BLOODY ROYALS & THE X FACTOR

Following are quotes from https://en.wikipedia.org/wiki/Tyrian_purple

Tyrian purple (Greek, πορφύρα, porphyra, Latin: purpura), also known as Tyrian red, ROYAL PURPLE, imperial purple or imperial dye, is a bromine-containing reddish-purple natural dye. It is a secretion produced by several species of predatory sea snails in the family Muricidae, rock snails originally known by the name Murex. In ancient times, extracting this dye involved tens of thousands of snails and substantial labor, and as a result, the dye was highly valued.

https://en.wikipedia.org/wiki/Tyre,_Lebanon

Lilith, Owls, Tyre, The Stone of Destiny & Queen Elizabeth https://spidercatweb.blog/2017/03/19/lilith/
Queen Elizabeth, The Daughter of TYRE?? https://spidercatweb.blog/2016/01/27/queen-elizabeth-the-daughter-of-tyre/

ROYAL HAEMOPILIACS

ROYALS & PORPHYRIA

A STRONG stomach is needed if you are going to look at some

King George III
Mary, Queen of Scots
James V of Scotland
James I and VI
Princess Charlotte Augusta of Wales
Prince William of Gloucester, who died in a plane crash in 1972. He was the eldest son of Prince Henry, Duke of Gloucester (son of George V). diagnosed with porphyria. Don’t know type or extent of his symptoms.

Grandson of George V; for the grandson of George II who was also known as Prince William of Gloucester, see Prince William Henry, Duke of Gloucester and Edinburgh for the son of Anne, Queen of Great Britain see Prince William, Duke of Gloucester

According to http://www.sussex.ac.uk/press_office…/article1.html “There is a one-in-two chance of any member of the Royal family with the faulty gene passing it on to each offspring. Of that number, around 10% will suffer symptoms.”

Daniel 4, the madness of Nebuchadnezzar (4th chapter of the Bible‘s Book of Daniel) tells how King Nebuchadnezzar learns the lesson of God’s sovereignty, “who is able to bring low those who walk in pride.” Nebuchadnezzar dreams of a great tree that shelters the whole world, but in his dream an angelic “watcher” appears and decrees that the tree must be cut down and that for seven years he, Nebuchadnezzar, will have his human mind taken away and will eat grass like an ox. This comes to pass, and at the end of his punishment Nebuchadnezzar praises God. (Daniel‘s role is to interpret the dream for the king).^[1]

The message of Nebuchadnezzar’s madness is that all earthly power, including that of kings, is subordinate to the power of God.^[2] It forms a contrasting pair with chapter 5: Nebuchadnezzar learns that God alone controls the world and is restored to his kingdom, while Belshazzar fails to learn from Nebuchadnezzar’s example and has his kingdom taken from him and given to the Medes and Persians.^[3]wiki

Nebuchadnezzar & porphoria

“Aside from boanthropy, other explanations for his behaviour include porphyria (a group of enzyme disorders that manifest with neurological symptoms including hallucinations, depression, anxiety and paranoia) or general paresis or paralytic dementia caused by syphilis.

The porphyrias are a group of rare inherited or acquired disorders of certain enzymes that normally participate in the production of porphyrins and haem. They manifest with either neurological complications or skin problems, or occasionally both.

The metamorphosis of humans into animals is known as therianthropy, the best known form of which is lycanthropy — transformation into a wolf or werewolf. The term “cynanthropy” dates back to ancient Greece and is applied to shapeshifters who alternate between human and dog form. A therianthrope, however, is a being that is part human, part animal. http://www.pharmaceutical-journal.com/opinion/blogs/nebuchadnezzar-and-boanthropy/11123165.blog

The European royal lines have always been prone to the odd loss-of-function mutation. An unlucky mutation in Queen Victoria’s Factor IX gene caused a nasty case X-linked Haemophilia B in her male descendants (a mutation that was only mapped in 2009 by sequencing the bones of the murdered Romanov branch).

More systemic genetic problems have been the result of heavy inbreeding; Charles II of Spain, with his distressingly bushy family tree (left), suffered from severe Habsburg jaw, along with a host of other genetic complaints. http://genomesunzipped.org/2011/04/inbreeding-genetic-disease-and-the-royal-wedding.php

http://mobile.abc.net.au/news/2004-12-18/gollums-precious-little-regard-for-his-health/605648 http://archive.is/u5rNK

PRINCE CHARLES RELATED TO DRACULA http://www.express.co.uk/news/royal/786300/Prince-Charles-Romania-royal-tour-Bucharest-Dracula

http://www.englishmonarchs.co.uk/scottish_kings.htm

BLUE BLOOD

Royal blue “The Phoenicians also made an indigo dye, sometimes referred to as royal blue or hyacinth purple, which was made from a closely related species of marine snail.^[18]“

“The colour-fast (non-fading) dye was an item of luxury trade, prized by Romans, who used it to colour ceremonial robes.”

Hemolymph, or haemolymph, is a fluid, analogous to the blood in vertebrates, that circulates in the interior of the arthropod body remaining in direct contact with the animal’s tissues. It is composed of a fluid plasma in which hemolymph cells called hemocytes are suspended. In addition to hemocytes, the plasma also contains many chemicals. It is the major tissue type of the open circulatory system characteristic of arthropods (e.g. arachnids, crustaceans and insects).^[1]^[2] In addition, some non-arthropods such as molluscs possess a hemolymphatic circulatory system. https://en.wikipedia.org/wiki/Hemolymph

Nobility https://en.wikipedia.org/wiki/Nobility
Rhesus Factor – RH Negative https://en.wikipedia.org/wiki/Rh_blood_group_system

Blue Baby https://en.wikipedia.org/wiki/Hemolytic_disease_of_the_newborn

The Rh factor was discovered by Landsteiner and Alexander Wiener in 1940 Before the prophylactic use of Rh immunoglobulins (anti-D globulin) was introduced, maternal anti-D antibodies frequently caused fetal brain damage, as a result of the increased levels of bilirubin (Kern icterus), and death. The mechanism underlying the prevention of maternal anti-D production after receipt of prophylactic Rh immunoglobulin could be due to antigen blocking or a central inhibition of the immune response. Prophylactic Rh immunoglobulins are usually given by intramuscular injection. Rh immunoglobulins are also used for treating idiopathic thrombocytopenia, when they are given intravenously. The primary mechanism of action for this indication is believed to be an immunological blockade of Fc receptors within the reticuloendothelial system, preventing entrapment of antibody-coated platelets with a subsequent rise in the circulating platelet count (Ware & Zimmerman, 1998). Today’s methods for obtaining Rh immunoglobulin for a therapeutic hyperimmunoglobulin preparation follow Wiener’s original 1943 procedures for obtaining anti-Rh antibodies for diagnostic purposes. In his search, Wiener found the most convenient source of anti-Rh sera were people already sensitized by pregnancy or transfusion. During World War II, Wiener prepared anti-Rh serum for the armed forces by injecting small Rh-positive red cells into people who were already sensitized and could induce a very strong anamnestic response. The best source of anti-Rh serum came from male Rh-negative volunteers immunized with a small dose of Rh-positive red cells. At least two injections, 4 months apart, for the production of specific high-titre anti-Rh antibodies were required (Wiener 1969) http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2141.2003.04295.x/full#ss4. http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2141.2003.04295.x/full https://archive.is/avONc

The Basque people of Spain have an unusually high percentage of Rh Negative blood, DNA tests have confirmed a link between the Irish and the Basques, Ireland and Scotland also have a high percentage of people with Rh negative blood,

The Rhesus Factor and Disease Prevention
https://qmro.qmul.ac.uk/xmlui/bitstream/handle/123456789/2748/TANSEYRhesusFactor2004FINAL.pdf?sequence=2

Purple, Prince, Riddled Royals & Chemtrails https://spidercatweb.blog/2016/04/21/prince-dead/

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According to this webpage archive the following supposedly all have RH negative blood- Liam & Noel Gallgher, Ozzy Osbourne, Fidel Castro, Kurt Cobaine, Janis Joplin, Marilyn Monroe

The following is according to their

Mar. 18, 1985 The regal donor of the precious stuff was Prince Charles, 36, who has become the first member of the royal family ever to give blood, in his case, O Rh-negative. http://content.time.com/time/magazine/article/0,9171,963393,00.html https://archive.is/zV5Pa

Genes on the Y Chromosome

Every human has 23 pairs of chromosomes – organized packets of genetic information (DNA) which code for all the necessary amino acids to create a human being. The twenty-third set of chromosomes determine the gender of a person: two X chromosomes create a female, and an X paired with a Y creates a male.

The Y chromosome is much smaller than a typical X chromosome, and contains somewhere between 70-200 genes (the entire human genome comprises approximately 20,000-25,000 genes). Some important genes on the Y chromosome include:

SRY: The SRY (Sex Determining Y Region) gene determines gender. This gene will bind to other DNA in the cell, distorting it out of shape. This single gene creates the male phenotype. In a very rare genetic event, the gene sometimes gets translocated onto an X chromosome. When this happens, the child carries a genome that should be female (46, XX), but develops as a male. Adult men with a 46, XX karyotype and a translocated SRY gene are often identified due to infertility or hypogonadism (underdeveloped testes).

SHOX: The SHOX gene (Short Stature Homeobox) is located on the X and the Y chromosome. This gene is responsible for skeletal growth. While many genes are located only on the X chromosome, this gene is present in both the X and the Y chromosome, so that each gender receives two functional copies of the gene.

USP9Y: This gene (ubiquitin specific peptidase 9, Y-linked) is found on the Y chromosome, and is only present in males. This gene is involved in the production of healthy sperm, and infertile males sometimes have a mutation in this gene.

The Y chromosome is not necessary for the male phenotype. The SRY gene is required, however, and it is almost always located on the Y chromosome. In a few rare cases, the SRY gene has been translocated (moved) to the X chromosome by accident. In these cases, the genotype is 46, XX – this would normally indicate a female genotype. In the rare case of translocation of the SRY gene, however, a man can be 46, XX: these men are often fully masculinized, but are infertile. This is sometimes called the “XX Male Syndrome.”

There are also reports of men who have a 46, XX genotype without the SRY gene. The causes of this rare occurrence have not been completely investigated. Like the men with the translocated SRY gene, these men are infertile.

Y Chromosome Disorders Klinefelter Syndrome XYY Syndrome Turner Syndrome

Irish and British DNA : a comparison

The Kingdom of Dalriada c 500 AD is marked in green. Pictish areas marked yellow. British and Irish DNA suggests that people on the two islands have much genetically in common. Males in both islands have a strong predominance of Haplogroup 1 gene, meaning that most of us in the British Isles are descended from the same Spanish stone age settlers.

The main difference is the degree to which later migrations of people to the islands affected the population’s DNA. Parts of Ireland (most notably the western seaboard) have been almost untouched by outside genetic influence since hunter-gatherer times. Men there with traditional Irish surnames have the highest incidence of the Haplogroup 1 gene – over 99%.

At the same time London, for example, has been a mutli-ethnic city for hundreds of years. Furthermore, England has seen more arrivals of new people from Europe – Anglo-Saxons and Normans – than Ireland.

Therefore while the earliest English ancestors were very similar in DNA and culture to the tribes of Ireland, later arrivals to England have created more diversity between the two groups.

Irish and Scottish people share very similar DNA. The obvious similarities of culture, pale skin, tendancy to red hair have historically been prescribed to the two people’s sharing a common celtic ancestry. Actually it now seems much more likely that the similarity results from the movement of people from the north of Ireland into Scotland in the centuries 400 – 800 AD. At this time the kingdom of Dalriada, based near Ballymoney in County Antrim extended far into Scotland. The Irish invaders brought Gaelic language and culture, and they also brought their genes.

Irish Characteristics and DNA The MC1R gene has been identified by researchers as the gene responsible for red hair as well as the accompanying fair skin and tendency towards freckles. According to recent research, genes for red hair first appeared in human beings about 40,000 to 50,000 years ago.

These genes were then brought to the British Isles by the original settlers, men and women who would have been relatively tall, with little body fat, athletic, fair-skinned and who would have had red hair. So red-heads may well be descended from the earliest ancestors of the Irish and British.

A spoof (and very funny) exploration into the characteristics of all Irish-blooded males can be read at this link: www.irishtimes.com/newspaper/weekend. Identified genes include IMG or the Irish Mother Gene and the GK (MF) S Gene Kelly-Michael-Flately-Syndrome which explains the inability of the Irish man to move his hips while dancing!

Irish origin myths confirmed by modern scientific evidence One of the oldest texts composed in Ireland is the Leabhar Gabhla, the Book of Invasions. It tells a semi-mythical history of the waves of people who settled in Ireland in earliest time. It says the first settlers to arrive in Ireland were a small dark race called the Fir Bolg, followed by a magical super-race called the Tuatha de Danaan (the people of the goddess Dana).

Most interestingly, the book says that the group which then came to Ireland and fully established itself as rulers of the island were the Milesians – the sons of Mil, the soldier from Spain. Modern DNA research has actually confirmed that the Irish are close genetic relatives of the people of northern Spain.

While it might seem strange that Ireland was populated from Spain rather than Britain or France, it is worth remembering that in ancient times the sea was one of the fastest and easiest ways to travel. When the land was covered in thick forest, coastal settlements were common and people travlleled around the seaboard of Europe quite freely.

Medieval map of Ireland, showing Irish tribes.

But where did the early Irish come from? For a long time the myth of Irish history has been that the Irish are Celts. Many people still refer to Irish, Scottish and Welsh as Celtic culture – and the assumtion has been that they were Celts who migrated from central Europe around 500BCE. Keltoi was the name given by the Ancient Greeks to a ‘barbaric’ (in their eyes) people who lived to the north of them in central Europe. While early Irish art shows some similarities of style to central European art of the Keltoi, historians have also recognised many significant differences between the two cultures.

The latest research into Irish DNA has confirmed that the early inhabitants of Ireland were not directly descended from the Keltoi of central Europe. In fact the closest genetic relatives of the Irish in Europe are to be found in the north of Spain in the region known as the Basque Country. These same ancestors are shared to an extent with the people of Britain – especially the Scottish.

DNA testing through the male Y chromosome has shown that Irish males have the highest incidence of the haplogroup 1 gene in Europe. While other parts of Europe have integrated contiuous waves of new settlers from Asia, Ireland’s remote geographical position has meant that the Irish gene-pool has been less susceptible to change. The same genes have been passed down from parents to children for thousands of years.

This is mirrored in genetic studies which have compared DNA analysis with Irish surnames. Many surnames in Irish are Gaelic surnames, suggesting that the holder of the surname is a descendant of people who lived in Ireland long before the English conquests of the Middle Ages. Men with Gaelic surnames, showed the highest incidences of Haplogroup 1 (or Rb1) gene. This means that those Irish whose ancestors pre-date English conquest of the island are direct descendants of early stone age settlers who migrated from Spain.

KING TUT’S DNA ~ WESTERN EUROPEAN

Haplogroups are assigned letters of the alphabet, and refinements consist of additional number and letter combinations, for example R1b or R1b1. Y-chromosome and mitochondrial DNA haplogroups have different haplogroup designations. In essence, haplogroups give an inisight into ancestral origins dating back thousands of years.

By entering all the STR data inadvertently shown on the Discovery video, a 99.6 percent fit with the R1b haplogroup is revealed.

The significance is, of course, that R1b is the most common Y-chromosome haplogroup in Europe reaching its highest concentrations in Ireland, Scotland, western England and the European Atlantic seaboard — in other words, European through and through. http://www.eutimes.net/2010/06/king-tuts-dna-is-western-european/ https://archive.is/yX4Ex

We’ve got the same mummy! Up to 70% of British men are ‘related’ to the Egyptian Pharaoh Tutankhamun http://www.dailymail.co.uk/sciencetech/article-2022313/Up-70-British-men-related-Egyptian-Pharaoh-Tutankhamun.html https://archive.is/kborD

MORE BRITISH ROYAL FAMILY