A View of Autism, Pineal Gland, Phytoestrogens and Nutrient Inhibitors from God's Blueprints:

This Hypothesis takes a view of Autism, the Pineal Gland, Phytoestrogens and Nutrient Inhibitors through the eyes of God's Blueprints. It is just my individual perception on how excessive consumption of substances that contains nutrient inhibitors and phytoestrogens in the process food-chain is the culprits behind the catastrophic events which are creating the Autism Epidemic as well as the Auto-immune Disease Epidemic... I believe what is happening is the excessive consumption of phytoestrogens such as are found in Soy, is triggering the onset of early puberty, or at least triggering abnormal hormonal changes in the body's internal environment... Couple this together with excessive consumption of nutrient inhibitors, also said to be found in Soy, that disrupts the body's ability to pick up Calcium, Iron and other nutrients, debasing the pre-puberty Pineal Gland development by altering the tissues Chemical Composition, and inhibiting its ability to perform its physiological functions....I am NOT a doctor and this contains absolutely NO medical advice... I believe this is only a small portion, just one little isolated piece of the puzzle, of the catastrophic disruptions taking place... A person cannot absorb this information and get the whole chaotic picture... This is just food for thought to open the door to the pathway of discussion, so cures can be found that afford real relief to the suffering ..

Nutrient inhibitors causes deionization, which stops the cells from being able to utilize a portion of ingested Calcium, Iron, Trypsin and other nutrients... This leads to an imbalance in the electrolytes concentration, which ends up destabilizes the Homeostasis balance of other nutrients such as Oxygen, Iodine, Zinc, Magnesium, B12, Phosphates, Hydrogen, etc.. This altered concentrations of electrolytes creates a hostile environment that denatures functional proteins and disrupts the body's ability to perform chemical reactions necessary for metabolic processes.. This limited access to electrolytes, nutrients and vitamins begins a complex network of disruptions that effects all "God's Internal Systems" such as: the Immune System, Cardiovascular System, Metabolism System, Digestive System, Endocrine System, Hormone System, Autonomic Nervous System, Reproductive System, Chemical Reactions, Chemical Composition of the (CSF) Cerebrospinal Fluid in the brain, Muscle Contractions, Cellular Respiration Electron Transport Chain, ATP Metabolism, ph Balance, Cell Maintenance, Negative and Positive Feedback Systems, Chemical and Pressure Receptors, Rapid Eye Movement (REM) Sleep Cycle Phase, Reticular activating System (RAS), Reticuloendothelial System (RES), etc... (It just stands to reason, deionization of a portion of nutrients would destroys the cells ability to perform physiological and metabolic functions, which would create an unstable environment which would destroy the Homeostasis balance in the body... This Internal destabilization, I believe, is the root cause of Autoimmune diseases: Aids, Alzheimer's, Autism, Arthritis, Brain Disorders, Birth Defects, Bone Diseases, Blood Disorders, Cancer, Diabetes, Epilepsy, Heart Disease, Lupus, Multiple Sclerosis(MS), MD, Myasthenia Gravis, Parkinson's, Scleroderma, Peripheral Neuropathy, Osteoporosis, Rare Diseases, etc....

A cow can eat stressed Johnson Grass and get Prussic Acid Poisoning and die quickly because it disrupts the electron transfer in the Cellular Respiration Electron Transport Chain... Yet it is reported, that when Cyanide Poisoning which is also called Prussic Acid Poisoning is treated with Methylene Blue it creates an inactive compound that is slowly broken down and detoxified out of the body.. This is not medical advice this is just a reported treatment found in an animal book, but emphasizes the point that deadly disruptions in the internal systems can be repaired by bringing the cause and the right treatments together to nullify the problem and render it harmless..

Sheep can winter over on a pasture with plants that contains high Oxalic and Phytic Acid and they can get a fatal ion imbalance..
(I am convinced the same thing is happening in people who unknowingly consume Nutrient Inhibitors in excessive amounts for prolonged periods of time, without compensating for the blockage of the nutrients... By the time a person realizes something has happened, disease is at a critical point and symptoms are manifesting themselves... The only thing different between the dying sheep and disease in humans is, in the sheep the disruption of cell nutrients is viewed as an ion imbalance caused by plant toxicity, but in the human form it is referred to as Auto-Immune Disease/ Disease with no known cause and no known cure.. Auto-Immune Disease is simply a disruption in mankind's ability to understand what God's Immune Systems are Automatically doing... The toll from consuming excessive amounts of nutrient inhibitors over an extended period of time has been a very slow, methodical and accumulating one, and so the human deaths have escaped unnoticed, because the speed has been far too slow, to ring an alert bell... I ask, what is the point of putting a substance, such as Soy with known nutrient inhibitors, in approximately 90% of the products in the processed food chain... In things such as "Tuna in Water", "Lard" or Vitamins and Calcium Supplements.. If you are going to take a calcium supplement or a multi-vitamin why would it contain a known calcium and iron inhibiting substance... Lard should simply be animal fat such as hog lard, so why has a calcium inhibitor been placed in it... Tuna fish canned in water, should be just that, so why has a calcium and iron inhibitors been placed in it... When food is saturated like this with "Nutrient Inhibitors" it doesn't take long and you have surpassed the moderation threshold and you are just saturated with "Nutrient Inhibitors"... This is like intentionally taking a substance with every meal to suppress the absorption of part of your nutrients, this makes no logical sense to me, at all.)...

Metabolism Disruptions:

Saturating the food chain with nutrient inhibiting substances, means over-time our bodies own internal resources for making chemical compositions will be exhausted, altering the chemical reactions available for cell usage.... The Internal Systems have to have precise chemicals to function properly, this is God's design for Metabolism.. (It would seem to me a depletion of nutrients could be a disruption passed on from one generation to the next... The statements like "This is the generation that the children will die before the parents" or " It is in the Genes" is true if the body is being starved of "Nutrients". Each new generation is arriving equipped with less and less "nutrient resources" to draw from.)...

Acidosis, Deficient ATPs and Denatured Proteins:
(When Iron inhibitors hinders the body's ability to utilize Iron, this would disrupt the balance between the Aerobic (Oxygen -requiring )/Anaerobic (without-oxygen)processes... 90% of the ATP metabolism would be susceptible to disruption... Iron is responsible for transporting Oxygen to the oxygen-requiring Cellular Respiration Electron Transport Chain... Sufficient Oxygen has to be available in this process to except the hydrogen passed down through the chain.. If Oxygen is insufficient the last cytochrome is stuck with hydrogen.. So the hydrogen cannot be passed off and the system becomes blocked at the NAD stage.. This stops the Electron Transfer and ATP metabolism becomes blocked in this system... A cell is unable to survive on just the small amount of ATPs produced without-oxygen, and they will die.. Similarly, Cyanide (Prussic Acid) poisoning disrupts the tissues ability to use Oxygen and results in suffocation... It does not disrupt the Oxygen-carrying ability of the hemoglobin, instead Cyanide attaches to the last cytochrome and blocks the electron transfer, and death occurs.. This is far faster then the accumulating Nutrient Inhibitor's effect of partially blocking Iron's availability, gradually depleting the Oxygen stores, leading to a slow and methodical disruption in the electron transfer.. When ATP metabolism is disrupted this causes excessive Hydrogen, Pyruvic and Lactic Acids, which disrupts the body's pH balance causing acidity .. An acidity environment denatures functional proteins such as antibodies and hemoglobin..

Pathway to Diabetes :

ATP transfers and stores energy released in the metabolic process known as catabolism.... This destructive metabolism releases the energy by converting complex molecules into simpler ones.. The body's preferred fuel source for producing ATP, comes from the destructive metabolism of Glucose... (So insufficient ATP metabolism would result in a diminished supply of cell energy, this would trigger a "Stress Response" by the Sympathetic Division of the Autonomic Nervous System (ANS)... In an attempt to restore Homeostasis the Sympathetic Division is able to over-ride normal processes... Deficient ATPs would trigger the assembly of Glucose into the blood to be utilized as fuel to make the ATPs... This process would stay triggered until the ATP was once again sufficient... But in the case of Nutrient Inhibitors obstructing the use of Iron, it is the lack of Oxygen that is disabling the ATP metabolism in the Cellular Respiration Electron Transport Chain... So fewer and fewer ATP would be available to carry out the process of metabolizing the Glucose to make more ATPs... When the body is in need of ATPs the "Stress Response" is to put strict limits on the use of Glucose for anything other than to be used as fuel to make ATPs, till Homeostasis is obtained.... In this case, the General Adaptation Syndrome (GAS) takes charge and resets the normal controls limits on the internal environment.. This creates a situation where the Blood Glucose or Blood Pressure can rise to abnormally high levels.. High levels of Blood Glucose is a known Diabetic Symptom)...

Pathway to Autism and Brain and Nerve Disorders:

Even a minute variation from the Homeostatic range of calcium ions can cause severe problems from hyper-excitability to inability to function and even death..

The Autism statistic has sky-rocketed once again, striking 1 in every 120 children.. Common sense would tell you, that if a woman is unable to absorb sufficient nutrients for her own body how could the same body be expected to serve as a good resource pool to build a fetus during pregnancy... And when the infant is born, in all probability the baby will hit the deck a running with insufficient nutrients to build and grow during the crucial developmental years and the "Internal System" will be unable to sufficiently develop... If the mothers nutrients are disrupted to the extent that the proteins are denatured, this could have a devastating effect on the fetus or newborns' own immunity, right out the gate... When functional proteins are denatured this disrupts antibodies in the immune system... So if the Mom is passing on insufficient antibodies to the fetus during the "Naturally Acquired Passive Immunity" process, this could rob the fetus or newborn of its early protection.... A fragile ill-developed Immune System would make them ill-equipped to be ready to fight the battle against toxins and diseases... Their little systems could easily be over-whelmed when exposed to such things as vaccines, inoculations, viruses and bacteria in this fragile state.. A persons' immune system hinges on precise chemical substances being available to carry out the process... If a pathogen invades the tissue it will trigger and inflammatory response.. This process utilizes lysosomes which are the cells garbage disposals...

Pathway #1.. Cell Garbage Disposals (Lysosomes) Dysfunction:
(If the nutrient inhibitors limit the cells' ability to use Iron then it is reasonable to think that the ability to get oxygen is also limited).. When the cells' garbage disposals (Lysosomes) are deficient in oxygen they become fragile rupture and burst, spilling out their nerve cell destroying enzymes.... The brain is an area that is particularly venerable to oxygen deficient garbage disposals.. Myelin sheaths and joints are other areas that are adversely effected by oxygen deficient lysosomes.. In the Brain, the nerve-cell destroying enzymes destroy neurons and neuroglia... Neuroglia are the brain glue that bathes, protects, supports, nurtures and holds the neurons together and maintains Homeostasis in the (CSF) cerebrospinal fluid. Neurons specialize in thinking, sensing, remembering, controlling the secretions of the glands and muscle control .. If neurons are lost the neuroglia move in to fill up the empty space... (So if deficient oxygen causes a lysosome dysfunction this could result in situations that are manifesting in symptoms like : Autism, Alzheimer's, Parkinson's, Multiple Sclerosis, HIV breach of the Blood Brain Barrier, Nervous System Disorders, Brain Disorders, Toxicity and Infections of the Brain, Brain Tumors, Learning Disorders, Disruption in Motor Skills, Arthritis, Osteoporosis, Joint Problems, Electrical conductor problems, Impulses Transmission Disruptions, etc.)..

Pathway# 2: Phytoestrogens and early puberty (Precocious Puberty):

Exposure to excessive phytoestrogens in the food-chain could be a double whammy... Phytoestrogens, are rumoured to be found in Soy, and are believed to be initiating early puberty as early as the age of three.. Puberty causes fluctuations in hormones that should normally start taking place around the age of 10... By the age of 10 all the key aspects would normally be in place to deal with the hormonal fluctuation, that start to occur about 2 years before the onset of puberty... If a child is going into puberty at 3 years of age, this means straight out of the womb, the infants hormonal changes are being activated... Major unnatural hormonal fluctuations would have to be detrimental to the developmental phase of the Internal Systems, and in all probability would weaken the development foundations of the Internal Systems....

Pathway #3: Pineal Gland Disruption and the Sleep Cycle Distuption:

One system that could possibly be disrupted by insufficient calcium and by early onset of puberty is the Pineal Gland, which has a connection to the reproductive function, the Biological Clock, the Sleep Cycle and Serotonin and Melatonin Hormones ... The Pineal Gland is involved with the Epithalamus System which also contains the Cerebrospinal Fluid Forming Mechanism.... Before the onset of Puberty the Pineal Gland starts to shrink in size and Calcium Carbonate and other minerals start collecting in its tissue.. The gland contains a very high concentration of Serotonin and contains an enzyme that converts Serotonin into Melatonin.. The Pineal Gland secretes the hormone, Melatonin... Melatonin is thought to be a sleep promoter.. Melatonin plays a role in setting the timing of the Biological Clock... Difficulty in sleeping long enough to be rested can be due to insufficient production of Melatonin.. Melatonin resets the daily rhythms... Secretion of Melatonin is regulated by the Daily Dark-Light Cycle... Sunlight inhibits Melatonin release and causes a lack of sleepiness.... Norepinephrine released by the Sympathetic Division of the Autonomic Nervous System during sunlight, inhibits Melatonin secretion from the Pineal Gland... But in darkness, the absence of Norepinephrine triggers the secretion of Melatonin from the Pineal Gland and causes sleepiness....(So with excessive estrogen-like substances coupled with deficient Calcium ions, it is quiet possible this could cause the Pineal Gland to go haywire and starts the Biological Clock far to early, activating the puberty processes and disrupting the "Sleep Restoration" Cycle.. This coupling of excessive Phytoestrogens and insufficient Calcium Ions are culprits that could possibly be attributed to excessive Soy consumption.. So if excessive Phytoestrogens are putting the puberty process on fast-track that would mean the process of small bits of Calcium Carbonate and other minerals that are gathering in the Pineal Gland Tissue before puberty, when it is growing smaller, is also put on fast track.. The problem would be the resources of Calcium Carbonate and minerals would be diminishing simultaneously, due to the Nutrient Inhibitors effects, so in all probability the foundation from which the Pineal Gland's chemical composition is established, is being debased... This Debasement as well as a Stress Response to the deficient Calcium Ions could activate a prolong Sympathetic Release of Norepinephrine, which would suppress the secretion of Melatonin and disrupt the Sleep Cycle even farther.)...

Pathway#4: Possible Serotonin Disruption and the Blood Clotting Process and Calcium:

The name Serotonin suggest that it serves as an antitoxin energiser in the blood serum...
Serotonin is a chemical neurotransmitter derived from the amino acid Tryptophan ... The name Tryptophan suggest it has the appearance, qualities and basic fundamentals of Trypsin... Tryptophan is an amino acid found in fibrin...Fibrin is an insoluble protein produced by the liver from the soluble protein fibrinogen in the blood clotting process... Estrogen activates the collection of Fibrin and makes its fibrous network even greater... Estrogen can neutralize the effects of Vitamin E.. Vitamin E is an anticoagulant and reduces clotting and it is an Oxygen Conserver, prolonging the amount of time oxygen remains in the blood.... (So excessive estrogen like substances could be over activating the release of Fibrin, but that would be disrupted by the lack of Calcium Ions.. The excessive phytoestrogen substances would enhance the "Stressor" by removing the Vitamin E's inhibiting effects on Oxygen Depletion)...

Disrupted Clotting process:
A chemical reaction between Calcium Ions and Prothrombin produce the enzyme Thrombin..
A chemical reaction between Thrombin and fibrinogen produce Fibrin.. Fibrin is one source of Tryptophan.. Serotonin is created from the amino acid Tryptophan..
(It is said that Soy starts out containing the anticoagulants Oxalic acid which is a Calcium Inhibitor.. Oxalci Acid deionises or isolates calcium ions in the blood and is a known disrupter of the Clotting Process... It just stands to reason, since the Blood Clotting Process hinges on the availability of Calcium Ions, then the supply of fibrin would hinge on the availability of Calcium Ions... So deficient Calcium Ions would inhibit the production of Fibrin, which would limit one of the body's resources of Tryptophan which would limit the production of Serotonin... And Serotonin is converted to Melatonin, so Melatonin also would be limited.. Couple this with the fact that Soy is also known to contain Trypsin Inhibitors, this could possibly lead to a Serotonin and Melatonin Hormone shortage.. Tryptophan appears to have the same basic fundamental qualities of Trypsin... Trypsin is the pancreas enzyme which accelerates the digestion of proteins into peptides.. It is quiet possible that a disruption in the ability to utilize Trypsin would force the body to commandeer the Tryptophan resources to accommodate for the lack of Trypsin resources.)...

The digestive process releases Serotonin into the blood..(The digestive process would be highly restricted by the Sympathetic Division in a prolonged Stress Response to Cell Starvation, so the release of Serotonin could be diminished, in this process also.).

Serotonin is also synthesized from the amino acid tyrosine.. Tyrosine is precursor of epinephrine, thyroxin and melanin.. Tyrosine chemically reacts with oxidized Iodine to synthesis T3 and T4 thyroid hormones... A Sympathetic Division "Stress Response" extremely diminishes Thyroid Gland secretions..(It has been stated that over consumption of Soy causes a disruption in the Thyroid Gland.. I feel that the Tyrosine resources could become depleted in a prolonged activation of the Stress Response to Cell Starvation and the excessive need for Epinephrine.. This could exhaust the supply of Tyrosine for constructing other hormones such as Thyroxin, Melanin, Melatonin and Serotonin... This could be an explanation for Soy's effect on the Thyroid Gland.)..
(So it just stands to reason, a disruption of Serotonin would inhibit one of the reining in mechanisms for controlling the Reticular Activating System (RAS)..
A disruption in the regulation of the Reticular Activating System could disrupt the "Sleep Restoration Cycle" and possibly the Reticuloendothelial System since this system is also associated with the Reticular Fibers)..

Pathway # 5: Disruption in the Reticular Activating System and Sleep Cycle:
(First rattle out of the box, an essential components of the Reticular Fibers, is Glycoproteins and collagen... Although, Glucose might be plentiful, the construction of Glycoproteins could be hindered by the need for ATPs in a Sympathetic Division "Stress Response" coupled with a hostile deionised environment resulting in denatured proteins .. This could deplete materials needed to maintain the Reticuloendothelial System and the Reticular Activating System... A Stress Response to "Cell Starvation, or "Nutrient Deficient Blood" would trigger a prolonged release of Norepinephrine and Epinephrine from the Sympathetic Division )..

Excessive release of Norepinephrine and Epinephrine could have an adverse effect on the Reticular Activating System (RAS), disrupting the "Sleep Restoration Phase" in the Sleep Cycle and possibly the part of the immune system called Recticuloendothelial System aka (Mononuclear Phayocytic System).. These hormones are capable of resetting the arousal system, which is known as the Reticular Activating System (RAS)... During a "Stress Response" they lower the arousal threshold in the (RAS), in order to maintain alertness until the "Stressor" subsides...(RAS) regulates the state of alertness and sets the attention span, controlling the ability to stay focused on specific ideas.. As long as the (RAS) is stimulated the neurons in the Cerebral Cortex remain stimulated.. Intense and prolonged stimulation of neurons causes anatomical changes...

Sleep is the partial state of unconsciousness..

There are four stages of sleep that bring about Slow-wave "Restorative" Sleep, which allows the unwinding of the neural system and lets it relax to its basic levels.. During the 1st stage the alpha brain waves begin when the temperature, blood pressure, pulse and respiration are in a normal, relaxed, idling slow synchronized, low amplitude setting .. In the 2nd stage a spurting irregular pattern begins to develop... In the 3rd stage as a deep sleep starts taking hold, dreams start, skeletal muscle relax and vital signs diminish, and irregular Theta waves and high-amplitude Delta waves appears... In the 4th stage the RAS activity diminishes allowing the high-amplitude Delta waves to become dominate, this is the Slow-Wave Sleep Phase... The brain becomes inactive and many of the neurons are firing together in synchrony.. Muscles are extremely relaxed, the Gastrointestinal motility is enhanced, and the vital signs go down to their lowest normal levels.. (In my opinion, these change mimics the Sympathetic Division of the (ANS) relinquishing dominate power and allowing the Parasympathetic Division to take over.. If this is the case, I believe the stress from needing "Cell Nutrients" would override the ability to go into the "Slow-Wave Sleep Phase").. The Rapid Eye Movement (REM) sleep cannot begin until this "Slow-Wave Sleep" has taken place..
During(REM) phase things start rapidly changing, becoming very irregular... Once again temperature, respiratory, heart and blood pressure rates rise and the movement in the gastrointestinal system diminishes... Once again the idling wakefulness from the Alpha Waves return.. This is a sign that the REM phase has begun... (In my opinion this mimics the Parasympathetic Division relinquishing dominate power back to the Sympathetic Division of the ANS).. Brain's use of oxygen is very great at this time, even more oxygen is used in this phase than in an awakened state.. The (RAS') threshold of arousal rises to its peak during the REM Sleep Phase.. Through the sleep cycle these patterns are fluctuating... But it is chiselled in stone, when the rise in the core body temperature takes place, then the midbrain Reticular Formation Dorsal Raphe Nuclei neurons are firing at their best possible rates...

(With Nutrient Inhibitors involved this disrupts the Core Temperature... Lack of usable Iron would create a deficiency in Oxygen, which would disrupt the processes taking place during the (REM) Sleep Phase which uses excessive amounts of oxygen.. Plus deficient Oxygen, disrupts ATP metabolism... ATP metabolism is the process by which heat is supplied to maintain the temperature.. A prolonged stress response to deficient nutrients would release excessive cortical which would suppress the production of IL-1.. IL-1 is the trigger mechanism for activating the secretion of Prostaglandins, especially the E series.. Prostaglandins are the hormone-type substances responsible for resetting the thermostat which activates the temperature regulating reflex mechanisms to raise the core body temperature... This would mean a prolonged Stress response would disable the Core Temperature Regulating Mechanism.).. During this sleep cycle not only the brain waves change but also neurotransmitter levels changes in certain areas of the brain... In deep sleep Serotonin levels increase and Norepinephrine levels decrease.. (Since the Pineal Gland contains the high concentration of Serotonin, I would assume it is stimulated in the deep sleep phase)... Norepinephrine is the Alert Neurotransmitter and Serotonin is the Sleep Neurotransmitter in the slow-wave sleep... In the (REM) phase Acetylcholine and Norepinephrine both rise in nuclei that are stimulated at this time... Norepinephrine induces transient paralysis in REM Sleep.. Acetylcholine in the Reticular Formation triggers the REM sleep arousal state ...
(I believe the "Cell Starvation" Stress Response would have the Beta Waves continual activated... Beta waves are present when we are mentally alert and concentrating on some stimuli or problem, and are more irregular, rhythmic and higher frequency.. This would lower the threshold for the activation of the Reticular Activating System maintaining an over-stimulated state of arousal which would disrupt the entrance into the Sleep Restoration Cycle)...

The (RAS) and the Cerebral Cortex together serve as dampers and normally, ignore up to 99% of all sensory stimuli as unimportant... This prevents sensory overload in which you would become totally aware of each and every shape, sound, color, odor etc..(It is quiet possible the "Stress" activated resetting of the (RAS) Threshold, could lead to a sensory over-load in the Autisic child's brain making them overly aware of unimportant stimuli in their environment, which would be disregarded with a normally functioning RAS threshold)...

Inhibitors of the (RAS) are the Hypothalamus Neural Sleep Centers and Serotonin... (These Mechanisms can be over-ridden in a Stress Response by the Sympathetic Division of the Autonomic Nervous System, in a bid to bring about Homeostasis.)...
Norepinephrine is a simulative hormone responsible for awakening up from a deep sleep, dreaming and controlling moods... During the (REM) phase the (RAS) releases Norepinephrine, transmitting impulses to the Cerebral Cortex.. (So it just stands to reason, in a prolonged Stress Response induced by Cell Starvation, impulses to the Cerebral Cortex would remain abnormally high keeping it in a continuously aroused state, due to the trigger happy excessive epinephrine and norepinephrine, which would reset the RAS Threshold down, lowering the activation starting point.).
(REM) sleep is essential for the maturation of the brain in infants and children.. A baby needs as much as 50% (REM) sleep.. 2 year olds needs as much as 35% and adults only need 25%...

Pathway # 6: Vaccines and a disruption in the Reticuloendothelial Immune System Response:...
(In my opinion, if Autism happens to be a delayed hypersensitive reaction or an immune response to a vaccine, the answers to a cure will lie in God's Blueprints of the Reticular Activating System and the Recticuloendothelial System aka Mononuclear Phayocytic System.)...

Disruption in the Immune Response and the Reticuloendothelial System:

Concerning Vaccines:
Gamma Globulin are protein components that contains antibodies in the blood and are the mechanisms that deals with immunity and disease resistance... Gamma (y)Globulin are the only globulins formed in the Reticuloendothelial Tissue by lymphocytes and plasma cells....Gamma Globulin is manufactured as a solution of immunoglobulin prepared by injecting a certain virus into animals, then harvesting antibodies from the blood to use in vaccines for humans..(So it appears there could be a connection between the the Reticuloendothelial System and the Vaccines)....In grown-ups Red Blood Cells (RBC) are normally, formed in the red bone marrow.. But in the fetus, RBCs are also produced from the lymph nodes, spleen and liver.. RBCs are destroyed after 3 or 4 months and the debris is cleaned up and recycled by the Reticuloendothelial System..(In my opinion, right here a connection is established with the fetus' RBC produced in the lymph nodes, spleen and liver, and the formation of the Gamma (Y) Globulins which are only formed in the Reticuloendothelial tissue by the lymphocytes and the plasma cell.)...

A calf's odds of surviving, when deprived of the Passive Immunity from its mother's milk, are quiet slim. The first milk (Colostrum) contains colostral corpuscles.. They turn into fat engulfing-cells in the Reticuloendothelial System... This milk has antibodies against pathogens the Mom had previously been exposed to... Through this milk the calf acquires passive immunity until his own antibodies have had time to develop..(This connects the animal babies Immune System with the Reticuloendothelia System and the necessity of giving the baby's Immune System the boost it takes until their own immunity has had time to become established... So it just stands to reason if a human Mom is deficient in nutrients and is passing on a Naturally Acquired Passive Immunity that has been deprived of its full potential, the infant would be facing great odds in mustering up an Immune Response to defend off toxins and treats to the Immune System.)..

Serotonin is also concentrated in the Brain the Raphe Nucleus.. Serotonin is not only associated with sleeping, temperature regulation and mood control but also with sensory perception.. Serotonin eases the transmission of impulses between neurons..

Types of Hypersensitive Reactions:
#1. Anaphylaxis is extreme sensitivity to specific substances such as drugs or proteins.. It can be a localized or a systemic reaction.. But this reaction usually only takes a few minutes to occur after exposure.. But again the treatment for such a life threatening reaction is Epinephrine.. (It seems that a vaccine could qualify as a drug and Serotonin could possibly be responsible for regulating the sensitivity perception of the vaccine.. So it just stands to reason, a depletion of any kind in the resources of Serotonin could allow a disruption in the sensitivity perception of a Vaccine.. If a Stress Response to Cell Starvation is in process the Epinephrine would be activated already in excess, this could minimize a life threatening reaction somewhat and maybe mask this type of hypersensitive systemic reaction to a vaccine).. Anaphylaxis takes place when an allergen is able to cross-link with IgE antibodies located on mast cells or basophils.. This activates the release of platelet-stimulating substances, Serotonin, Heparin, Histamine and chemo tactic factors, thus triggering the inflammatory response...

Histamine is a substance released by the Immune System Cells during an allergic reaction that causes irritation, smooth muscle contractions, blood vessel dilatation, and stimulation of gastric secretions.. Histamine's name means it is a blend of histidine and amine.. Histidine is an amino acid that functions as the Iron-binding site for hemoglobin.. (So if the Nutrient Inhibitors are binding the Iron and blocking it from completing its normal binding to Hemoglobin, this could mean that the normal balance between Histamine and Serotonin is disrupted. The resources of Serotonin could be skimpy while the resources of Histamine could be well in excess.. (It is widely stated, that Soy infant formula contains Trypsin inhibitors... So if the infants food chain is saturated with this Tyrpsin Nutrient Inhibitor, then it just stands to reason that, the materials to construct Tryptophan would be limited and the ability to construct Serotonin would also be limited. In which case this would mean the chemical composition involved in the extreme sensitivity response is altered.)...


#2. Cytotoxic Reactions: IgG and IgM antibodies cause this kind of reaction, and are aimed at antigen located on RBC, tissue cells, platelets and lymphocytes... This activates the Complement System, which means the reaction is enhanced.. In this reaction lysis leads to cell damage.. (The Nutrient Inhibitors disruption of Oxygen could be a Key player enhancing a disruption in this reaction... The Lysosomal membrane becomes fragile when deficient in Oxygen, they rupture easily causing Autolysis which is self-digestion of the cell.. Another connection to this type of reaction taking place would be the fetus' utilizing lymph nodes, spleen and the liver to produce RBC and then after 3 or 4 months those RBCs being recycled back into the Reticuloendothelial System.).. The IgG immunoglobulin are the only ones that are able to cross over to the fetus in order to provide this Passive Immunity.. And IgG causes the Complement Fixation.. Meaning it causes a certain complementary group of blood proteins to bind to a specific yoked antibody-antigen pair and enhances the Immune Response to foreign cells... (If Trypsin is being blocked then the protein digestion would be disrupted and proteins are the essential components of the Complement System.. So it just stands to reason the Complement Immune Response could be disrupted.)...

#3. The Immune Complex Reaction: This reaction also involves the IgG or IgM antibodies and activation of the Complement System.. If a special ratio of antibody to antigen happen, the interconnected whole can be small enough to escape phagocytes.. They can then get trapped in the basement membrane beneath the endothelium of blood vessels, this activates the Complement and results in inflammation.. (Combine this with the previous information on possible Cytotoxic Reaction disruptions... If a mother has passed on a weakened Immunity because a lack of nutrients, this could alter the normal ratio between Antibody an Antigen... The Reticular Fibers are used in the construction of the basement membrane.... There is a possibility that the resource of Reticular Fibers could be limited by a limited resources of Glycoproteins.. This would hinge on the fact if the materials to produce Glycoproteins has been hindered by the need for ATPs in a Sympathetic Division "Stress Response" coupled with a hostile deionised environment resulting in denatured proteins...

#4. Cell-mediated delayed Type Hypersensitivity Reaction: Macrophages that have been stimulated by the T cells causes this reaction... This type of reaction can be transferred through blood transfusions..
Delayed hypersensitivity reactions have an accumulation of fibrin deposited at the inflamed site and permeated with large numbers of lymphocyts and macrophages.. This type of reaction is triggered by the tuberculosis skin test or intracellular bacteria.. It usually appears within 72 hours after exposure.. The reaction happens when the allergen is escorted to the to the lymph nodes, by the antigen-presenting cells, and presented to the T cells...This causes the T cells to be sensitized and start proliferating and part of them start migrating through the lymph and blood.. At the place the allergen entered thy began secreting gamma-interferon this stimulates macrophages and Tumor Necrosis Factor (TNF) and this triggers the Inflammatory Response...
Tumor Necrosis Factor:(TNF) cause the neutrophils and macrophages to gather at sites of inflammation.. Also activates the macrophages to make IL-1... And functions to induce a fever.. (Several disruptions could be taking place in this type of reaction.. During a fever Iron is isolated by the liver and spleen so it will not be available for bacteria to utilize.. And with the Nutrient Inhibitors depleting the usable supply of Iron, the fever process could be caught up in a Fight or Flight Stress Response.. In a prolonged Stress Response, the Immune System is switched on by the IL-1 but the prolonged release of Cortisol suppresses the production of IL-1 and IL-1 is the co-stimulator necessary to put helper T cells and a good portion of the rest of the Immune System in gear so it can do its job and shut off.. IL-1 suppression would inhibit the Thermostat regulating process by not stimulating the Prostaglandins (PGs) to reset the core temperature.. (PGs)E and A reduce blood pressure, F group increases it.. When released by injured cells,(PGs) especially the series E intensifies the effects of histamine and kinins... (With deficient nutrients the blood pressure would be reset to a higher level this would inhibit the E and A series of (PGs) while increasing the F group of (PGs).

Autoimmune thrombocytopenia.. Is a condition where the thrombocyte (which are an import part of the clotting process)are destroyed. Proteins which have become altered or distorted for some reason are suddenly recognized as an enemy.. This can be triggered in some people by drugs, which bind to the thrombosis membranes and creates new antigens (This could possibly have a connection to an Immune reaction gone haywire.. Because the Nutrient Inhibitors disrupting the Clotting Process by inhibiting the ability to utilize Calcium Ions... And thus altering the concentration of electrolytes, which creates the hostile environment of which denatures Proteins.. Thus causing the Proteins to become altered.).. This response degrades the IgG antibodies and this altered IgG is then targeted for destruction by the IgM antibodies.. When the IgM binds to the IgG the complement is triggered causing local tissue destruction.. This is a form of Immune-Complex Hypersensitivity...

Pathway #7: Nitric Oxide Disruptions:
Nitric Oxide (NO)is a highly reactive free radical, which normally only last less than 10 seconds, then oxygen and water combine with it to deactivate into nitrates and nitrites.. Thus insuring that its actions are brief because in large amounts (NO)is highly toxic... (I believe the resources of oxygen could have become so depleted that the (NO) could accumulate in large enough quantities to become Toxic and cause a destructive effect in the Brain.).. (NO) is released from the Phagocytic cells such as macrophages... (NO) is a neurotransmitter that is made on demand and acts instantly.. (NO)is made from Arginine by the Nitric Oxide Synthase (NOS) enzyme.. The Autonomic Neurons that release Adrenal Medulla hormones, Epinephrine and Norepinephrine and activate relaxation of the smooth muscles of the abdominal area, have a very high concentration of (NOS)... (I believe there is a possibility that the prolonged Stress Response, could be releasing excessive amounts of the high concentration of (NO) in the Adrenal Medulla Hormones, in an attempt to bring the deficient blood back to Homeostasis)... (NO) released by neurons enters into close neurons and activates an enzyme which stimulates the production of cyclic GMP which serves as a second messenger.. (NO)is thought to play a part in learning and memory.. (NO) is involved in the automatic regulation of Blood Pressure... (As would take place in the Negative Feedback Systems and the Autonomic Nervous System, if tissue was not being supplied with Nutrient Rich Blood).... (NO) is the endothelium-derived relaxation factor (EDRF) which is one of the most important chemicals involved in altering blood vessel diameter...(Substances that alter blood vessel diameters would be released in excessive qualities in the Stress Response). The Long-term memory phenomenon known as Long-term potentiation (LTP) depends on (NO) being released from neurons that have been activated by the neurotransmitter Glutamate.. (Due to the lack of oxygen to deactivate the (NO) it could become toxic to the memory process.)...

Again I am not a doctor and this contains no medical advice just food for thought..

06/14/2009

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