I am a rebel in healthcare and I know it. I personally love Dr. Google because it tells me which of my patients are fully engaged and care and who want aggressive input by me instead of just applying conservative paradigm algorithms. These patients help me identify who really needs me and who really just wants conventional advice. It really is a time saver for a quantum mitochondriac clinician. I want my patients to be collectors of information based upon their conditions and come to me with it so we can go over it and I can discuss with them why I agree with it and why I may not. I trust my patients to make the decision when they hear both sides of the argument. It seems many of my fellow MD’s don’t have my perspective and look at Dr. Google as a “problem.” I don’t feel this way at all. Here is the account of another MD. I’d like to hear your comments below out these two perspectives.
Dr. Homere said, “In a world of cyberchondria and a web polluted with unlimited medical data, patients are searching their symptoms, diagnoses and treatment options even before going to a physician. Nowadays, at least one third of patients go on the Internet for self-diagnosis — or, often, self-misdiagnosis.
After searching for a symptom, understanding e-medical facts is not as simple as reading hotel amenities or reviewing a pizza place. This paradigm introduces new patient behaviors that physicians are not prepared to deal with in medical school, nor during training years.
Data showed that more than fifty percent of patients do not share with their doctor that they searched the topic on the Internet. How do patients react if the physician gives them different information than what they read on the web? Do they trust him and ignore their research? Or would they go to another physician thinking this one is wrong and outdated?
Unfortunately, this is now a fact — we cannot fight it anymore or control it. All we can do as physicians is to be aware of it and understand patient’s fears and thoughts, after they have been “manipulated” by the Internet.
Physicians are compelled to make the effort of not only following valuable medical information in peer-reviewed journals and professional societies sites, but also they need to be aware of the set of data available for the public, data often put together by non-doctors. This will make doctors understand better patient’s concerns and try to build on or correct “common e-knowledge” when sometimes this knowledge is wrong, inaccurate, or does not apply to the patient’s actual situation.
On another note, since we cannot convince our patients not to go on the Internet as they “can’t help it.” Providers should not be shy to direct their patients on how to use this tool, by recommending accurate keywords that apply to their disease and suggest specific procedures to look up on video sharing platforms.
With millennials seeking more medical care, social media revolution and Internet-mania will further impact patient behavior. Providers have non-conformal tasks: to be aware of these new trends and influences, in order to integrate them in their practices and reinforce patient-doctor relationships; we mention in this article following public data from unconfirmed medical sources and counseling patients for accurate web searches.”
Who do you agree with it? Do you have a different take on this topic ? I’d like to hear your ideas below. Share it, if you feel compelled
Homere Al Moutran is an otolaryngologist in NYC. He can be reached on LinkedIn and Twitter @DrHom_NY. I am Dr. Jack Kruse and I can be found on Linkedin and on twitter @DrJackKruse or at www.jackkruse.com
You need to watch the last 5 minutes of the video above and makes sure you get the impact of Dr. Doug Wallace’s statment of where disease really comes from. Now I want you to fully understand how coupling works in humans using light. The coupler humans use is called an ‘ interactive controller’ . It turns out our non coding DNA is the seat of epigenetic control over our genome and the knobs of the system are light frequencies. When a system loses negative feedback control you uncouple cycles from one another. Let me give you a clear example of a LOSS of negative feedback control: in this type of coupling mechanism two components of the system have opposite effects on one another. Consider prey and predator as a couple. Consumption of prey by predator has a positive effect on the eater, and a negative on on the eaten animal. The negative effect on predators on prey prevents uncontrolled growth of the predator’s population. This stabilizes the population sizes of both groups when they are coupled. Blue light is a major uncoupler of mitochondrial biology because in natural sunlight blue light is ALWAYS coupled to the 42% of IR-A light present in sunlight.
Those artificial blue lights are killers for mice and men because they are never found with red light or with UVA light in a proper diurnal frequency as this cites shows……….http://www.pnas.org/content/112/21/6748.abstract
Blue light from artificial bulbs and LED screens uncouple electron and protons spin from ECT flow speeds to release massive amounts of light while also radically altering free radical signaling. If you re-watch my Vermont 2017 talk you will see a slide called a Jablonski diagram where I tell the audience that all of life is explained on this one slide. It turns out the first thing that is made in a cell as an excited electron falls to the ground state is a free radical. That free radical is made when the excited electron releases its energy in the form of light. This signal is quantized and it allows the epigenetic programs to get their marching orders to tell DNA and the cell how it should react. How does this happen? Free radicals are capapble of changing the size and shape of all the matter in DNA and they can affect the proteins that compress DNA called chromatin. These radicals also have massive effects on methylation and histone modification which sets the stage for how DNA works via electromagnetic signaling. Light is the force carrier for the electromagnetic force and we’ve known in biophysics literature for quite some time now that DNA emits electromagnetic signals to water that surrounds it by proton tunneling in the hydrogen bonded water networks. That water is absorbs this radiation and records a record of the process so that other areas in the nucleus gets the information on how DNA signal will proceed. One of the key areas in the nucleus that needs this data is the nucleolus. This is a place that makes our many types of ribosomes that make protein once the cell deciphers the light message of the cell’s circular dynamic couples. People maybe shocked to know that in 2015 the NASA Ames research laboratory has published papers showing that pyrimidine is fully programmable using UV light. For those of you who don’t know pyrimidine is one of the bases in human DNA. It is also one of the organic molecules normally found on meteorites and asteroids in our solar system. They found that under the right environment UV light could transform pyrimidine buried in ice into uracil, cytosine, and thymine which are the only base pairs used in both DNA and RNA on Earth. Think about this for a moment. The base is found in cold ice in space. This is how far back cold thermogenesis really reaches my patrons. I’ve never mentioned this anywhere before. UV light alone with cold can do this to a base that is criticial in human DNA. What else do I want you to know right now? All cells normally release ELF-UV light as they go on about living. In any stressed situation human cells release EVEN MORE ELF-UV light. This tells you that as the environment varies so does the amount of UV light. It implies that the change in the environment is the stimulus to change DNA base pairs. What might this means to a mitochondriac? What should it mean to molecular biology? Free radicial signaling in a mitochondria is what makes a cell release a specific amount and frequency of UV light.
There is EVEN more to this story for the curious mind. UV light is the only part of the visible spectrum of light that is capapble of changing the structure in a cell via ionization. It can do it electrically and magnetically. This means what ever electrifies and magnetizes DNA is the real controllr of life. Did you know that UV light changes the magnetic fields within bases of DNA and RNA? Did you know that UV light can effect the electrons in the ring structure of all the bases in RNA and DNA to alters their electric fields and their excited state? Do you think this is how DNA transfers information and energy about its double helix? Does DNA and RNA use water to communicate to the mitochondria in a bidirectional fashion? Might mitochondrion and DNA be the most important coupled system in biology? It appears that water is how these systems communicate with one another.
How does this happen thermodynamically? Anytime anything with structure changes its size or shape it changes is ability to handle energy. How does this transfer to what we know about mitochondrion today?
At the same time the respiratory proteins stretch out because the size of the mitochondria changes and gets larger and this engages the allometric scaling laws of metabolism. This is a power law in mathematics. In Nick Lane’s latest book, “The Vital Question”, he mentions it in there. Every one Angstrom increase in the distance between the respiratory proteins slows electron and proton tunneling by a FACTOR of ten. Anytime you slow electron chain transport (ECT) you are closer to death because illness show up. This is exactly what Wallace said in the last 5 minutes of the video above isn’t it? Do we know this is true experimentally when we stop ECT completely? Yes we do. Cynanide stops ECT hence, it kills us. When ECT is not stopped completely, just slowed down, we get phenotypical changes in tissues due to energy flux modulation. This energy flux change cause size and shape changes in RNA and DNA to alter the non coding apsects of our genome that are made up mostly of viral DNA/RNA, and this results in humans getting mitochondrial diseases. This is how the light we allow our mitochondrion to sense to give us the reality we experience. In this way, health is simply the slowest form of death we create on the inner mitochondrial membrane. When these respiratory proteins stretch out in dimension and lenght we call this increasing heteroplasmy rate. We normally want our heteroplasmy rate low. Keeping a lid on ELF-UV light release is the key to keeping our genome as quiet as possible. The more DNA expression we have the closer we get to some disease.
Because of the false narratives in dietary dogma, most people think food dominates functionality in biology. A mitochondriac knows that we build optimal function and health first, when we alter the size and shape of things in a mitochondrion to shape the thermodynamics to make function meet optimal form and marry to appearences we observe.
We’re a colony of two genomes, nuclear and mitochondrial. DNA methylation is the nuclear on/off switch for genes. Histone modification is the volume controler of the nuclear genome, while the long non coding RNA is the amplifier in our system. Small RNA called miRNA is the key that alters mitochondrial respiratory proteins. Ultimately in this symphony, the mitochondrial genome is the “conductor” who controls the flow of photoelectric power from the sun to power up each knob to create an opus we call life.
We’re all masterpieces of epigenetics and not our genes that code for only proteins. Every cell has the exact same code in it but every cell has a unique epigenetic markings that is unique and made by the local mitochondrion in our different tissues. These markings sculpt our long non coding RNA and use miRNA as its colony of ants to carry out the changes to our nucleic acids that our environment dictates. These things change segments of nucleic acids and our mitochondrial genome in each tissue to change our pattern of methylation, alter acetylation of histones, which tweak the genome’s information capability just by changing the flow of energy through a bacteria we stole millions of years below. As mitochondrial heteroplasmy rises in our “stolen circular genome”, the telomeres shorten in the nuclear genome. Forces of nature changes the gears of biology in every living cell. Push and pull forces buried into light waves give life the action to move in both genomes to explain fully. what life is at the most fundamental levels of nature.
What is the linkage to these coupling events? Sunlight builds redox potential and buries it in water a mitochondrion makes as we burn fat. A cell cannot make a lot of water using glucose as a fuel source. This is why glucose metabolism never made bacteria or archea complex for 3 billion years. The loss of redox power is the linkage seen in loss of ciracdian coupling in cells because of an increase of heteroplasmy of mitochondria in tissues. The redox potential is the critical linkage of the first two biologic cycle of energy conservation, namely ubiquitin and the cell cycle. These two processes are control by the light information harvested in the central retinal pathways and the skin to couple to growth and metabolism cycles in the entire organism. The coupling of the mitochondria to the nucleus how light controls biology at all levels. This is precisely how light from our surfaces couples cell growth via ubiquitin rates via our surfaces.
Consider the quote above. Now I want you to consider another part of light therapy that “experts” are telling you is completely safe. That light is nnEMF in the RF/microwave ranges. This also alters free radical signaling and makes cells emit massive amounts of ELF-UV that is fully capable of changing your DNA code. Do you think this is perfectly safe?
Blue and red light in the solar frequencies are like predator and prey in the analogy I made above……..they each perfectly balance one another in nature. The life we lead today creates and imbalance in this system. Today, modern artificial light has 4 times the amount of blue and no red really present to speak of. This destroys the coupled cycle of every cell in the body and cause mitochondrial havoc. This is why I said in the Vermont video I believe cancer is a blue light disease. Why is this idea so critical to understand? Because ubiquitin is the major stabilizer of negative feedback control on cell growth and it works via melanopsin and blockade of blue light post sunset. Blue light destroys melatonin at night to ruin the tight relatioship of the respiratory proteins. Melatonin is made during AM sunlight but is active when the sun has set. Melanopsin is the key opsin of the central retinal pathways and tells melatonin when to act to help optimize mitochondrial biogenesis. The actor of ubiquitin is LIGHT frequencies that affect long segment non coding RNA and miRNA!!!! That is what affects epigenetic expresion of the human genome that controls expression. I also believe that blue light has a massive effect on small coding RNA segments called miRNA’s to lead to cancers. This is especially true of melanoma in humans. This explains why light is the most powerful drug we have. When you uncouple blue light from all the other frequencies you create an asymmetry that can be used to help or hurt you based upon the use of that blue light and it leads to some mitochondrial disease phenotype.
Patrons you got a mouthful today……………ponder it all.
