any questions, I hope that you find this a helpful and supportive place to help you manage your tinnitus.

We have some resources that you might like to check out in addition to our home here:

tinnitus.org.uk

- especially tinnitus.org.uk/hyperacusis and tinnitus.org.uk/tinnitus-an... where you will see jaw problems - which includes dental issues - can frequently trigger tinnitus

takeontinnitus.co.uk

Helpline 0800 018 0527 (Monday-Friday 9am-5pm) (outside the UK you can call +44 (0)114 250 9922)

Warmest wishes

Nic (BTA Communications Manager and Forum Administrator)

SyntaxError profile image
SyntaxError in reply toNicTinnitus

Thank you so much for the helpful information.

Not what you're looking for?

You may also like...

Tinnitus/Hyperacusis

After having T after a concert in around 2000 I have managed to cope with it very much in the...
Gemlord profile image

SEVERE TINNITUS AND HYPERACUSIS

3 months ago my life changed. My manageable T became severe along with H. I posted for help on this...
lifeseeker profile image

Tinnitus and Hyperacusis

Hi I posted on here recently about my increase in tinnitus. I also have Hyperacusis . Does...

Hyperacusis, reactive tinnitus

As the title says my tinnitus worsens if there is noise around (reactive). On top this I have...
Alfonso42 profile image

Tinnitus gone (for 2hours) the sound of silence!

I have had Tinnitus and Hyperacusis since Nov 2019, I am resigned to having this forever and do my...

Moderation team

See all
TinnitusUKInes profile image
TinnitusUKInesAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.