THE HUMAN BRAIN IS 95% NON-FUNCTIONAL

1. The human brain is 95% non-functional.  It is an antenna for the wireless mind.  You are remotely controlled, unless you escape inwards.
2. The eyes do not and cannot see. It,  like the brain,  is cyber attacked by photon reflections of size, color etc. So who and how does one see reality?

3. Humans have 22+1 chromosomes and most 95% run on Rhesus positive blood.  It doesn't and won't work out because Rhesus positive apes have 24-chromosomes.  Something went amiss.

4. Intelligence  by the 1% are due to their spiritual elevation due to the fact that the brain cannot do the job, but the soul can do it right.

The Pyramids Orions Belt by Nassim Haramein

Brien Foerster - Ancient Civilizations Presentation

COVERUP Of Alien Activity In Our Oceans Exposed 2/26/16

MAJOR Discovery Of Alien Base Installation On Mars & More! 2/24/16

MODERN HUMANS ARE FABRICATIONS BY ADVANCED EVIL BEINGS.

All primates, apes, hominids, neanderthal:, cromags 48 (24 pairs) 
Humans (Homo sapiens): 46 (23 pairs) 

There is no natural evolutionary way: 

1) Evolution from ape to human just "looses" two chromosomes (1 pair). It is impossible. 
2) Chromosomes 2 and 3 just "fuse" into one long jumbo doubled-up chromosome 

Somehow, humans have 46 chromosomes (23 pairs) and primates have 48 chromosomes (24 pairs). If two chromosomes less doesn't sound like a stark difference to you, well consider the fact that dolphins have 2 chromosomes less than humans, too, and look how different they are from humans! 

So what happened? To have caused both a SPLICING of hominids' chromosome 2 and 3 in one pair, and the loss of a whole chromosome pair?? 

Ancient GE! Only genetic engineering can explain that. It's like someone took a female earth hominid with 24 pairs of chromosomes, and wanted to impregnate it with their own sperm but their own species happens to have 23 pairs. So what do you do in order to make this hybridization work? You take the female earth hominid's egg's chromosome 2 and 3 and fuse them, that way eliminating one chromosome half-pair. With your sperm, you provide your 23 half-pairs, and now the genetically engineered female hominid egg with its doubled-up chromosome 2&3 provide 23 half-pairs, instead of the incompatible 24 pairs all other earth primates & hominids have. 

Problem solved, the female hominid's egg with chromosome # reduced by one, accepts fertilization from your sperm and the fertile hybrid offspring is born with your chromosome number and thus can, when mature, successfully reproduce with its hybrid siblings, other hybrids created as per above, and with your extraterrestrial species directly, too! 

However it cannot ever again successfully reproduce with the native earth hominids because of the reduced chromosome number. But that's not a problem since you already have 50% native DNA, that's more than enough, you don't want them to breed back into the native population for then they will end up reverting to mostly neanderthal/cromag/hominid race all over again. 

And so the human race was created some 150,000 yrs ago and then free to interbreed and reproduce with each other as well as directly with the extraterrestrial species that caused this 

Above Top Secret.

Lloyd Pye (RIP) and Human Origins.

The murder of Lloyd Pye, death from Weaponized Cancer

 If you are an enemy of the secret government of the united states stay away from your doctor. He will inject you with Cancer virus and irradiate you to activate it.See my more than 400 videos on you tube covering a vast array of similar subjects.Chanel Donations via paypal of any amount accepted to keep my research going.

THE MURDER OF LLOYD PYE, DEATH FROM WEAPONIZED CANCER.


Repeated DNA of the human Y chromosome.

Smith KD1, Young KE, Talbot CC Jr, Schmeckpeper BJ.

Author information

Abstract

A significant fraction of the human Y chromosome is composed of DNA sequences which have homologues on the X chromosome or autosomes in humans and non-human primates. However, most human Y-chromosome sequences so far examined do not have homologues on the Y chromosomes of other primates. This observation suggests that a significant proportion of the human Y chromosome is composed of sequences that have acquired their Y-chromosome association since humans diverged from other primates. More than 50% of the human Y chromosome is composed of a variety of repeated DNAs which, with one known exception, can be distinguished from homologues elsewhere in the genome. These include the alphoid repeats, the major human SINE (Alu repeats) and several additional families of repeats which account for the majority of Y-chromosome repeated DNA. The alphoid sequences tandemly clustered near the centromere on the Y chromosome can be distinguished from those on other chromosomes by both sequence and repeat organization, while the majority of Y-chromosome Alu repeats have little homology with genomic consensus Alu sequences. In contrast, the Y-chromosome LINE repeats cannot be distinguished from LINEs found on other chromosomes. It has been proposed that both SINE and LINE repeats have been dispersed throughout the genome by mechanisms that involve RNA intermediates. The difference in the relationship of the Y-chromosome Alu and LINE repeats to their respective family members elsewhere in the genome makes it possible that their dispersal to the Y chromosome has occurred by different mechanisms or at different rates. In addition to the SINE and LINE repeats, the human Y chromosome contains a group of repeated DNA elements originally identified as 3.4 and 2.1 kb fragments in HaeIII digests of male genomic DNA. Although the 3.4 and 2.1 kb Y repeats do not cross-react, both exist as tandem clusters of alternating Y-specific and non-Y-specific sequences. The 3.4 kb Y repeats contain at least three distinct sequences with autosomal homologies interspersed in various ways with a collection of several different Y-specific repeat sequences. Individual recombinant clones derived from isolated 3.4 kb HaeIII Y fragments have been identified which do not cross-react. Thus, the 3.4 kb HaeIII Y fragments are a heterogeneous mixture of sequences which have in common the regular occurrence of HaeIII restriction sites at 3.4 kb intervals and an organization as tandem clusters at various sites along the Y-long arm.(ABSTRACT TRUNCATED AT 400 WORDS)