I will let you know if I am accepted for treatment in November. From what I have read about Susan Shore's device she has had better results for people that had tinnitus for longer periods of time. I know it is a different device, but still the same concept.I wonder if Lenire will ever fix a person's tinnitus whose had it for longer than one year.
One of the test patients (Patricia) had had her tinnitus for 4-5 years and she had a complete recovery. You can see patient testimonials on this link: https://www.neuromoddevices.com/stories.I wonder if Lenire will ever fix a person's tinnitus whose had it for longer than one year.
Source?From what I have read about Susan Shore's device she has had better results for people that had tinnitus for longer periods of time. I know it is a different device, but still the same concept.
In the TENT-A2 trial (191 participants) people with tinnitus up to 10 years were included. (Source Inclusion Criteria: Subjective tinnitus more than 3 months and less than 10 years)The 500 sample trial had patients with tinnitus for up to 5 years.
Kind of discouraging that of all their participants there's only one where it went completely away. Maybe that's because they only had the device for 12 weeks though? Had they continued even longer maybe it would eventually disappear altogether?One of the test patients (Patricia) had had her tinnitus for 4-5 years and she had a complete recovery. You can see patient testimonials on this link: https://www.neuromoddevices.com/stories.
That's the most significant question we don't have an answer too: would continued use of the device reduce tinnitus further?Kind of discouraging that of all their participants there's only one where it went completely away. Maybe that's because they only had the device for 12 weeks though? Had they continued even longer maybe it would eventually disappear altogether?
I'm getting antsy about getting my hands on one of these devices as I've just hit two years and it's been bothering me more the past six months than it did the first year and a half. I didn't even look up tinnitus or seek out treatment until this year because it was mild enough that it didn't interfere with my life. Now it's all I think about.
I would assume so, simply because I recall one of the users here state their tinnitus didn't go away until two months AFTER treatment, and I believe they used their device for longer than three months. So, I'm trying to stay positive about it working, but I sure wish they had more testimonials from people who found complete relief instead of just symptom reduction.That's the most significant question we don't have an answer too: would continued use of the device reduce tinnitus further?
From the interview, the CEO said that it was a 3 months use because simply there had to be a start and end.
So this question is still up in the air.
That could be TOTALLY coincidental.I recall one of the users here state their tinnitus didn't go away until two months AFTER treatment, and I believe they used their device for longer than three months.
Tinnitus at a level of 1-3/10 is completely livable.I would assume so, simply because I recall one of the users here state their tinnitus didn't go away until two months AFTER treatment, and I believe they used their device for longer than three months. So, I'm trying to stay positive about it working, but I sure wish they had more testimonials from people who found complete relief instead of just symptom reduction.
That being said, I wouldn't hesitate to buy it once it becomes available because even a chance is better than nothing.
It was @kelpiemsp in reference to the device in Minnesota being used for 9 months and from what I gather they've had tinnitus prior to this their entire life.That could be TOTALLY coincidental.
One person sample size is not enough to draw any conclusions from.
Ah yes, thank you! And while the other person above said this could be totally coincidental, I hardly think so for someone who has had it for as long as @kelpiemsp. Obviously it's always possible, but very unlikely. So that's encouraging, even if it's only a sample size of one.It was @kelpiemsp in reference to the device in Minnesota being used for 9 months and from what I gather they've had tinnitus prior to this their entire life.
Did you ever even look at the clinical trial page? @Autumnly was even nice enough to post the info here for you, and you're still not getting it. The inclusion criteria for the trial was up to 10 years. The sample size of their trials are over 500, and clearly not everyone will have complete remission. That was never the claim, but that most will get some relief. It's no wonder your emoji looks all confused.That could be TOTALLY coincidental.
One person sample size is not enough to draw any conclusions from.
I watched a presentation from Susan Shore where she explains that. If you dig a bit, you'll find it.I want to see a cellular level explanation of exactly how this would work. If there is hyper activity in the DCN, I want to know why the hyperactivity is there and why electrically stimulating it with noise and shocks would fix that, and why the timing matters etc.
I have noticed that there is zero explanation for that.
Hi Valeri, I'm still doing okay. It's good to still see some familiar people here and hope you're doing well also.Good to see you again! Hope you're still doing ok!
It is an inherent assumption of the model. You would have to go back to neuromodulation theory, and we are discussing applied methods. It wouldn't make any sense to talk about it in that detail. But page two, paragraph one, bullet point three gives you a layman's example.I want to see a cellular level explanation of exactly how this would work. If there is hyper activity in the DCN, I want to know why the hyperactivity is there and why electrically stimulating it with noise and shocks would fix that, and why the timing matters etc.
I have noticed that there is zero explanation for that.
I want to see a cellular level explanation of exactly how this would work. If there is hyper activity in the DCN, I want to know why the hyperactivity is there and why electrically stimulating it with noise and shocks would fix that, and why the timing matters etc.
I have noticed that there is zero explanation for that.
It's the same concept Dr. Shore is working on, and she seems to have it down better than Neuromod. She explains some of it here in this interview with the ATA:I want to see a cellular level explanation of exactly how this would work. If there is hyper activity in the DCN, I want to know why the hyperactivity is there and why electrically stimulating it with noise and shocks would fix that, and why the timing matters etc.
I have noticed that there is zero explanation for that.
Progressively fade.@kelpiemsp
Did your sensitivity to sounds go away AFTER your treatment, or did it progressively fade step-by-step during each treatment session?
Well, with Neuromod's track record of communication I doubt we'll ever get one.I have noticed that there is zero explanation for that.
They cannot just communicate whenever they feel like it.Well, with Neuromod's track record of communication I doubt we'll ever get one.
The underlying mechanisms of how many medical things work are unknown. Antidepressants notoriously are not known how they work. I agree their conclusions are based on the results of the experiments rather than on understanding the mechanism.What I've been able to glean from all this is that the underlying mechanism is poorly understood to the point where they have to sort of fumble around via trial and error with the parameters. Now, if you read a research paper it will be all dressed up in scientific lingo but at the end of the day they don't really know whether it will work until they test it... i.e. trial and error.
Because of this, I really don't find the theoretical end of the equation to be what inspires confidence but rather the statistical results of the trials. The theory makes for an interesting intellectual exercise but no matter how rigorous the science, theory is still ultimately theory. It's a mental trap you can fall into where latch onto and dig deeper and deeper into a theory based on how rational it sounds only to discover that it simply doesn't work.
See the strange thing is, with Lenire this doesn't seem to be the case.Progressively fade.
That's how I feel about it, bimodal stimulation will work for a lot of people, but I think it's the 'first' treatment of it's kind that's 'poked it's head out of the ground first'.What I've been able to glean from all this is that the underlying mechanism is poorly understood to the point where they have to sort of fumble around via trial and error with the parameters. Now, if you read a research paper it will be all dressed up in scientific lingo but at the end of the day they don't really know whether it will work until they test it... i.e. trial and error.
Because of this, I really don't find the theoretical end of the equation to be what inspires confidence but rather the statistical results of the trials. The theory makes for an interesting intellectual exercise but no matter how rigorous the science, theory is still ultimately theory. It's a mental trap you can fall into where latch onto and dig deeper and deeper into a theory based on how rational it sounds only to discover that it simply doesn't work.
How did it get worse?I'm getting antsy about getting my hands on one of these devices as I've just hit two years and it's been bothering me more the past six months than it did the first year and a half. I didn't even look up tinnitus or seek out treatment until this year because it was mild enough that it didn't interfere with my life. Now it's all I think about.
Good question. I was exposed to some chemicals at my (now former) workplace and things just started going haywire in my body from there. I've had nerve pains in my head and all other sorts of stuff going wrong ever since. Then the tinnitus just started bugging me more. Since then I've had ear issues on and off for months and no ENT can see a reason for it. Test results show I have reactivated Epstein-Barr virus. Not sure if that's what giving me all these issues but I have not felt well in many months.How did it get worse?