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CANCER
 What is cancer?
A Cancer cell is described as a being
undifferentiated. Cancer cell has no useful Action.
The cancer cell just sit inside the tumor tissue,
doing nothing except multiplying and refusing to
die. Spreading of Cancer cells kills the patient.
 People think p53 gene that regulates apoptosis
which is found abundantly available in cancer
tumors.
Aerobic Vs Anaerobic Respiration
 Cancer dose not cause cells to turn anaerobic
but rather it is stabilized anaerobic respiration
that is the single cause that turns the normal
cells that depends on aerobic respiration into
cancer cells
-Dr. David Greck
 It is lactic acid accumulation due to anaerobic
respiration that inhibits the cell from receiving
oxygen. Calcium and oxygen are used to
buffer this acid, this enables Cancer cell to
stabilize.
Cancer loves Sugar…
 So in order for a cancer cell to obtain the same the
energy as a normal cell it must metabolize at least
18 times more glucose called cancer loves sugar.
Since Cancer cell is very week it can’t Process
more sugar it helps in preventing prote4ctive antioxidant enzymes , SOD (Super Oxide Dismutaze),
Glutathione
Peroxidase
(GPx),
Glutathione
Reductase (GR) and Catalyze does leaving the cell
wide open to oxidative attack by Ozone.
Lack of Oxygen is a cause….
 Cancer cell can’t extract oxygen form Hemoglobin
since anaerobic respiration doesn’t produce CO2
which is required
to get Oxygen out of
Hemoglobin.
 Dr.P.G.Seeger proved by blocking respiratory
chain normal cells turned to cancer cells within
few days.
 Based on this Dr.Abul Kalam a professsor of
Pathology at University of Mary land reverted
cancer cells into normal cells by using IP6 , a B
vitamin inositol
Lack of Oxygen is a cause….
 Dr. Otto warburg a noble laureate in Medicine
discovered when cells denied 60 % of oxygen
requirement they exhibit anaerobic respiration
resulting in cancer cells due to fermentation.
 Over 70 % of our bodies are water , aerobic
respiration burn oxygen and glucose. In order to
create energy body also needs 500gms of pure
Hydrogen, even our DNA is held by Hydrogen
bonds. When the pH is alkali they have greater
potential to absorb hydrogen which results in
more oxygen delivered to the cells.
Lack of awareness in daily diet….
 Our blood must maintain a PH of 7.35 to transport
oxygen there is a buffer system in the body to
maintain this PH despite considerable addition of
acids.
 However due to poor diet junk foods fast foods
processed foods and cool drink our alkali reserves
get depleted. This leads dumping of excess acids
in the cells. As more and more acid getting
accumulated less oxygen is absorbed resulting in
fermentation of glucose.
Acidic environment is a cause….
 According to Dr. Keiichii Morishita.
 Many cells in the environment die but few cells
survive by becoming abnormal cells. These
abnormal cells are called MALIGNANT Which
stops corresponding brain with our own DNA
memory code.
 Therefore malignant cells grow indefinitely and
without order this is called CANCER.
 Hence cancer cells thrive on acidic PH and
hypoxia.
Acidic environment is a cause….
 It means alkaline PH and oxygen should make
cancer cell revert to be inert and harmless.
 A soda/cool drink as a PH of 2. which is 100000
times more acidic than water. Which reduces
immune response by 15% for a period of 6 hours.
 Hence general rule of thumb as per
Dr.
Robert Young to have diet containing 80% alkaline
and 20% acidic forming ingredients.
Statistics….
 Three Indians die of cancer every minute, one
American die of cancer every minute.
 Cancer is blooming, glowing, growing day by day.
Facts of modern living….
 Consider these facts What we eat is contaminated
heavily by more than 287 Xeno biotic chemicals
that are detected.
 These were detected with in the umbilical cord
blood of American newborns with an average of
200 chemicals.(July 2005 EWG study)
 108 of these chemicals are potential cancer
causing agents, 217 are toxic to the brain and
nervous system, 208 cause birth defects and
abnormal development.
Facts of modern living….
 18 are poly aromatic hydrocarbons (PAHs), 12 are
poly
brominated
dibenzo
dioxines
and
furans(PBDD/Fs), 17 are Poly chlorinated di benzo
dioxines and furans(PBCD/Fs), 28 Organo
chlorine pesticides(OCs), 46 are Poly brominated
diphenyl ethers(PBDEs),70 are Poly chlorinated
napthalenes(PCNs), 209 are Poly chlorinated
biphenyls(PCBs) and a range of heavy metals
aluminum, arsenic, cadmium, cesium, mercury,
nickel and strontium.
Facts of modern living….
 Tons of antibiotics used to farm animals and
poultry.
 Cattle injected with loads of Oxytosin harmone
every day and growth harmones to grow quickly.
 Grains we eat contaminated myco toxins
contaminated drinking water with chlorine fluorine
and other chemicals
 Using x-rays, CT scans etc exorbitantly
 Smoking cigarette, drinking alcohol on one side
cool drinks and diet sodas that contain aspartane
on the other side.
 Eating Junk food, Fast food. Processed food etc.
What causes CANCER ?
 A tumor is just an uncontrolled growth of cells and
is just a symptom of cancer not the cause.
 How ever tumors do have the ability to migrate to
different parts of the body and grow out of control.
They oftentimes interfere with the function of
organs such as Brain, Liver, Kidney and Lungs
thus resulting in death.
 In other words cancer is a problem with the entire
system of the interrelated parts of the body.
 Appropriate treatment must be for the total
environment of the body.
What causes CANCER ?
 There are many different theories on what
actually causes CANCER
1. The External Toxin Theory
The proliferation of cancer cells is caused by
external toxins such as chemicals and other
materials created largely from industry and
carelessness. These chemicals have saturated
our water, food, and the air we breath. We don’t
realize their effects until we come down with a
chronic disease like CANCER after years of
exposure. The link between external toxins and
cancer cells is irrefutable.
What causes CANCER ?
2. The Microbe Theory
The CANCER is caused by pleomorphic (shape
changing) microbes, such as fungi, yeasts,
bacteria, and parasites. It is well documented that
some
fungal
infections
were
actually
misdiagnosed as leukemia. Many researchers
have observed cellular pleomorphism with the aid
of dark field microscopes. Pleomorphism is based
on the belief that fungi, molds, yeasts, and
bacteria are all merely different stages in the life
cycle of microbes.
What causes CANCER ?
3. The Immune System Theory
The CANCER is fundamentally a disease of the immune
system. When your exposure to contaminants gets too
high the strength of your immune system drops too low.
As part of the normal metabolic process a human body
produces a few hundred to as many as 10,000 cancerous
cells each and every day. If immune system is functioning
properly it has the ability to recognize the aberrant cells
and remove them from the body. The reason that every
body doesn’t get cancer is because their immune system
are designed to prevent it. ”Thus just what a healthy
immune system does”
What causes CANCER ?
4. The Hypoxia Theory
According to Dr. Otto Warburg CANCER is caused by a
poor diet and lifestyle which results in toxic buildup thus
over loading the body’s self- cleansing mechanism.
CANCER is believed to be a manifestation of long term
nutritional and environmental irritation as well as a
deficiency in the immune system resulting in cellular
oxygen starvation (hypoxia) leading to uncontrolled cell
replication.
Oxygen is our main life force lack of it would cause
damage to our bodies and organs.
What causes CANCER ?
5. The Internal Rebel Theory
The wild overgrowth of cancer cells is a kind of
genetic rebellion with in the body, where one’s
own cells rebel and destroy the body which
produced them. This is why doctors try to cut and
burn the cancer out of the body or poison the
cancer with toxic medicines or send radiation
throughout the body to kill these internal rebels.
According to this theory the standard CANCER
treatment protocols are SLASH, POISON and
BURN.
What causes CANCER ?
 From the above theories we can summarize or in other
words hypoxia (lack of oxygen) at the tissue level and
immune failure resulting from toxicity and are the prime
causes of cancer.
 According to Dr. Saul pressman “ The cause of cancer is
clear : poor diet, lifestyle and poor mental attitude result in
toxic buildup which overloads the self-cleansing
mechanism. Cancer is manifestation of long term
nutritional and environmental irritation resulting in cellular
oxygen starvation, leading to uncontrolled cell replication.”
What causes CANCER ?

According to Dr. Stephen Ayre “.. Cancer cells get their
energy by secreting their own insulin and they stimulate
themselves to grow by secreting their own insulin-like
growth factor(IGF). These are their mechanisms of
malignancy.”
 Resent research by Dr. Gregg L. Semenza at johns
Hopkins University in Baltimore has shown that the
reason why the cells replicate is not necessarily
because there is damage to the P53 gene , but rather
because the exposure of cancer cells to IGF causes
them to self stimulate and also induces the expression
of hypoxia-indicible factor 1 (HIF-1) transcription factor,
which controls the oxygen delivery and also the
metabolic adaptation to hypoxia.
What causes CANCER ?
 UK Researchers from the Gray Laboratory Cancer
Research Trust concluded “ Cells undergo a variety of
biological responses when placed in hypoxic conditions,
including activation of signaling path ways that regulate
proliferation, angiogenesis and death. Cancer cells have
adapted these path ways, allowing tumors to survive
and even grow under hypoxic conditions…”
When the solid tumor is large enough and the disease
progresses, cancer starts to invade other tissues. This
process is called metastasis.
 According to M.Kunz and S.M Ibrahim, “ Tissue hypoxia
has been regarded as a central factor for tumor
aggressiveness and metastasis.”
CANCER Growth Stages
G0 Phase (Stage 0): Carcinoma INSITU cancer cells are not actively
replicating and therefore resistant to chemotherapy medications cells in
this phase cam function as a reserve pools of cells, reactive and
become part of the proliferative pool even as the total no. of cancer
cells decreases.
G1 Phase (Growth): Cancer cells are proleferating, synthesizing RNA,
Enzymes, Structural proteins and cell organelles. The G1 phase is
reerred as ‘first’ gap or first growth period.
S Phase (Synthesis): After suficient quantities of RNA, enzymes and
proteins are produced in G1, cells profress to the S Phase where DNA
is synthesized.
G2 Phase (Growth): After DNA synthesis concludes, RNA and protein
synthesis resume.
M Phase (Mitotic): This is the final phase of the cell cycle, during which
the cell undergoes mitosis (Cell division) and two of spring cells are
formed.
Types of Tumors
Carcinoma: Malignant tumors derived rom surface
(Epithelial) cells. The most common cancers fall
into this group, including breast, prostate, lung and
colon cancer.
Sarcoma: Malignant tumors derived from
connective tissues.
Lymphoma and Leukemia: Malignancies derived
from blood forming cells.
Diagnosis of Cancer
Breast Cancer
Mammography in 2008, A group of physicians opposed
general practice of giving for women between 40 – 49
stating that women in that age group are not at a uniform
risk of cancer and that mammograms themselves could
expose them to harm from needless treatment because of
false evaluations.
Group of health cooperative of Seattle examined 35,895
mammograms evaluated by 123 radiologists between
1996-2003 and found that 40% of them misdiagnosed
existing tumors.
Use of full body ionizing radiation scans like CT scans ca
expose you to radiation equivalent to a person standing
with in 2 kilometers of the atomic blast at NAGASAKI and
HIROSIMA.
Digital Infrared Thermography
This much superior in diagnosing breast cancer with 90%
accuracy unlike 60-80% cancers diagnosed by
Mammography.
More than 800 peer reviewed study on breast cancer.
90% detection accuracy
Abnormal breast thermogram is the single most significant
marker of high risk for the development of breast cancer.
Can detect first signs of pre cancerous development upto
10 years in advance of any diagnostic procedure. Since
most breast cancers take 8-10 years to grow in size of 1
cm, after reaching this size in 1.5 year it can become size of
3.5 cms.
Breastthermography.com, iact-org.org, thermologyonline.org
Magnetic Resonance Spectroscopy
(MRS)
Visually after abnormality detects by Mammogram or MRI,
a needle biopsy is performed which is cold standard
method of differentiating malignant from non malignant
tumors. 80 % breast tumors are benign means most
biopsies are unnecessary.
Proton Magnetic Resonance Spectroscope (1HMRS also
called 3.0 Tesla MRI)
Can detect elevated levels of choline compounds which are
present in cancerous tumors.
Anti-Malignin Antibody Serum
(AMAS)
Developed by Husband and Wife team Samuel and Eleanor Bogoch of
Boston University School of Medicine. They isolated ‘Malignin’ antigent
from most of Malignant cancer cells.
This is 99% accurate ever compare to CEA test and can detect
common and uncommon varieties of cancers of anus, brain, breast,
cervia, colon, esophagus, kidney, lung, overy, prostate, skin, stomach,
testes, thyroid, urethra and uterus. Clasification of Malignancies
detected are fibrosarcoma, hemangioblastoma, limyosarcoma,
leukemia, liposarcoma, lymphoma, melanoma, mesothelioma and
osteogenic sarcoma.
AMAS will be negative in case there is no Malignancy, the disease in
terminal / final stages of Malignancy since there is no production of
AMA.
AMAS < 77 mcg/ml healthy, > 135 mcg/ml shown positive of cervix, skin
alcerative colits with no Malignancy.
www.acam.org
Breath Test
Dr. Linus Pauling, a two time NOBLE winner analyzed
compounds contained breath by gas chromatography. More
than 200 volatile organic compunds (VOCs) are found in
breath which of them are markers of disease.
Menssana Research of Newyork, Newjercy developed a
portable “Breath collection apparatus (BCA) which can be
used in any location.
BCA has identify new and comprehensive set of markers of
Oxidative Stress known as ‘ Breath Metlylated Alkane
counter (BMAC)
Many diseases can be diagnosed today using Breath Test.
Chemotherapy drugs are designed to be either cell
cycle specific or not. They attack cancer cells at
specific phase in the cell’s cycle for example
common chemo drug Taxol works between G0 and
G1 phase.
Other chemo drugs function in general way or noncell cycle specific.
Interestingly many chemo drugs are plant
derivatives/extracts like Amino Lamptothelin,
Docetaxel, noxoresinin, oncovin, taxol, adriamycin,
vinblastine.
Stopping Metastasis
Dr. H.V. Honn stated that
– The lymphatic systems, where in malignent cells
can spread to both local and distant lymph
nodes
– The CV system where in cancerous cells can
detach from the tumor site of origin travel
through out the body and invade any organ.
Thus seeding a new growth.
– Cancerous cells bind to cells on the outer
membrane (Vascular endothelium) of healthy
organs and in time penetrate to the interior of
the target organ.
What is the cure?
Strategy 1: preventing adhesion with modified citrus pectin:
Malignant cells have a particular “stickiness” that allow
them to stick to the cell walls of distant organs. The ability
of these cancerous cells to adhere to secondary sites is
related to the ability to clot. Therefore so many
anticoagulants are tried to reduce thickening.
The culprit is Galactin -3 or protein that clumps cancer cells
together. Those molecules occupy receptor sites on the
surfaces o many cells types, including cancers of breast,
colon, prostate, glialblastoma, laryngeal epidermoid
carcinoma, lymphoma and melanoma.
It is glue like substance which allows malignent cells to
adhere to each other, as well as to normal cells o the blood
vessels and vital organs distant from the primary site of
origin.
Modified Citrus Pectin (MCP)
Contains large amounts of galactose (Galactosides and galactosyl residues). The
sticky galacten-3 have very high affinity or galactose and bind with it within blood
stream and lymph.
The binding process of galactose with galectin-3 blocks the cancerous cells from
being able to adhere to each other and to other sites throughout body.
Because the malignant cells are isolated without being able to clump together to
form colonies, they eventually atrophy and eliminated from the body.
While MCP may not be able to stop cancerous cells from detaching from the original
site, it does inhibit the chemical fool holds needed to colonize the other organs.
1992- Study in JNCI shown human B16-F1 Melanoma cells in lung colonificaion –
metastases decreased by 90% with injection of MCP.
1995 – JNCI article shown 1% MCP injection developed only one tumor colony
compared to 9 colonies in controlled group in Prostate cancer
2000 – study shows reduction in Colon-25 tumors implanted in mice when MCP is
given at 1.6 mg/ml on daily basis. 70% reduction in tumor size found.
Wayne State Researchers studied in Vivo in mice injected with MDA-MB-435 Breast
Cancer cells given MCP in drinking water the angiogenesis and metastasis were
reduced by 72.1%
The most effective molecular weight ranges from 10,000 – 20,000 kilodaltons
econugenics.com
What is the cure?
Strategy 2: Tissue strengthening and collagen dissolving enzyme blocking:
1996 – JAMA (Journal of American Medical Association) all Flatin drugs can
damage cellular structure
Warning issued all stations can be carcinogenic – damage to DNA, cells genetic
software which can trigger two processes that facilitate the inception of cancer
growth:
– Uncontrolled cell multiplication – cell becomes reprogrammed to reproduced and
multiply without restraint. This is first step in formation of cancer.
– Mass production of collagen dissolving enzymes the increased number of cells
begins to produce tissue, degrading enzymes which allow the malignant growth to
spread.
The rate of spread of a primary cancerous growth is its aggressiveness; is a
direct function of the amount of collagen dissolving enzymes it produces. This
mechanism plays major role in the process of metastasis.
The Mathias Roth, renowned German Physician:
–
–
Strengthening the stability of normal healthy tissues so that they provide a strong defence against
the movement of cancerous cells
Further preventing the offensive advance of cancer cells by blocking the effectiveness of their
collagen dissolving enzymes
Vitamin-C, Liacin and Proline
natural healthshoppe.com
Cimetadine
British Journal of Cancer – 2002 study conducted by 15
Japanese clinics shown colorectal tumors given 800mg of
oral Cimetadine daily for one year survived by 10 years.
Found to prevent metastasis, cimetadine boosts immune
function, inhibit formation of tumor blood vessels
(angiogenesis) and increases apostasis (cell death) of
cancer cells
To prevent secondary blood vessels formation in secondary
tumors
Curcumin, Green Tea extract, Quercetin, Resveratrol,
Selenium, Vit- D3
Therapies
Radiation Therapy:
– EBT, IMRT, Gamma Knife, Cyber Knife, Proton Beam, Seeding
Techniques and IV Administration of Liquid radiation like Bexxol.
HIFU (High Intensity Focused Ultrasound):
– HIFU raises temperature at cancer site to 80 – 1000C in 1 sec
without damaging the tissue
Chemo Therapy:
– Protocol Therapy
– Cesium High pH Therapy
– Dr.Budwig Protocol
Treatment methods
Dr. Navarro Six self-treatments
1. Immune-system stimulation:


Transfer Point Beta-1, 3D Glucan
One 500mg capsule per 23Kg of body weight daily in the morning,
30min before eating or drinking anything.
[Source: www.AboutBetaGlucan.com/bspecial]
2. Flax oil/Cottage cheese “smoothie”

1/3rd of a cup of flaxseed oil mixed with 2/3rd s of a cup of cottage
cheese. Ass berries, almonds and walnuts and little stevia in the
blender. Add a little fresh water. Adjust to taste. Blend on the
liquefy setting. Eat it as soon as it’s blended.
[Source: www.barleans.com]
3. Heart Plus and Green Tea Extract

Six capsules of Heart plus (2 at a time, 3times a day) & 3 caplets
of green tea extract (1 caplet, 3 times a day)
[Source: www.MakingHealthAffordable.com]
Dr. Navarro Six self-treatments
4. Barley Powder
 20 tablets/day, take 6 or 7 about 15min before each meal
[Source: www.GreenSupreme.net]
5. Cancer-fighting diet

Avoid these five foods:
1)
2)
3)
4)
5)

sugar in all forms
Processed food in all forms
Animal protein
Dairy (except for cottage cheese/flax oil mixture), and
Gluten.
Maximize raw, whole vegetables. For variety, eat gluten-free,
sprouted bread products, flaxseed crackers, cereals (millet,
quinoa, etc., without gluten and with almond milk)
6. Vitamin/mineral supplement
 Take 2 packets of Daily Advantage daily.
[Source: www.DrDavidWilliams.com]
CANCER
 CANCER is a 4-Letter word and that word is
"ACID". Cancer is a systemic disease that has
localized and metastasized to the weakest point
in the body, whether it is in the breast, prostate,
uterus, ovaries, colon, liver or lungs.
STOOL SELF TEST
 Is it soft, firm?
 Color... is it light brown, medium?
 Is it free from foul smell and odors?
 Does it float?
 Do you have to strain?
 Does elimination take place 15-20 minutes after a
meal?
 Is it 5 to 7 inches long?
 Is it 1 to 1-1/2 inches in diameter?
 Is it banana-shaped?
STOOL INVESTIGATION
 Bright red blood means that the blood is from the anus. It could be

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
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

from an internal hemorrhoid or from a fistula or other rectal problem.
Dark red blood has come from farther up in the digestive system... it
could mean ulcers or colitis in the splenic flexure area.
Blackish-red blood indicates ulceration and bleeding around the
hepatic flexure.
Blood totally black in color could be from the stomach.
High protein diets with mostly meat produce a dark colored stool.
Spinach and other vegetables containing chlorophyll can stain stools
green; dark colored food such as blackberries or cherries will stain
the stool a darker color.
Yellow or orange stool indicates insufficient bile and is mixed with
intestinal contents, or a sign of jaundice or liver disease. Carrot juice
can also make stools turn orange color.
A reddish wine colored stool can be caused from eating beets.
STOOL INVESTIGATION
 Iron medication or anemia could cause slate grey or blackish stool.
 Excess protein stool is black.
 Very dark, olive blue stool may indicate a diet too rich in protein and
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fat – too much putrefaction within the bowel.
Dark, hard, offensive smelling stool may indicate very severe
bleeding high in the intestinal region. It may come from an ulcer in
the stomach, duodenum, colitis, or Crohn’s Disease.
Grey or chicken soup-like stool can indicate liver or gall bladder
trouble.
A hard, black stool means constipation.
Flat and thin-like stool indicates an obstruction in the lower part of
the bowel or spastic colitis (usually around the splenic flexure of
sigmoid area).
A stool with many small bubbles (bead-like) shows fermentative
conditions.
A slick, slimy stool could be caused from jaundice.
STOOL STATUS CHECK (Regularly)
SPIT TEST
 When you awake in the morning, before you put anything into your
mouth, work up some saliva and spit it into a clear glass of water.
Within 1-30 minutes, look in the glass. If there are strings coming down
from your saliva, or if the water turned cloudy, or if your saliva sank to
the bottom, YOU MAY HAVE A CANDIDA CONCERN! Healthy saliva
will simply float on the top!
CANDIDA SELF-TEST
PARASITES – Uninvited Guests
 Parasites are organisms that live by feeding upon another
organism. Parasites living in the human body feed on our
cells, our energy, our blood, the food we eat, and even the
supplements we take. There are many types of parasites
from single-celled organisms that are only visible under a
microscope to tapeworms that grow up to about 39 feet
(12 meters).
 It is a common misconception that parasites exist only in
third world countries. Over 200 types of parasites have
been found in North America. Parasites are transmitted
from person to person, pets, insects, soil, unfiltered water
and even tap water.
SYMPTOMS OF PARASITES
 Abdominal pain
 Memory loss
 Dry cough
 Allergies
 Mucus in the stools
 Fever and chills
 Anorexia
 Muscle pain
 Flatulence
 Appetite changes
 Nausea
 Gas
 Arthritis
 Poor appetite
 Gastrointestinal
 Asthma
 Poor digestion
symptoms
 Bloating
 Poor immunity
 Headaches
 Bloody stools
 Rectal bleeding
 Heartburn
 Brain fog
 Rectal itching
 Hives
 Cancer
 Skin rash
 Insomnia
 Colitis
 Tapeworms
 Intestinal cramps
 Constipation
 Unexplained weight loss
 Irritable bowel
 Dermatitis
 Malabsorption
 Joint pain
 Diarrhea
 Lymph blockage
 Leaky gut
HOW TO GET RID OF PARASITES?
 Internal parasite and Candida cleanse
 Strict diet
 Drink only clean, restructured and electron
charged water
 Replenish the good intestinal bacteria
 Supplement with a fiber supplement to
absorb toxins from cleansing
 Supplement with enzymes to digest food
and kill parasites in the stomach
PARASITE SELF-TEST
Answer ‘yes’ or ‘no’ for each question below. If you answer yes, give yourself 1
point, if no, no points are awarded.
Do you experience unexplained muscle aches and pains?
2) Do you experience normal bowel movements with bouts of
intermittent diarrhea or constipation?
3) Do you have unexplained weight loss and/or fever?
4) Do you have a distended belly?
5) Do you grind your teeth while you sleep?
6) Do you have dark circles under your eyes and/or acne?
7) Do you have insomnia or disturbed sleep?
8) Have you traveled outside of the United States?
9) Do you regularly eat unpeeled raw fruit and/or vegetables?
10) Do you have pets that sleep in bed with you or do you eat after
contact with your pets?
TOTAL SCORE
A score of 3 or higher indicates you may be suffering from parasites.
1)
latest updates and late-breaking
research on new breakthroughs
in the fight against cancer
THE LACTOFERRIN MIRACLE
 From the moment you were born, lactoferrin — an iron-
binding protein found in breast milk (colostrum) — was
your first shield against infection and disease and your
primary source of immune-system chemicals.
 The primary task of your immune system is to survey your
body—organ by organ, tissue by tissue, cell by cell — to
make sure that only the cells that are supposed to be there
. . . are. When a healthy immune system recognizes a
foreign substance — a virus or cancerous cell — it
immediately fights to eliminate it.
 Researchers discovered the significance of lactoferrin to
the immune system while researching another mysterious
biological phenomenon: pregnancy.
What’s so mysterious about pregnancy?
 Until recently, scientists had been baffled by the fact that a
woman’s body doesn’t normally reject a fetus, which naturally
contains the foreign antigens of the father. Science has
discovered that shortly after conception, a woman’s immune
system is down-regulated.
 This is why her body does not reject the fetus as “foreign”
matter. (For this reason, pregnant women should not take
lactoferrin) Immediately after delivery, however, her body
produces colostrum, or the first milk, which restores her immune
system and provides powerful immune chemicals to the infant.
Lactoferrin is the primary immune-system chemical in first milk.
 Studies have shown that the mother’s or first milk is the only
source from which an infant can get these ignificant immune
substances. Synthetic formulas can’t offer the same nutritional,
immunological, or physiological value, despite efforts to produce
formulas that mimic breast milk as closely as possible.
The Healing Mystery of Lactoferrin
Lactoferrin has at least two specific immune boosting functions:
 It binds to iron in your blood, keeping it away from cancer
cells, bacteria, viruses, and other pathogens that require iron
to grow. The lactoferrin protein is able to sequester and
release iron as needed, under controlled conditions. This
property helps prevent harmful oxidative reactions, making
lactoferrin a powerful antioxidant.
 It activates very specific strands of DNA that turn on the
genes that launch your immune response. This is such a rare
and surprising action that there is no other kind of protein like
it. Lactoferrin is in a class by itself.
The Healing Mystery of Lactoferrin
 Lactoferrin also contains antibodies against a wide range of
bacterial, fungal, viral, and protozoal pathogens. In effect, the
lactoferrin protein backs budding cancer cells or bacteria into
a corner . . . starves them and sends out a signal to your
white blood cells that says, “It’s over here! Come and get it!”
 State-of-the-art techniques in cellular and molecular biology
have recently allowed us to isolate lactoferrin from the “first
food of life.” The commercially available preparation is in a
form in which the food hasn’t been chemically altered.
 Other case histories indicate that the negative effects of
conventional treatments like chemotherapy and radiation are
drastically reduced or eliminated with supplemental
Lactoferrin (The amounts of lactoferrin used in these reported
cases range from 500 to 1500 mg a day).
The Heart Disease Test
that detects CANCER
 C-reactive protein (CRP) blood test that can help predict heart disease
risk, may also be a good indicator of risk for a very common type of
cancer.
 C-reactive protein is produced by the liver in response to inflammation.
Over the years, researchers have found high levels of CRP to be
associated with various chronic health problems, including stroke and
diabetes. A team headed by researchers at the Johns Hopkins
Bloomberg School of Public Health, reported on a population-based
study designed to see if there’s a link between elevated CRP levels and
colorectal cancer. The highest levels of CRP indicated double the risk of
developing colorectal cancer and two and a half times the risk of colon
cancer.
 Thomas P. Erlinger, M.D. noted in Journal of the American Medical
Association, that elevated CRP was clearly linked to colorectal and
colon cancer risk.
Vitamin D for Colon Cancer
 A study of more than 3,000 subjects, aged 50 to 75 years,
who were screened for colon cancer. Using dietary
questionnaires, researchers found a clear association
between vitamin D intake of more than 645 IU per day and a
reduced risk of colon cancer. Those who had the greatest
protection also used multivitamins, exercised regularly, and
had diets with high fiber content. Moderate sun exposure,
wild salmon and cod liver oil supplements are excellent
sources of vitamin D.
 Exactly how CRP levels may be affected by dietary factors,
multivitamin use and vitamin D remains to be seen. In the
meanwhile, it appears that the growing importance of CRP
now includes a novel way to help predict colorectal cancer.
Modified Citrus Pectin
 Metastasis has been referred to as the most lethal process on
earth. If it happens in your body, most doctors will consider you a
grim case, at best, because it refers to the spread of tumor cells
from their point of origin (say, the prostate) to other organs in your
body (say, to your lungs). Rarely do cancer patients die before
their cancer has begun to reach out to other body parts (or
metastasize). Once cancer has begun to metastasize, however, it’s
not easy to stop.
 Researchers have discovered that modified citrus pectin (MCP),
which is rich in certain simple sugars, acts as an “antiadhesive
agent” to prevent the cell interactions necessary for the transport
and growth of tumor cells to secondary sites in the body. Simply
put, MCP targets compounds in your body that help tumor cells
grow and spread.
 The recommended amount is 15 grams (or 3 rounded
teaspoons) per day.
Modified Citrus Pectin
 Prostate cancer:
 In an experiment at the University of Michigan Medical Center, rats
were injected with a million prostate-tumor cells. Normally, metastasis
would occur 10 to 12 days after injection and they would die 13 to 15
days after the cancer had affected the lungs and lymph nodes.
 And the truly promising and fascinating news is this: The cancercausing compound that MCP destroys in rat prostate cancer cells
(galectin-3) is also present in human tissues, including human
prostate tumors. In other words, MCP may prove to work exactly the
same way in human male prostate tumors as it does in rat prostate
tumors.
 Skin cancer:
 Skin cancer is the fastest-growing cancer in the world. MCP may one
day help us slow the progress of this deadly disease. In a study where
they also injected MCP, metastasis was decreased 90 percent. In
those mice who did not receive MCP along with the cancer-causing
substance, tumor colonies increased as much as 300 percent.
Guacatonga
 Guacatonga a small tree that grows in the wilds of the Amazon can fight
cancer. The bark, leaves, and roots of this tree have long been part of the
herbal medicine traditions in the lands where it grows.
 Taxol® which is derived from a plant source: the bark of the Pacific yew
tree, is a prescription drug used to fight cancer, particularly cancer of the
ovary, breast, and lung.
 The RTI research identified three new clerodane diterpenoids, which they
labeled casearvestrins A, B, and C. And the effects of these three newly
discovered compounds were quite impressive. All showed cytotoxic
effects against lung, colon, mouth, and ovarian cancer cells in laboratory
tests, when compared to controls.
 There are still many unanswered questions about exactly how the
phytochemicals in this rainforest plant fight cancer. Some studies have
suggested that the clerodane diterpenoids in the plant may kill cancer
cells by damaging their DNA. Another study found that the leaves and
twigs of guacatonga contain another phytochemical called lapachol, the
active ingredient in yet another Amazonian anticancer plant called pau
d’arco.
“Off the shelf” cancer cure emerges
 Silymarin, a constituent of milk thistle (and artichokes), has
been used for 2,000 years to treat liver disorders––and that’s
still what it’s most commonly known for today. But in 1994
researchers discovered that it was also a powerful killer of
colon and skin cancer. Since then, laboratory tests and
animal studies have shown silymarin’s anticarcinogenic effect
against breast and prostate cancers, as well.
Hybridized Mushroom Extract
 For the last five years in Japan, people with cancer, AIDS,
and other life-threatening illnesses as well as healthy people
who want to stay that way have been revving up their
immune systems, destroying tumor cells, and preventing
cancer and other illnesses with a powerful extract called
AHCC (activated hexose correlate compound).
 AHCC is an extract of a unique hybridization of several kinds
of medical mushrooms known for their immune-enhancing
abilities. On their own, each mushroom has a long medical
history in Japan, where their extracts are widely prescribed
by physicians. But when combined into a single hybrid
mushroom, the resulting active ingredient is so potent that
dozens of rigorous scientific studies have now established
 AHCC to be one of the world’s most powerful and safe
immune stimulators.
AHCC - Remarkable immune system
boost in multiple ways
 Scientific studies of the extract AHCC, published in respected peer-
reviewed journals such as International Journal of Immunology, AntiCancer Drugs, and Society of Natural Immunity, have established the
health benefits and safety of AHCC more conclusively than nearly any
other natural supplement. What is especially remarkable about AHCC is
that it consistently and effectively boosts immune system function.
Specifically, AHCC:
 Stimulates cytokine (IL-2, IL-12, TNF, and INF) production, which stimulates
immune function.
 Increases NK cell activity against diseased cells as much as 300 percent.
 Increases the formation of explosive granules within NK cells. The more
ammunition each NK cell carries, the more invaders it can destroy.
 Increases the number and the activity of lymphocytes, specifically increasing
T Cells up to 200 percent.
 Increases Interferon levels, which inhibits the replication of viruses and
stimulates NK cell activity.
 Increases the formation of TNF, a group of proteins that help destroy cancer
cells.
AHCC – Dosage
 After years of successful use in Japan, AHCC is available in the
United States as the active ingredient in a product called
ImmPower. Distributed by American BioSciences, ImmPower
comes in gelatin capsules containing 500mg of AHCC (proprietary
blend).
 For prevention, the recommended dose is one gram per day taken
as one 500mg capsule in the morning and again at night. This
dose will help increase NK cell activity and support immune system
functioning for good health and general well-being.
 For those with cancer, AIDS, or other life-threatening conditions,
the research indicates a therapeutic dose of two capsules in the
morning, two at mid-day and two at night for a total of 3 grams per
day to jump start NK cell activity. After three weeks, the dose can
be reduced to 1 gram per day (one capsule in the morning and one
at night), to maintain the increased NK cell activity level.
News of astounding natural cancer
killer nearly squashed forever
 Since the 1970s, the bark, leaves, roots, fruit, and fruit seeds of the
Amazonian Graviola tree have been studied in numerous
laboratory tests and have shown remarkable results with this
deadly disease.
 A study, published in the Journal of Natural Products, showed that
Graviola is not only comparable to Adriamycin but dramatically
outperforms it in laboratory tests. Results showed that it selectively
killed colon cancer cells at “10,000 times the potency of
Adriamycin”.
 Graviola has been combined with seven other immune-boosting
herbs in a product called N-Tense. As a dietary supplement, you
should take six to eight capsules of N-Tense per day. Graviola and
N-Tense are completely natural substances with no side effects
apart from possible mild stomach upset at high dosages (in excess
of 5 grams) if taken on an empty stomach.
Brazil’s “Mushroom of God”
Mushroom, the botanical name Agaricus Blazei Murill (ABM),
could be a potent immune-builder and cancer-fighter.
ABM contains a host of health-promoting components:
vitamins B1 and B2, niacin, phosphorous, iron, calcium,
protein, amino acids, and ergosterol (which converts into
vitamin D2 when the mushroom is dried). But most
importantly, the researchers discovered that ABM contains
large quantities of active polysaccharides, complex
carbohydrates, most commonly found in foods like wheat,
rice, and potatoes that stimulate the immune system to fight
off bacterial and viral illnesses.
ABM Stimulation
 ABM stimulates the immune system by triggering the
production of:
 T-cells, which directly attack cells that have been taken over by
viruses or cancers
 Interleukin, which bolsters the immune system by stimulating the
growth and activity of white blood cells
 Tumor necrosis factor (TNF), which activates white blood cells and
fights tumors
 Macrophages, which protect the body from infection by consuming
foreign material.
Major experiments with ABM
 At Japan’s Ehime University School of Medicine, researchers tested ABM’s impact on
tumors. Twenty days of treatment with certain ABM extracts (800 mg/kg per day taken
orally) retarded tumor growth in cancerous mice between 80 and 90 percent. The
researchers determined that the tumor-retarding agent was ergosterol, a steroid alcohol
that occurs naturally in mold and yeast.
 So they conducted a second experiment, giving oral doses of ergosterol (between 100 and
800 mg/kg) daily to tumor-bearing mice for 20 days. The treatment “significantly reduced
tumor growth” in a dose-dependent manner. Mice given the largest doses experienced
85.5 percent less tumor growth than mice treated with placebos. The ergosterol, however,
did not destroy cancer cells directly. Instead, it inhibited the development of new blood
vessels within the tumor a process that can stop and eventually reverse tumor growth. The
treatment also produced another benefit: After 20 days of treatment none of the mice were
suffering any of the side effects typically induced by chemotherapy drugs.
 Cancerous guinea pigs experienced even greater recovery rates over 99 percent when
they were treated with ABM. Researchers from Tokyo College of Pharmacy, Tokyo
University, and Japan’s National Cancer Center Laboratory injected cancer cells into the
femur (thighbone) of each pig—a procedure that normally causes cancer to spread
throughout the animal’s body within four to five weeks.
 Twenty-four hours later (once the cancer cells were embedded in the animals’ tissue), the
researchers gave the pigs ABM injections and continued to give them daily injections for
10 consecutive days. Five weeks later, 99.4 percent of the guinea pigs had fully recovered
from the cancer.
MEMBER SOURCE DIRECTORY
ABM (Agaricus Blazei Murrill)
www.virtuvites.com
Guacatonga
www.rain-tree.com
Graviola and N-Tense
www.rain-tree.com
ImmPower (AHCC)
www.theharmonyco.com
Immunoguard (lactoferrin)
www.goldshieldusa.com
PectaSol
www.econugenics.com
Alternate Therapies
(Non-toxic treatments)
Non-toxic treatments
 The difference between conventional cancer treatments
and alternative cancer treatments is
 The conventional cancer treatments are all toxic, while
all successful alternative cancer treatments are nontoxic.
 The successful alternative treatments target cancer
cells and do not harm healthy cells. While incase of
conventional treatments not selectively toxic it kill all
cells including healthy cells
 Alternative cancer treatments focus on cleansing the
body and stimulating the natural immune system with
special diets supplementation, detoxification and
oxygenation.
Non-toxic treatments
 There are over 300 non toxic alternative CANCER
1.



treatments are available. But we focus on the most
effective of these 300 treatments.
ALOE ARBORESCENS
All natural recipe derived from the Aloe arborescens
plant which used to promote supreme immune health.
The recipe:
Half kilo of pure honey
350 grams of Aloe arborescens leaves
40-50 ml of distillate (whisky, cognac or other pure
alcohol) to preserve the product and open the path for
the main treatment to get all over the body by dilating
the blood vessels. The distillate is only 1% of the
formula but it is very important.
Non-toxic treatments
Dosage:
 One tablespoon is a single dose. Three table spoons
daily three times.
 The doses are taken 10-20 minutes before a meal on an
empty stomach.
 It is important that the patient does not stop the protocol
until the cancer is completely in remission. Otherwise
the cancer will likely come back.
 This is an excellent supplemental treatment to be used
in conjunction with other protocols.
 This protocol can be combined with chemotherapy and
may considerably reduce the side effects.
Non-toxic treatments
 There has been much publicized scientific research and




literature on the synergistic benefits of the 300
phytotherapeutic biochemical and nutrient constituents
of Aloe vera to aid the body’s defenses to enhance the
immune system and protect against diseases.
The book written by Zago entitled “ Aloe Isn’t
Medicine and Yet…. It cures”
To Zago’s books
www.truthpublishing.com.
For the products
www.aloeproductscenter.com
Non-toxic treatments
2. BIO-OXIDATIVE THERAPIES.
Otto Warburg noble laureate believed that all
degenerative diseases are result of lack of oxygen at
the cellular level. He quoted “ Cancer has only one
prime cause. The prime cause of the cancer is the
replacement of normal oxygen respiration of body cells
by anaerobic cell respiration.”
This therapy uses the principles of oxidation to bring about
improvements in the body
There are two natural substances whose clinical use has
been documented in medical literature since the 1920’s
and which have been proven effective in treating some
of our most common serious diseases including heart
disease, cancer, and AIDS. They are Hydrogen
peroxide and Ozone
Non-toxic treatments
 Dr. Charles H Farr was nominated for noble prize in
1993 for this work.
 Hydrogen peroxide or ozone breaks down into various
oxygen sub species which contact anaerobic viruses
and microbes as well as diseased or deficient tissue
cells. Where these cells get oxidized while leaving
healthy cells intact. When body becomes saturated this
special forms of oxygen all disease causing micro
organisms are killed and the underlying toxicity is
oxidized and eliminated.
 Ozone found to blast holes through membranes of
viruses of HIV, fungi, yeast, bacteria and abnormal
cells before killing them without harming normal tissues.
Non-toxic treatments
 Administration of Ozone
Saturated fluid with Ozone is administered through
intravenously or 10-15 ml of blood is removed from the
body, saturated with Ozone and then infused into body.
Even Ozone sauna’s are available.
 Dr. Hans Nieper, used Ozone in Hanover, Germany, On
president Ronald Reagan, sir Antony Quinn, William
Holden, John Wayne, Yul Brynner and princess
Caroline of Monacco
 Dr. Saul Pressman the Ozone guru
[email protected]
Non-toxic treatments
 Hydrogen peroxide
Colostrum the first milk of delivered mother contains
tremendously high concentration of hydrogen peroxide
which fights invading organisms such as parasites etc.
Dr. Charles Farr shown that hydrogen peroxide stimulates
Oxidative enzyme system throughout the body which
triggers increase in metabolic rate causes small arteries
to dilate and increase blood flow, clears out toxins,
raises body temperature and enhances the body’s
distribution and consumption of oxygen. (BOM
international conference in 1992 ).
Dr. Reginald Holman in 1950 added H2O2 in drinking water
of rats that had cancerous tumors. Tumors completely
disappeared within 15-60 days.
Non-toxic treatments
 Dr. Kurt Donsbach wrote “One ounce of 35 % hydrogen
peroxide per gallon of water in a vaporizer every night
in a emphysemic’s bed room, and they will breath freer
than they have breathed in years i do this for my Lung
cancer patients”
 Administration of H2O2
0.0375% hydrogen peroxide in salt water or sugar water
given intravenous 50-500 ml into a large vein slowly
over a period of 1-3 hrs just like saline. Usually it is
given daily incase of HIV and CANCER. Only food
grade 35% should be used. It should not be used with
BUDWIG protocol.
 Oxycyclene is a liquid that helps in production of H2O2
within WBC resulting in destruction of both the disease
organism and the harboring white cell.
Non-toxic treatments
3. BRANDT/KEHR GRAPE CURE
Dr. John Pezzuto of the University of Illinois at Chicago
found that Grapes contains several nutrients that are
known to kill cancer cells, such as Selenium, Gallic
Acid, Quercetin etc.
The Brandt/Kehr diet involves twelve hours of fasting
followed by twelve hours of grape consumption. During
consumption period, supposed to consume absolutely
nothing except for grapes, grape mush and fresh
squeezed grape juice. To maximize the effectiveness of
grape mush, divide it into eight equal portions to be
eaten slowly every one and half hours of the twelve
hour consumption period.
Non-toxic treatments
While consuming be sure to drink at least a gallon per
day of pure spring water or well water, spread out over
both twelve hour periods and taken with the grape mush
during the consumption period.
The grape juice mush should include crushed seeds
and the skins, and the grapes should be purple Concord
grapes. In case of non-availability of organic grapes, be
sure to wash your grapes in warm spring water for at
least fifteen minutes and rinse.
Cancer cells consume eighteen times more sugar than
normal healthy cells. Thus, the grape cure diet is one of
the ultimate ways to kill Cancer Cells.
Non-toxic treatments
The following supplements can be taken with the
Brandt/Kehr Grape Cure
a) Grape Seed Extract
b) Grape Skin Extract
c) Quercetin
d) Vitamin C
e) Cayenne Pepper
f) Niacin
Both Cayenne Pepper and Niacin increase blood flow
which helps get the grape juice to the cancer cells.
Brandt/Kehr Grape Cure uses the glucose as a
transport agent for the cancer fighting nutrients.
Non-toxic treatments
4. BUDWIG DIET
This is the theory behind the Budwig Diet: the use of
oxygen in the organism can be stimulated by
lipoproteins (sulfur-rich proteins and linoleic acid).
Excellent sources of sulfur-rich proteins are nuts,
onions, chives, garlic and especially cottage cheese and
yogurt.
The blend of Flaxseed oil and cottage cheese should be
a part of every cancer patient’s diet. The blending of
this will convert the oil-soluble omega-3 in to watersoluble omega-3.
Dr. Dan C. Roehm, “What she (Dr. Budwig) has
demonstrated to my initial disbelief but lately, to my
complete satisfaction in my practice is: CANCER IS
EASILY CURABLE, the treatment is dietary/lifestyle, t
Non-toxic treatments
Dr. Dan C. Roehm, “What she (Dr. Budwig) has
demonstrated to my initial disbelief but lately, to my
complete satisfaction in my practice is: CANCER IS
EASILY CURABLE, the treatment is dietary/lifestyle,
the response is immediate; the cancer cell is weak and
vulnerable. The precise biochemical breakdown point
was identified by her in 1951 and is specifically
correctable, in vitro (test-tube) as well as in vivo (real)…
This diet is far and away the most successful anticancer diet in the world.”
Non-toxic treatments
5. CELLECT-BUDWIG
This is one of the most potent non-toxic and highly
effective alternative cancer treatments.
The key product in this protocol is a powder called
CELLECT. Cellect is a multi-mineral, multi-amino acid,
multi-vitamin supplement, with some anti-cancer
products.
Cellect occasionally causes constipation, be sure to
take three of the Cod Liver Oil capsules (included with
the Cellect) with each serving. Psyllium husk and fresh
vegetable juice also helps to alleviate constipation.
www.cellect.org
Non-toxic treatments
According to Dr. Krebs, cancer patients should start with
a few apricot seeds a day and build up to around thirty
apricot seeds per day preferably eaten on an empty
stomach and spread throughout the day between
meals, taking around ten seeds between breakfast and
lunch, then ten more between lunch and dinner, then
ten more at bedtime.
Cancer patients should drink Organic Vegetable Juice
with a dosage of 1 litre per 100 kg of body weight. It is
recommended that the juice should be consumed in
several smaller amounts instead of drinking the entire
juice at one sitting.
Non-toxic treatments
According to Dr. Kelley’s treatment, coffee enemas are
recommended, since the coffee will open up the bile
ducts and stimulate the production of bile in the liver.
Most of us have livers that are overloaded with toxins,
so it’s quite likely that you will need three or more
enemas per day.
This
particular
protocol
website
:
www.CellectBudwig.com
Non-toxic treatments
6. DMSO/MSM/CESIUM CHLORIDE (“DMCC”)
Dimethyl Sulfoxide (“DMSO”) is a highly non-toxic,
100% natural product that comes from the Wood
industry.
Methyl Sulfonyl Methane (“MSM”) is basically DMSO
with an additional oxygen atom attached to the sulphur
atom, forming a molecule with a total of two oxygen
atoms.
MSN occurs in fresh fruit and vegetables, raw milk,
wheat grass juice and aloe vera.
Non-toxic treatments

A research team headed by Stanley W. Jacob, M.D.,
at the University of Oregon Medical School, a study was
conducted in which DMSO was mixed with
haemotoxylon ( a purple dye) and injected in to patients
with cancer. They learned that DMSO has an affinity for
cancer cells. As a matter of fact, some of the cancer
patients were cured during this study. The study also
showed that DMSO could not only dissolve substances,
but it could also penetrate human skin and carry the
dissolved substances along with it.
Non-toxic treatments
According to Dr. David Gregg, “In the body DMSO
forms equilibrium with MSM, and the combination
becomes an oxygen transport system, enhancing
aerobic metabolism. This operates at only one point,
the respiratory chain (at the inner membrane of the
mitochondria).”
 According to Dr. R Barefoot in his book, The Calcium
Factor: The scientific secret of Health and Youth,
“Cesium chloride is a natural salt, and where it is found
cancer does not exist. This is because cesium is the
most caustic mineral that exists and when it enters the
body, it seeks out all of the acidic cancer hotspots,
dousing the fire of cancer, there by terminating the
cancer within days.”

Non-toxic treatments
 According to Dr. R Barefoot “when dimethyl sulfoxide
(DMSO) is rubbed near a painful cancer, the pain is
removed, and the DMSO causes the cesium to
penetrate the cancer tumor much faster, thereby
terminating the cancer much faster.”
 According to Dr. David Gregg, the cesium cancer-kill
mechanism is one the following.
a) It changes the osmotic pressure in the cancer cells
relative to the surrounding media, causing them to swell
and burst. This is why the tumor swells, which can be
dangerous in some cases.
b) It results in an opposing cesium and potassium
concentration gradient that arrests the continued
operation of the sodium-potassium pump, arresting the
sodium-glucose co-transport system feeding glucose
into the cancer cell, thus starving the cancer cell.
Non-toxic treatments
c) It results in an accumulation of negative ions inside
the cancer cell, cancelling the potential gradient across
the cell membrane, which is required to energize the
sodium glucose co-transport system, thus starving the
cell.
d) It results in a breakdown of the cancer’s disguise
which deceives the immune system, thus the cancer cell
is made visible and is attacked/destroyed by the
immune system.
However one can understand that any level of swelling,
inflammation, and/or congestion can be very dangerous:
thus the DMCC protocol is not recommended for
everyone.
Non-toxic treatments




7. ENZYME/METABOLIC THERAPY
The building blocks of this protocol were Pancreatic
enzymes.
Dr. kelley had a cure rate of ninety-three percent in
patients that lived at least 18 months after starting his
treatment.
He instructed to patients to eliminate pasteurized milk,
peanuts, white flour and sugar, chlorinated water, and
all processed foods.
Dr. kelley developed a line of over 50 nutritional
formulations for different types of cancers, and he
always individualized plans for patients according to
their own metabolic type.
Non-toxic treatments
 Dr. Kelley diet restricts protein, is 70% to 80% raw, and
emphasizes whole grains, friuts, vegetables, raw juices,
sprouts and pancreatic enzymes. Coffee enemas are
taken to help the body detoxify and to eliminate toxins
secreted by tumors as they dissolve.
 Dr Kelley was astonished to find case after case of
appropriately diagnosed advanced cancer patients who
were healthy and active 10-15 years after their
diagnosis.
 Dr Kelley treated 22 pancreatic cancer patients between
1974 and 1982.
Non-toxic treatments
 The twenty-two patients fell into three categories:
a) 10 patients consulted with Kelley only once and
never went on the protocol- All died.
b) 7 patients followed the protocol only partially and
sporadically – All died.
c) However 5 patients followed the protocol completely
– All achieved long term remission. The median survival
rate of these five pancreatic cancer patients was nine
years.
 One answer to cancer can be found at this website:
www.drkelley.com/CANLIVER55.html
 Dr. Kelley died in 2005 before he died he wrote a book
entitled Cancer: Curing the Incurable Without
Surgery, Chemotherapy or Radiation.
Non-toxic treatments
8. ESSIAC TEA
 An Indian doctor quoted “If people would use this weed
there would be little or no cancer in the world”. This
weed was one of the Herbs in the Medicine man’s
formula.
 In 1924 a Canadian nurse named Rene Caisse wanted
to test the Tea on her aunt, who had been diagnosed
with Terminal Stomach cancer and was given less than
Six months to live. She has advised to take the Herbal
tea daily for two months. Amazingly she recovered and
lived for 20 more years.
 She also tested the Tea on her mother who had been
diagnosed with Terminal Liver Cancer and had been
given less than 2 months to live, remarkably her mother
lived another 18 years.
Non-toxic treatments
 Dr.Fisher and nurse Caisse immediately began treating
cancer patients with the magic tea, which she eventually
named “Essiac” which is “Caisse” spelled backwards.
She healed thousands of terminal cancer victims with
‘Essiac’ in her clinic in between mid 1920’s and the late
1930’s.
 For “Essiac” formula visit www.octagonalhouse.com
 The formula :
A) 6 ½ cups cut up Burdock Root (cut into pea-sized
pieces).
Non-toxic treatments
•
Burdock root has been regarded as an effective blood
purifier that neutralizes and eliminates poisons form the
body. Studies have shown anti-tumor activity in
burdock. Japanese scientist have isolated an antimutation property in burdock, which they call the “B
factor”.
• A memo form the WHO reveled that burdock is effective
against HIV.
B) 1 pound (0.45 Kg) powdered sheep sorrel (including the
roots)
•
it is the main “Essiac” herb dissolves cancerous
tumors. It contains aloe emodin, a natural substance
that shows significant anti-leukemic activity. It contains
anti-oxidants is diuretic and has been used to check
hemorrhages.
Non-toxic treatments
C) ¼ cup powdered slippery Elm Bark
• It is well known for its soothing properties. It reduces
inflammations such as sour throat, diarrhea and urinary
problems. It contains Beta-sitosteral which has shown
anti cancer activity
D) 1 Ounce powdered Turkish Rhubarb Root
• It has been shown to have anti tumor activity. It is
diuretic, anti-inflammatory, and antibacterial.
Non-toxic treatments
Usage:
• 1 to 2 ounces per day diluted with about ½ cup of hot
water.
• If you cancer you should take “Essiac” three times per
day.
• Do not eat or drink (Except water) 1 Hr before & after
taking Essiac.
• Essiac tea is compatible with other alternative cancer
treatments except for Cancell.”Do not take Cancell
Protocol with Essiac tea”.
• For
more information on Essiac Tea visit
www.healthfreedom.info/canceressiac.htm
Non-toxic treatments
9 FREQUENCY GENERATORS:
 The term “electromedicine” has a very specific meaning
in the alternative cancer world.
 Dr. Royal Raymond Rife, a microbiologist who did
research in 1930’s designed a frequency generators to
vibrate the microbes (inside he cancer cells) to death.
 Very
low
amperage
electrical
currents
or
electromagnetic waves which drive through the body
and are able to revert cancer cells into normal cells.
10. GERSON THERAPY:
 It is a metabolic therapy which use uses a special diet,
along with supplements and coffee enemas.
Non-toxic treatments
10. GERSON THERAPY:
 Developed by Dr. Max Gerson, a German refugee
physician. It is a metabolic therapy which use uses a
special diet, along with supplements and coffee
enemas.
 What you eat on overall basis:
• 13 total glasses of fresh, raw carrot/apple and greenleaf juices prepared hourly from fresh, organic fruits and
vegetables.
• 3 full vegetarian meals, which typically include salad,
cooked vegetables, baked potatoes, vegetable soup,
and juice.
• Fresh fruit and fresh fruit dessert as snacks in addition
to regular diet.
Non-toxic treatments
 A Typical Day on the Gerson diet:
 BREAKFAST: 1 glass orange juice, Large portion oat




meal (with out milk), Bread
LUNCH & DINNER: 1 glass carrot-apple juice, Raw
vegetables salad, 2 cups Hippocrates soup, 1 large
baked potato, Cooked vegetables
DESSERT: fruit (Stewed or raw)
SNACKS: 6 additional carrot-apple juices, 5 green
juices, fruit & Vegetables.
Extra Supplements and Detoxification: aside from
diet another very important piece of Gerson therapy is
detoxification of tissues and blood.
caster oil packs helps in stimulating bile flow and
enhances the liver’s ability.
Non-toxic treatments
11. INSULIN POTENTIATION THERAPY
 The therapy which revolutionized effectiveness of
chemotherapy by making the drug available 100 times
to a tumor site example a drug like Cyclophosphamide
which required 20 mg but given 2 grams IPT increased
effectiveness of methotrexate by 10000 fold.
 This great therapy developed by a surgeon Donato
Perez Garcia, Cancer cells have 6-15 times more
insulin receptors on their cells they can take 15 times
more glucose.
 The 300 IPT trained doctors world wide
 IPTforcancer.com
Non-toxic treatments
Dr. Moss Reports:
 He has written more than 11 books in medicine
including cancer therapy, antioxidants against cancer,
Questioning chemotherapy and The cancer Industry. He
got PBS film the Cancer war an award winning
documentary.
 Dr. Moss now provides reports to individuals and their
family about treatment possibilities and each mass
report provides the client 400-450 pages of specialized
discussion of 1 out of some 200 different types of
cancers. It includes conventional and alternate
therapies in the world.
 Cancerdecisions.com