I’ve found that delivering high doses of 1070nm near infrared light directly to the scalp increases ATP and blood flow to the brain. This in turn can slow, stop and reverse neurodegenerative processes including the ones that are associated with Parki so sons and Alzheimer’s and ALS. I designed a device to provide this stimulation that is now being marketed under the brand names Nauradiant and Neuromatrix. I provide consultation and am conducting g ongoing research to improve outcomes. UVB and near infrared light energy are aming the most direct ways to enhance brain health and prevent c of price and physical decline. Seek professional guidance to optimize results.
marvinberman@quietmindfdn.org
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mhberman
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"I’ve found that delivering high doses of 1070nm near infrared light directly to the scalp increases ATP and blood flow to the brain."
Please provide the methodology and scientific processes that YOU personally used to make the determination that "ATP and blood flow" increase due to the use of near infrared light.
Please do not quote someone elses so called studies. I want to see YOUR work.
People who stand to profit from the gadgets they invent invariably hype their effectiveness.
I wouldn't have commented except you said, "This in turn can slow, stop and reverse neurodegenerative processes including the ones that are associated with Parkinsons and Alzheimer’s and ALS." which is dubious, at best.
I completely agree that without real evidence no one should take claims veryseriously. I do however have published research showing significant improvement from use of the 1070nm transcranial photobiomodulation for Dementia and Parkinson’s. The Neuradiant unit I designed, now marketed by Neuronic and improved on by Sanjay Manchanda with the Neuromatrix, available through Quietmind Associates, was used in a 2023 pilot study on Long covid brain fog. The results were significant t in that all subjects’ symptoms were reversed to baseline or better than before they got infected.
I’m happy to share the papers, email me at Info@quietmindfdn.org
near infrared wavelengths from 700-1200 will stimulate ATP synthesis, the 1070 does it better than 800 based on laser and led studies done at UT-Arlington in Hanli Liu’s lab. Our research was more clinically oriented toward showing improvement in cognition in folks with Alzheimer’s and Parkinson’s.
Upon reviewing the Neuronic website (or maybe I was accidentally on the Neurotic website), I am now even more skeptical.
Here's the main disclaimer at the bottom of the primary web page:
Neuronic helmets are therapeutic infrared lamps that emit energy in the near-infrared spectrum. They are designed for use on the head to promote energy and relaxation. The helmets are intended for general wellness purposes and should be used as directed in the user manual.
Product Disclaimer: Neuronic devices are not intended for the diagnosis or prevention of any medical condition. Neuronic does not provide medical advice. Neuronic products are designed to support wellness and should not replace professional medical guidance. Always consult a qualified healthcare professional for your health or any specific medical concerns.
Our product cannot guarantee the same effects on each individual. There are no known side effects of using our device. We advise you to consult a medical professional and conduct your own research before using our devices. The information presented on our website is not a substitute to the advice of a licensed healthcare practitioner.
And another disclaimer from a so-called collegiate study of the product linked on the Neuronic website:
Neuronic devices are not medical devices under any jurisdiction and are not intended to diagnose, treat, cure or prevent ant disease. These statements have not been evaluated by the Food and Drug Administration.
SO HERE IS MY OFFER: As a Parkinson Disease sufferer, I will conduct a thorough and unbiased test of a new Neuradiant or Neuronic helmet (whatever the official name is) that you will provide free of charge, and I will commit to provide a concise and robust experience report to the HEALTH UNLOCKED members, touting the benefits and improvements I experience for the Parkinson Disease symptoms I suffer from, based on the use of "your" product. In the event that I experience "all" of the improvements both you and Neuronic claim, then after my personal and honest study has ended, I will keep and pay the current and fair retail price of the product.
If no benefits are experienced, then I will equally report out the findings to the members and I will return the product in its original packaging.
DEAL ??????????
I do have one question regarding Neuronics first and main disclaimer -- how did they measure the "wellness" of said individuals who have used the product ??? Wellness is very much a subjective feeling and observation correct?? Very hard to measure and very much a potential for a placebo effect.
Also, please respond to my question of how "improved blood flow"was measured. This one really has me curious.
You are welcome to extend your offer to the folks at Neuronic as I’m no longer operationally involved and haven’t been for over a year. My research is more in the objective scienctific domain. We do offer a single subject study program for 1-2 years. We provide both the photobiomodulation and neurofeedback equipment and all testing and supervision services. The fee is $10,000 for one year and $15,000 for 2 years.
This is a single subject open label study and we’d submit the results for publication as a case study.
If you send me your email address I’ll forward some papers that relate to using photobiomodulation to improve Parkinson’s disease symptoms.
It is a simple matter to post your papers on the internet. Why have you not done so?
As to paying these large fees, I could not help but notice you could not be bothered to properly edit your original post for spelling. not about to sign up With someone who is so sloppy, not that I would have been tempted In any case. If you cannot be bothered two properly edit I see no reason why I should spend the time either.
I almost never comment in this space and am being reminded why. You can look up the papers on researchgate.com and pubmed. I don’t see a way to post papers here, do you?
I said: It is a simple matter to post your papers on the internet, Not Health unlocked.
If your papers are posted, why not provide links? Instead you are suggesting I search for papers on the subject matter, and then try to determine which ones are yours.
I offered to send them if you send me an email so I can attach them. There is no way to post attachments to these messages that I could find. All my papers are available by typing my name when you go to researchgate.
You seem by your other posts to be trying to make a serious effort to contribute so I’m responding without reacting to your astonishingly disrespectful prose style. If you want to engage in civil discourse please write back or better yet, I’m old enough (74) that I actually can enjoy talking on the phone
Okay I'll give you credit for trying, but do you mean to tell me you do not know how to post a link? Here is what I get when I search for your name on Researchgate:
if you look at our website Quietmindfdn.org we are S 501c3 nonprofit and work with people regardless of their ability to pay. The devices we promote we provide at discounted prices and folks can donate to our research fund and write off a portion of the device’s cost from their taxes.
Somebody’s getting rich by playing on others desperation, especially with these prices.
And rest assured, there will be some ill or unadvised individual out there who is not savvy to the vetting we apply to individuals like this on this website, and they will fall prey to this scam.
Your previous comment about “never responding in this space and now you are reminded why” alludes to the fact that you do not like to go through the rigid process of being scrutinized by a bunch of highly pessimistic Parkinsons sufferers, who by the way are very intent on protecting their own.
Your responses (just on this forum alone) are not passing the smell test. Wait, I have Parkinson’s and I can’t smell. In this case, then my eyes do not deceive me.
Not a model for studies with placebo group which this is not. The program is designed this way as it is not grant funded. it is an equipment fee and for exclusive use over the study period. Subjects can opt for ongoing support for $5000/year and we continue to collect data and supervise treatment.
is it possible that we have all been so wounded that we cannot accept that someone may actually be trying to help? I agree that the prices are high but it sounds like there are ways to participate with some kind of financial support . Can you please elaborate more on that?
We all struggle to cope with our earliest unresolved traumas resurfacing when our defenses weaken from age and infirmity. The cultural climate and sterility of the online experience make this all much harder to manage. The photobiomodulation unit we offer now can support 4 unique protocols at the same time. This allows 4 people to use the device in sequence. The protocols can be modified by the user with supervision in minutes. Everyone has to work out a treatment process that fits their available time, energy and resources. The consultation process either a competent consultant should result in a plan that optimizes results given what can be invested. We should stop throwing spaghetti at the wall and work with professionals who know the range of options and can support you having a long term recovery strategy. Peer support is absolute essential but not to replace clinically experienced professional consultation.
Thanks for that and it is damning. This person was trained in psychology and had his license revoked. No training relevant to Parkinson's. Lest there be any question of identity the person described at the link is affiliated with the same website as the poster here.
Sadly, I am that person and that debacle 15 years ago was the result of a political purge and isn’t related to my research. I hope you check out the research I did and that of my colleagues who worked with me. Google Paul Chazot chair of Pharmacology Durham University UK.
The research stands on its own. Check out the reviews on Trust Pilot under Neuronic or the Quietmind Foundation website.
Still waiting on a link to at least one of your research papers. Do you not know how to post a link?
If you do not know how to post a link you could post a citation, you know, title of the paper, name of the journal, authors, date, etc.
I went to your website and under research: ttps://quietmindfdn.org/research.html there was nothing other than a discussion of your own institutional research board.
Under resources at your website there were four papers discussing photo biomodulation for covid. That's good but that's not Parkinson's. quietmindfdn.org/resources....
I also see under the guise of participating in a research study an intranasal device for sale for $290: quietmindfdn.org/store/p21/...
Found this paper on treatment of dementia using near infrared: Transcranial Near Infrared Light Stimulations Improve Cognition in Patients with Dementiaquietmindfdn.org/uploads/2/...
Apparently this is the basis for asking patients to enroll in treatment under the guise of a "single patient trial" at a cost of $12,000 - $18,000. The study itself used patients with Alzheimer's and Parkinson's who had dementia, but fails to disclose how many patients with each condition were treated. This is a fail because without breaking out results separately for Parkinson's versus Alzheimer's we have no idea how Parkinson's patients actually did. The author of this post could have linked to this paper right up front and saved a whole lot of wasted time and effort
Ok thank you both. The most important thing to me is that we be willing to believe people have good intentions. And at the same time be willing to question everything too… including websites that claim to have absolute truth.
Rental is $500 a month and $150 for 45 min. Video consultation to review history and create an initial protocol. Rental fees are deducted from purchase.
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