Cancer should not exist. Part 2

[rtexanssane]

NOTE. When the medical authourities tell you that there is no evidence that Vitamin B17 prevents cancer all that means is that it has not been proven to the satisfaction of the FDA and NOT that insufficient research has been done. Vitamin B17 was first isolated in 1810 and was first used in cancer therapy as early as 1845 so there is well over 100 years of research.
The problem is that to for a new treatment to be approved by the FDA will cost upward of 250 million dollars in research which makes all medical research the exlusive domain of the large pharmecutcal corporations.
These corporations never carry out research on anything which cannot be patented or that you can buy on asupermarket shelf. When was the last time you picked up a prescription for fruit an vegetables if you dont beleive me.
In the 100 or so years since the isolation of B17 it has been demonstrated that cultures who have a diet rich in this vitamin are cancer free. The Huzas, The Escimos, The Abkasions, The Hopi and Navaho Indians of North America and some native populations of South America and South Africa all have in common that the degree to which they are free from cancer relates directly to the degree to which they have Vitamin B17 in their diet.
In other words as long as the adher to there native diet the cancer rate is zero. It is only when they become westernised and take on our diet that they become prone to cancer.
The Hunza's are of particular interest because they are an Apricot culture and their favourite delicacy is the the Apricot kernal. Although B17 is found in over 1200 different foods the kernals of fruit seeds other than citrus contain the highest concentration of B17 known to man Bitter Almonds being the richest source.
The Average Hunza has 200 times the intake of B17 in their diet than that of the average American.
At one time Millet used to be the staple grain for cattle. It is rich in B17 but has been replaced by wheat which is virtually devoid of it so there is no longer ressidual B17 in the meat we eat. Our Great grandmothers used to grind up the seeds of fruit in jams an preserves which they no longer do and mass production certainly does not utilise it in our food.
So over the last hundred years or so B17 has been gradually whittled out of the western diet and its during this same period that cancer has risen to the point where one in three people will be affected either directly or through a loved one.
In fact its more than one in three because the figure is only relevant if you count only those individuals whose cancer will develop to the point where it is diagnosible before they die by other means. There is an alarming number of autopsied males that are found to have prostate cancer after they have died by other means.

Before explaining how B17 tackles cancer i am going to go into a bit of detail about how cancer works and the first defence that our body has against this disease and then show how B17 works as the secondary back up.

THE TROPOBLASTIC THESIS OF CANCER

In 1902 Professor John Beard an embriologist from Edinburgh University discovered that there is no discernable difference between cancer cell and Trophablast cells which occur in early pregnancy.
If you could see a speeded up film of trophablast in early pregnancy you would see it behave in exactly the same way as cancer. It does not become a part of the individual it is purely parasytic in nature. It grows and multiplies as it eats its way into the Uterice to prepare a place for the phoetus. This is the difference between a malignant lump and a benign one. The benign lump pushes away the sorrounding tisses wheras a milignant tumour eats its way into the surrounding tissue.
So why is it then that every pregnant woman does not end up with cancer.
Beard noted that aroud week 8 of early pregnancy that these cells begin to die off: Why.. He discovered that after 8 weeks the phoeutes pancreas becomes functional and that the pancreas secreates the enzyme Tripsin which plays a vital role.
normally the white cells responsible for fighting off didease will attack anything foreign to the body but because trophoblasts are not foreign the outer membrane contains a negative electro-static charge which the white cell also carries and so they repel each other like two magnets.
The enzyme Tripsin eats through the outer wall of the trophoblast leaving it fully exposed to the white cell which then destroys it.
With reguard to this it is interesting to note that the upper intestine near the point where the pancreas enters into it is the one place in the human body where cancer is almost never found and that also diabetics who suffer from a pancreas malfunction are 3 times more likely to contract cancer than non-diabetics.
Different cancer tumours have varying degrees of malignancy but baird noted that the more malignant the tumour the more it took on the characteristics of pregnancy trophoblast and that the most malignant tumours of all are indistinguishable from trophoblast or as Professor beard pointed out over 100 years ago they are one and the same.
So when the Stem cell combines with eastrogen to produce trophoblast in pregnancy the result is an ambilical cord and a placenta, but when this process occurs as part of the general healing process where tissue has been damaged by carcenogens then the result is cancer.
Well not quite. To be more accurate when this alternative healing process produces more trophoblast cells than the bodies natural defences can keep up with then the result is cancer.
And this is where Vitamin B17 comes in. This is natures secondary back should the first one fail. Here is how it works.

The B17 molecule contains 2 units of sugar 1 unit of Hydrogen Cyanide (Not to be confufused with industrial pottasium Cyanide) and 1 unit of Benzaldehide.
These ingredients are locked inside a membrane and are completely inert until the molecule comes into contact with a cancer cell.
There is only one enzyme that can unlock these ingredients. It is called Beta Glucosidase the unlocking enzyme and it does not appear in living tissue to any great decree except at the cancer cell where it appears in large quantities.
There is another enzyme called Rhodenese the protecting enzyme which occurs in all living tissue except the cancer cell which is consequently unprotected.
So when the B17 molecule comes into contact with a cancer cell the Cyanide and benzaldehide are released. Cyanide which as everyone knows in large enough quantities is deadly as too is benzaldehide. In fact these two acting together are 100 times more toxic than either acting alone. The toxicity is so great that it has been observed under a microscope that no cancer cell can survive, whereas when these ingredients come into contact with heathy normal tissue the Rhodenese breaks down these deadly toxins and converts them into by-products that feed and nourish the healthy cell.
It is a perfectly balanced mechanism of nature that has been observed for over 100 years that could not have been an accident.

It should be noted at this point that the greatest strengh of B17 is in its ability to prevent cancer from ever ocurring in the first place.
When you conduct research into its effectiveness in cancer therapy although there have been many astounding results there are factors that limit its success and this is mainly due to the politcs of cancer therapy.
In 1952 Dr Earnst T Krebbs junior was the first person to develop the concentrated form of B17 for cancer therapy which he caled Leatrille.
He personally reported almost 100% success rate for virgin cases which means cases where the patient had no prior treatment from conventional medicine.
And there is the problem. Most of the people who have been treated with Leatrille are not virgin cases, many of them being cases that have been told they have only a short time to live after conventional treatment has failed. When they die as many of them do they are counted as statistical failures for Leatrille when in reality it is a victory for Leatrille that any of them survive under these circmstances.
Added to this is the fact that early diagnosis is rare because in order to to diagnose cancer under current medicine you need a biopsy which is an expensive proceedure for which you cannot nip down to your local GP and have as part of a routine medical. Even in Britain where we have a health service you will have to go on a waiting list unless you have the money to go private.

For anyone who is suffering from cancer or knows somebody who is check out Metabolic Therapy (not to be confused with nutritional therapy)
It combines the use of Leatrille and enzyme therapy i was talking about earlier. The one is to boost the bodies own natural defence specifically against cancer while the Leatrille adds a huge backup.
If you cannot afford such treatment you can always ask the therapist for a recommended daily intake of Apricot kernels to give you the best chance possible.

Because of these factors relating to therapy i urge people to focus on the original statement that i made at the beginning.

CANCER WOULD NOT EXIST IF WE ALL HAD VITAMIN B17 AS PART OF OUR DAILY DIET.

Dont wait to get cancer and then be cured. By applying this knowledge now cancer can become a disease of the past like Scurvy and Co.

Good health to you.