True friendship is like fluorescence, it shines better when the situation darkens. It opens our mind to the possibilities of MAYBE



NEW BLOG OUT: Fluorescence is the emission of light by a substance that has absorbed light or other electromagnetic radiation. It is a form of luminescence. In most cases, the emitted light has a longer wavelength, and therefore lower energy, than the absorbed radiation. The most striking example of fluorescence occurs when the absorbed radiation is in the ultraviolet region of the spectrum, and thus invisible to the human eye, while the emitted light is in the visible region, which gives the fluorescent substance a distinct color that can be seen only when exposed to UV light. Fluorescent materials cease to glow nearly immediately when the radiation source stops, unlike phosphorescent materials, which continue to emit light for some time after.



Fluorescence has many practical applications, including mineralogy, gemology, medicine, chemical sensors (fluorescence spectroscopy), fluorescent labeling, dyes, biological detectors, cosmic-ray detection, and, most commonly, fluorescent lamps. Fluorescence also occurs frequently in nature in some minerals and in various biological states in many branches of the animal kingdom.



https://www.patreon.com/posts/24770650

 

Electromagnetic fields can activate voltage-gated calcium channels (VGCCs) via molecular resonance in the plasma membrane of cells. When electromagnetic fields activate these channels, large amounts of intracellular calcium (Ca2+) are produced. The amount produced is subject to the wave physics of the emitted light wave from the point source. If the wave is polarized this also changes the calcium efflux and its ionic resonance. Calcium is the key secondary messenger in cells for these antigens on the surface and they interact and react with RNS species like peroxynitrite (RNS radical).
This excess calcium within the cells produces a chain of free radical chemical reactions from the mitochondria which changes the physiology of the cell at a femtosecond basis. This leads to the production of a VARYING free radical signal that causes organizational chaos in the cell. That chaos is manifested by the disruption of the incident EMF that excites and activates the voltage-gated channels in the cell. A highly variable incident EMF with produce a highly variable ROS/RNS mitochondrial signal and this results in unpredictable biochemistry in the cell. This is associated with the production of chronic oxidative stressor chemicals in the living system that cannot be buffered by the normal quenching chemicals in cells. All of this results from an environment that produces an altered electric and magnetic field around an animal/human.
The chaotic free radical signal is capable of culminating in DNA damage and or the change in the plasma membrane to lead to pathologic symptoms and eventual disease.
The calcium efflux causes excess calcium directly in and around the cell and in its local environment. So with respect to RBCs, it also means that this effect of electric and magnetic fields will also affect the surface of the blood vessels. Peroxiredoxins are the key peripheral circadian controller that remove CpG Island from the fragmented DNA and mtDNA that enter the blood when nnEMF is destroying cellular biology. Tight control of RBC circadian cycles links RBC antigen clearance to the innate immune system via C4. RBC become more permeable to toxins in this case and as a result, the RBC ages faster and more antigens pass through the circulatory system. This is really what happens in all mold and biotoxin disease. It is not the mold or toxin that is critical in this case, it is REMOVAL of the nnEMF field that is critical to get right. Most of the clinician out there never get this advice to their patients or the public.
All of these mechanisms of nnEMF field exposure alter melanopsin biology in the blood and arteries to a chaotic release of nitric oxide (NO) within cells and in arteries to cause disease when it occurs chronically and affects mitochondrial function when other frequencies of sunlight are subtracted from this photic dance.
The increase of nitric oxide is a chameleon event in the blood plasma. Endothelial nitric oxide synthetase has a quantum superposition effect on sulfur atoms in the skin, arteries, blood, and gut to protect us from dangerous nitrogenous groups in these antigens.
This means that any pulsed or polarized non-native man-made electromagnetic signal can have a variable non-linear effect on sulfation and nitrosylation pathways in any of these organs. I covered this last night in my Feb 2019 webinar Q & A.
It can result in therapeutic effects or detrimental effects in the blood plasma depending upon the nnEMF stimulus. This will lead to highly variable chaotic mitochondrial energy flux and fidelity signal dynamics. This is very damaging to the matrix and directly affects what biochemistry can or cannot occur. This is one reason why non-thermal electromagnetic fields (PEMF) are increasingly used in medical therapies, but they are being used without any proper understanding of how they truly operate.
Today the sellers and purveyors of these devices think and believe that their RF/microwaves effect is always beneficial therapeutically in a wildly variable world of surrounding nnEMF. THIS IS PURE FALLACY AND MARKETiNG BuLLSHIT.
Moreover, they fail to realize that this eNOS switch in cells is very sensitive to any variable PEMF RF pulse. This is why PEMF devices need to be strictly avoided in a 5G world. Yes, that includes all the Oura rings and PEMF devices pushed by BEMER and Dr. Havas based upon the latest NTP study on RF radiations.
For example, if one is in an environment that fosters chronic nitric oxide release this means there will be a relative lack of sulfation of the skin, arteries, and gut and RBC's and this would favor the activation of the reactive nitrogen species of chemicals. This is particular devasting to the microbiome because NO and H2S work in unison to control the constitution of the microbiome.
In fact, we now know that nitric oxide can also interact with the superoxide pulse (OO-) created in cytochrome one (NAD+/NADH) form altered mitochondrial function to create peroxynitrite (ONOO-) to do further damage. This is why people with gut and microbiome conditions relapse so often in toxic nnEMF environments loaded with blue light. Most of the doctors are not sophisticated enough yet to understand that things like SIBO and adrenal fatigue are adaptative and not pathologic symptoms tied to altered and highly variable EMF fields that their patients live in.
It has been found that when peroxynitrite breaks down, it creates reactive free radicals and oxidative stress within cells and this likely leads to many of the symptoms of CV and neurodegeneration on longer timescales. In this way, both atherosclerosis, CV, and neurodegeneration can be thought severe chronic adaptive mechanisms employed by cells who have developed an innate immune allergy to nnEMF. My Q & A last night was epic in this regard.

 

Do you think pulses and polarization from a smart meter have no effect on the electrical activity that is going on inside of you? This video is for that skeptic. Smart meters us a combination of RF and microwaves so they very much mimic what 5G mm waves can do. This video will serve as a warning why Uncle Jack said that the new spikes in coronary calcification lesions, widow makers, and acute onset A-fib with clotting is coming to every ER in 2019 in 5 G cities.
The uninformed masses are hooked on cardiotoxic devices that require limitless RF/microwave pollution documented to incrementally obliterate the blood, heart, and brain and their colonies of mitochondria. This is why heart disease, atherosclerosis, and neurodegeneration all seem to be linked fundamentally. As a group, they may appear energetic and viable. But examine each person individually and uncover a resplendent array of physical impediments, abnormalities, and danger signs that plague even the very young. Within the cells, the DNA and the blood of microwave addicts there is vast evidence of radiation sickness long before they receive a clinical diagnosis.
https://www.youtube.com/watch?time_continue=1234&v=UIobFr3m8kk

 

Many people argue that blue light in the day is needed so why block blue light from your digital devices!?

☀️ The issue with blue light from your screens is it’s unbalanced against other colors and at a specific intensity throughout the day, it doesn’t change intensity like with the sun

The study below now proves that artificial blue light from your digital devices in causing apoptosis (cell death) in the human eye and is a complete game changer

The study used blue light at 449 nm, 458 nm, and 470 nm. The results showed the lower the number nm (more high energy) then blue light the more cell death occurred in the eye.

This shows that wearing blue light reducing glasses during the day is essential for your health when using digital devices or under artificial light indoors.

If this causes cell death in the eye I am sure we will see future studies address my thoughts that blue light also induces aging and cell death in the skin.
https://academic.oup.com/ib/article/9/5/436/5115388

 

When will they compute the link to blue light and nnEMF to excitotoxic damage?

When anal candling becomes mainstream at Catholic schools?

A Computational Model of Loss of Dopaminergic Cells in Parkinson's Disease Due to Glutamate-Induced Excitotoxicity
https://www.frontiersin.org/article...T&utm_campaign=ECO_FNINS_XXXXXXXX_auto-dlvrit

 

Low Vitamin-D3 and reduced exposure to sunlight were significantly associated with increased risk of Parkinson’s disease
Vitamin-D supplements had no significant benefits in improving motor function for patients with Parkinson’s disease
There is no replacement for the Sun for mitochondrial diseases!
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352758/

 

The wisdom of MAYBE is a small glimmer of hope...........for that other person in your tribe or your circle of six.

Because all of biology and life is non-linear and no one thinks about it deeply enough.

Never become addicted to certainty. In human affairs, it's a healthy thing now and then to hang a question mark on the things we have long taken for granted. Nature commands us to embrace MAYBE and few of us realize it --The Wisdom of Maybe. #BlackSwanWisdom

What your future can be..........if you are open to the wisdom of MAYBE
I want you to see your future………………I see it in your current situations........often times way before you see the real etiology of your issues.



What is most obvious is also often most concealed in nature. Much of what we think we know has depths never ventured to because we mistake the surface for the bottom. Such is the case, especially, with human diseases today. So many "smart people think Parkinson’s Disease begins in the gut when it is an optical illusion of how the photoelectric effect is not being used in its proper non-linear fashion by our neuroectoderm derivatives in our cells. A lack of solar redox and way too much artificial light Light sculpts the microbiome and this is why it appears PD begins in the gut. We now live under alien man-made artificial light and not sunlight. It begins with melanopsin dysfunction on our skin, eyes, gut and lung surfaces and all this photonic damage leads to a lowering of the DC current in the brain and a loss of magnetic flux in our mitochondria to cause the electrical short circuits in all those tissues. I love when non-neurologic experts think they know the foundational truths of a disease they really do not have a clue about it at all.........that is called the Dunning Kruger effect. All DBS devices work to replace both electric and magnetic fields and when you see it in operation as the video above shows you’ll begin to realize that light is made up from electric and magnetic fields…………..and you’ll see really where your PD came from. Your choices around light and dark. The first loss in PD is a loss of the circadian mechanism linked to light and dark for cells. https://www.genengnews.com/topics/omics/circadian-rhythm-alters-gut-microbiomes-response-to-diet/

 

The best and most truthful thing I heard during my neurosurgical residency: "Charity Hospital offers the best training available in the world today. The problem is it's administered without an anesthetic for the patient and doctor." This is why you'll never forget its lessons.

 

I am chuckling hard right now............TOLD YA'. PD is a light-mediated disease that destroys mitochondria.
https://www.eurekalert.org/pub_releases/2019-06/uob-ncn062619.php
New contents: Neuronal Parkinson inclusions are different than expected
UNIVERSITY OF BASEL
"We used correlative light and electron microscopy and other advanced light microscopy methods to take a closer look at the brain of deceased Parkinson's patients and discovered that the Lewy bodies consist mainly of membrane fragments from mitochondria and other organelles, but have in most cases no or only negligible quantities of protein fibrils," says Stahlberg. "The discovery that alpha-synuclein did not present in the form of fibrils was unexpected for us and the entire research field."

 

HOW ARE PD AND FIBROMYALGIA THE SAME BUT DIFFERENT? The answer is in how both affect muscle function and physiology. Both come from a lack of light at a particular surface. = PD = lack of dopamine in the RPE........this is why Parkinson people lose muscle mass and it even causes their special non-expressionless faces...........PD is usually related to a lack of full-spectrum sunlight getting to the eye to build dopamine and melatonin locally in the retina.
If the eye doesn't get the stimulus of UV/IR light neither does the frontal lobes nor the brainstem = substantial nigra = PD.
What happens if you live your life 99% indoors and always around fake light always covered up with clothes or fake light? Fibromyalgia = skin surface defect = this implies PD and FM are somehow linked in quantum fashion doesn't it? HOW? Where do skin and brain come from in a zygote? NEUROECTODERM.................BOOM


DETAILS: When the water in your cell can not carry the right amount of energy life can not grow. Think of a plant. If it has little water and lots of suns will it grow and live well? No. Realize water and the level of potassium (K+) in a cell are linked. Energy is tied to K+ ion concentrations and this is connected to ATP levels at cytochrome 5, the ATPase. K+ also links to water molecules and in turn to ATP molecules stochastically. For every 0.3 mEq below 3.8 mEq that potassium is on a standard blood lab draw, means there is 100 mEq deficit of potassium INSIDE a cell. This deficit causes mitochondria to consume more calcium and magnesium and it swells. This is the same effect we see with 1G-5G environments. The result is that both oxygen tension and free radical signaling also change when this occurs. The amount of IR light released from mitochondria is also affected adversely because the ATPase F0 rotating head also slows down. The collateral effect of this slowed Fo head rotation is ECT flow slows.

This slows ECT because it increases the distance of the respiratory proteins. The atomic size change altered the local geometry below your skin where your muscles are. This is where muscle pain and FM come from. This is linked to the redox potential in a cell (amount of UV light confined) because it is linked to the electrostatic attraction in a cell. This is huge for potassium because its K+ ion has the unique ability in “gluing of water”. People forget the water a mitochondrion makes is done at CCO. Gluing = EZ of Pollack or the AI hypothesis of Ling.

Potassium ions are able to glue water because the ion's atomic radius allows it to polarize in sunlight. Sunlight is unpolarized..............K+ ions is the initial polarizer of sunlight inside cells. When somebody is in an environment that causes the dielectric constant of water to lower from 78 for any reason (LOTS IN MODERN WORLD), the polarization of the ion becomes smaller than cell water. This lessons the cells ability to become a battery in sunlight.

This causes a huge electric problem in the cell because the polarization energy of K+ is subtracted from Coulomb energy. Normally K+ is more polarizable than water, so polarization is added to the Coulomb energy in a cell. When fluoride or bromide, from toothpaste or grains, for example, are added to a cell dielectric collapse occurs. The same is true with glyphosate and many supplements and drugs used today. This is precisely how the dielectric constant in water is destroyed by supplements, pills, drugs, and chemicals, and pesticides.

In the normal state of affairs in wellness in the sun, this allows potassium to function as the optimal "photo-electrical adapter" to transfer energy throughout the cell coherently. It is also massively important in patients with dielectric collapse because intracellular dehydration from non-native EMF completely ruins this relationship and this is why they find it so hard to get better fast. ATP is designed to unfold proteins fully to open their carbonyl and imino side chain groups on all amino acids to intracellular water. This action allows binding and polarization to separate water into subatomic particles that are positively and negatively charged. This action is called building or expanding the exclusion zone (EZ) of water. Dr. Gerald Pollack's experiments showed these effects. Dr. Gilbert Ling proved by experiment that each molecule of ATP in a cell controls 8,800 water molecule binding sites and 20 potassium ions to allow water to become structured inside every cell of your body.

The first step in photosynthesis and in mitochondrial oxidation/phosphorylation of electrons is to charge separate water...........now you know the why K+ and sunlight help muscle pain and fatigue reverse. UV and IR light build dopamine and melatonin which stimulate muscle growth and entrain properly function by maintaining the respiratory proteins in muscle mitochondria. Light is the most powerful drug we have.............especially for muscles. Get some.

 

Dopamine increases the signal to noise ratio in the brain, facilitating pattern recognition both in space and across time. This can affect thinking in those with an acute TBI just like it affects those with mental diseases on a more chronic basis. Schizophrenics lose focus and attention because they have too many neuronal circuits firing at once and this creates chaos. Focus and attention come easier when one’s brain is not being pulled down multiple pathways. This is why many with TBI report depression and an inability to concentrate cognitively. We call this cognitive haze and lethergy. Paying attention, establishes traction between your internal frequencies and the external world, synchronizing with it, using it to help calibrate your internal pace. This is why circadian coupling is always a key feature of mental illness and in suicides too. It often manifests in TBI’s. We’ve seen this in NFL and NHL injuries with CTE which is a more chronic form of TBI.

A brain going in a million different directions has trouble hanging onto external processes long enough to synchronize with them. Thus, unable to follow a trail outside of oneself, one can get stuck bouncing around inside, making it difficult to learn and follow through. That defines the schizophrenic phenotype. It also explains the cognitive issues we see in TBI patients. The human experience of time is a construct, and it is shaped by anatomical and dynamical constraints of the nervous system built around dopamine and melatonin and how they couple with our SCN. Schizophrenia is a persistent, often chronic (due to chronic poor lit nnEMF environment) and serious mental disorder affecting a variety of aspects of behavior, thinking, and emotion. TBI is more of an acute injury to the eye clock mechanism. Patients with delusions or hallucinations often are described as psychotic. Thinking is usually disconnected and illogical from reality.

Peculiar behaviors may be associated with social withdrawal and disinterest.



Dopamine changes the antenna function in the neocortex and basal ganglia to augment the signal to noise ratio in the brain. It increases pattern recognition, even for things that may not be there, as in paranoid schizophrenia cases. People do not realize how dopamine affects a schizophrenic brain and an ADHD brain. Dopamine deficit lowers the signal to noise ratio, making the signal difficult to distinguish from the background noise, and patterns harder to detect. With ADHD’s dopamine deficit, following one conversation or train of thought can prove tricky because all conversations or thoughts sound equally loud, making it hard to pick out a continuous stream, instead of picking up bits and pieces from several different streams of conversation or thought. This makes ADHD have its disruptive attention spans.

Random firing neurons make up the background noise in the brain, like all the voices at a party not part of your conversation. The person whose voice you focus in on, ignoring all the others, is the signal amidst the noise. A low signal to noise ratio means distinguishing one’s conversation partner’s voice from the surrounding voices proves difficult; all the voices sound equally loud, making it difficult to determine which voice to follow. When the signal to noise ratio increases however, the background noise fades and your conversation partner’s voice become distinct and easy to follow. Dopamine turns up the volume on the audio signals at the party as compared to the background noise making it easier to decipher the conversation and act properly on it.

Drugs that stimulate the dopamine system treat the dopamine dearth of ADHD. ADHD treatment stimulants–Ritalin, Adderall, and Vyvance–increase dopamine production, enhancing focus and learning. Ritalin boosts dopamine activity and returns the brain functioning to “normal” levels increasing a person’s level of engagement. In my opinion, drugs cannot replace a proper solar environment with a connection to Earth and the lunar cycles. NOTHING REPLACES NATURE.

Drugs that block dopamine in order to treat schizophrenia or amphetamine overdose can cause Parkinson’s like symptoms in long-term users. Chudler, Eric H. Neuroscience for Kids. 2009. Schizophrenia. http://faculty.washington.edu/chudler/schiz.html (accessed Nov. 14, 2009)

 

Do you still think PD is not a photoelectric quantum based disease that destroys dopamine?

I'm laughing at you.


https://neurosciencenews.com/parkinsons-vitamin-d-14665/

 

This post extends this post..........https://www.facebook.com/drjackkrus...otif_id=1566033637773272&notif_t=feed_comment

 

The probable REM sleep behavior disorder negatively affects health-related quality of life in Parkinson's disease with bilateral subthalamic nucleus stimulation.https://pubmed.ncbi.nlm.nih.gov/33129010/

 

Deep brain stimulation is exactly what it sounds like — a pacemaker-like implant delivers electricity to misfiring brain cells. Scientists are only beginning to tap into its potential for treating puzzling brain conditions.https://www.discovermagazine.com/he...imulation-and-why-does-it-work-for-parkinsons

 

PD is always associated with a sleep defect because of mtDNA damage that destroys melatonin autocrine production. This sets up the circadian cycle loss that destroys dopaminergic neuron destruction.
Sleeping less than six hours a night when you're in your 50s, 60s, and 70s increases your risk of dementia by 30%, a long-term study has found.
https://edition.cnn.com/2021/04/20/health/sleep-dementia-risk-study-wellness/index.html

 

PD and IRA light podcast: https://www.breakingthegrey.com/post/dr-marvin-berman-is-healing-the-mind-with-red-light

 

https://link.springer.com/article/10.1007/s00401-021-02324-0

 

In Parkinson’s disease, LC3B becomes trapped in protein aggregates and becomes inactive.
"Without degradation, the cells eject the aggregates, which then spread to nearby neurons, propagating the disease throughout the brain."
https://neurosciencenews.com/lc3b-parkinsons-18524/

 

https://pubmed.ncbi.nlm.nih.gov/34114509/