CLAN OF WORMS PART 6: AHEPA & ANEMIA

In part 5, I covered how AHEPA & Sons Of Pericles President Stephen A Scopas escaped conviction in NY for operating an international orphan-stealing/dealing ring.

Here's his obituary: https://www.nytimes.com/1999/01/12/classified/paid-notice-deaths-scopas-stephen-s-sr.html

"Mr. Scopas served until his death as the National Chairman of the Ahepa Cooley's Anemia Foundation"

What is Cooley’s Anemia? It’s a genetic mutation that causes red blood cell irregularity. As a result, the blood is less capable of holding oxygen and iron.

http://www.thogde.org/c5/index.php/thalassemia-aid-without-borders/thalassemia/the-origins-of-thalassemia/

Thalassemia, also known as MEDITERRANIAN ANEMIA, is an ANCIENT group of diseases that have existed for over 7,000 years. The name thalassemia comes from the ANCIENT GREEK word for sea, thalassa, as the ancients believed it was an "illness that came from the sea". In 1925, pediatrician Thomas Benton Cooley published a work on thalassemia. This was the first description of the disorder, and for a long time it became known as Cooley's anemia.

Traditionally, beta thalassemia major is particularly prevalent in a belt stretching from West Africa through the Mediterranean, the Arabian Peninsula and the Black Sea to India, South China and South-East Asia. However, due to global mobility in modern times, sufferers are now found nearly everywhere. Throughout the world, it is estimated that 4.6 million children and adolescents are affected by thalassemia and every day hundreds of babies are born with this inherited disorder. A high number of CARRIERS of the thalassemia genetic trait are found in countries where MARRIAGE BETWEEN RELATIVES was, and still is, common practice and in third-world or emerging countries. Little or no schooling, social or religious stigmatization, and a lack of useful information and education all help to spread this genetic disorder. In many cultures, sick children, particularly girls, are often hidden away, abandoned or killed.

http://www.whonamedit.com/synd.cfm/2157.html

Countries like ITALY, GREECE, and Cyprus have the highest frequency of thalassaemia cases in the world, 10 percent of the Mediterranean population are carriers of this gene. There exists a thalassaemic "belt" that includes the Mediterranean passing through West and Central Asian countries like Turkey, Iran, Afghanistan onto Pakistan & India and passes on to the South East Asian countries like Indonesia, Burma & Thailand. Cooley and B. Lee (American physician) described the disease in children of Italian immigrants in the USA.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1521431/?page=1 (1952 article describing Mediterranean Anemia)

https://www.sciencedaily.com/releases/2005/06/050620003719.htm

Children's Hospital Oakland, a world recognized center for treatment and research of thalassemia, has formed an international network treating patients throughout the world. Thalassemia is the WORLD’S MOST COMMON GENETIC BLOOD DISORDER and it is RAPIDLY INCREASING. SEVEN PERCENT of the world's population are CARRIERS, and 400,000 affected babies are born each year. The World Health Organization (WHO) predicts a DOUBLING of these STATISTICS within the next few decades. Once rare in California, it has become the most frequent disorder detected in the state newborn screening program of over 700,000 annual births. Thalassemia is usually FATAL IN INFANCY unless ONGOING TRANSFUSIONS are initiated.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333734/ (study describing the ancient origins of Anemia in the Meditteranean, and (((Akzhiv-Israel)))...though it puts forth the totally unsupported claim that it developed in Africa)

http://www.pnas.org/content/88/1/310 (Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan 1991) “The present study constitutes an extensive molecular characterization of this disease in a small, highly inbred ethnic group with a high incidence of beta-thalassemia--the Jews of Kurdistan. An unusual mutational diversity was observed. In 42 sibships 13 different mutations were identified”

http://www.saintbarbara.org/our_parish/ahepa/

In 1972, the chapter joined hands with the Connecticut Campaign Against Cooley’s Anemia, and with Ahepan Congressman Robert Giaimo in introducing the Cooley’s Anemia Research Bill Act before the U.S. Congress, resulting in the National Funding for Cooley’s Anemia Research.

https://ahepa.org/programs/publichealth/

AHEPA Cooley's Anemia Foundation Cooley’s Anemia, also known as “Thalassemia”, is a rare but fatal genetic blood disorder. It mostly affects people of Mediterranean descent. In its most severe form it requires bone marrow transplants but usually those who are diagnosed experience symptoms of fatigue, weakness, paleness, and slow growth. Many are unaware they are carriers of the genetic disease until either their child suffers from it or a DNA test result is acquired. In it’s major form, Thalassemia “Cooley’s Anemia” is fatal and requires bone transplant surgery. In 1990, after the son of one of our chapter members was in need of this surgery, it quickly became obvious that an even greater need existed, thus the AHEPA Bone Marrow Donor Registry was incorporated. Today, there have been incredible breakthroughs in gene editing that may allow for children to live Thalassemia-free! Since 1947, AHEPA has supported the Aristotle University of Thessaloniki with the AHEPA Hospital wing. It has helped over 10 million patients and continues to serve the community of Thessaloniki today.

AHEPA-COOLEY ANEMIA partnered with NHLBI (leading blood researchers)

https://ahepa.org/wp-content/uploads/2018/06/ahepa-public-policy-priorities-115th-Congress.pdf

https://clinicaltrials.gov/ct2/show/results/NCT01319552?cond=%22beta+thalassemia%22&draw=3&rank=161 (Cooley-Anemia study: FRESH BLOOD IS BETTER ...National Heart, Lung, and Blood Institute (NHLBI-Partner with AHEPA-Cooley Anemia foundation) Steven L. Spitalnik, Columbia University)

What Vampires have long known, Medicine has proven. Blood transfusions are more effective when they are transfused within hours from when the blood is drawn. This creates the imperative for literal human blood banks. UNDERGROUND MEDICINE IS HUMAN TRAFFICKING

https://www.vampirerave.com/forum/message.php?message=28501&group=1&catid=1 (Vampirism Enthusiast forum: Anemia, is it related to vampires? Forum discusses Anemia being a source of Vampire legends, Individuals who practice Vampirism often have a form of Anemia, and inbreeding of families to keep wealth often led to Anemias)

All in all, I suspect that much of the PizzaGate, Ritual Sacrifice, Vampire/Werewolf Lore, Blood-letting and other blood-based cult activity has some biological, eugenic imperative. Religious orders have long been obsessed with Blood-Lines which led to inbreeding. Inbreeding led to genetic diseases in wealthy families. These same organizations founded hospitals and have been doing inter-country medical research and population-wide genetic testing.