Would You Recommend TMS for Me?

Beste

Member
Author
Mar 3, 2016
409
Tinnitus Since
02/16/2016
Cause of Tinnitus
Benzo/Clonazepam, Stress
Hello,

It's been almost one month since I got tinnitus. My tinnitus changes volumes and does not seem to go anywhere soon. Do you guys recommend TMS for me at this stage? Or is it too soon?
 
Hello,

It's been almost one month since I got tinnitus. My tinnitus changes volumes and does not seem to go anywhere soon. Do you guys recommend TMS for me at this stage? Or is it too soon?
Transcranial magnetic stimulation? Where would you get it? Do you think it helps tinnitus?
 
Transcranial magnetic stimulation? Where would you get it? Do you think it helps tinnitus?
I've spoken with a TMS specialist in my country Turkey and he said this is only way I may help with T. They tested TMS on 2500 people and got great success on 1800. Just in case I'm new to T, I just wonder if it works on me. He says how sooner it is better it gets.
 
@Beste
Speaking from experience: I wouldn't do it. At least not after a month.
A month is pretty much nothing in terms of T. You still got a lot time to get better.
My first "normal" T got a lot better after a year. Even with hearing loss. (I assume you have normal hearing so your chances are even better)

(r)TMS. You will find my (very negative) rTMS experience/report somewhere on the board here. I dont want to repeat it every time because im a very unique case and already had multiple extreme T before doing it, so it was kind of last resort thing for me.

I wouldn't believe in the numbers your specialist is giving you. And "great success" seems very sugarcoated.
Theres another study (its linked in some threads where I posted my experience) and it says the 50% of the people who did had a partial reflief for about 6months or more. Thats all.

And not to forget, these numbers don't mention the people who got worse from rTMS (like me). This therapy is pretty blunt. It will stress your brain and auditory cortex.
I still regret it every day and I have much hate for the TRI doctors which performed this and didn' really advise me on the risks of this treatment. The german TRI just cared for lab results, they didn't even do loreta EEG scans like they do at the Brai²n clinic. Seems they just use brute force on the brain and hope for the best. Thats the German Tinntius Research Initiative.

So in your case, you dont have extreme T and you're just a month in. Keep away from it. (Dont forget that its pretty expensive if you have to pay it yourself)
 

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