I'm sorry but that's drivel. There are loads of reasons why someone could be rejected - this isn't because I know about Neuromod's policies or have any knowledge of audiology / tinnitus beyond anyone else on this forum, but come on, think man. Impacted earwax, otosclerosis, psychological trauma / crisis, acoustic neuroma, probably more.
Yes, that's the only reason I've heard of yet for rejecting someone, if you select less than 3 months in the questionnaire. I'm not saying that's the only criteria, just the only one I've read.
I've been guessing that the US release would be offset a little less than a year from Europe. I have no basis to that guess, but it's just my hunch, as Neuromod hasn't issued any guidance that I'm aware of.
I agree, I find it rather insulting that someone who became aware of a treatment because of Tinnitus Talk would then tell Tinnitus Talk to fuck off and not return the favor.
I think the concern is this:
Don't worry about that. There might be a few people like that but based on my many years of hanging around Tinnitus Talk the vast majority here feels a deep kinship with their fellow sufferers and will do everything to report back, myself included. There will be no shortage of credible user reports.
The people who have had their initial assessment have nothing to report yet. They would be bombarded by loads of questions that they cannot yet answer. I am sure we will all have more information when the device starts to be used.
@ruud1boy thanks for answering.
Unfortunately Regensburg is an eight hour drive for me, Dublin is closer (I'm from the Netherlands).
You think this is the concern or you're trying to manufacture the concern?
No one has the device yet so there is nothing to report yet. Also once people start using it it may take many weeks/months for any change to occur so it's going to be a while.
People in the trials signed NDAs.
Though I respect people wanting to remain anonymous, I can't help but cringe that people are refusing to post their experiences on their own accounts. The fact that they are afraid of Neuromod finding it or somehow jinxing themselves by talking about on an anonymous forum it is so cringe.
Why don't you concentrate on posting your audiograms and your history with PRP and Dr. Shim, which you have been teasing about for months. And stop "cock-blocking" our hopes over here!!
Aluminum foil hats don't even block EMF. You need a Faraday cage which has to be grounded.Though I respect people wanting to remain anonymous, I can't help but cringe that people are refusing to post their experiences on their own accounts. The fact that they are afraid of Neuromod finding it or somehow jinxing themselves by talking about on an anonymous forum it is so cringe.
They don't want to post themselves, but tell @Markku to post for them because apparently that cancels out the jinxing voodoo?
We are already anonymous on here, why are people going through two hoops? Soon people will be buying VPNs and creating new accounts to post.
This is actually funny / sad.
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But hang on - you're the person who has been saying that any talk of Neuromod discouraging any public posting by members was nonsense. Yet the evidence is now pretty clear that several members who have decided to buy Lenire are reluctant to talk directly about their experiences for fear of "jeopardizing their relationship" with Neuromod.
...or these people do not feel comfortable to post on a forum in general. Lots of people "lurk" on forums and don't post.
Not posting publicly because of a fear of Neuromod finding out or "jinxing" is illogical and irrational.
Or it could be that it takes a week or two to take effect or for some up to 6 weeks.
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