MASS Ischemia: Cellular Injury and the ischemic Penumbra – the progression of hypoxia in the Brain – “Cores” neural tracts from the inside out – This creates a series of disconnections to the brain’s wiring – locally and or systemically (autism) to progressively (dementia) and intermittently (Multiple sclerosis, CIDP, ADEM)..and more..including autistic enterocolitis and bowel disorders..ischemia again
MASS ischemia induces hypoxic “coring” of the nerves within tract systems inside the brain(and autism, dementia, Multiple sclerosis, etc…). Nerve tracts (white matter) in the brain are collections of individual nerve axons (like wires inside an insulated cable) that carry electrical messages within the brain (thinking, perceiving, feeling, remembering axons), to the brain (sensory axons), and away from the brain (motor axons). These “wires” are bundled into cable groups (fasciculi) within a larger nerve tract. Tiny blood vessels (vasa nervosum) course through and alongside nerve tracts along the outside of fasciculi that carries individual “wires” of motor and sensory and thinking information to, from, and within the brain.
MASS ischemia coring lesions to neural tracts: The ischemia unfolds within the fascicular cables at the centre core first and foremost as this is the area furthest from the perfusing blood vessels (vasa nervosusm) that traverse along the outside of the fascicular bundles within the nerve tract. It is this arrangements of microscopic blood vessels relative to the fasciculi that creates the pattern of neural deficits we see post vaccination. For example, pressure lesions (tumor, swelling etc..) in the brain will damage the third cranial nerve in all of its functions (the pupil will become large, eye-lid will sag, eye will deviate outwards). However, when the damages to the third nerve is microvascular and ischemia based from relative impairments in blood flow, then the eye will deviate outward (the central core of the 3rd nerve fasciculus carries the "wires" for controlling medial movements of the eye), but the pupil will be spared and will NOT enlarge (dilate) since the "wires" that control pupil dilation are aligned along the outer fringes of the 3rd nerve fasciculus and are closest to the blood vessels that have decreased blood flow (MASS ischemia) and will receive oxygen and not be harmed, whereas cells and tissue at the core of the fasciculus (furthest from the blood vessel) will be "starved" and begin to die as the impaired blood flow translates into impaired oxygen perfusion to areas furthest from the impaired blood vessel flow.
When blood flow is de-railed by MASS ischemia (and repeat vaccines), these tiny blood vessels alongside and within the nerve tracts will have impairments in blood flow and the delivery of oxygen to tissues and cells. Since oxygen diffuses from the blood vessels to the tissue – the further a tissue area is away from the blood vessel supplying it, the greater the ischemic injury will be since partially impaired blood flow allows oxygen to reach tissue immediately adjacent to the blood vessel that has impaired flow, but the cells ad tissue furthest from the vessel will experience ischemia first.
MASS ischemia "coring: lesions are from hypoxia (low oxygen) delivery to the nerve wires within fascicular bundles furthest from the micro blood supply that traverses along the outside of the fascicular bundles within nerve tracts - this creates partial palsies and various "disconnections" to neural signalling - disconnections.
MASS ischemia creates “coring” damages to the “wires” at the central core to fasciculi traversing through nerve tracts. These are minute strokes that effectively partially cut (disconnect) “wires” within the fasicular sub-cables within neural tracts. These cuts will create partial palsies to some motor functions and other deficits in sensory processing, integration, thinking, language, attention, concentration, perception, speaking, and relating to the world in general…autism for example.
Re: Reference to Pupil Sparing Ischemic 3rd nerve Palsy: Archives of Neurology – Click here
ALL of these disorders are MASS ischemia states - same clinical signs of ischemic brain damage - vaccine induced I am sorry to share...just as repeat vaccines can cuase Type 1 Diabetes, or Wild Polio virus can cause paralysis and respiratory failure. 3rd cranial nerve ischemic lesion sparing the pupil - Gardasil influenza, and MMR vaccines....
MASS FLO ischemia - the common cause of disease and disorder - from vaccinations to toxins to innfectious diseases to heavy metals to immuological tolerance - acquired or "inherited"
- MASS ischemia derails blood flow, creates hypoxia, and can “burn-out” micro circulation blood vessels mostly in end vascular watershed territories – in the brain or in the organs and tissues of the body – including the hand as seen here in soldier who suffered MASS Ischemia (Gulf War syndrome ) after a series of anthrax vaccines that created Tourettes syndrome (a MASS ischemia disorder), his right eye deviating outward while sparing the pupil (ischemic 3rd nerve palsy), loss of hair (end vascular areas to the scalp), burning semen syndrome (end vascular areas to the penis are rendered hypoxic “burning” upon ejaculation (an ischemic neuropathy), and permanent “white areas” in his hands where the micro circulation has been destroyed. When we squeezes his hand, the hand stays white for protracted periods as the perfusion to the hand is impaired by the loss of multiple micro circulation blood vessels form the MASS ischemia state from repeat vaccines. This “capillary burnout” in the hand is ALSO what has happened in the brain to create his Tourettes syndrome, and in children post vaccinations to create autism spectrum -the damages happen after every vaccine received.
Within the ischemic cerebrovascular bed, there are two major zones of injury: the core ischemic zone and the “ischemic penumbra” (the term generally used to define ischemic but still viable cerebral tissue).
In the core zone, which is an area of severe ischemia (blood flow below 10% to 25%), the loss of inadequate supply of oxygen and glucose results in rapid depletion of energy stores. Severe ischemia can result in necrosis of neurons or nerve tracts and also of supporting cellular elements (glial cells) within the severely ischemic area.
MASS ischemia results in relative decreases to complete blocks in forward progression of blood flow – largely in end vascular capillary units (the smallest blood vessels in the circulatory system at the level where oxygen is dropped off to cells).
MASS ischemia coring -the cause of autism neurobehavioral deficits
When a large blood vessel is blocked by a clot or debris, an area of hypoxia (low oxygen) extends outwards from the blood vessel into the tissue area representing areas of tissue and cells that are dead or dying form lack of oxygen and fuel (glucose). This is called the ischemic (impaired blood flow) penumbra (the surrounding tissue in which oxygen exists in a progressively lesser to greater degree).
MASS ischemia to the micro circulation to the bowel creates "autistic enterocolitis". This is pain from ischemia to the micro circulation to the bowl. The brain has no pain receptors when the same process unfolds in the central nervous system - so no pain sensation is created. Germs (fungus, bacteria, virus, parasite...) will sequester to "pockets" within the bowel that have been rendered avascular and the relative oxygen deficits created will also de-stabilize the normal bowel flora. Avascular areas in the body are uniquely susceptible to pathogenic infiltration by opportunistic organisms. For example, the mastoid bone behind the ear is a hollow, avascular (no blood vessels0 structure. If bacteria from a middle ear infection gain access to the mastoid bone it becomes a medical emergency since the bacteria will flourish in the avascular environment as there is no blood vessel network to bring the body's immune system to the area to eradicate the infection - and the mastoid bone can be eroded from the inside out by the proliferation of the pathogen relatively unopposed by any immune system counter-attack to eradicate it. You cannot heal, sustain life, or eradicate germs 9or heavy metals) if the blood supply is damaged or "cut-off" on a macroscopic level (i.e diabetic foot ulcers) or a microscopic level (bowel or brain or bone).
The Ischemic Penumbra
Brain cells within the penumbra, a rim of mild to moderately ischemic tissue lying between tissue that is normally perfused and the area in which infarction (no oxygen) is evolving, may remain viable for several hours. That is because the penumbral zone is supplied with blood by collateral arteries anastomosing (interconnecting) with branches of the occluded (blocked or impaired) vascular tree .
However, even cells in this region will die if reperfusion is not established during the early hours since collateral circulation is inadequate to maintain the neuronal demand for oxygen and glucose indefinitely.
In this example, the ischemic penumbra is shown as a rim of tissue surrounding the severely ischemic core lying within the vascular territory of the pre-Rolandic branch of the left middle cerebral artery. The Rolandic artery is occluded by a thromboembolus. The extent of the penumbra varies directly with the number and patency (openness and unimpeded flow) of collateral arteries.
MASS ischemia - the Penumbra Core and transition from Harm to heal - MASS ischemia "locks" healing at the "injury" phase; in order to recover from MASS ischemia (autism, dementia etc...) the MASS ischemic state must be "dis-lodged" from remaining stuck in the "injury" phase -this requires as step one -treating the blood flow "spiral" state and addressing the oxygen deficit and pH imbalance in all of these "MASS ischemia anoxia" zones" - this is achieved by re-establishing the colloidal stability of blood flow fluid dynamics so that greater flow can be established to the micro circulation where varied capillary networks remain but have been "crimped" back and blood "sludging and skimming" in these areas is rectified - this improves flow - step one on the MASS recovery protocol - for everyone. BrainGuardMD directly addresses this phase of the healing response with our "BrainGuardMD MASS Charge Flow Crystals" which instill negative charge into consumable water (distilled) taken three times daily. This is step one..and everyone requires this phase to be in place for the other recovery phase solutions to work. Without the proper charge, carrying capacity, and dispersion forces in the human blood (and its flow) nothing will heal in micro circulation and diseases will progress and or never recover fully. BrainGuardMD MASS Charge Flow Crystals available by calling: 1-877-MOULDEN
The penumbra is where pharmacologic interventions are most likely to be effective. However, it may also be possible to salvage cells within the severely ischemic core zone. Although severe ischemia kills selectively vulnerable neurons, glial cells may be spared if blood flow is restored early. Therefore, timely recanalization of the occluded vessel should theoretically restore perfusion in both the penumbra and in the severely ischemic core. Partial recanalization should markedly reduce the size of the penumbra as well.
Microvascular Ischemia Cranial Nerve "Coring" lesions partial palsies from hypoxia
Know the signs - MASS ischemia - Brain damages on a continnum of silent induced harm - subtle to profound - ALL vaccines - Ischemic strokes to the nerves (and body)
