Frequency Therapeutics — Hearing Loss Regeneration

Why is it called fx-322? I have several Masons in my family and some of the Masonic regalia features a skull and cross bones with the number 322 under it. I wonder if Masons run Frequency Therapeutics and they named it that to glorify their fraternity.
TRT shill detected, isn't it funny when Pawel Jastreboff himself makes an account on TinnitusTalk pretending to make the good guys look like they are part of the conspiracy.
 
TRT shill detected, isn't it funny when Pawel Jastreboff himself makes an account on TinnitusTalk pretending to make the good guys look like they are part of the conspiracy.
I'm no shill. I think TRT is worthless crap too. My only hope of curing my tinnitus at this point is the fx-322, or whatever Decibel Therapeutics is working on. That or my own neuro plasticity kicking in and re-wiring my auditory cortex. I've known about the Masons for almost 2 decades, I'm just throwing stuff out there because I make connections. I could care less if Masons run these pharmaceutical corporations or not. They aren't going to make me sell my soul to the devil, they just want my money, and if they can cure my tinnitus, they can have all of my money.
 
I'm no shill. I think TRT is worthless crap too. My only hope of curing my tinnitus at this point is the fx-322, or whatever Decibel Therapeutics is working on. That or my own neuro plasticity kicking in and re-wiring my auditory cortex. I've known about the Masons for almost 2 decades, I'm just throwing stuff out there because I make connections. I could care less if Masons run these pharmaceutical corporations or not. They aren't going to make me sell my soul to the devil, they just want my money, and if they can cure my tinnitus, they can have all of my money.
i dont beleive in anything super natural, but yeah MPP MPP MPP
 
i dont beleive in anything super natural, but yeah MPP MPP MPP
dude, I've been following the forums on this site for about 2 months and I agree with every post you've made. I'm not pushing any TRT or other false cures. My primary hope lies in just getting over it, which I don't think is going to happen because every morning when I wake up and realize I still have this monstrous disease it hits me like a ton of bricks. I sincerely believe our best bet currently is fx-322, and maybe the Susan Shore device. I have e-mailed Susan Shore and asked her to drop some information and she hasn't yet. But Constrast, I am on your side. I too despise these fakers pushing fake cures. I think they need to be humiliated and punished for their greed and taking advantage of people like us that are suffering.
 
Frequency Therapeutics isn't the only game in town. It's just the furthest along the track. I've found about five projects along very similar lines. I haven't been keeping score so please don't ask me to list them. My point? If it's not fx-322 it will be something else.

My other point is this. It seems like a soul-destroying thing waiting for a cure. Have you tried mindfulness training (https://www.tinnitus.org.uk/mindfulness-for-tinnitus), yoga, cbt,... Stuff that may not be a cure, but may help? I've done mindulness training in other contexts and it's a powerful thing. Apologies if this makes you roll your eyes. It's well-intentioned. All the best.

Anyway, trt = testosterone replacement therapy? Edit: Should have searched first. Got it.
 
I have called them. I am from Maine and willing to fly. The reason you might not get a response from the email that is on the flyer, is because the person is on vacation until August 1st. I called the phone number in which case on his voicemail he just says to call the ENT number. I have done that and they have been very responsive. They were just waiting for some doctor who is doing the study to also come back from vacation. He has now. My hearing loss is over 8khz. The receptionist still wants me to send the audiograms for the Dr to review to see if I qualify. I will be doing that soon and have the receptionists email to send them to. I am not going to ask lots of questions because I feel like too many things are unknown. If I get in, then great. If not I live near Boston and hopefully Decibal has something soon. I hope soon that everyone has a quiet night sleep.
THE G O A T
 
I have called them. I am from Maine and willing to fly. The reason you might not get a response from the email that is on the flyer, is because the person is on vacation until August 1st. I called the phone number in which case on his voicemail he just says to call the ENT number. I have done that and they have been very responsive. They were just waiting for some doctor who is doing the study to also come back from vacation. He has now. My hearing loss is over 8khz. The receptionist still wants me to send the audiograms for the Dr to review to see if I qualify. I will be doing that soon and have the receptionists email to send them to. I am not going to ask lots of questions because I feel like too many things are unknown. If I get in, then great. If not I live near Boston and hopefully Decibal has something soon. I hope soon that everyone has a quiet night sleep.
@TomBradyGOAT just to clarify, in my opinion you are the GOAT because you're effectively trying to get UHF hearing loss into Frequency TX trial. :):)
 
I called and spoke to the the receptionist as I'm in Houston TX ,and thats only about a 2 hour drive for me to location. They want me to send my Audiogram. I have a slight 20 db dip a 2k, but most of my hearing loss is over 8K. So I probably wont qualify , but i'm going to send it anyways. Will keep everyone posted.
 
I have been quietly watching, I called and sent audio grams. They said my hearing loss is not significant enough. Mine dips at 6k to 30db and 8k to 50db. Again as other stated an my personal opinion ents are morons. They dont care about higher frequency loss they think you dont need it. So my guess is those of us with high frequency loss will be last in line even when this gets released. Sorry for the news.
 
If there's money to make, we'll be able to get it, no doubt! Even if we only suffer from high frequency loss.

But all costs will be ours. Health insurance will not cover it for (high frequency-related) tinnitus only.
 
I have been quietly watching, I called and sent audio grams. They said my hearing loss is not significant enough. Mine dips at 6k to 30db and 8k to 50db. Again as other stated an my personal opinion ents are morons. They dont care about higher frequency loss they think you dont need it. So my guess is those of us with high frequency loss will be last in line even when this gets released. Sorry for the news.
Are you serious?? That's nuts!
 
If there's money to make, we'll be able to get it, no doubt! Even if we only suffer from high frequency loss.
Really, really hoping you're right, but I'm not so sure...I think it would depend on how regulated the treatment is.
 
Wait, as in they have already administered the treatment to two people?
Simply means they administered them to the trial which in phase 2 could still be placebo. The biggest issue they have right now is finding the correct paitences willing to participate. That will determine how long this takes ultimately.
 
Really, really hoping you're right, but I'm not so sure...I think it would depend on how regulated the treatment is.
Speculation at this point is only that. They (and us) simply need people willing to try it. So instead of that lets focus on getting people aware of it. So they can hopefully get into trial. I know I was willing to fly there. This could be a problem for many people. A funding account or something to help people who want to but cant affoard to would be the best thing, I think any of us could do an promoting awareness.
 
As much as I want to blame medical industry greed conspiracies for the delay of some cure, I also realize that I have not power over this and all I can do is be patient to become a patient. Just live as well as you can muster and be strong and soon we may have a cure and this will be our pre-Heaven. Just please march on and call out for a cure.
 
Hmmmm. I wouldn't believe what the receptionist says. And if the ent's are casually passing on information like that, it's strictly amateur hour. Also, they are testing a hearing loss treatment, not a treatment for tinnitus. They are going to be selecting participants with common types of hearing loss. Easy to measure and easy to compare against large populations.
 

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