I live in winterland. The Great White North. Canada.
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3. The Pineal Gland
Quote:
The Pineal Gland -also called the epiphysis- looks like a miniature pine cone and is situated in the middle of the brain beneath the two brain halves, surrounded by the ventricles, under the roof of the corpus callosum (cross-beam connecting the 2 brain halves). (see picture) This active organ has, together with the Pituitary Gland (see picture), the next highest blood circulation after the kidneys. It is not protected by the blood-brain barrier and therefore makes this gland fragile to any substance entering the bloodstream. It is, for instance, very sensitive to fluoride.
Another factor involved in affecting the Pineal Gland can be excessive high or even toxic levels of an SSRI-AntiDepressant in the bloodstream. Certain individuals have a metabolic deficiency in the metabolism of anti-depressant medication. In the liver, a group of enzymes named " cytochrome P-450" enzymes, particularly the "CYP2D6 enzymes" of this group of enzymes, metabolise SSRI-AntiDepressants. When not properly metabolised, because one has a metabolic deficiency, a daily therapeutic dose can build up to excessive high or even toxic levels in the bloodstream. Hence, the Pineal Gland would be an easy target, since it is not very well protected by the blood-brain barrier. It is it's connection to serotonin what makes this organ so very interesting.
3.a. The Pineal Gland-Serotonin connection
Nicholas Giarmin, a professor of pharmacology and Daniel Freedman, a professor of psychiatry, confirmed that the human brain manufactures serotonin at various sites in the brain. For example, in the Thalamus, they discovered 61 nanograms of serotonin per gram of tissue; in the Hippocampus, 56 ng.; in the Central Gray Section of the Midbrain, they found 482 ng. But in the Pineal Gland, they found 3140 ng. of serotonin per gram of tissue. The Pineal Gland was unmistakably the richest site of serotonin in the brain! This discovery implicates the Pineal Gland as an important site of serotonergic activity.
The neurohormone Melatonin & the Endocrine System
One of the neurotransmitters secreted by the Pineal Gland is Melatonin, also known as N-Acetyl-5-Methoxy-Tryptamine (NA-5-MT). In the Pineal Gland, serotonin converts into melatonin by enzymatic interaction. Melatonin is also an important hormone to the body, that's why it is called a neurohormone. It is necessary to regulate the function of all organs of the Endocrine System in the body. The organs or glands of the endocrine system are: the Pituitary Gland, situated in the brain; the Thyroid + Parathyroid Glands; the Thymus; the Pancreas; the Ovaries/Testes (see image). All of these endocrine organs/glands secrete their hormones to the blood. The Pituitary Gland stimulates the secretion of these hormones, while the Pineal Gland apply the brakes on them through it's neurohormone melatonin. If the endocrine organs/glands release too much of their hormones, for instance when we are stressed, then the Pineal Gland releases melatonin to counteract these hormones. Also serotonin gets released when stress is involved. The increased serotonin triggers the release of adrenaline, which allows the body to work through the stress.
The Pineal Gland is a magneto sensitive organ, what means that it is sensitive to electromagnetic fields (EMF). It is sensitive to electromagnetic waves from computer monitors, cellular phones, microwave ovens, high voltage lines, etc.. Electromagnetic fields suppress the activity of the Pineal Gland and reduce melatonin production. EMF also affect serotonin.
The neurohormone Melatonin & the Eye-SCN-Pineal Gland Axis
The Pineal Gland is also a photosensitive organ, what means that it is sensitive to light. It normally releases melatonin when it no longer receives light impulses. Just like serotonin, also melatonin has it's own day & night cycle (circadian rhythm) which begins where the cycle of serotonin normally ends. When serotonin reaches it's lowest level at night (in the dark) during slow wave sleep, the Pineal Gland starts to convert it's store of serotonin into melatonin to be released prior to REM sleep. Melatonin has it's peak around 02:00 AM. During daytime, the daylight inhibits the release of melatonin. This works as follows: when, during daytime, light reaches the eyes, then it's presence gets translated into nerve impulses, which travel through the optic nerve between the eyes and a region of the Hypothalamus called the "Suprachiasmatic Nucleus" (SCN). (see picture) The SCN in it's turn sends it's nerve impulses to the Pineal Gland. These impulses inhibit the Pineal Gland's production of melatonin until it gets dark, when it's to be released again. Melatonin is not only present in the brain and body but also in the eye! One has speculated whether or not high melatonin levels in the eyes during daylight exposure, may bring damage to them over time. Visual/eye problems (light sensitivity, spots, blurred vision) are other symptoms, frequently reported by (former) SSRI-AntiDepressant users. I questioned myself if these problems could be related to elevated melatonin levels in the eye. When serotonin accumulates in the Pineal Gland, on account of an SSRI-AntiDepressant, then it would come under pressure to produce more melatonin out of the excessive amounts of serotonin. Hence, during daytime, melatonin levels in the eyes would be significantly higher then normally would occur... But, I had to revise this hypothesis. In a PubMed study, SSRI-AntiDepressants were found not to elevate melatonin levels in humans. Although "Luvox" and "Paxil" increases melatonin to a more or lesser amount, apparently this seemed not to be the case for the other SSRI-AntiDepressants. However, since the Pineal Gland does contain a complete map of the visual field of the eyes, could there be a correlation between visual/eye problems and a dysfunctional Pineal Gland?
A case, noted by Dr. Berman, could give us some more insight into this matter:
A child was brought to a German clinic suffering from eye trouble and headaches. He was five years old and very mature, and apparently had reached the age of adolescence. He was abnormally bright mentally, discussing metaphysical and spiritual subjects. He was strongly group-conscious and only happy when sharing what he had with others. After his arrival at the clinic, he rapidly grew worse and died in a month. An autopsy showed a tumour of the pineal gland. - Berman, Louis, M.D., The Glands Regulating Personality, p. 89. Could it be that the visual/eye problems (light sensitivity, spots, blurred vision), frequently reported by (former) SSRI-AntiDepressant users, are caused by some element of Pineal Gland dysfunction?
They are really fucking with us man - on every fucking despicable level.
They know what flouride is doing to us - and microwaves.
Fuck fuck fuck this means war.
Another hilarious read brought to you by internet scholars.
hooray
my non confrontational, generally easy going post was completely ignored.
styles, you are pretty much a 5%er in philosophical terms.
its just interesting to me, that you oppose others so much, and then come up with this...
Stylemaster in inhumanely dim.
what the fuck is sino-american economic system?
cheap toys?
you said every nation can't follow the american system of "stepping on other ppls toes" to get what they want.
i said, every nation steps on peoples toes to get that why want
you said china didn't, it's isolationist
i said china did, as the country China, is han china, or essential the Chin section of han china, taking over everyone around it.
since korea, mongolia, vietnam, tibet and various other locations have a history of chinese imperialism, i really don't see how difficult it is to sink the one in.
those ppl you mentioned, are, indeed, chinese, not because they're ethnically chinese, but cause they're members of a chinese nation build on the kingdom of Chin, taking over it's neighbors and making them chinese, which would equalify as being a toe stepper on'er
the system of dicking your way to the top is not an american invention, and you, again, can't find a country that didn't dick its way to the top.
again, not difficult to sink in, i'd find examples if i were you because the next conversation in line after this one is how toothpaste n microwaves are killing the black community's melanin(soul).
^^Scientific blogs by brain scientists are hilarious to you?
I can honestly say man that I felt what u do because at first I was looking at a lot of this as a bunch of bullshit. Basically I looked at it like black propaganda to uplift people in dire state.
But now the facts are in. More to come...
Melanin Pigments in Human Pineal Gland
Author(s): Koshy, S. & Vettivel, S.
Vol. 50, No. 2 (2001-07 - 2001-12)
Department of Anatomy, Christian Medical College, Vellore, India
Abstract
Masson-Fontana staining confirmed the presence of melanin pigments in the human adult pineal gland. In 1-10 years age group, the pigments were present within the pinealocytes. In 11-20 years age group also, the pigments were in the pinealocytes only. In 21-30 year age group, the pigments were in the pinealocytes and appeared in the stroma in the areas of glial fibre predominance. In 31-40 years age group onwards, the pigments were present, in addition to pinealocytes, in the stroma among the fibres. As age advanced, the amount of extracellular pigments gradually increased, extracellular pigments were more concentrated, and the extracellular pigments were more clearly seen. There was no gender difference in the amount of melanin pigments. The background comparative anatomy also is discussed.
Key words: melanocyte, melanin, pinealocytes, pineal gland
Introduction:
Melanocytes are melanin-pigment synthesizing pigment cells derived from neural crest and widely distributed in vertebrates. They are stellate cells with long processes with numerous dark brown or black granules of melanin in their cytoplasm. There function is generally, to prevent light from reaching adjacent cells. In humans, they are present in the epidermis and its appendages, oral epithelium, some mucous membranes, uveal tract of eye ball, parts of middle and internal ear, and parts of leptomeninges in the base of brain. The cells of retinal pigment epithelium, neurons in locus ceruleus and substantia nigra also synthesize melanin. Melanins are high molecular weight polymers, attached to a structural protein, to form melanoproteins, and in the humans, there are two classes, the brown-black eumelanin and red-yellow pheomelanin, both derived from a substrate tyrosine (Dyson 1995).
Pineal gland (epiphysis cerebri) was once considered to be a phylogenic relic, a vestige of a dorsal third eye, and of little functional significance; the mammalian pineal is now regarded and accepted as an endocrine gland of major regulatory importance, modifying the activity of the adenohypophysis, neurohypophysis, endocrine pancreas, parathyroids, adrenal cortex, adrenal medulla, and gonads. (de Vries and Kappers 1971; Klein 1978; Haulica and Coeulescu 1981; Reiter 1983, 1985, 1987; Malendowicz 1985; Dyson 1995).
The pineal in the big brown bat is pigmented and intensified with constant darkness (Bhatnagar and Hilton 1994). Pigmented cells in the cat pineal gland show a preferential localization at the ventral surface of the pineal gland near its distal end and the pineal pigment is melanin (Calvo et al. 1992). Presence of pigment cells is a constant characteristic in the adult dog pineal gland; the pigment is melanin (Calvo et al. 1988). Embryo ovine pineal gland has pigment cells containing melanin (Regodon et al. 1998). Pineal glands of neonates consist of cords of dark, nucleated cells, which are frequently pigmented (Min et al. 1987). In the human adult, melanin pigments gradually accumulate within the parenchymal cells with increasing age in males, whereas in females, the maximum pigmentation is noticed in 30-40 year age group and then there was a fall (Tapp and Huxley 1972). The present study was done to find whether or not the human adult pineal gland showed gender difference and age changes in the amount of melanin pigments.
Materials and Methods:
Forty pineal glands were collected from South Indian subjects (31 males and 9 females) who were accident deads, within five to six hours after death during autopsy. There were no histological postmortem changes. Age of the subjects ranged from one to eighty years. Age groups of the subjects were 1-10, 11-20, 21-30, 31-40, 41-50, 5160, 61-70, 71-80 years.
Pineal glands were removed from the brain along with the superior colliculus so that the pineal recess of the third ventricle was also included. These were put in Bouin's fluid. After fixation, the specimens were processed for light microscopy. Eight-micron serial sections were cut and stained. Staining methods used were (i) haematoxylin and eosin, (ii) Masson-Fontana method for melanin, and (iii) Mallory's phosphotungstic acid haematoxylin method for neuroglial cells and nerve fibres. The arrangement of the parenchyma and stroma was observed. Melanin pigments were visually studied for location and quantity with regard to gender and age.
Observations:
Pineal gland had a well defined capsule (piamater) and septa extended from the capsule into the parenchyma dividing it into complete and incomplete lobules. Parenchyma consisted of light and dark pinealocytes and glial cells. Corpora arenacea were a constant feature (Koshy and Vettivel 2001). Melanin pigments were present in the pinealocytes and in the stroma. In 1-10 years age group, the parenchyma was highly cellular, predominantly of pinealocytes. Within the pinealocytes, melanin pigments were present. There were no extra cellular pigments. In 11-20 years age group, the parenchyma was highly cellular with the presence of pinealocytes. Pigments were present as in 1-10 year group, within the pinealocytes. In 21-30 years age group, abundant dark melanin pigments were inside the pinealocytes and in the areas of glial fibre predominance. The pinealocytes were not abundant as in 11-20 age group but extracellular pigments were in the transition areas from pinealocytes-predominance to glial fibre-predominance (Fig. 1). In pineal glands of higher age groups, 31-40, 41-50, 51-60, 61-70 years, melanin pigments were seen as clear granules, more among the fibres. The pinealocytes also had melanin pigments within them. The extra cellular pigments were more clearly seen as age advanced. There was no gender difference in the amount of melanin pigments. A gradual increase in melanin, more concentrated extracellularly, occured as age advanced.
Discussion:
Pineal gland projects from the roof of diencephalon. A recess of third ventricle extends into its stalk. The pineal was formerly considered a vestigial organ with no function but now it is known to be an active endocrine gland. Its activity is influenced by the daily cycle of light and dark and it is a link between environment and physiology of an organism (individual). It responds to annual changes in day-length and influences gonadal activity in seasonal breading species but has, though less apparent, significant effect on the reproductive system of other species that breed throughout the year. Its innervation is exclusively via sympathetic fibres that originate in the superior cervical ganglion and enter the cranial cavity accompanying blood vessels supplying the brain (Fawcet 1994).
Paired eyes of vertebrates are organs to focus a clear image upon a film of sensory cells known as retina, and these cells convey the impulses to the brain, giving their interpretation of intensity, colour, or movements. In some primitive vertebrates, there are also two different median organs, which serve as receptors for light, although not necessarily to obtain visual images. There are indications, from elasmobranch embryology, that the prevertebrates possess a metameric series of paired visual organs on the roof of the head; most of them rapidly disappear as the lateral eyes become perfect; but two pairs of dorsal eyes still hang on, almost to the cyclostome level. In lamprey, one member of each of these supposed pairs might be seen as a small bulb, attached by a stalk, to the root of the diencephalon. The anterior one (parietal stalk) does not quite reach, but the posterior (pineal eye) does reach a semitransparent spot in the skin of the head. Possibly, both bodies were present in primitive amphibian, for in frogs, the pineal is found, nearly reaching the skin; yet in some modern reptiles (sphenodon and lizards) a parietal eye is present, with the pineal redued. Among early vertebrates, the evidence of these organs is simply a foramen in the roof of the skull in ostracoderms, some placoderms, crossopterygians, primitive amphibians, and some of the early reptiles, including Therapsids. It usually lies between the parietal bones. The parietal eye of the Sphenodon is well covered, and no function has been demonstrated, but it contains a retina and a lens; the neurosensory retinal cells synapse with neurons, which go directly down the stalk. In birds, the pineal stalk is reduced but often distinct and with a complicated structure distally. Mammals have a minute epiphysis (pineal organ), which has been suspected to have an endocrine function (Eaton 1960).
In most fish, and amphibians, the pineal organ is a single sac. In the more primitive fish, tail-less amphibians and lizards, there is a second component, the parapineal organ or parietal organ, which arises as an anterior evagination of the pineal organ or as a separate outgrowth of the roof of diencephalon. In frogs, parapineal component lies just beneath the epidermis on the dorsum of the head, where it can be seen. Numerous nerves and nerve endings are found in the pineal organs of lower vertebrates. Pineal organs of lower vertebrates reveal presence of photoreceptor cells that resemble those of the mammalian retina in having a lamellar portion of the apex and a receptor synapse at the base. The most elaborate pineal is found in the primitive lizard, Sphenodon. It contains a simple retina, consisting of photoreceptors backed by supporting cells that contain pigment, and its parietal component includes a lens-like structure. It thus constitutes a vestigial parietal eye. Probably, the parietal eye of the Sphenodon was functional because of the large size of the pineal foramen in the fossil reptiles (Fawcett 1994).
Pineal gland contains cords and follicles of pinealocytes and neuroglial cells among which ramify blood vessels and nerves. Pinealocytes form the pineal parenchyma; neuroglial cells, partially separating the pinealocytes, are like astrocytes. Ultrastructure of human fetal pinealocytes indicates their secretory function in early intrauterine life (Moller 1974). As in adults, they contain all the appropriate organelles together with abundant microfilaments, microtubules, and a few cilia with a 9 + 0 microtubular pattern. Cilia of this type are associated with secretory cells in other endocrine glands (Barnes 1961; Andersen et al. 1970). Extending from the cell body are one or more processes (Knight et al 1973), which end in terminal buds near blood vessels or ependymal cells of the pineal recess. The terminal buds contain electron dense cored vesicles, which store monoamines and polypeptide hormones (Sheridan and Sladek 1975), release of which requires sympathetic innervation. The polypeptide hormones combine with specific protein carriers, termed neuro-epiphysins (Lukaszyk and Reiter 1975). They are released by exocytosis together with exocytotic debris. When released, the complex dissociates, hormones being exchanged for calcium ions. The calcium-carrier complex so formed is, in the pineal, deposited concentrically around exocytotic debris as corpora arenacea or brain sand. It is often supposed that the pineal gland atrophies with age, corpora arenacea being a sign of atrophy; on the contrary, these corpuscles may indicate continued secretion. There was no evidence of pineal degeneration in the elderly (Wildi and Frauchiger 1965).
The pinealocytes of mammals evolved from the photoreceptor cells of the pineal organ of primitive vertebrates. In the course of their evolution from light sensitive elements to endocrine cells, the region of the cell, specialised for photoreception was lost, together with the sensory nerves connecting it to other regions of the brain. The synaptic ribbons of mammalian pinealocytes may be vestiges of the special synapses that are characteristic of photoreceptors. Whether they have acquired an alternate function, related to secretion, is not known (Fawcett 1994). Pinealocytes of some mammals contain synaptic ribbons, perhaps involved in transmission; vesicles near them contain neurotransmitters such as - aminobutyric acid (Krstic 1976). Similar arrangements of organelles occur in mammalian retinal photoreceptors and simpler submammalian photoreceptors, suggesting that mammalian pinealocytes are derived from photoreceptors (Kappers 1976; Relkin 1976). Transient similarities exist between pinealocytes and retinal photoreceptors in neonatal rats (Zimmerman and Tsi 1975).
Melanin pigments are associated with light and are found in association with photoreceptors. This association, probably, exists with photoreceptor cells-derived pinealocytes also. It is possible that the pigments, corresponding to those (rodopsin) in photoreceptors and those in the supporting cells in Sphenodon pineal gland, are in the pinealocytes and stroma in the human pineal gland. Increase of melanin pigments is due to the action of pineal indole-melatonin. Melatonin suppresses the melanocyte-stimulating hormone and prevents dispersion of melanin granules. Therefore, the melanin pigments become concentrated in the pineal gland.
The sphenodon pineal has pigments in the supporting cells of the photoreceptors. Mammalian retina has pigment cell layer. Melanin pigments have been shown to be present in animal and human fetal pinealocytes. Correspondingly, the present study, light microscopically, has shown melanin pigments in the human adults. Melanin pigments gradually accumulate within the parenchymal cells with increasing age in males, whereas in females, the maximum pigmentation is noticed in 30-40 year age group and then there is a fall (Tapp and Huxley 1972). The present study shows that there is no gender difference in the amount of melanin pigments, that a gradual increase in melanin pigments, more concentrated extra cellularly, occurs and that melanin pigments are more clearly seen as age advances.
Acknowledgement:
The help of Dr. Valsamma Mathew, Department of Anatomy and Dr. Radha Krishnan, Department of Forensic Medicine of Kottayam Medical College, Kottayam is acknowledged.
it is propaganda
i won't say black propaganda cause the only black ppl the buy this shit are Stylemaster, Poppa Wu, Sunnywinters and his secondaries.
it's a disgusting field of thought, to become what you hate in white supremacist culture, meaning your striving to be the lowest example of socialization your 'enemy' has to offer.
it all comes from self hate and self-esteem voids and will do nothing but cause it's suscribers to live in a world of hate and frustration that will eat their insides and lead them to believe the world outside of their illusion is forever hopeless.
a sad way to die.
YAY! articles that I myself could have written and called scientific fact and nobody, including the poster will ever read!
why commity suicide when you have green font!?
additionally the amalgamation of science, psychology, history, politics, sociology etc. which is somehow fluently integrated into conversation, is ridiculous.
some of the above might be linked, maybe all of the above.
but the extent to which people here state a scientific "fact" and from there go on to explain the entirety of history and then go on to explain current societal and political ills, is illogical and bizarre.
Regards,
You can find "research" to support any argument, from conspiracy theories to this.
When I look at a piece of information I want to know if it's been peered reviewed, and adheres to a strict set of scientific guidelines for experimentation, otherwise I'm not buying it. This way, subjectivity and bias in data are eliminated a best as is possible.
There is a lot of misinformation on the internet from so-called scientific sources that haven't been exposed to this type of scrutiny. So unless I can see that the information presented is credible in the way I described I won't be paying it much attention. In fact, whenever I want to get up to date on a particular issue I always go through the university I attend to find published work (ie peer reviewed etc) on the topic.
Furthermore, a great number of KTL posters stay losing because they are unable to comprehend whether a source is credible or not beyond their radical opinion. It is great to look at all points of view on a topic, I am not disputing that. However, when someone strongly and often rudely argues their case, citing unproven "scientific" data combined with conspiracies about the government etc I don't see how it can be taken seriously.
For me, it isnt even that.
Ive taken the time (and it wasnt even wasted time, because some of these sources provide credible information) to read most of the 'research' posted.
Unfortunately, from this 'research' wild conclusions are drawn which do not logically follow the information presented in sources.
They idea of sourcing material is to back up an argument which you are making, as oppose to outlining 'facts' and then going off on a tangent about what you 'think' is scientifically correct.
All the actual 'research' which stylemasterr posted is acceptable i feel.
However, he used this in order to lay the foundation for his subsequent argument, instead of provided supporting evidence.
This is a common trend with his posts i find.
He will outlay 'facts' which seem acceptable, and then launch into a flawed, quasi scientific philosophical argument, which minimally references the original source.
And this isnt even the norm in KTL.
Style is going far beyond the general standard of 'proof' here.
Normally people write paragraphs of opinion and post at the end "if you dont believe me, look here *insert several webpages*.
Whats more, why havent you called me rahbart?
what is the plan?
im at uni...
when are you leaving?
should i get home some time soon?
fanx.
Soon my friend. I understand what you mean. It's all about taking information out of context. This often happens when people don't understand the scientific terms. None of that information presented proves Style's point.
and VAD3R, I have no qualms with you but you did exactly what am talking about in a previous post, the one where you mentioned fluoride.
enswur duh phfohn plase.
calcified flouride inhibited testicular glands.
So you dont believe there is an elite agenda to kill off some 80% of the planet so be it...
but I presented some facts on how this directly affects the pineal gland.
If you dont want to acknowledge the possibility that some insecure powerful men do feel threatened to lose out a lot with things like a black president that might do something about Reparations or actually do meaningful things for people of color...thats on you.
Aids - fluoride - syphilis - what else man? What the fuck else is fucking us up that is man-made death?
just stopping by to check what's new and damn ... this thread is good
see ya in a month!
fuck yall. you ain't black so you will never "get it".
why does it even matter to any of yall?
i mean really yall aussies don'/t even know any black people. why do you care?
TSA included you uncle tom oreo cracker worshipping onion armpit african reject. stay suckin those redneck dicks. stay indoors and get you vitamin D that way you fuckin loser.
pat idk what to tell you man. i started my style career talkin this same shit.
see whites and savagery vol 1 & 2 , my 1st threads.
and said "if a white person can accept the fact that i feel this way we can be the best of friends"
i have had brotherly friendship with white guys but will tell them in a min that crackers a fucked up and i have to know them in order to trust them.
i thought that's where we were. a mutual understanding that style thought whites were biologically inferior to people of color, but have the same capacity for greatness as anyone else.
no?
ain't that a kick in the nuts
i feel like befriending a white person is like having a pet cobra. if it bites you, you can't be mad at anyone but yourself.
ouch
fuck it.
it's a subject of maturity.
that's what's wrong.
you and pat said you read those articles.
i don't, they're fuckin stupid can come from places like TheBlackNubianAlliance, which is the last place i would send my kids to actually learn something
therefore, KTL posters get frustrated when the argue with me because i present actual facts that we both actually know. nothing elaborate and nothing far fetched but by making it clear that im not gonna read pathetic articles written by people that are internally hurt asserting their false superiority as a means to redeem a shattered and empty sense of self worth it kills them inside more cause ALL THEY CAN DO is post these articles.
it's pathetic.
really, really, really pathetic.
between that, stylemasters current state of anger, and sunny winters secondaries is easy to see why KTL is pure garbage.
all i do is come on here, present truths that all posters know and they have a hard time arguing it so they start talking about how africans smell while trying to assert black people are a super natural race of superior people, which they're not, they're poor.
so as i was saying. China engages in the world system, the only evidence presented against me is the fact that China has a lot of ethnicities but they're overwhelmed by the han chinese population.
those ethnicities were conquered by the han chinese and are under their domain till this day.
china also has a history of imperial dominance over vietnam, korea, tibet, various Gobi desert or people of western china, and mongolia, which till this day the majority of mongol land and people are artificially place behind chinese boarders.
you mad?
Peace.
This is to those who are in the know. You know who I'm talking to.
Pay very close attention to whats going on here. We have original people, black people, people of color, non-whites who are showing serious signs of being sick.
Because the devil taught him how to eat the wrong foods.
He likes the devil because the devil gives him nothing.
The statement above is very important....those who know it and understand know why.
Look how he big ups white people but continues to put down original (black) people. He want to be a part of the devil's social equality but the devil will never let that happen.
He's being used as a tool and also a slave.
What does a person when they don't love themselves? The destroy self and everything that reminds them of self!
Why did Musa have a hard time civilizing the devil......?
The 85% believe in the 10% on face value.
Anything black, he's against. Anything white, he's for.
It's not about truth. It's not about freedom, justice, or equality. It's about him being other than his own self.
He's going under the study from 35-50 years to try and learn and do like the colored man hoping that he'll be able to take the heads of 4 gods wanting free transportation to the vatican to see his unrighteous brother.
what are these wrong foods and why do africans proudly eat them?
pork?
the national food of Cameroon
i would also like to add that the devil gave me 10 dollar last week and traded me my skateboard for civilizations III
i played Civ III until early this year when i uninstalled it to free up computer space and the trade was made in 2000.
the devil also game me Wu Chronicles II and The Pretty Toney album
Doesn't the devil wear Prada?
If the devil ate swine and vomited in the waters of the Nile then 85% of the original man would be infected.
Of the remaining 15%, 10% would avoid infection and die from dehydration. The other 5% would transcend food and water and become master to self, swine and slave.
Supreme Math.
Is there a way to tell Black Man cases that their thinking is bullshit from roots?
For real.
Y'all 5%'s are so much into science - well, PROVE ME THAT YACUB EXISTED AND CREATED US DEVILS TO TORTURE BLACK FOLKS. Prove me.
Prove me rationally or empirically ANYTHING you said in the post #106 about devils fucking up blacks. About poisoning with wrong food and shit.
Prove.
^^^ it would be better to prove the theory if you can instead of avoiding it or sayin people aren't ready, etc. it only makes people REALLY think its bullshit if you refuse to give any proof. im sure u annoyed with people askin you so just give an answer
BEFORE YOU CAN ADD AND SUBTRACT, DON'T YOU NEED TO KNOW HOW TO COUNT FIRST? IN ORDER TO COUNT IN THE RIGHT ORDER, DON'T YOU NEED TO KNOW WHAT THE NUMBERS ARE?
I SEE PEOPLE DON'T KNOW HOW TO KEEP THINGS IN ORDER. THAT'S WHY THEY WON'T UNDERSTAND BECAUSE THEY KEEP SAYING 2 COMES BEFORE 1.
YOU CAN'T PROVE SOMETHING TO A PERSON THAT DON'T KNOW NOTHING, AND ISN'T WILLING TO DO WHAT IT TAKES TO ACTUALLY FIND OUT.
YOU'LL NEVER UNDERSTAND THE SCIENCE OF YACUB WITHOUT HAVING A SOUND UNDERSTANDING OF WHO THE ORIGINAL MAN IS.
WHEN DID I SAY PEOPLE WEREN'T READY? OK, I'LL SAY IT NOW.....YOU'RE NOT READY!
I DON'T CARE WHAT PEOPLE THINK OF ME. I KNOW WHO I AM.
You boys and girls don't know who the Original Asiatic Black Man is?
Yup. The Black Man, the black Adam and Eve, from which all the mankind spread out. Am I correct?
Excellent. It's just a long version of a sentence: "You are stupid and I am smart".
Ah, yeah, this too: "And I won't help YOU to become smart, for it'd diminish my superiority complex".
Is this what Honorable Allah and First Borns wanted from you? To keep your knowledge for yourself instead of spreading it?
Or is it because I'm just the usual devil that wants to keep YOU down? I don't even know you, motherfucker!
when you avoid questions it usually means you don't have an answer
People Want Lesson 88 But Don't Know Shit About Lesson 1. Nope, You Won't Understand Because You Don't Know The Basics.