1. What becomes of oxygen we breathe?
Oxygen plays a role in a variety of cellular processes, including sterol and fatty acid synthesis, and is critical for oxidative phosphorylation (8). Thus, it is not surprising that changes in oxygen availability can have drastic effects on the function of a cell. Several studies indicate that low-oxygen conditions can induce apoptosis (76, 86). This occurs when oxygen levels decrease to at, or below, 0.5% (anoxia). When oxygen levels are 0.5–3% (hypoxia), cells do not undergo apoptosis. Instead, hypoxia activates a variety of cellular events that can ultimately lead to cell survival depending on the light associated with the hypoxia signal.
The reduction of oxygen to water by mitochondrial respiration may represent the integration of two essential functions for aerobic life: coupling to oxidative phosphorylation for bioenergetic benefits and elimination of the essential ROS substrate for maintaining genomic stability. This may surprise you.
Low oxygen in mammals triggers signal-transduction pathways involved in both cell death and survival. For example, anoxia activates proapoptotic BCL-2 proteins and caspases to initiate apoptosis.
The adaptive cellular events that occur in response to hypoxia are mediated largely by the transcription factor hypoxia-inducible factor-1 (HIF-1).
HIF-1 induces the expression of multiple antiapoptotic BCL-2 proteins to promote cell survival. Interestingly hypoxia increases production of mitochondrial reactive oxygen species (ROS), which serve as signaling molecules to activate HIF-1. This link shows you ROS is not always a bad situation inside a mitochondria. Inside mitochondria, oxygen role has changed because of how experiments have shown us how redox chemistry is really run. It is now seen to give rise to copious amounts of "diffusible reactive oxygen species" known as DRS/DROS.
Implications? In the field of enzymology, murburn is a term coined by Kelath Manoj that explains the catalytic mechanism of certain redox-active proteins. The term describes the equilibrium among molecules, unbound ions and radicals inside a cell simultaneously. This process signifies a process of "mild unrestricted redox catalysis".
Murburn is abstracted from "mured burning" (connoting a "closed burning", an oxidative process), and implies equilibriums involving diffusible reactive oxygen species (DRS/DROS/ROS) created inside of mitochondria. Though akin to the oxygen assisted combustion of fuel, unlike the flames produced in the open burning process, the biological reaction occurs in enclosed premises, is mild and generates heat alone without flames. The heat is used by water and by melanin. Heat increases melanin's ability to be an electrical conductor in mammals. Exogenous dark skin melanin uses this and endogenous melanin makes use of this in uncoupled haplotypes. Such a reaction can also incur selective and specific electron/moiety transfers quantum mechanically that are not acounted for in biochemistry books.
Further, though burning is a reaction that usually involves oxygen (aerobic process), "burning flames" produced by anoxic oxidants are also well-known. Therefore, the enzymes working via murburn scheme (aerobic or anaerobic) can now be called murzymes and the region around the biomolecule where the DRS interacts with the final ‘substrate’ is called ‘murzone’. Melanin and water are key chemicals allowing murzones to operate.

2. Since oxygen is paramagnetic, what are the effects of oxygen with cell phone use?
Cells phones generate magnetic fields. Paramagnetic atoms are drawn to magnetic fields.
What is the magnetic field strength of a cell phone?
The magnetic field strength transmitted from the antenna of the majority of all cellular phones, about 7.5–10 cm from the antenna, is well over 2000 nT. When a cellular phone is held to the user's head, it emits a magnetic EMFs of 1000 to 6000 nT.
Cell phones not only expose the user to radiofrequency (RF), but also to a magnetic field (MF) of extremely low frequency (ELF: 1 Hz—100 kHz according to the ICNIRP. The ICNIRP tries to minize the physics. So you need to realize all tech use close to your body makes you HYPOXIC.

3. The electromagnetic pollution of technology is produced by either the RF signal envelope or the hardware itself (e.g., battery management). Consumption of electrical current produces Magnetic Fields in the vicinity of the wires, which can also have a significant impact on ELF exposure. This is why wired earpods are a problem. Different hardware architectures may cause different exposure among cell phone models. Magnetic fields emitted from wirless earpods are WORSE. This means they create more magnetic fields and this will decrease your cerumen production and this affects melanin in the integument and in the endogenous regions of the cochlea.
The nature of the cell phone ELF signal has been described.
A. Tuor M, Ebert S, Schuderer J, Kuster N. Assessment of ELF exposure from GSM handsets and development of an optimized RF/ELF exposure setup for studies of human volunteers: Final report. Zurich: IT IS FoundationBAG Reg (2005). No. 2.23. 02.-18/02.001778.
B. Gosselin M, Kühn S, Kuster N. Experimental and numerical assessment of low-frequency current distributions from UMTS and GSM mobile phones. Phys Med Biol (2013) 58:8339–57. doi:10.1088/0031-9155/58/23/8339
The second generation Global System for Mobile Communications (2G GSM) uses eight time slots. The basic frame has a period of 4.61 ms sending information every 0.57 ms. Then the signal envelope creates a 217 Hz EMF component. Every 26th frame is omitted in GSM protocols, resulting in a 8.3 Hz EMF component in the output signal. The time frame used in the third-generation Universal Mobile Telecommunications System (3G UMTS) is 10 ms creating a 100 Hz component. This field has huge implications for mitochondrial oscillation. A 50 Hz component follows from the 20 ms speech frame (except for the main power supply). This is why the NTP toxicity study results so interested me and this is when tinnitus and brain tumor risk seemed to begin to rise. It was a clue to me to look deeper into melanin biology.

4. Non ionizing radiation has implications for melanin biology and the spocrine glands of man. Both are controlled by melanin creation and destruction.
Adey WR. Tissue interactions with non-ionizing electromagnetic fields. Physiol Rev (1981) 61(2):435–514. doi:10.1152/physrev.1981.61.2.435
Cell phones expose significant parts of the human head and other parts of the body to ELF MF classified by the IARC as a 2B carcinogen. The MF values measured in the LCD “off” mode were slightly higher compared to the LCD “on”. However, the MF in both modes were comparable to the background. The standby MF were approximately 20- to 60-fold lower compared to active phone use (listening and speaking mode). For the 2G, the highest RMS values were detected in the listening mode, front side (70.03 µT) within the range of 5 Hz–200 Hz and in the speaking mode, front side (12.67 µT) within the range of 120 Hz—10 kHz. For 3G, the highest RMS values were detected in the speaking mode, front side (16.82 µT) within the first range and the listening mode, front side (12.31 µT).
The 3G cell phones consistently emitted a lower ELF MF as compared to the 2G ones. The measured and also simulated ELF MF were comparable with MF values that have been reported to induce biological and health effects, including those related to carcinogenesis.
Another detrimental effect can occur under chronic ELF exposure even in standby mode (airplane mode). Therefore, it should be recommended to not keep cell phone on the body or in its proximity at any time. We also do not recommend charging the phones while using them as far as the charger can increase the exposure to MF ELF in the standby mode. According to our simulations, about 35 cm distance between body surface and a cell phone is needed to ensure the ELF MF values recommended by the EUROPAEM.
This was all derived from Front. Phys., 27 January 2023
Sec. Biophysics Volume 11 - 2023 | doi.org

5. As a neurosurgeon I have to be aware of changes to magnetic field strength emission by tech gear used around the CNS and PNS.
5G systems emit higher magnetic fields than 2G phones.
The magnetic fields warming is the major organic consequence of the electromagnetic fields radiofrequency radiation emitted from 5G network installation especially at a very high frequencies.
Why is this a big deal in neurosurgery?

6. My team has to be aware of sources of external magnetic fields.
Potential magnetic field interference can come from cordless drills, cell phones, electronic tablet devices, metal detectors and earbuds/headphones. In fact, in 2018, the FDA noted, “it is reasonable to assume that a ventriculoperitoneal shunt valve that is manipulated by a hand-held magnetic tool may also be vulnerable to other external magnetic sources (in the environment),” noting that more research is needed on the subject. These shunts are now used in neurosurgery. I have noticed that people with new phones in 5G cities have to have their shunt valves checked more frequently. Many come in with new symptoms of shunt valve slippage.
This makes me wonder what is happening to the melanin sheets inside their heads at the same time.
To date, FDA studies done by INDUSTRY conclude that magnetic handheld devices are safe as long as they are kept at least two inches away from the shunt valve, although the agency notes that differences in body physiology and magnet characteristics may affect results. The FDA advises that hydrocephalus patients using earbuds or a cell phone should use these on the opposite ear from where the shunt is located. This warning concerns me as a surgeon.
I know the FDA has not been relaible partner in COVID so why would I trust my patients with their data on magnetic fields from tech gear?
This is why I look at retinas and inside ear canals of all my patients now. I'm looking for nnEMF damage.

7. What else concerns me? My team now takes and makes note of internal magnets. What am I talking about?
Magnetic hearing devices (such as cochlear implants and bone conduction and middle ear hearing devices) may interact with VP shunts if the two are placed too close to each other. In this case, magnetic field interference could be avoided by putting the programmable CSF shunt valve on the contralateral side of a hearing device.
In a study of magnetic field strength of four bone conduction hearing devices and interaction with programmable shunt valves concluded it was safe to use the devices together but recommended at least a 5 mm distance in the case of one hearing device. Again this study makes me wonder what is going on internally with melanin sheets in the brain and sense organs. I can see the effects on the skin around these devices. Most have a lack of melanin associated with them. People who use ora rings often have less melanin on the finer they wear it on.
Why else am I concerned? Moreover, the FDA recommends checking shunt valve settings after placement or adjustment of other devices that contain magnets to ensure that the setting has not changed.
For patients requiring bilateral hearing implants after acoustic neuroma resections, the implanting physician should position the CSF shunt valve and the ipsilateral hearing implant at a maximum distance from one another to avoid issues with magnets and shunts for hydrocephalus, according to the FDA. This advice tells me there is clearly a biological effect of non ionizing radiation from tech use.

8. An MRI does not use ionizing radiation but it has a strong external magnet. Did you know that MRIs may pose a risk to certain shunts’ valve settings?
Before a patient has an MRI, they should tell the MRI technologist about any programmable shunts. Their doctor should arrange to have their shunt setting checked after the MRI, and reprogrammed if necessary.
Free radicals are magnetic inside of mitochondria because of their unpaired electrons. This tells me all these devices create an alien magnetic footprint inside of patients.

9. Neurosurgeons know that this is a problem because during informed consent we talk about these things with patients. Unintended magnetic shunt valve changes can lead to serious neurological issues.
Signs of shunt malfunction may include headache, lethargy, vomiting, vision changes and behavioral changes. Symptom severity depends on how much the setting changed, for how long and how sensitive the patient is to pressure changes. Overdrainage symptoms can include severe headache, nausea, vomiting and seizures and underdrainage may cause a recurrence of hydrocephalus symptoms.
Parents and caregivers of children with magnetic CSF shunt systems should be told of possible non ionizing electromagnetic interference. They need to keep children away from magnets in older TVs and older video games, encourage use of cell phones on the opposite side of the head from the shunt, know symptoms of magnetic interference and how to get help.

10. In three bench studies done in labs, and not on people, Codman Certas® Plus programmable valves demonstrated no setting changes from common household magnets in over 2,200 exposures at close proximity (<5 mm).
Life is not lived in a lab. Humans now use technology at close proximity to their heads and bodies.
Any unintended CSF shunt valve changes should be reported through the FDA MedWatch Program or the FDA Medical Product Safety Network (Med Sun) if your facility participates in the program.
The agency advises including the following information with any report:
The suspected distance of programmable shunt from the magnetic source
Identification of suspected magnetic source(s)
Severity of patient symptoms
Change in valve setting value from intended setting
Manufacturer and brand of the CSF shunt or brand of hearing device
Patient age, gender, underlying diagnosis for shunt
Other medical devices in region of shunt (for example cochlear implant)
Device evaluation post-explant, if available.
The agency also advises vaccine injury reporting and this has not been accurate at all and I make sure my patients know the track history of the FDA and their reporting metrics.

11. I also inform all my patients that use of these devices comes with contraindications. For example, these devices are contraindicated in patients receiving anticoagulants or known to have a bleeding diathesis. Why? Many people do not know that clotting and drugs that effect clotting work via electric and magnetic field generation. Therefore, we need to use older shunts that are not programmable.

12. I also avoid their use in cases of neurodegeneration for similar reasons. Protein folding is affected by electric and magnetic field manipulation.
I have recently begun to ask if patients use Starlink because I think there is a risk of magnetic manipulation of their systems as well. I do the same thing with use of Teslas. This is now part of my decentralized informed consent.

13. In April of 2018, I did a webinar to give my members a clue what they should expect from extensuve uses of 4G-6G technology and their potential risks. Today, in 2024 I have updated my consent forms to include NEURALINK/TESLA use in my consent forms on aneurysms, AVMs, and cavernomas. I now believe the science is being published in biophysics journals to show that disease perturbation is feasible via a disrupted Auger effect in cerebral blood vessels where melanopsin, neuropsin, melatonin, and nitric oxide all reside.  I have told neurosurgeons to stay vigilant for observation of these problems in VP shunts, vagal nerve stimualtors, pain pumps and with cochlea implants.
In these patients I look for Auger effect anomilies.
I look in their eyes at the iris, retina, and in their ear canals. I look at their skin close to their tech devices. I am looking for color change and the type of ear wax they have to assess the risk. I also sometimes will smell their ear wax.
Sounds bizarre until you know why I do it.

14. Ear wax is not what it seems from a decentralized quantum perspective. Ear wax is not wax. It is exfoliated skin and secreations from your apocrine glands that uses the Auger effect. Decentralized science teaches us something centralized science does not know. Cerumin operates using the Auger effect to protect us from electromagnetic waves we are not used to. This cerumen substance is a combination of skin cells that have fallen off from inside of the ear, bits of hair and secretions from the ceruminous glands in the outer ear canal. Keratinocytes undergo apoptosis as they go from the basal membrane of the skin to the surface. DNA becomes more exposed to the environment as the skin cells die. The DNA has electromagnetic protective effects ---> Auger effect.

15. Did you know that earwax has a circadian basis tied to latitude and mitochondrial biology? Most people are ignorant of these things. At Kruse Longevity Center we make it our business to know these things because we begin where allopathic and functional medicine end in their understanding of human biology.
There are two different types of earwax: wet and dry.
A. Dry earwax is usually crumbly and lighter in color from tan to light grey. People that have North-Eastern Asian and Native American ancestry often have this type of earwax due to mtDNA thermodynamics
B. Wet earwax is sticky and yellow to brown in color and can even have a nasty odor. This earwax is normally found in people that are more likely to have European or African ancestry. See the video below for the data.
youtube.com

16. The primary purpose of earwax to a decentralized clincian is to protect your ear canal and eardrum from foreign materials and foreign electromagnetic waves seen in Earth 4.6 billion year history.
For example cloudy days allow more cosmic radiation into the ionosphere. This means life has to have an answer for the electromagnetic insult. In water, whales are mammals that have an exquisite hearing mechanism that uses cerumen because they use echolocation. This is how cerumen protects them. web-static-aws.seas.harvard.edu

17. So why do I look in places where melanin is to get a clue? Stress or anxiety can actually increase or decrease your earwax production. Light stress and sound stress can do it.  The glands in the ear that assist secreting wax are a class of glands called the apocrine glands. The human female breast is an apocrine gland. This is why some women cannot breast feed because their gland do not make secretions. These glands are the same glands that are responsible for your apocrine glands to create sweat. The leptin melanocortin pathways control these glands.
This is why a return of sweat creation is part of the Leptin Rx I wrote 20 years ago. When you cannot sweat properly or control the flow of kerotinocytes to apoptosis properly via ultra weak UV light release during mitochondrial respiration you get diseases like diabetes. 
Go back and look at the Leptin Rx closely.  These diseases are associated with melanin loss and too much entropy gain from nnEMF exposure.

18. How does the biophysics operate, Uncle Jack?
The polarizing force that protects us begins with DNA in skin cells that are in the process of dying as they come to the surface in mammals.  This polarizing force is formed from the Debeye force in biophysics.  DNA has massive Debeye forces due to its AMO physics.  Debye forces are caused by the interactions between permanent dipoles and other atoms/molecules, which results in the formation of induced dipoles. For example, an induced dipole can be formed from the repulsive forces between electrons that belong to a molecule in a cell and they induce a permanent dipole.  When ROS/RNS is generated by an exogenous EMF people forget these chemicals have unpaired electrons and these electrons repell one another.  Think Pauli exclusion principle.  The same thing happens in RNA/DNA.

19. The DNA double helix provides a beautiful and easy to understand example of how intermolecular forces combine to determine the AMO physics that determine macromolecular structure. A simple consideration of hydrogen bonds, dispersion forces, and ionic interactions explains why DNA is most stable as a double helix.  DNA and RNA are naturally polarized molecules containing large electric dipole moments due to the presence of a significant number of charged atoms at neutral pH.  Charge can be induced or rediced by light frequencies.  DNA is massively negatively charged because of the presence of phosphate groups in nucleotides. The phosphate backbone of DNA is negatively charged, which is due to the presence of bonds created between the phosphorus and oxygen atoms. I covered all this science in the Cameron Borg podcast released 48 hours ago on YouTube.
A Russian scientist named Gariaev has experimentally documented the DNA has an ability to use sound and light to repair DNA damage. The research carried out by Gariaev and Vladimir Poponin, has showed that DNA has a special ability to attract photons causing them to slide along the helical molecule of DNA instead of along a linear pathway because of its electric and magnetic polarizations of the base pairs inside the double helix.  This exists because of the Debeye forces present in DNA atomic molecular organization.
This finding tells us that DNA likely has the capacity to bend light endogenously when it is created by mtDNA metabolism or melanin release.  It also hints at how DNA works as a sunscreen in the skin in degenerating keratinocytes using the Auger effect. 
My members have learned about these ideas long ago.  This mimics gravitational lensing of light and draws photons to DNA and bends the biophoton field around itself for messaging or fidelity.  This idea  is buried in Montagnier water experiment in 2009.  I mentioned this to Huberman in the Tetragrammaton podcast only see his eyes glaze over. This mechanism is likely how holograms,  consciousness, transgenerational epigentics occurs quantum mechanically in cells.  Light programs DNA our mitchondrial DNA programs.

20. HOW?
According to the laws of physics, the motion of electrical charges in a polarized molecule produces a magnetic field at 90 degrees and results in the emission of electromagnetic waves. Thus, each DNA can radiate various types of electromagnetic waves depending on the nature of its interaction with biological material like DNA and RNA.  Thes waves DNA emits can be absorbed by melanin and water.
So this is why if you are a tech abuser you will get a different informed consent form from me and why I will show interest in your skin, ears, and retina as a neurosurgeon.