Pauling Therapy Synopsis

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PAULING THERAPY Synopsis:

The Reader's Digest Version

 

 

Linus Pauling invented a cure for Heart Disease in 1991 which was

announced 1993-1994.Pauling claimed that specific non-toxic

substances called Lp(a) binding inhibitors taken orally will prevent and

even dissolve existing atherosclerotic plaque build-ups. Three United

States of America Patents have been granted on the Pauling/Rath method.

 

Pauling's announcement is based on experimental proof with guinea pigs

who like humans can not make their own vitamin C.

The three primary " Lp(a) binding inhibitor " substances are

vitamin C, lysine and proline.

The Pauling Therapy works by itself, but in theory, Pauling's protocol

makes an ideal oral adjunct to EDTA Chelation therapy and other more

conventional therapies for all forms of cardiovascular disease, except

radiation.

Early scientists recognized that plaques form in the same places. Usually

near the heart where the blood vessels are stretched and bent,

implicating high blood pressures and the mechanical stress caused by the

heart beat. These scientists were ignored.

Today the majority of heart surgeries only replace a few inches of blood

vessel near the heart (coronary arteries). It is unlikely that the

primary cause of the lesions leading to heart disease are

" poisons " circulating in the blood because plaque does not form

randomly throughout the blood stream. (Note: In a heart bypass, veins

from the leg are used which are without plaque.)

We know now that atherosclerotic plaques deposit in response to injury

and that plaque is part of a healing process. The 1985 Nobel prize was

awarded for the discovery of the Lysine Binding sites. Mainstream medical

science has known since 1989 that Lp(a) (not LDL cholesterol) binds to

form atherosclerotic plaques. Pauling and Rath have identified Lp(a) as

an evolutionary surrogate for low vitamin C in humans. Mechanical stress

then, not cholesterol or other " poisons in the blood, causes the

lesions that lead to heart disease.

Modern medicine has been misguided about vitamin C since the 1940s.

VItamin C is required and used up making the super protein collagen.

According to the Pauling/Rath Unified Theory, the root cause of

atherosclerotic plaque deposits is a vitamin C deficiency: chronic, not

acute. The correct terminology for cardiovascular (heart) disease is

" chronic scurvy " or " sub clinical scurvy " .

Heart disease is unknown in most animal species. Pauling and Rath think

humans are less resistant than other animals to arterial damage from

mechanical stress (caused by the heart beat) because they become

deficient in a specific protein caused by a specific vitamin deficiency.

A vitamin deficiency that is impossible in most animals!

The Pauling mega-nutrient therapy to counter Lp(a) increases blood

concentrations of important substances that will:

 

Strengthen and heal blood vessels,

 

Lower Lp(a) blood levels and keep Lp(a) levels low,

and

 

Inhibit the binding of Lp(a) molecules to the walls of blood

vessels.

Vitamin C is required for healing the lesion, primarily through the

collagen pathway.

Lysine and proline work to unbind Lp(a) from the arterial wall.

Unlike ordinary drugs, there are no health risks. These substances are

required for life.

The Pauling Therapy is so safe, and the medical condition so grave, there

is no reason why any physician should resist it, especially in otherwise

hopeless cases.

By " cured " we mean that as first described on the LINUS PAULING

VIDEO ON HEART DIEASE: End-stage CVD patients report the complete

cessation of their angina pain, color returns, blood pressure drops,

blood flow increases, blockages disappear, heart rates drop, lipid

profiles normalize, energy increases as does the sense of well being.

Patients who had failed now pass treadmill stress tests without surgery

or any other medical intervention. Patients barely able to walk before

the Pauling therapy report that within months they can dig fence post

holes and cut down trees. Over time, elevated Lp(a) lowers. Some doctors

have even told such patients that new blood vessels have

" grown " as an explanation for the increased blood flow to the

coronary arteries feeding the heart.

Linus Pauling's 1992 video describes these findings.

CONGRATULATIONS: YOU NOW KNOW MORE ABOUT HEART DISEASE THAN THE

AVERAGE CARDIOLOGIST IN THE UNITED STATES OF AMERICA.

A great amount of money is at stake. This discovery is ignored. We can

only speculate why. Regretably, not a single study has been conducted to

investigate the high-dose Pauling protocol. Instead, all this is

dismissed a priori as " quackery. One

reason may be that every pharmaceutical company, cardiologist and heart

surgeon has a vested interest in their part of the $326 billion spent

annually on heart disease. Should the Pauling

discovery become widely known, there will be a revolution in medicine.

Certainly cardiology and heart surgery will not survive in their present

form.

We are not doctors. In 1995, when we reported what

Pauling had said and written, we did not know if

Pauling was correct.

We now know.

Pauling nailed it.

Intelisoft Multimedia is now willing

wager against others who might think otherwise. Amount negotiable. Winner

takes all. Should any person or entity wish to accept this challenge

and pit any competing therapy, treatment or protocol against Pauling's,

in a clinical trial setting with end-stage cardiovascular patients,

contact us.

Terms negotiatable. There are only two up-front stipulations:

 

The competing protocol may not include vitamin C (above the RDA),

lysine or proline (or synthetic analogs),

and

 

 

The subjects in the Pauling Therapy group must not have been

treated with any intra-arterial radiation therapy to stem

restenosis.

 

 

 

We will fund the Pauling protocol subjects.

Antagonist fund the patients on their

protocol.Our Prediction: 90% of the

patients on the high dose Pauling vitamin C/lysine protocol will be

" cured " within 30 days as measured by: lowered Arterial

Stiffness (ASI measured using FDA approved Cardiovision), reductions in

Chest pain, increased mobility, improved sense of well being, etc.