I got a response back from Neuromod this morning. It came back from an Audiogram Review email address. There was not much information in the email other than saying we look forward to seeing you at your appointment in November.I sent in my audiogram last night. This audiogram was taken within the last year. Based on their criteria I should be fine. I have no loss up to 3kHz then a slow drop up to 8kHz which my left ear is at 45 dB loss and right is around 40 dB loss. I would be considered to have mild/moderate loss. Though I feel my tinnitus is so loud it masks the upper range. I will post here if I hear anything back.
That's pretty vague. If I were you I would get them to state that they see nothing in the audiogram that would reject you (which isn't necessarily an auto-approval, just NOT an auto-reject).I got a response back from Neuromod this morning. It came back from an Audiogram Review email address. There was not much information in the email other than saying we look forward to seeing you at your appointment in November.
I'm a little hopeless but I think we should wait longer.How's everybody feeling with the new Lenire, and the information so far provided? Myself, I am not feeling at all confident but I suppose it's early days.
I saw a comment on Facebook. Somebody has been using Lenire for 2 months and reports zero effect :-(
I still think the majority of people will get some kind of reduction from this.How's everybody feeling with the new Lenire, and the information so far provided? Myself, I am not feeling at all confident but I suppose it's early days.
I saw a comment on Facebook. Somebody has been using Lenire for 2 months and reports zero effect :-(
She actually is saying hers has been worse but she mentioned that they told her that would probably happen in the beginning. She also mentioned that they said it won't work for everybody, unfortunately she might fall in that small percentage that doesn't get any or much help.How's everybody feeling with the new Lenire, and the information so far provided? Myself, I am not feeling at all confident but I suppose it's early days.
I saw a comment on Facebook. Somebody has been using Lenire for 2 months and reports zero effect :-(
Do you know what was the cause of their tinnitus?I saw a comment on Facebook. Somebody has been using Lenire for 2 months and reports zero effect :-(
Markku, how was the conference/expo?@Hazel, @Liz Windsor and @Steve are confirmed to be attending the networking event, the conference, and the expo. I believe @Candy may attend as well, not confirmed though.
We'll also have a booth, this time for both the conference and the expo (last year we only had a booth for the expo).
Here's our thread about it:
2019 Tinnitus Expo in London on 14 September
We may be crossing paths with Neuromod and having a chat
I'm with you on that sister. My comfort level of spending what will be a lot of money on travel (I live just to the left of the ends of the earth) will be much assuaged by seeing a little data. Certainly the write up given in Tinnitus Talk makes it sound like the study structure itself is pretty solid, so if the results are anything like what has been suggested I am going to open up my wallet and hope for some relief.So I would assume it will be a good 2-3 months minimum before the publication of the trial data.
I look forward to that and will be more likely to go ahead with trying Lenire after.
I attached a photo of the Neuromod stand. Nothing new, same info as you can read on their website, etc.Markku, how was the conference/expo?
Anything interesting to come from Neuromod?
I didn't ask them about the A2 trial I'm afraid.I'm with you on that sister. My comfort level of spending what will be a lot of money on travel (I live just to the left of the ends of the earth) will be much assuaged by seeing a little data. Certainly the write up given in Tinnitus Talk makes it sound like the study structure itself is pretty solid, so if the results are anything like what has been suggested I am going to open up my wallet and hope for some relief.
Is there any suggestion that their Stage A2 data will ever be released?
18 weeks, not 12 weeks? A surprise for me.I had my six week review and device update. The treatment is going to last 18 weeks, so there'll be another update to the parameters end of October.
They defined an 18-week period?I had my six week review and device update. The treatment is going to last 18 weeks, so there'll be another update to the parameters end of October.
She said it's likely to be more effective and they are learning all the time. I didn't enquire beyond that.Did they say why the treatment will last 18 weeks? Is it the same for all patients?
Did they have new information about the efficacy of the treatment on other patients?
My interpretation is that they on an ad-hoc basis have asked some people who didn't get a significant benefit to continue using the device. But we cannot know if those people ultimately benefited or not.She said it's likely to be more effective and they are learning all the time. I didn't enquire beyond that.
Do they change the timings @BigNick? Mine's on Friday.I had my six week review and device update. The treatment is going to last 18 weeks, so there'll be another update to the parameters end of October.
How is your tinnitus lately at the 6 week checkpoint? Is your tinnitus now better than it was before starting the treatment?Do they change the timings @BigNick? Mine's on Friday.
That's awesome news. Maybe it'll be of help to do it a fourth time, or maybe even indefinitely until the tinnitus is basically gone? That would be amazing.She said it's likely to be more effective and they are learning all the time. I didn't enquire beyond that.
Yes, definitely better, still sucks tho!How is your tinnitus lately at the 6 week checkpoint? Is your tinnitus now better than it was before starting the treatment?