Blood. And Blood curses?!?! Its all in the blood. Why is that some races have included in their genetic patterning obstacles to a long and healthy Life? I have been prompted to offer this post today as a few synchronicities are coming together and this might help someone out there. After watching the previous post where Bashar talks about the early stage of manipulation by Annunaki... with their genetic tinkering to inhibit human being's development in order to keep them subservient and worshipping them, the 'creator gods', that they imposed themselves as...So at the same time I was also looking into a blood condition that occurs with a certain group of races with the same genetic burden that goes mainly undetected, until symptoms around the age of 40/50 become very problematic...

Okay this is a different kind post that I'm offering today. It will be synchronous to some but not to all. Its to do with a blood condition that is not very well highlighted and it can be the cause of so many symptoms that worsen as they get misdiagnosed and even undiagnosed because the awareness of this condition, as far as I am aware personally, IS NOT in many families 'health stories'. But the families I am referring to are from, or have origins from Northern European genes that have been impacting blood for generations. So For Irish genes mainly, but not only, as these genes could have come in at any time through ancient history. The condition is Haemochromatosis and refers to the iron in blood as being overloaded...due to over absorption of iron and its continuous overabsorption. But as its not generally well known as is for example, diabetes or arthritis, (which are in themselves also indicators of this condition). Its symptoms go undetected and patients go down other lines of health investigation ignoring the possibility of treatments that would relieve this condition, and so therefore would eliminate treatment of the symptoms. This condition is known as the Irish Curse and is as synonymous with the Irish as Sickle cell is to people of black races. But awareness of sickle cell is high, and symptoms can be quickly observed and taken under the canopy of the local health systems. But when I asked my family in ireland what they know of haemochromatosis and its link to the irish people, I was met with blank faces. Which might explain why my family, mother, father brother, and quite a few cousins had very differing but serious health situations which they died off, or died young or maintained a death later in life but with very little quality of life and that needed care throughout. The reason I am speaking about this is because if I didn't know better, it would seem that certain family lineages would be the victims of a curse...to be linked to a blood condition that remains so obscure, hidden as to be undetected and that can sadly give rise to complicated problems that if undetected result in a long slow death due to organ failure caused by continuous, unstopped absorption of iron to toxic levels. Enlarged spleens, (that can and do rupture), pancreatitis, enlarged livers (that could have had iron toxicity levels monitored if known of genetic problem) mistaken for being caused by other means....The reason I am sharing this, (apart from the obvious questions HOW WHY and WHERE did all this start???) is that simple blood tests asked for by GP after the obvious routine tests are not revealing anything conclusive, can act to raise new questions that are not being asked. Knowledge of Now INTERNET-accessible material makes this so that we intervene on our own behalfs. If it is mainly an Irish or north european condition, not many doctors in UK will actually know about it, and so will not be tapped in on how to investigate. The populations in UK are so diverse and there are (were and radiating outward) huge populations of the Irish, now intermingled with other unsuspecting peoples, that can make this gene alteration mishap a far wider consequence than we knew. Even the Irish in Ireland, and in general those of populations originating with Northern Europe genes don't seem to be aware of it and so it continues to go undetected. Misdiagnosed or Not diagnosed at all. The information regarding the past seems to say that it would not be a THING really because it was a survival mechanism to keep keep the young of reproductive age able to reproduce before the usual death age of 30 -40. Preservation of Iron in the blood during harshest of living conditions such as famine and stavation but even before that during migration and seeking food out. As conditions now are generally considered to be food in abundance then the Iron continued increased iron absorption leads to the toxicity and debilitating symptoms that come from it. SYMPTOMS can be seen in Early Young Adulthood, but without the correct blood test will be misdiagnosed and therefore conditions become then serious problems for life. Usually the symptoms shout out loudly in Adult Middle Aged years, only when the toxicity levels, undetected throughout youth have become harmful. Only When you have cause for concern with your own symptoms and their undiagnosis or misdiagnosis do you look into the Internet-accessible vaults. When you read the long list of symptoms, and can tick the boxes do you realise that WOW, thats me, and sadly see that your wider families collection of health problems including, brain fog, mental health, depression, menstral problems, heart problems, early onset osteoporosis, arthritis stomach, swelling and painful body parts etc in varying combinations....could have been due to high iron toxicity held in the cells in the heart/liver/stomach/pituitary gland and that it is down to a combination of genetic snakes and ladders. But the thing to take away here is that we are still...very much so..unaware of the truth about the knowledge of the Body and its health systems...'pharmaceuticals and co' will have us believe that whatever the symptoms are..there is always a PILL for it. Without taking responsibility and accountabilty for ourselves... we believe them, and acquiese... as they want us taking 70 pills a day by the age of 70. Even when we think of the technology that is available to the world at Large, we are still largely crawling around in the dark in terms of education about ourselves and the health of our brain body mind complex. If you are interested in investigating this condition further, and learning the best way to deal with it ONCE A. you have found a doctor who is a agreeable to ask for the blood test to see if there is iron overload in your blood and B. the doctor helps you get a genetic test to see if Iron overload is due to Genetic Haemachromatosis. THEN Once diagnosed, IT IS HELPFUL THAT THE DOCTOR REMAINs to be helpful in arranging and monitoring the treatment of reducing iron overload by frequent blood letting...i.e giving up a pint of blood regularly to reduce the toxic levels back to normal levels...So if interested a few links to copy and paste. here...https://medical-news.org/early-signs-of-iron-overload-few-patients-recognize/120660/... https://www.ruh.nhs.uk/pathology/blood_test_info/docs/gpquickguidetogenetichaemochromatosis.pdf ...https://www.youtube.com/watch?v=36n37AaVVLc ...https://www.youtube.com/watch?v=bPu7gliKuYU ....