Tinnnitus in PD: Hi all This is a link to... - Cure Parkinson's

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Tinnnitus in PD

Ianfrizell profile image
7 Replies

Hi all

This is a link to my vlog about tinnitus in PD.

youtu.be/WawM71HvUww

Cheers,

Ian

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Ianfrizell profile image
Ianfrizell
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7 Replies
RS313 profile image
RS313

I actually was diagnosed with this before parkinsons and had to get steroid injections.After i found out i had parkinsons and started meds it went away and never had to get shots after that.

Rhyothemis profile image
Rhyothemis

My father had tinnitus; he was diagnosed with Menier's, and then a few other things, and finally, a few years and many doctor visits later, Multiple System Atrophy.

They also say that neuropathy is not a symptom of MSA, but they mean that it is not useful diagnostically, though I think I read that 40% of MSA patients experience neuropathy. It was the symptom my father mentioned most often and presumably had the biggest impact on his quality of life.

~

I have tinnitus, though fairly mild; it is only really bothersome in the evening for some reason. I noticed after doing auricular TENS for vagal nerve stimulation on my right ear that the tinnitus is gone on that side. {I don't have PD}

GBAMIGOD profile image
GBAMIGOD

Hi. So is Tinnitus in PD curable or treatable?How do you deal with this.Once in a while I get cracking sound in my ears,especially when I wake up in the mornings.I take a benzo for sleeping as well,and I have read that the wearing off of benzo meds could cause tinnitus as a side effect.Due to this,I am not sure if my tinnitus is a symptom of my PD,or a side effect of benzo.For people with PD,who experience tinnitus,what kind of sound do they experience in the ears?

Ianfrizell profile image
Ianfrizell in reply to GBAMIGOD

I believe tinnitus is not treatable, but some people have said that it has lessened when they started taking PD meds...

My tinnitus is a high pitched tone which varies in volume, apparently randomly!

Dtwolfe63 profile image
Dtwolfe63

I am 55 and was diagnosed with PD about a year ago. I was unaware about some of the signs... I lost my sense of smell almost entirely about 6 years ago. Around that same time I began having tinnitus and it has gotten much worse as time goes by. It can be quite bothersome and often causes migraine.

horsplay profile image
horsplay

I'm t0 and have pd and tinnitus. I never considered the two were related.

M1tz1 profile image
M1tz1

I don't have PD, Ian, though I have some symptoms in common. I started with tinnitus many, many years ago but always felt that it was caused by exposure to my son's playing the bagpipes!

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