tinnitus: Just trying to figure out if there is a... - Thyroid UK

Thyroid UK

141,182 members166,423 posts

tinnitus

tinthy profile image
14 Replies

Just trying to figure out if there is a connection between thyroid & tinnitus. I was diagnosed with a thyroid problem 2 yrs ago and prescribed 50mcg Levothyroxine , about 4 months later the tinnitus started. Doctor said it was just a coincidence . I have been tested to see what could have caused tinnitus and was told i have a collapsed ear drum but I have always had this. So why now. It is without doubt one of the worst conditions and all you get told is you need to learn how to deal with it. Thanks for that docs. It seems a lot of you out there also have had similar experiences. My question is why is someone not doing something about this awful condition.

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

The NHS is useless at treating chronic conditions; they are geared towards treating injuries however. It costs money to manage chronic conditions: GPs get an "allowance" per patient from the council. Anything more they spend on you comes out of their profits.

Also, different conditions are worth funding points. The point system does not correlate with the degree to which the chronic condition debilitates you. So some diseases are worth zero points. Thyroid disease is a low value disease, while hypertension is the highest value diseases, or it was last time i checked.

So if you have hypertension you will be managed more efficiently than if you have Hashimoto's for example.

Anyhow i have had tinnitus since 2012. I have Hashi's and P anaemia. It got better for a while on b12 injections but for the last year it has been really bad again.

Charlotte1234 profile image
Charlotte1234 in reply to

Hi :)

I have been having strange neurological symptoms for 8 months now - awaiting a neuro appointment. I have developed tinnitus, pins and needles in my hands, cold hands and feet, 2 episodes of vertigo and muscle twitching all over my body. My B12 was 380 and ferritin 32.

Does any of this relate to PA or any of your symptoms? X

Hello tinthy,

Soon after starting levothyroxine 4 years ago, I felt some psychological changes in my head and behaviour. Some changes were positive but I also suffered vertigo for about a month and then sudden dizzy spells and tinnitus on and off ever since. I am convinced it is all related with starting thyroid meds and other thyroid issues.

flower007

tinthy profile image
tinthy in reply to

Hi, Flower007 , Yes its too much of a coincidence that a lot of people have both.

ROMM53 profile image
ROMM53

Tinnitus can be a sign of hypothyroidism or a sign of under treated hypothyroidism.

Could you tell us how much ? Levothyroxine you take, how you feel generally and could you post your most recent thyroid function test results so we can see if you are optimally replaced? Thanks 😀

tinthy profile image
tinthy in reply toROMM53

Hi, I take 50mcg a day , so quite a low dose. couldn't tell you my latest results at the moment. But i also take Naproxen for a back problem at the moment and this also is on the list of suspects . Trying to lose some wight too but not having much luck there either.

ROMM53 profile image
ROMM53 in reply totinthy

Good idea to always ask for a copy of your thyroid blood results, for your own records.

You could ring your GP surgery and ask for a copy of your last TFTs. You may have to pay a small charge but it is a perfectly legitimate request. Post the results with ranges on here for advice. 😊

helvella profile image
helvellaAdministrator

tinthy,

Have a read here:

healthunlocked.com/thyroidu...

greygoose profile image
greygoose

You are probably low in magnesium - most people are because the soil is depleted, and being hypo makes deficiencies worse because of absorbtion issues. I have had tinnitus for many, many years - long before l was diagnosed and started levo. But I firmly believe that, not only have I been hypo since l was a small child, but that I have also had magnesium deficiency for most of my life.

Since I started supplementing with magnesium about a year ago, the tinnitus has diminished considerably and is mostly unnoticable now - unless I listen for it. :)

in reply togreygoose

I wouldn't listen for it. You may hear it again.

greygoose profile image
greygoose in reply to

lol Yes, know what you mean. But when I read this thread, I thought, Ooo! I haven't heard it for a while, Wonder if it's still there... And it is, but the volume is very low. So, I can live with that. :)

tinthy profile image
tinthy in reply togreygoose

Thanks for that I will look into it. :)

greygoose profile image
greygoose in reply totinthy

:)

Klagh profile image
Klagh

DEFINITE connection. I had VERY BAD tinnitus for years while on porcine thyroid. I have Hashimoto's. Now I'm on cytomel only. I supplement with bovine adrenal glandulars (8 caps daily). I still need more T3 (it can be very difficult getting it in the States). HOWEVER, my tinnitus has reduced dramatically.

Not what you're looking for?

You may also like...

Tinnitus Revisited

I thought that I would pass this along. It will not match everyone’s problem, but it might help a...
LAHs profile image

thyroid and tinnitus

I was diagnosed with under active thyroid about 9 years ago and take 75 mg levothyroxine daily. I...
Rockyport profile image

Tinnitus after RAI

I am just curious and throwing this out there! Did anyone else have onset of tinnitus after RAI...
Shaf3938 profile image

Hearing loss, tinnitus and vertigo... my journey update

I just wanted to update this forum on the latest outcomes I have experienced since joining last...
FIT2018 profile image

Hashimotos, labyrinthitis and tinnitus

Hi I had thyroidectomy 41 years ago and been on Levothyroxine since. Had (for the first time ever)...
Lottyplum profile image

Moderation team

See all
Jaydee1507 profile image
Jaydee1507Administrator
PurpleNails profile image
PurpleNailsAdministrator
SlowDragon profile image
SlowDragonAdministrator

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.