Category Archives: Medicin

Happy Toothpaste Recipe That Will Put Dentists Out of Business!

Honey, himalayan salt, baking soda, boron. (Feel free to swallow it, unlike conventional fluoride toothpaste, recommended by dentists, that could literally kill a small child if they ingest too much… it is hard to believe in this day, that dentists still recommend people brush their teeth with rat poison… fluoride, placing that industry itself into it’s own special hazard to public health and wellbeing.)

You can try equal amounts of the first three ingredients, followed by sprinkle of boron… then again, most people are deficient in boron their entire lives, soooooo…. 😉

By the way… the boron will make your teeth so hard (in tandem with alkalinity and minerals of the honey)….no more brittle teeth… your dentist might not be able to afford the lavish lifestyle for much longer… darn eh?)

Maybe you have heard baking soda is too abrasive for teeth… It is the alkalinity that is needed to protect enamel… brushing teeth is basically a gentle job, it is not like scrubbing floors to get them clean, it is more akin to wiping the counter. One Pleiadian Commander said he never brushes his teeth ever… only rinses. 😉

Honey: Chock full of minerals… and will help create a HEALTHY BIOFILM… something chemicals do not do. Realize that any toothpaste that does not put in a natural biofilm on the teeth, is not going to help you to naturally rebuild the enamel.

Himalayan salt: One of the great mineral salt sources for human health… spend the extra money and get the extra minerals.

Baking soda: Look at it this way… an acidic mouth means softer teeth, that will dissolve the teeth slowly but surely… an alkaline mouth means harder teeth.

Boron: From what I hear, the workers at the largest boron mine, remain healthy… no cancer, which is unusual for industrial mining. Also, have ever heard of someone dying from boron poisoning? Have you ever heard of boron building up in toixic amounts in the body? It doesn’t…. however simply just use a tiny bit if this is of concern, and continue to do research, so that you are comfy with what you are doing. 😉

How I do this?: I dip my tooth brush in honey… then I add sprinkle a premix of himalayan salt, baking soda, and boron… easy and it is fresh everytime.

What about coconut oil? While great for oilpulling, I do not like my toothbrush having an oily film on it, which doesn’t feel clean…. so leave the oil for the oilpulling.


Boron helps keep your teeth and gums healthy through reducing inflammation and improving bone and tissue repair. There’s an interesting study that came out in 2013 that found boron would helps the tooth building cells in such a way it’s believed thatboron could be used in bone and tooth tissue engineering.

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Cancer affects all of us. Its growing pervasiveness forces us to think hard about the current state of health care and the future of medicine. Have any of these questions weighed on you? What is the cause of all cancers? What is cancer—a mutant cell, a virus, a mold or an acidic liquid? Is cancer a noun or is it actually an adjective that explains what’s happening to the body cells? Are tumors bad or good? These questions have certainly weighed on me.

Most of the last 30 years of my cancer research has been focused on what is happening to the cells as it pertains specifically to the environment around those cells. Because medicine should not solely focus on the diagnosis and treatment of a disease but also endeavor to prevent illness by the promotion of health and fitness. Why? Because disease is an illusion! In reality, what we call disease is the manifestation of the body struggling to prevent over-acidification/fermentation/breakdown of the body’s cells, tissues, organs or glands. Disease is the body in preservation mode straining to maintain the homeostasis of its internal, alkaline fluids.

Cancer and an alkaline body are often brought up in the same sentence. The question that always follows is can cancer survive in an alkaline environment.

All cells in the body have an optimal ph which is acid alkaline and an optimal temperature at which they function. If your body were to cool down to between 90 – 92 degrees you’re not going to be moving around.

Our bodies function best at a ph of 7.4 and when you get up to a ph of 7.5 or 7.6, cancer cells just can’t do their thing. Part of a cancer cells requirement is acid production and in an alkaline environment they can’t produce those acids.

As an example, remember when trying to stick your head out of the car window and the wind is pounding you in the face as you’re going 60 mph and you can’t breathe so you have to turn your head to the side. It’s the same thing for cancer cells, it’s too much alkalinity and they can’t handle it.

So What Is Cancer?
Cancer is the body attempting to maintain alkaline homeostasis. Cancer is the body in preservation mode trying to maintain its natural healthy alkaline design. So first, you must understand that cancer is unequivocally not a disease, but a symptom, or better yet an effect of gastrointestinal, respiratory, environmental and metabolic acids that build up in the blood and then thrown off into the tissues poisoning and suppressing our immune system, making it increasingly difficult to maintain the alkaline pH of the internal fluids of the body.

Cancer is not a cell, but an acidic, toxic liquid that spoils and degenerates the body cells that make up our tissues, organs and glands. This happens when toxic acidic waste products are not properly eliminated through the four channels of elimination, which are urination, perspiration, respiration, and defecation.

Your body is like a car. You’re motor runs 24/7, which requires energy. And when energy is being used, a waste product is produced. Just like a car produces exhaust, your body produces carbon dioxide, carbon monoxide, lactic acid, or uric acid when it uses energy. So acid is constantly being created by the body cells, which has to be eliminated. If not, it will cause cancer!

When energy is being used to think, to move, to breathe, at the same time an acidic waste product is being created. If the acid is not eliminated, it is pushed out into the connective tissue. It is your connective tissue that becomes the ‘acid catcher’ in order to maintain the purity and alkalinity of the blood. The blood has to maintain its purity and alkalinity. If the blood varies even just one-tenth of one point, from its healthy pH of 7.365, you can have ill effects. When the blood pH starts dropping or if it starts going up, the body will do whatever it can to maintain its delicate pH. This is very significant in order to understand the cause and treatment of cancer and why it’s not a cell but the spoiling of the cells by dietary and metabolic acids, which have not been properly eliminated through normal elimination. When you are enervated or fatigued you do not have the energy to move the acidic waste products out of the body to maintain the purity of the blood. When this happens the blood pushes these acidic waste products out into the connective and fatty tissues in order to preserve its alkaline 7.365 balance.

For example, when acidic waste elimination takes place through the mucus membrane of the nose, it is called a cold—catarrh of the nose. And when this crisis is repeated for years, the mucus membrane thickens and ulcerates, and the bones enlarge, closing the passages. At this stage hay fever, then asthma develop. When the tonsils or any other respiratory passages become the seat of the crisis of acidity then we have tonsillitis, laryngitis, bronchitis, asthma, pneumonia, and finally cancer. You see, it’s progressive. It’s the same disease at different levels of acidity. All of these symptoms are happening in different progressions from the same thing—varying levels of acidosis.

Hence all cancerous conditions are the expulsion of acids from the blood and then the tissues, organs and glands and are essentially the same character evolving from the same cause, namely systemic acidosis—a crisis of toxemia.

Cancer is not a noun but an adjective expressing the process of cellular transformation. Sugar is the waste product. In fact, that’s why a banana gets sweeter and sweeter as it ferments. So sugar cravings are the body’s signal that the body needs more sustainable energy. However, sugar stimulates and gives the body a deceptive quick-fix—an illusion. Whereas salt provides the matrix of life and gives your body the rise in sustainable energy, over a longer period of time, without the high and extreme lows that come from eating an acid—whether it be sugar or any other acidic food or drink.

How Do I Fight Cancer?
If you don’t want cancer, if you want to prevent cancer, you have to eliminate your acidic wastes through defecation, urination, respiration or perspiration. Because cancer is not a cell, but a poisonous acidic liquid. A cancer cell is a cell that has been spoiled or poisoned by this acidic liquid—the metabolic, respiratory, environmental and/or gastrointestinal acids that are produced internally, or may be taken in via the lungs or skin. When this condition develops within us, the body will go into the preservation mode. One preservation tactic the body employs is to form fibrous materials, which cross-link, to encapsulate the spoiled cancerous cells, thus forming a protective tumor. Hence, the tumor is the body’s protective mechanism to encapsulate spoiled or poisoned acidic cells which have not been properly eliminated—isolating them from healthy cells that make up the tissues, organs and glands of the body.

So, the tumor is not the problem. Let the tumor go. Let it do its job. The focus must be placed not on the tumor but on the internal environment around the tumor, which is full of acidic cells. Think of any cancerous condition as a systemic acidic condition that affects first the weakest parts of the body.

The composition of our body fluids, that bath the outside of our cells, must be controlled very carefully from moment to moment and day to day with no single important constituent varying more than one percent. The good news is that this condition of health can be controlled and you can do it yourself!

All conditions of cancer potentially can be reversed if the treatments are focused on the fluids and not the cells of the body. Therefore it doesn’t matter what the cancerous condition is, because cancer is not the cause but the effect of an over-acidic lifestyle and diet which is the cause of cancer. You do not GET cancer, you DO cancer with your daily lifestyle and dietary choices!

The future is here and NOW. My hope is that The pH Miracle for Cancer will expand your knowledge and protect you from the acidic condition medical science calls cancer.

The pH miracle program follows the COWS protocol, which is.

C – Chlorophyll
O – Oils
W – Water
S – Salts

How much weight does the alkaline water trend really have in the medical world? Let’s take a closer look.

Wouldn’t it be lovely if all you had to do to avoid getting cancer was crack open a bottle of your favorite alkaline water and start chugging?
Jorge J. Nieva, MD, associate professor of clinical medicine at the USC Norris Comprehensive Cancer Center of Keck Medicine of USC for his expertise insights.

The internet rumor is that cancer is caused by extra acidity in your body, and that by drinking alkaline water you can “neutralize” your body’s acidity. While we wish cancer prevention was that amazingly simple, science comes down on the side of “not very likely.”

Here, we dive deep into the reasons.

pH and Your Body

Healthy bodies have a pH of about 7.4, which is slightly alkaline. (In liquids, 7 is neutral, anything lower is acidic, while anything higher is alkaline or basic.) Your body is really good at maintaining that pH of 7.4. It has to be. “Your body’s PH is not going to change from 7.4 to 7.6, explains Dr. Nieva. “If it changes much out of that range, you’re in the ICU.”

“Your lungs and kidney don’t let your PH change; that’s what they do,” he explains. Carbon dioxide (CO2) is the most common acid in your body and is a constantly being produced by your cells. When you produce CO2 in excess (for example, after an intense workout), your body is designed to eliminate it. Your blood carries the acid away from your organs and you breathe the excess out of your lungs. That is why you breath faster when you exercise, it is to keep your body’s pH normal and remove the excess CO2. Your kidneys also get in on the act, eliminating acid in the urine, but at a much slower rate than your lungs.

So where did the idea come from that alkaline water can prevent cancer?

Cancer cells can’t live in a high alkaline environment and the immediate areas in your body surrounding the cancer cells can become acidic. The thinking follows that if your body is more alkaline, you won’t get cancer.

Wait, that sounds like fans of alkaline water may be onto something. They aren’t?

While cancer cells can’t survive in high alkaline environments, neither can any of the other cells in your body.

And while the tissues immediately surrounding the tumor are more acidic, it’s a result of the way it use oxygen and create energy, not because the tumor itself is inherently more acidic. Researchers don’t know exactly why this process happens and are studying it, as it may lead to the discovery of more effective cancer treatments.

Now onto alkaline water…

Everything you eat or drink goes straight your stomach, where it is greeted by your stomach acid, which has a pH of 3. It sounds redundant, but your stomach acid naturally has to be acidic to break down the food that you’ve eaten or liquid you’ve drunk. The acidity also makes your food sterile so that you don’t get infections from the bacteria on the surface of foods. From there, it’s onto your intestines where the whole mix gets neutralized back to slightly alkaline by your pancreatic secretions and enzymes. Your intestines are the great leveler and everything you eat ends up at the same pH, regardless of the pH it had while still on your plate or in your glass.

If you’ve been chugging alkaline water by the gallon, you’ll just pee it out in the end, anyway. “You take in alkaline water, you make alkaline urine,” Dr. Nieva says. “That’s all you’re going to do.”

Your body is an efficient machine and it’s designed to maintain a safe, slightly alkaline level of 7.4. The good news is, that unless you have a kidney problem, you’re not doing any harm by drinking alkaline water.

There’s so much information surrounding cancer and diet that it can be hard to separate the myths from the facts. That’s especially true when it comes to trendy diets.

The alkaline diet is one such trendy diet that often comes up in conversations about both cancer treatment and prevention.

What is the alkaline diet?

The alkaline diet is based on the theory that eating certain foods can change the body’s acid levels, also called the pH levels. Some believe that changing the body’s pH levels can improve your health and help you lose weight or even prevent cancer.

But there’s no way the foods you eat can alter the pH level of your blood. The body’s pH is a very tightly regulated system. If you change your diet, you may see changes in the pH of your saliva or urine because these are waste products, but there’s no way you could ever eat enough that it really impacts your blood.

What is alkaline water?

While we can’t comment on specific brands, most alkaline water is just like bottled water with different mineral content. Alkaline water also can’t change the pH of your blood.

What is the link between the alkaline diet and cancer?

Some studies have shown that acidic environments help cancer cells grow. So the idea is that a diet high in alkaline foods (high pH) and low in acidic foods will raise the body’s pH levels (make the body more alkaline) and prevent or even cure cancer.

It should be noted that these are studies of cancer cells in a dish and do not represent the complex nature of how tumors behave in the human body. And food cannot change the pH of your blood.

What should cancer patients know before changing their diets?

Research shows that there’s no one diet or food that can cure cancer. But proper nutrition can help you feel your best during cancer treatment – or at any time.

That’s why it’s so important to talk to a doctor or a dietitian before beginning a new diet. This is true regardless of whether you have cancer. Different diet plans work for different people, and your doctor or dietitian can help you determine if a new diet will help you reach your health goals.

Ask your doctor here to refer you to a clinical dietitian. Each clinic has an assigned dietitian who is available to help patients at all stages of cancer treatment.

Your dietitian can assess your nutrition and talk with you about your nutrition goals, which may change at different stages of treatment. Your dietitian can help limit your diet’s adverse effects on your treatment, minimize side effects and help you cope with new food sensitives that you’ve developed since your diagnosis.
Now, the most important piece is how to you make all the cells in your body alkaline. Well, you do that in a number of ways and the first place to start is nutrition and the food you’re putting in your mouth.

The more food you consume that is alkaline, the healthier you will be. Also, remember there are some foods that are acidic but once consumed become alkalizing in the body like lemons.

Alkaline Juice Cleanse Recipes

Our alkaline juice cleanse recipes provide a good way of helping your body to maintain a slightly alkaline state. Alkaline diet theory is gaining more and more attention every day and nutritionists are starting to take it much more seriously.

Our natural healthy state is a ph balance of 7.35-7.45, which is slightly alkaline. It’s known that when your body starts veering towards an acidic state it has to work extra hard to bring it back into a state that is slightly alkaline. One of the ways this is done is by sapping calcium reserves, as well as other minerals out of our bones in order to help buffer this imbalance.

Some nutritionists now, as well as many others are also seeing a link between acidity in our bodies and many poor health conditions that are plaguing our modern world. Many chronic health conditions are being connected to this acid/alkaline balance, and while there is still debate as to what the absolute truth is. There are many that are convinced that this imbalance is at the bottom of a myriad of health problems.

The alkaline juice recipes below use a good mix of vegetables and fruit that are known to be highly alkalizing for your body. Many alkaline juice recipes use fruit that is higher in sugar, which according to the top researchers in this field are acidic due to this sugar content. In keeping in tune with this, I have done my absolute best to use only alkaline ingredients that are lower in sugar and that are also found in the lists of the top authorities relating to this field.

Carrots and coconut juice have been found by many authorities in this field to be among the few types of fruit and vegetables with sugar to have an overall alkalizing effect once inside of the body. For this reason I have chosen to include them in some of the alkaline juice recipes that are listed here.

(If you are looking for a way to get alkaline more optimally, you should really consider The Complete Guide To Doing A 7 Day Juice Cleanse. Our eBook provides a whole lot of value, and will give you all of the information you need to do a good alkaline juice cleanse.)

If you have any questions or comments at all please feel free to leave them in the comments section below!

For specific instructions how to prepare your produce for our juice cleanse recipes click here!

Recipe #1.

Tropical Alkaline Breeze

Simple recipe.

1 Young thai coconut
8 Carrots
2 Stalks Celery

If you want something more precise.

Young thai coconut juice= 11 ounces juice
(4 and 1/2 cups carrots chopped) Carrots= 9 ounces juice
(1 and 1/2 cups chopped) Celery= 4 ounces juice

Yields about 24 ounces of juice.

This alkaline juice cleanse recipe makes a moderately sweet juice that is just awesome! When using the young coconut you do not juice any of the actual flesh. You simply open the coconut and then pour the coconut water into your juice mix. Happy juicing!

Recipe #2.

Refreshing Green Energy

Simple recipe.

1/2 Bunch (7 leaves) Kale
1 Large handful Basil
1 Cucumber
2 Stalks (bulb part leaves included) Fennel
4 Large Carrots
1 Knuckle Ginger

If you want something more precise.

(2 and 1/2 cups chopped) Kale= 2 ounces juice
(1 cup chopped) Basil= 1 and 1/2 ounces juice
(2 cups chopped) Cucumber= 6 ounces juice
(1 cup chopped) Fennel= 3 ounces juice
(3 cups chopped) Carrots= 7 ounces juice
(1 and 1/2 inch square) Ginger= under an ounce of juice

Yields about 20 and 1/2 ounces of juice.

When it comes to the fennel in this juice you want to cut two stalks including the bulb part on the bottom. This will give you the stalks, leafy part, and the bulb part. This recipe is among the alkaline juice cleanse recipes that creates more of a vegetable juice, which is not really sweet at all. The flavors do balance each other out well though and this juice is lower on the glycemic index. This juice is also very alkalizing and makes a great addition to an alkaline diet.

The kale we used when creating this recipe was a curly variety of kale, but you can use whatever type of kale you like.

Recipe #3.

The Green Cooler

Simple recipe.

3 Ounces fresh squeezed wheatgrass juice
1 Juice of Coconut
1 Large Cucumber

If you want something more precise.

3 ounces fresh squeezed wheatgrass juice
8 and 1/2 ounces coconut juice(water)
(2 cups chopped) Cucumber= 6 and 1/2 ounces juice

Yields about 18 ounces of juice.

This alkaline juice cleanse recipe makes a juice that’s not really sweet, yet you can taste the coconut and wheatgrass juice through the cucumber. Young coconut juice generally is much better than the typical coconut juice, but I did not have access to that when I made this juice. Whatever type of coconut you have will work as it will still contribute to the alkalinity of this juice recipe when it comes to alkaline juice recipes and also juice cleanse recipes in general. You have to be creative as you want to keep them lower in sugar, yet also tasty enough to enjoy. I compiled a start to finish picture below of my little adventure on the morning this juice was made. I just love making myself a nice tall alkaline juice in the morning! What a way to start the day!


Recipe #4.

The Mini Super Alkaline Juice!

Simple recipe.

1/2 Large Cucumber
4 Stalks Celery
1/2 Large Lemon (or 2 small lemons)

If you want something more precise.

(2 cups chopped) Cucumber= 6 ounces juice
(2 cups chopped) Celery= 5 ounces juice
(3/4 cup chopped) Lemon= 1 and 1/2 ounces juice

Yields 12 and 1/2 to 13 ounces of juice.

As far as alkaline juice cleanse recipes go, this one definitely has a lemony juice taste to it. The cucumber, as well as being very alkaline, helps to level out the flavor though and makes this an easy juice to enjoy. When juicing the lemons, use the entire lemon (peel and all)!

Cucumber, celery, and lemon alkaline juice cleanse recipe


Recipe #5.

Leafless Alkaline Salad Juice

Simple recipe.

3 Heads Broccoli
8 Carrots
3 Stalks Celery
1/2 Large Cucumber

If you want something more precise.

(5 cups chopped) Broccoli= 8 and 1/2 ounces juice
(4 cups chopped) Carrots= 9 ounces juice
(1 and 3/4 cups chopped) Celery= 5 ounces juice
(1 and 3/4 cups chopped) Cucumber= 4 ounces juice

Yields about 26 and 1/2 ounces of juice.

Alkaline juice cleanse recipes need to tie together nutritious alkaline ingredients in a way that is palatable. This juice makes a very nutritious alkaline blend and is also easy to drink.

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Vaccines found to contain pig virus DNA and monkey kidney cells… the “dirty” little secret the vaccine industry doesn’t want you to know

(Natural News) A list of vaccine excipients released by the CDC provides insight into some of the most toxic ingredients that big pharmaceutical companies use in manufacturing vaccines. With the FDA and CDC insisting on the safety of these vaccines, larger drug firms continue to use these ingredients to cash in on their products while simultaneously disregarding public safety.
Vaccines heavily-laden with infected animal cells

The CDC’s list includes an array of excipients that use various vero cells taken from animal hosts. These cells have undergone great scrutiny as various clinical studies raised concerns about possible infection. An excipient found in polio vaccine, for example, contains cells from African green monkeys. Vero cells taken from this species of ape are known to be infected with Simian Virus 40, a DNA tumor virus associated with the onset of different types of cancer. Further analysis also revealed that the virus has a slow-moving an archetypal strain that drug manufacturers and regulators failed to monitor. The use of this infected vaccine excipient resulted in a significant increase in cancer rates since the 1960s.

A rotavirus vaccine also came under fire for using this excipient. A 2010 study published in the Journal of Virology found that the rotavirus vaccine contains a live simian virus, with researchers noting a 96 percent matching certainty. Another study confirmed the presence of an endogenous baboon virus in the same vaccine. The results appear in the journal Advances in Virology. Infected cells taken from diseased monkeys have also been feared to have tainted a smallpox vaccine. Warning indications for said vaccine include a host of adverse health conditions such as cardiac disease, blindness and encephalitis.

Bovine serum is another potentially lethal excipient found mostly in MMR and rotavirus vaccines. The inclusion of this excipient in vaccines has raised concerns of Creutzfeldt-Jakob disease (CJD) contamination. While different health agencies — including the World Health Organization, the CDC and the Australian Therapeutic Goods Administration — have refuted this, there were rare, documented cases of CJD infection in humans in the U.K. These cases were associated with ingestion of products infected with mad cow disease.

Experts have also raised concerns about the use of porcine vero cells in vaccine production. A rotavirus vaccine was in a bit of hot water a few years back after regulators found out that the treatment contained very high levels of porcine circovirus 1. The vaccine was proven to contain more than 100,000 porcine circovirus 1 DNA molecules in each dose. However, it remains uncertain how the virus directly affects humans, which makes it all the more disconcerting.
Drug firms deliberately add carcinogens, neurotoxins to vaccines

Highly toxic chemicals are not uncommon in vaccine production. In fact, the CDC’s list of vaccine excipients includes at least one industrial-grade chemical. Benzene, for example, is a key component of food dyes used in vaccines. Benzene is a highly toxic carcinogen associated with the onset of different types of cancer such as acute myeloid leukemia, non-Hodgkin’s lymphoma and multiple myeloma. Other carcinogenic compounds found in vaccines include formaldehyde, acetone and ethanol.

Thimerosal, a neurotoxin, was also present in most vaccine excipients listed in the CDC document. Thimerosal contains mercury, the second most toxic element in the world next to plutonium. Various studies have found a correlation between thimerosal and the onset of autism spectrum disorder in children.

Despite the apparent health hazard, big pharmaceutical companies insist on using aluminum hydroxide as a key component to vaccine production. Aluminum hydroxide is tied to a host of adverse medical conditions including rhabdomyolysis, encephalopathy and osteomalacia. The asthma-inducing glutaraldehyde also appeared to be a staple in vaccine production. Data from the CDC list showed that at least eight vaccine excipients used the toxic compound as a disinfectant. Glutaraldehyde was linked to chemical colitis, rectocolitis and eczema.

Sources include: [PDF]

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USA Opioid overdoses now deadlier than car crashes

Americans are now more likely to die from an opioid overdose than from a vehicle crash for the first time in history, according to a new report.

The National Safety Council released new data this week that found Opioid overdoses are now the fifth most likely cause of death, with the odds of dying from an overdose at 1 in 96.

The odds of dying in a motor vehicle crash are 1 in 103.

The council cited an increased influx of the drug fentanyl in a statement on the data, according to NPR.

Fentanyl, a synthetic drug often trafficked on the black market from Mexico and Canada, is often combined with heroin or another drug, and has been repeatedly tied to the nationwide opioid crisis.

The Centers for Disease Control last month named fentanyl as the deadliest drug in the U.S., saying it was involved in nearly one-third of deadly overdoses in 2016.

U.S. life expectancy declined overall in 2017 due to an increase in drug overdoses and suicides. The National Safety Council data found that the chances of death by suicide are 1 in 88.

The most likely cause of death for Americans remains heart disease, with 1 in 6 odds, closely followed by cancer.

Fentanyl is smuggled into the United States across its insecure southern border with Mexico. As long as that border remains insecure, tens of thousands of Americans will continue dying from smuggled fentanyl.

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How to Cure Cancer and How Not to Do it: It’s More Complex Than Just Killing Cancer Cells & 10 Natural Cancer Treatments Revealed

Cancer is a disease of the tissue, not of the cell, let alone, of the gene. The latter is the official dogma and did not get us very far. Cancer is a wound that never heals, a regeneration that fails to stop. Treatment that slaughters cancer cell populations (thus, essentially all treatments except immunotherapy) further damages the cancer tissue which further stimulates an abnormal, never-ending wound healing process: generation of more abnormal cancerous stem cells that keep dividing. So why add injury to injury with treatment that kills cells? It perpetuates a vicious cycle. Recognizing that cancer treatment can be a doubled-edged sword that shrinks the tumor while promoting cancer progression will open a new vista on new treatment strategies that stop the vicious cycle.


What do all (non-surgical) cancer treatments, be it radiation, chemotherapy, or modern targeted therapy or even the latest immunotherapy have common? Answer: They seek to kill the cancer cells. But there is another commonality: They also all fail to eradicate the tumor most of the time. If we are brutally honest with ourselves, these conventional treatment strategies essentially do not work. But wait, wait: this is not yet another quackery opinion about how conventional chemotherapy is just “poison”. It is about the latest rigorous research results and biological thinking. There is a much more subtle aspect to brutal mass-killing of the cancer cell populations that I will explain here. Understanding it will change how we think about cancer therapy and help explain the occasional stunning successes of immunotherapy.

More precisely: current treatment does not work as desired and as expected in terms of the underlying scientific rationale. Modern “precision” therapy that targets the specific mutation in cancer cell, the putative root cause of cancers, should in theory work but doesn’t. Almost invariably, advanced tumors, even after treatment with targeted drugs that dramatically shrink the tumor, will regrow (“progress”), typically within one to two years. By logical necessity then, one may infer from the two commonalities of all therapies –designed to kill and failing to cure– the following:

Could the very act of killing cancer cells, that is, poisoning, suffocating or precision-targeting, be the problem, not the solution? (The exception is immune therapy which in a minority of cases can lead to “durable remission” but more later on this exception that confirms the rules that I will explain here.)

We are quite good at developing cancer drugs that can reduce tumor size by killing cancer cells. However, what kills the patient is not the primary tumor but the recurrent tumor and metastasis. After the initial regression to barely detectable size (“complete pathological remission”, CPR) the tumor can regrow from the cells that survive the treatment and then metastasize. The recurrent tumor is almost invariably more aggressive and harder to kill; its cells are now therapy-resistant.

Many things in life are not 100% but that does not matter: A glass that is “99% full” is essentially “full”. Getting 99% of the questions correct in an exam is a splendid achievement. Killing 99% of the enemy soldiers affords a decisive victory in battle. Not so in cancer treatment. Here we need a 100% kill rate. A tumor of the size of a pea (1g or 1cm3) may contain 10E9 (one billion) cancer cells. Killing 99% of the cells that it contains is actually not a success: you are left with 1% of surviving cells, which still corresponds to a whopping 10E7 (ten million) cells which can divide and multiply, driving a near-exponential re-growth of the cancer cell population. One reason why it is so hard to kill 100% of cells is the enormous heterogeneity of the cancer cell population with respect to the intrinsic drug-sensitivity and accessibility of individual cells.

But all is not as simple: why are recurrent tumors almost always MORE malignant (=“tumor progression”) and why do they also exhibits therapy-resistance, precluding that doctors simply re-apply the same treatment again and again? The old thinking was that the cells that survive the first treatment and regrow are cells that carry pre-existing chance mutations in their genomic DNA that make them inherently therapy-resistant. Because of this Darwinian selection, therefore, more and more potent drugs must be developed and deployed — so goes traditional thinking. But that is the wrong strategy. Darwinian selection could explain why cells become resistant –but why are cancer cells of recurrent tumors more aggressive, that is, more invasive and migratory? Why are they more resilient and versatile, resembling stem cells (=the normal cells in the tissue from which regeneration occurs)? This will become automatically clear later.

In life when we only achieve partial success in any task, for instance scoring not 99% but much less than 100% in a test, or killing only an insignificant fraction of enemy troops, the reflex is that we will need to double-down: We work harder or deploy more troops and more powerful weapons. Unfortunately, currently the sole strategy in cancer research applies the same principle: We double-down by developing more and more potent drugs that act with higher precision to target the mutated cancer cells. But instead of doubling down, it may be good to back down and rethink our strategy. Why?

We now learn that, despite prevailing dogma, new mutations are not the sole culprit for tumor progression, as cancer DNA sequencing increasingly suggest. But if so, the most powerful “precision medicine” drugs would be blunt — because the 1% or even 0.1% surviving cancer cells are not just “inherentlymore resistant”. They become an entirely different animal after having gone through a near-death situation imparted by the initial cell killing (“cytotoxic”) treatment. This qualitative change in the remaining tumor is the consequence of two processes: (a) First, conventional cytotoxic drugs or irradiation cause cell stress, which activates stem-cell functions that normally serve to initiate regeneration but in cancer cells only produces more “cancer stem cells”which instead can (re)initiate a tumor. (b) Second, the treatment damages the tumor tissue as a whole, leaving behind a battle-field littered with dead cells, which we call “cell debris”.

Let’s focus here on the latter process (b): What happens in the “tissue micro-environment” of the partially destroyed tumor following treatment


Instead of zooming in on the genetic mutations within the cancer cells’ genome, let’s zoom out. Let us consider the tissue micro-environment of the cancer cells in a tumor. The non-mutated “normal” cells surrounding the cancer cells, which comprise the so called “tumor stroma”, are not innocent bystanders in tumor development and progression. But they become (un)willing co-conspirators that nurture the initially tiny “dormant” tumor into a vigorously growing tumor that is clinically manifest. Thus, cancer is not simply a disease of incessantly dividing mutated cells that cause the tumor to expand and “take-off” as its tumor cells exponentially multiply. Cancer is even less a “genetic disease” as many textbooks present it. No, for many years now, it has been recognized by academics (but rarely acted on by practitioners) that cancer is a disease of the entire tissue, and is comprised of a heterogeneous population of a variety of cancer cells and of non-cancerous supporting cells: immune cells, including its first line defense cells, the macrophages, as well as blood vessel cells, and cells that normally constitute the structural framework of organs: the “fibroblasts”. Such cells are attracted to the clump of tumor cells and they are mixed in with the malignant cells. These non-cancerous “stromal cells” are recruited by the tumor via chemical and mechanical signals and become activated. They begin to communicate with each and with the tumor cells via a network of precisely wired communication channels.

The tumor is not just a clump of cancer cells (pink). It takes a village to grow a tumor. The village consists of the stromal cells: Immune cells (light blue), blood vessel cells (purple) fibroblasts (green) and others. The red arrows are the communication lines between the various cells — embodied by a large array of various ‘micro-hormones’ released by specific cells and addressed to specific cells.

Information is exchanged via a large array of specific signaling molecules secreted by cells: the so called “cytokines”, growth factors, small peptides and lipid autacoids. These “micro-hormones”, as we shall call them altogether, are sent by cells of one type, and addressed to specific cells of other types that carry the receptor molecule for the respective signaling molecule. These signal carry an instruction for the receiving cell to change its activity in particular ways, for instance, to increase cell division rate. A complex inter-cellular communication network thus is erected that coordinates the action of all the stromal cells and that also stimulates tumor growth in a concerted manner. This is the support from its tissue environment that the tumor needs to grow. Many of the more avantgarde cancer researchers have thus long proposed apt metaphors: the tumor is a new (pathological) organ. It takes a village (of cells) to grow a tumor. Here, we will take one more step into the metaphorical to explain a complex process.

Mutated cancer cells alone, without the help of the activated stromal cells, often stay silent in the tissue as harmless, dormant or “occult” micro-tumors for decades, and do not “take-off”. This is akin to the many nascent hurricanes in the Atlantic, many of which never make it to become full-blown hurricane that call our attention but instead die off while still above the Oceans because conditions for the self-reinforcing vicious cycles of warm air and low pressure are not met.

But there is more to this similarity: tumors also require a vicious cycle of reciprocal causation: Only when the network of stromal cells and the tumor cells establish a relationship of mutual reinforcement, where stromal cells stimulate tumor cells and tumor cells stimulate stromal cells, thus creating a self-propelling vicious cycle of reciprocal activation, will the mutated cells drive the net growth of the tumor. Unfortunately, the general phenomenon of bidirectional causation and associated “non-linearity” lies outside the domain of comprehension of the linearly thinking scientists that dominate in the community of cancer researchers.

But dealing with such non-linear mutual causation confronts us with this question: How does the self-sustaining chicken-egg system get started in the first place? What triggers the attraction and activation of immune cells and the other stromal cells to build this self-propelling, growing society of communicating cells that lock-in the tumor in a robust expansion mode?


Rudolf Virchow, the German pathologist and father of scientific medicine proposed more than 100 years ago that the tumor is a wound that does not heal. Wound healing is a very complicated process. It is initiated by tissue injury, a damage of the specialized cells in the tissue (e.g. skin cells, liver cells etc. — that are the building blocks and the functional elements of organs) and the associated disruption of the highly ordered tissue architecture by a mechanical or chemical injury or an infection by a microorganism. The lesion of cells and the destruction of the nicely layered cell arrangement triggers the attraction and activation of an army of immune cells to fight the infectious agents. Blood vessel cells also migrate in the zone of damaged tissue to form new capillaries and nearby fibroblasts proliferate, thus providing the logistical and structural support for tissue repair. This process of increased blood and cell supply is known as inflammation. Along with inflammation, the nearby specialized cells of the tissue are converted into immature stem cells which then (along with resident tissue stem cells) regenerate the damaged tissue.

Now we can see: all those non-cancer cells of the “village”, which we said above supports tumor growth, are part of a (pathological) version of a wound!

Virchow was even right in that wound healing is coupled with tissue regeneration because a pathological version of it is manifest in tumor growth. As we now know for 20 or so years, tumor growth is largely driven by the“cancer stem cells” –the malignant version of the normal stem cells. (The very concept of cancer stem cells is debated because they are not fixed entities.)

In normal wound healing and regeneration, these tightly coordinated cellular processes of inflammation come to an end when the invading agent is eliminated and the tissue damage is fixed. The complexity of wound healing program includes the central but of neglected feature of being self-limited. Once the damage is contained, the immune response is suppressed, growth of new blood vessel ceases, and the army of inflammation cells retreats. The tissue stem cells differentiate and mature to functional tissue cells and thus, regeneration stops.

As we will see, of crucial importance, but often forgotten, is that in this stage specialized immune cells, the “clearing macrophages” (a subtype of macrophages), arrive and eat up the cell debris (from the dying cells) to clean up the battle zone, and the tissue heals –restitutio ad integrum.

Because inflammation drives diseases and cause pain, much research has been devoted to understanding what starts the inflammation and what drugs can block it. But very little is known as to what ensures the self-limiting nature of normal wound healing — the process now referred to as “resolution”. Because of resolution, a normal wound healing does not enter the endless vicious cycle of mutual stimulation by its component parts.

In the tumor tissue, as Virchows suggested, a wound healing-like process also takes place. It is thought to be triggered by a local disruption of the tissue architecture by the dormant micro-tumors along with the abnormal biochemistry of the malignant cells that is sensed by the tissue. In fact, disruption of the “glue” (matrix) that separates the specialized organ cells (epithelium) from the stromal infrastruture (where the fibroblasts reside in the normal tissue), followed by a pathological overproduction of a thick matrix is often the very first tissue reaction and perhaps the very first step of malignancy –at least from the unorthodox point of view of a tumor as a disease of the tissue. This increased tissue density is what is detected by mammography in the case of breast cancer. But additional tissue damage of unknown origin, perhaps due to chronic irritation, likely contributes to wound healing activities surrounding the tumor –creating the village of cells that is required for tumor growth.

New cancer DNA sequencing data suggest that, contrary to conventional wisdom, the awakening of tumors from the dormant state may not even require additional “cancer-driving mutations”. (This may be one explanation for why many chemicals suspected of causing cancer are not necessarily mutagens.)

But a key difference to normal wound healing is that the wound healing process in the malignant tissue runs on an abnormal program that leads to the vicious cycle. Here are the three key abnormalities:

· [1] First, since the growing tumor further destroys the tissue architecture, it embodies eo ipso THE tissue damage with all the consequences: it triggers the inflammation which in turn stimulates the conversion of cancer cells to cancer stem cells which proliferate robustly following their inborn instinct to replace damaged tissue. But they do so not faithfully following the architectural needs of the tissue because these cells are mutated. This uncoordinated growth in turn causes further tissue destruction, which further provokes repair mechanisms — a strong vicious cycle.

· [2] Second, the stromal cell reaction in this abnormal inflammation is poorly orchestrated; the inflammatory cells recruited to the site of damage are akin to an army of soldiers entering into the battle following an attack signal but incapable of hearing the signal for retreat in the cacophony: inflammation does not resolve and the wound cannot heal.

· [3] Finally, not only do cancer cells multiply rapidly, but they do so more than the new blood vessels can sustain. Running out of oxygen many cancer cells die (even if many cancer cells, notably the cancer stem cells, become specialists for survival in low oxygen). The tumor tissue is thus littered with dead cell bodies, the debris. And this debris material itself, by exposing the inner content of cells to the tissue, represents one of the most potent stimulator of inflammation. This is biologically plausible: What stronger an alarm signal of destruction is there than dead cell bodies and the release of the cells’ entrails? In many organisms and in many tissues, death of the cell will trigger the neighboring cell to briefly become a stem cell and divide to fill the gap, the machinery of self-repair that guarantees tissue integrity. But in tumors, this regenerative process is uncontrolled. In fact, experimental injection of dead tumor cells into small tumors grown in mice can boost tumor growth by up to 100-fold, as long known and as more recently shown for many ways of producing dead cells, with a variety of drugs and for a variety of tumor types.

Thus, unlike in normal tissue, if the continuously generated cancer stem cells in tumors are the seeds, then the stroma is the soil, continuously fertilized by inflammation and dead cell debris. No wonder, with this self-seeding and self-fertilizing, the tumor is a wound that does not heal, and a regeneration that does not stop. It has only one fate as a whole system (despite cell death): to expand and progress to higher malignancy.


We started with a logical deduction –an intellectual process that many cancer researchers have abandoned in favor of a blind chase for new cancer-driving mutations as explanation of the dreadful nature of cancer. We can now follow up with another logical deduction: treatment kills cells, thus it will increase the debris in the tumor, and debris in one of the key elements that spins the vicious cycle of mutual stimulation between stromal cells and tumor cells that drives tumor growth. In a more refined mathematical analysis this scenario represents a so called “bifurcating instability” in which there is no middle ground, no grey zone (or very unlikely) , but a binary “either-or” outcome: (a) Yes, if we manage to kill the overwhelming majority of cancer cells (very close to, if not 100% of cells) then too little tumor mass remains to sustain the self-stimulating vicious cycle and the tumor will die away as a whole. (b) But if we manage to kill only much less than 100% of the cells there is sufficient tumor mass to be stimulated by the debris and inflammation, such that the very act of killing can, after initial shrinking of the tumor cell population, in fact stimulate the tumor.

This seems paradoxical, but may the following metaphoric stretch be allowed here: human societies sometimes behaves similarly: Hiroshima and Nagasaki city reemerged with latency from the ashes after the nuclear bomb detonation to new glamour and are arguably more flourishing than before.

Thus, cell killing tumor treatment adds injury to the injury that initially triggered the inflammation. This is exactly the scenario that Friedrich Nietzsche had in mind about human nature: What does not destroy me, strengthens me. This phenomenon of course applies to the war on terrorism, the suppression of political dissent, etc. as I wrote here. This Nietzschean principle that allows good people to reemerge stronger from life crises, that empowers bad guys after half-hearted attempts to contain them, that enhance resolve and resistance in those under attack, is also coopted by malignant tumors. It is the reason why the recurrence of tumor after treatment is not just the Darwinian selection of cells that happen to be insensitive to treatment but presents a different, in many ways more aggressive cancer.

Unfortunately, the cancer research community has, in the otherwise laudable effort to find simplicity, evolved a culture that makes it blind to all kinds of complex processes that involve the non-linear dynamics that is at the core of any vicious cycle. Instead, the modern cancer researcher, unlearned in basic biology and untaught in the analysis of complex systems, suffers from the habitual assumption of linear causation and the associated doubling-down mentality, believing that more effective killing is always better.

If cancer is a wound that never heals and if it is nearly impossible and too risky to aggressively seek a 100% kill rate (except in the case of the very uniform childhood tumors), applying a therapy based on the principle of mass-killing (but still unintentionally sparing many cells) will most of the time be a double-edged sword: the impressive initial remission (“shock and awe”) actually promotes later recurrence. If stimulation of cancer progression is built-in into the treatment, then no wonder that none of the drugs approved by FDA or by its European equivalent (EMA) in recent years for cancer treatment have prolonged life by more than a year (median survival). Yet, we keep doubling down by deploying more potent, more precise cell killing drugs, now under the mantra or “precision oncology”.

So what are alternatives to the mass-killing of cancer cells with cytotoxic chemotherapy, precision drugs or irradiation? We present below two promising, scientifically plausible alternatives — one is a hot topic, and another one which is only emerging as an entirely new treatment modality of which most active cancer researcher have yet to hear.

Link to video: Natural Cancer Cures and Why You Don’t Know About Them



The first alternative to the mass killing of cancer cells by cytotoxic drugs, including the precision therapy targeting mutations, or irradiation is immune therapy. Although developers and promoters of immune therapy, the hottest cancer treatment fad at the moment, are agnostic of all the above theory of the consequence of cell killing and the vicious cycle, but instead hoped to simply harness the natural cell-killing capacity of the immune system as yet another way to kill tumor cells, they have picked up a wonderful weapon for the battle against cancer: The cytotoxic immune cells, notably the T lymphocytes (“CD8 T cells”, formerly also called “killer T cells”) are fundamentally different from drug molecules or the beams of irradiation.

First, the immune system cells are living “kill vehicles”, and thus, much more powerful than any chemical or physical treatment –to an extent that one may hope that they could defy the double-edged sword nature of cytotoxic drugs by killing nearly 100% of the tumor cells with minimal collateral damage. After all, therapeutic agents of immunotherapy, such as the CAR-T cells and other genetically engineered T cells, or the body’s own anticancer T-cells awakened by a new class of drugs (“check-point inhibitors”) can, unlike chemicals, actively multiply and migrate to chase the tumor cells far into their tissue hide-outs –potentially killing many more cancer cells than the passively diffusing and inevitably decaying drug molecules. One central limitation in the deployment of immune system weapons is that one must know the precise barcode (antigen) that tumor cells carry on their surface and that is recognized by the immune system as abnormal or foreign in order to direct the immune cells to the cancer cells. Often we don’t even know whether the immune system is sensitized to recognize the tumor cells as foreign and to attack them.

But there is a more interesting, oft ignored bright side of immune therapy, notably, the checkpoint inhibitor drugs which overcome the natural checks on the immune system. This new class of drug activates an anti-tumor immune attack by preventing the natural molecular breaks in the immune system from operating. These breaks (“check-points”) normally serve to avert the immune from running amok and destroying the normal tissue, the cause of auto-immune diseases. These breaks are coopted by the cancer cells to subdue the immune cells that may attack them. Assuming that the immune system is sensitized to regarding the cancer cells as foreign (which unfortunately is often NOT the case) and that the cancer cells are indeed already successfully suppressing an anti-cancer immunity, then (and only then) it is plausible that removing the check-points will activate the intrinsic kill machinery of the immune system which can be a wonderful weapon. Let’s assume now that we have such a fortunate scenario to see the neglected bright-side of immune therapy.

Again, one must take the more holistic and encompassing view of biology that often escapes the narrow minds of cancer biologists and drug developers: By unleashing the immune system’s kill apparatus, a natural and biologically integrated process of cell killing is launched. The immune system kills cells in a way that is different from the brutal manner in which man-made agents slaughter cancer cells. The immune system does not engage in mass-killing but has evolved to gently kill infected or foreign-looking cells with minimal damage to the tissue. An immune killer cell (CD8+ T cell) kills the target cells slowly, one by one, by applying the “kiss-of-death” after double-checking that a given cell in the tissue deserves to be killed (because it carries the antigen signal). But most importantly, this process of soft killing comes with its own natural “vacuum cleaner” to remove all the dead cell debris produced by killing. The T-cells that perform the killing also sends a signal (still being studied by researchers) to attract the clearing macrophages, which in sync with the killing will remove the dead cells, thus initiating the process of resolution. The slow killing may explain why the tumor does not immediately shrink after administration of check-point inhibitor immunotherapy, but only after some delay. But then, in the unfortunately still small fraction of patients in whom the check-point-inhibitors work, the remission is sustained — and patients can be free of recurrence appears up to two years (so far).



Now onto the second alternative to standard cell-killing treatment. Continuing our more encompassing biological thinking, one will readily see this plausible approach: Why not just artificially activate the resolution process along with cell killing? If tumor expansion is fueled by the vicious cycle in which incessant inflammation is sustained by continuing production of dead cells — why not disrupt this cycle by removing the debris, which is the source of or at least propels inflammation? Can we combine conventional cell killing therapy with a therapeutic activation of the clearing macrophages? That way we would not depend on the T cells which require that the cancer cells are immunogenic (carrying an antigen that stimulates the anticancer activity of the immune system) — a requirement for check-point inhibitors to work. What is it that the inflammed tissues releases to activate the army of the clearing macrophages?

In the 1970s, Charles Serhan, now at Harvard medical School, and Bengt Ingemar Samuelsson at the Karolinska Institute in Stockholm discovered a new group of lipid-derived micro-hormones that they would eventually call “specialized pro-resolving mediators” or SPM. Samuelsson had already discovered the prostaglandins, the lipid micro-hormone that causeinflammation and whose synthesis is blocked by aspirin, for which he received the Novel Prize in 1982 (along with S. Bergström and J. Vane). SPMs turn out to be a sort of opponents of the prostaglandins; they are at the heart of the self-limiting nature of inflammation. Ensuing studies of the biological message that SPMs carry in the cell-cell communication network of the stroma (red arrows in the Figure of the “Village of cells” in section 2.) suggest that SPMs activate the clearing macrophages –a subtype of scavenger immune cells (turquois in above figure) — to gobble up the cell debris. Interestingly, clearing macrophage act discretely, that is without releasing inflammation and tumor promoting signals. Thus, they embody to the mutual checks that balance the mutual stimulation in the dense interaction network of the “village of cells”.

One prominent family of SPMs are termed RESOLVINS, which are derived from the omega-3-polyunstaurated fatty acids (omega-3 PUFA), including EPA and DHA, that are famously found in healthy diet. In fact, the health benefits of omega-3 PUFA have been attributed to the anti-inflammatory effects of the SPMs and active research is still going on at this front. It is not entirely clear to what extent eating diet rich in omega-3 PUFA, including EPA nd DHA results a relevant increase in tissue levels of resolvins that could be protective against prolonged inflammation. But a recent large-scale study in mice carrying a variety of cancers showed that administration of resolvins has a drastic anti-tumor effect –notably in tumors set-up such that their growth is demonstrably fueled by dead cells from chemotherapy.



In view of the tumors’ Nietzschean response to treatment it is only natural that patients and advocates ask: If cell killing treatment (that is, essentially all forms of therapy) can promote instead of suppress cancer, should patients then receive cancer therapy with radiation, chemotherapy or targeted therapy at all?Clearly, forgoing traditional treatment is NOT an option at this moment.

There is no question that cytotoxic or targeted treatment has at least short-term benefits –if only to “debulk” the large tumor, which can anatomically and biochemically cause secondary medical problems, or to facilitate surgical removal. If treatment has a cancer promoting effect it would be hidden behind the net benefit seen across a cohort of patients in clinical studies. In other words, the double-edged effects prevented a theoretically better outcome (across a patient population) that is impossible to extract in current schemes of clinical studies.

But biologically there is the possibility that in some tumor constellations, as discussed above, we are lucky and the kill rate is so large, perhaps very close to 100% of the cancer cells, such that a massive reduction of the number cancer cells leaves barely viable cells behind that would benefit from the principles that “what does not destroy, strengthens”. For, if too few cells are left that are converted to cancer-stem cells by the additional tissue injury imparted by cytotoxic treatment, there is no sufficient critical mass of cancer cells for regrowth. This may be the case in some childhood tumors where the cancer consists of rather uniform cells that carry few mutations and have a high tendency to differentiate –the process that converts the stem-cell state into the mature functional cell state. For instance, the standard therapy of a form of childhood leukemia consists of aggressive “remission induction therapy” to eliminate as many leukemia cells as possible, followed by prolonged “maintenance” chemotherapy at lower dose. The detailed scheme for treatment decision is complex and depends on many factors, including the nature of the mutations in the cancer cells that in theory would determine whether there exists an open path (chreod) for the cells to enter the differentiated state so us to recapitulate healthy, self-limited regeneration.

The reason why in some childhood tumors an intervention can end up on the favorable side of the binary watershed/double-edged sword scheme, and thus trigger tumor collapse as opposed to stimulating its progression, as is the case of majority of adult cancer, remains a mystery. Does such a window of opportunity within the fateful catch-22 situation of treatment in adult tumors exist at all –but we have not yet found it? Unfortunately, most adult cancers have a too heterogeneous cell composition; this diversity of cells itself will allow a larger number of cells to survive the initial treatment, providing a robust playing ground for the Nietzschean principle to operate and to start the vicious cycle of the wound that does not heal.

There is a more encompassing category of thought that cancer researchers must learn to embrace from observing the binary Nietzschean response to treatment –either tumor dies or it is rendered stronger but little in between (see watershed figure in section 4): The possibility of a preordained “either-or” nature of outcomes when dealing with complex systems. Every interference with our body, with ecosystems and societies, or with any complex system of many interacting parts that dance the tango of mutual stimulation and of mutual checks, thus creating layers of vicious cycles but also of reciprocal constraint, is a double-edged sword. Such a system cannot NOT respond. It HAS to respond either favorably or unfavorably (from the interferer’s point of view). Overcoming such robust, regenerative, sensitive systems is not a zero-sum game in which partial victories add up, inviting a doubling down of our attacks. You can not just send more troops to finish of the enemy. This reminds us of fighting the multi-headed Hydra of Lerna in Greek mythology: with every head you chop, new ones growth. The regenerative power exceeds the damage of injury most of the time — but worse it is s further stimulated by the damage — unless you manage to kill them off with a massive lethal blow at once (as is perhaps what happens with the curable childhood cancer).

OK, back from concrete metaphors to some more abstract theory: As said now many time here — the mind of cancer researchers, like that of most biomedical scientists, unfortunately operates in a realm of simplistic, linear thinking in which linear causative relationships, e.g. “A causes B”, are used to explain the world. “A is the root cause of B” . Hence A needs to be eliminated to avert B, the undesired state, e.g., a disease state. But this is not how complex, multi-component, networked and multi-layered systems, such as tumors, the body, or human societies function. So called non-linear interactions among the component parts are mathematically the key ingredients that create hidden instabilities: they poise a system at watersheds which forces our intervention into becoming doubled-edged swords. Such systems exhibit two opposite self-propelling outcomes –tumor eradication or tumor promotion. In this framework, it becomes obvious how primitive the idea is of just eradicating the root cause (the malignant cells and even worse, the mutations they harbor). We must not be tricked into generalizing from the few fortunate cases where such primitive causal thinking has been successful.

Ironically, with modern immunotherapy we may have inadvertently entered the realm of the more holistic modulation of tissue processes that (in unintended ways) avoids the detrimental therapeutic wounding of the tumor tissue. Often in the history of medicine a treatment works (even if only partially) not for the reasons we think and we need to be aware of that. Unfortunately, in an act of intellectual complacency we rejoice at the superficial elegance of using immune cells as life kill vehicles and thoughtlessly follow the appealing fashion of immunotherapy. Currently hundreds of millions of dollars are committed to blindly test immunotherapy in over 800 clinical trials with minimal variation on the theme, minimal biological reasoning about the enormous intricacy of the immune response. In this echo chamber of simplistic ideas that ignores complexity and non-linearity, we may miss many opportunities for widening the narrow window for successful outcomes: To actively tilt the balance of the double-sword effect of therapeutic intervention, away from provoking tumor progression and towards restoring a quiescent tissue by soft killing and controlled elimination of cancer cells. The lever to do so is what “precision medicine” should identify and operate — not just that for “precision killing”.


Natural Cancer Treatments Revealed

Have you ever wondered how effective natural cancer treatments can be? Around 20 years ago, my mother was diagnosed with breast cancer. This was crazy for my family at the time because my mom was a gym teacher, swim instructor and was always considered to be “healthy.”

After her diagnosis, she took the advice of her oncologists at the Cleveland Clinic and underwent a mastectomy followed by many rounds of chemotherapy. I can still remember seeing my mom’s hair fall out and thinking she had aged 10 years in the few weeks following chemo.

Praise God, after all of her treatments, she was diagnosed as being “cancer-free” and healthy. But for the next several years, she was sicker than she’d ever been in her life and struggled with constipation, candida, depression and chronic fatigue syndrome.

Then, around nine years after her first diagnosis, a terrible thing happened: She was diagnosed with cancer again. At that point, I had experience working in the natural health field, so when I flew home, we prayed together and talked about the best healthcare strategy. She decided to pursue natural cancer treatments by focusing on diet and lifestyle changes.

My mom started following an all-natural plan that included vegetable juicing, probiotic foods, immune-boosting supplements, stress reducing techniques and prayer. And after only four months, the tumors on her lungs had shrunk significantly and one year after that, she was again diagnosed as being “cancer-free” and healthy. It’s now been 10 years and my mom recently turned 60 years old — and she is in the best shape of her life, regularly water skiing, running and still going strong.

I want to be clear: I am not claiming that what we did with my mother is a cancer cure. But I believe these natural therapies, either used by themselves or in conjunction with conventional medical treatments, may support the body in the healing process.

I am often asked, “What exactly did your mom do?” Here are the natural cancer treatments and strategies she followed to heal her body.

Most Effective Natural Cancer Treatments

  1. The Gerson Therapy and Juicing I see in him one of the most eminent geniuses in the history of medicine. Many of his basic ideas have been adopted without having his name connected with them. Yet, he has achieved more than seemed possible under adverse conditions. He leaves a legacy which commands attention and which will assure him his due place. Those whom he has cured will now attest to the truth of his ideas. ~ Albert Schweitzer, MD (Nobel Peace Prize Winner, 1952)

Who was Albert Schweitzer talking about?

He was referring to Dr. Max Gerson, the German-born American medical doctor who developed one of the most effective natural cancer treatments over 90 years ago. Coined the “Gerson Therapy,” Dr. Gerson helped hundreds of cancer patients activate their body’s extraordinary ability to heal itself by recommending:

Organic, plant-based foods
Raw juices
Coffee enemas
Beef liver
Natural supplements

In the words of the Gerson Institute:

With its whole-body approach to healing, the Gerson Therapy naturally reactivates your body’s magnificent ability to heal itself — with no damaging side effects. This a powerful, natural treatment boosts the body’s own immune system to heal cancer, arthritis, heart disease, allergies, and many other degenerative diseases.

How the Gerson Therapy Works

The Gerson Therapy targets the most significant metabolic requirements in your body. How? Believe it or not, this therapy allows you to reap the nutritional benefits of consuming 15–20 pounds of organically grown fruits and vegetables each day! Here’s the breakdown:

The Gerson Diet – Consisting of eating only organic fruits, vegetables and sprouted ancient grains, the Gerson Diet is exceptionally rich in vitamins, minerals and enzymes. It’s also very low in fats, proteins and sodium. The meal plan advises cancer patients to drink 13 glasses of freshly prepared juice, eat three plant-based meals, and only snack on fresh fruits each day. Also, the traditional Gerson Therapy recommends consuming raw beef liver since it is the most nutrient-dense food on the planet and extremely high in vitamin B12.

Juicing – According to the Gerson Institute, “Fresh pressed juice from raw foods provides the easiest and most effective way of providing high quality nutrition.” The cancer-fighting protocol calls for patients to drink fresh vegetables each day, including raw carrots or apples and green-leaf juice. To preserve the nutritional content, the juice should be prepared hourly using a two-step juicer or a masticating juicer used with a separate hydraulic press. This helps prevent denaturation — when vitamins, minerals and enzymes are destroyed. (Most commercial juicers spin so fast that they heat up juice to the point they are basically pasteurized!)

Detoxification – The Gerson Therapy utilizes coffee enemas as the primary method of detoxing the body by increasing the parasympathetic nervous system. For cancer patients, this may take up to five enemas each day. The importance of keeping the body free of toxins is stressed by Dr. Gerson’s daughter, Charlotte:

The moment a patient is put on the full therapy, the combined effect of the food, the juices and the medication causes the immune system to attack and kill tumor tissue, besides working to flush out accumulated toxins from the body tissues. This great clearing-out procedure carries the risk of overburdening and poisoning the liver — the all-important organ of detoxification, which, in a cancer patient, is bound to be already damaged and debilitated.

Supplements – The Gerson Therapy recommends the following organic medicinal therapies:
    Lugol’s solution
    Pancreatic enzymes
    Potassium compound
    Thyroid hormone
    Vitamin B12
2. The Budwig Protocol

    Over the years, I have been given a lot of different advice as well, so when I heard about Dr. Budwig’s protocol I too was very skeptical, until I tried it. Numerous, independent clinical cancer studies published in major medical journals world-wide confirm Dr. Budwig’s findings. Over 40 years ago, Dr. Budwig presented clear and convincing evidence, which has been confirmed by hundreds of other related scientific research papers since, that the essential fatty acids were at the core of the answer to the cancer problem.

    ~ Robert E. Willner, MD, PhD (The Cancer Solution)

In 1952, Dr. Johanna Budwig was the German Government’s Senior Expert on lipids and pharmacology and was considered one of the leading global authorities on fats and oils. During her research, she discovered that many of the conventional processed fats and hydrogenated oils were destroying the membranes of our cells, and this caused diseased cells and toxicity.

Developing a specific diet — in this case, the Budwig diet protocol — to counteract this cancer-causing process, Dr. Budwig claimed to have had over a 90 percent success rate with her protocol over a 50-year period!

How the Budwig Protocol Works

When you replace deadly processed fats and oils with life-giving unsaturated/saturated fatty acids, your cells rebuild and are rejuvenated. Dr. Budwig found that consuming a mixture of cottage cheese, flaxseeds, and flaxseed oil had the best results.

When cottage cheese (which is rich in sulfur protein and saturated fats) and flax (which is high in electron-rich unsaturated fatty acids) are combined this way, your body is able to absorb these vital nutrients easier and quicker.

My “Beyond Budwig” Recipe

Because of the changes in agriculture, I suggest this updated 21st century version of the Budwig Protocol:

    6 ounces cultured dairy (cottage cheese, goat’s milk kefir or amasai)
    4 tablespoons sprouted and ground chia or flax
    1 tablespoon flaxseed oil
    1 teaspoon turmeric powder
    1/4 teaspoon black pepper

Mix all the ingredients together in bowl or blender and consume once daily.

For more details, check out the article and video I posted on the Budwig Diet Protocol for Cancer.
3. Proteolytic Enzyme Therapy

In 1906, John Beard first proposed that pancreatic proteolytic enzymes represent the body’s main defense against cancer. Beard focused on high dose porcine-based pancreatic enzyme therapy and eating a holistic diet to create an internal environment in which the body can more thoroughly heal itself.

While it wasn’t researched for most of the 20th century, a few scientists picked up the concept in the 1960s. But it wasn’t until Nicholas J. Gonzalez, MD started to evaluate the concept at Cornell University Medical College in 1981 that people started to seriously consider this natural approach.

How the Pancreatic Proteolytic Enzyme Approach Works

The autonomic nervous system consists of the sympathetic (“fight” or “flight”) and autonomic (“rest” and “digest”) nervous systems. Basing his protocol off of Dr. Francis Pottenger’s research in the 1920s and 1930s, Gonzalez’s work centers on balancing these two systems, as they are suspected to be one of the major causes of cancer.

He discovered that a vegetarian diet suppresses sympathetic function, whereas the opposite is true with a meat-rich diet. So after dividing patients into different categories based of their metabolic differences, genetic and physical make-up, here are the recommendations:

    People with epithelial tumors like lung, pancreas, colon, prostate, uterine cancers are prescribed a largely plant-based diet with minimal to no animal protein.
    People with blood or immune based tumors like leukemia, myeloma or lymphoma are put on a high-animal protein, high-fat diet with minimal-to-moderate plant foods.

In addition, these physicians recommend taking 5 grams of proteolytic enzymes 3 times daily on an empty stomach between meals to reduce inflammation.

According to Dr. Josef Beuth, the research behind this natural cancer treatment is pretty airtight:

    These studies demonstrated that systemic enzyme therapy significantly decreased tumor-induced and therapy-induced side effects and complaints such as nausea, gastrointestinal complaints, fatigue, weight loss, and restlessness and obviously stabilized the quality of life.
  1. Vitamin C Chelation

Chelation therapy uses chemicals or natural compounds to remove toxic metals from the body. The word “chelate” means to grab onto something, which describes chelating agents’ ability to grab onto toxins.

Generally, only holistic doctors and naturopaths use chelation therapy because it is not an officially “approved therapy” for most conditions in medicine today. When it is employed in the medical system, however, it is most commonly used to remove calcium deposits from arteries.

In a study published in Free Radical Biology & Medicine, vitamin C chelation therapy was found to be highly pro-oxidant after just one hour of treatment. This benefit lasted more than 16 treatments in the absence of nutrient supplementation and even provided “beneficial long-term antioxidant effects.”

Pro-oxidation isn’t always good, but in this case it is.

It was discovered that, “Pro-oxidant effects appear to be responsible for destroying tumor cells. These pro-oxidant effects may also induce endogenous antioxidant systems in normal tissues that offer protection against carcinogenic insult!”

Along with vitamin C chelation, consuming more vitamin C-rich foodsmay also prevent and fight cancer.

  1. Frankincense Essential Oil Therapy

Dr. Budwig recommends frankincense essential oil (especially when it comes to fighting brain tumors). And now research trials highlighting frankincense’s potential canter-fighting abilities are filling medical journals. Specifically, Indian Frankincense (Boswellia serrata) has been shown clinically to being a potentially effective treatment for:

Brain cancer
Breast cancer
Colon cancer
Pancreatic cancer
Prostate cancer
Stomach cancer

According to researchers out of Baylor University Medical Center in Dallas, the potential cancer-killing effects of frankincense are due in part to its ability to influence your genes to promote healing. Baylor cancer scientists emphasize that this potency makes Boswellia serrata a viable candidate for both cancer prevention and treatment!

How Frankincense Essential Oil Therapy Works

Rub frankincense essential oil on your neck three times daily. Also, drink three drops in 8 ounces of water three times daily.

  1. Probiotic Foods and Supplements

Best known as “good bacteria,” probiotics are microorganisms that promote a natural balance in your intestinal microflora. The best way to include probiotics in your diet is in their most natural state, which includes raw milk products such as cheese, kefir and yogurt.

Recent research has suggested that probiotic supplementation may be able to stop tumor growth. And this makes perfect sense because 80 percent of your immune system is housed in your gut. In addition to supporting your immunity to disease, research has also shown that probiotics can improve digestive function and mineral absorption as well as aid in healing leaky gut, which all contribute to helping prevent cancer!

  1. Sunshine and Vitamin D3

Science continues to support the fact that high levels of heart healthy, fat-soluble vitamins and minerals are key to keeping your body free of cancer. And recently, there has been considerable progress regarding the role that fat-soluble vitamin D3 plays in cancer prevention.

Research studies are mounting and a 2007 randomized placebo controlled double blind clinical trial suggests that vitamin D may be a highly effective way to help prevent cancer.

The study, published in the American Journal of Clinical Nutrition, is truly groundbreaking as it evaluated nearly 1,200 postmenopausal women for four years and tracked how a 1,400–1,500 milligram supplement of calcium compared to a calcium supplement plus 1,100 IU vitamin D3 in preventing cancer.

The results were amazing. After just one year of vitamin D3-added supplementation, the risk of developing all cancer types was decreased by an astounding 77 percent! Compared to the 0 percent improvement in the placebo and calcium supplement only groups, this is truly remarkable!

The Best Way to Get Vitamin D

To best prevent breast cancer, research suggests you should supplement so that your vitamin D3 levels are at least 40-60 ng/ml and up to 80 ng/ml.

The sweet spot you’re shooting for is 50-70 ng/ml. Here’s the best way to get there:

Optimize vitamin D3 through 20 minutes of sun exposure everyday. This is best done by exposing 40 percent of your body to the sun between 10 am and 2 pm.

Take an oral supplement containing around 5,000 to 10,000 IU of vitamin D3 daily. Because they are fat-soluble, make sure that you take them with some healthy “fatty” foods containing coconut oil or a probiotic-rich drink like kefir.

It can be challenging to find a pure supplement on the market, so try to find a combination formula of astaxanthin, omega-3 fish oil and vitamin D3.

  1. Turmeric and Curcumin

While the link between curcumin and disease reversal has been widely examined, the use of this spice in relation to cancer is one of the most thoroughly researched topics.

A number of laboratory studies on cancer cells suggest that curcumin does have anticancer effects. It seems to be able to fight cancer cells and prevent more from growing. It seems to be most effective against breast cancer, bowel cancer, stomach cancer and skin cancer cells.

In fact, a 2007 laboratory study showed that the combined treatment of curcumin with chemotherapy eliminated more bowel cancer cells than chemotherapy alone.

Other laboratory studies have also shown that curcumin interferes with cancer development, growth and spread. And researchers have reported that curcumin blocked the formation of cancer-causing enzymes in rodents.

Bottom line: Evidence suggests that in general turmeric works well to help stop cancer in its tracks and is especially effective at helping to treat breast cancer, colon cancer and skin cancer.

  1. Oxygen Therapy and Hyperbaric Chambers All normal cells have an absolute requirement for oxygen, but cancer cells can live without oxygen — a rule without exception. Deprive a cell 35 percent of its oxygen for 48 hours and it may become cancerous. ~ Otto Warburg, MD (Nobel Prize in Physiology Winner, 1931)

Dr. Warburg made it clear that the root cause of cancer is oxygen deficiency, which creates an acidic state in the human body. He also discovered that cancer cells do not breathe oxygen and cannot survive in the presence of high levels of oxygen, as found in an alkaline state.

We’ve all heard that antioxidants kill free radicals in the body and reverse oxidative stress-causing chronic disease. This is one of the reasons why I love to use blueberries in my morning Berry Protein Smoothie! But is eating blueberries enough to cure cancer?

Probably not. That’s why supplementing with oxygen therapy and utilizing a hyperbaric chamber is highly beneficial for people seeking natural cancer treatments.

Because the air pressure inside a hyperbaric oxygen chamber is about 2.5 times greater than the normal pressure in the atmosphere, it causes your blood to carry more oxygen to the organs and tissues in your body. Thought to heal everything from infected wounds to radiation injuries, many people claim that it has cured them of cancer. While it’s not quite mainstream yet, a growing numbers of hospitals have purchased some units to help their patients.

Prayer and Building Peace

A joyful heart is good medicine, but a broken spirit dries up the bones.

~ Proverbs 17:22

In addition to the many research studies that have been conducted on the healing benefits of prayer, maintaining mental peace and a positive outlook are absolutely critical to cancer prevention and treatment.

Some people utilize Eastern techniques like practicing tai chi or simply feeling gratitude, and these are highly effective in their own right. My favorite forms of meditation, however, consist of prayer, gratitude and reading the Bible.

Whatever your preference, make sure your focus is on living a stress-free lifestyle filled with peace and joy!
Bonus Therapy: Immune-Boosting Mushrooms

Mushrooms have been used in Chinese medicine for over 4,000 years, and research regarding the cordycep and reishi species and cancer therapy has been pretty straightforward. They can:

Potentially increase survival
Help shrink tumors
Boost your immune system
Reduce radiotherapy and chemotherapy side effects like nausea and hair loss

Of course, these results all depend on which extracts you choose and their concentrations. Some sources even suggest that supplementing with a complementary dose of vitamin C is also necessary.

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Bookmark This: Over 400 Links Google Doesn’t Want You to Visit

The war on truth has reached a fever pitch as Google has made it their mission to annihilate the independent media. The ‘New Media’ lead by the likes of Infowars, Breitbart, Natural News and many other great independent sites will have an uphill battle when it comes to getting their content in front of readers. Google has announced they will be doubling down on their ‘Orwellian’ practice of making stories disappear from their monopolistic search engine. Outlined in their Gestapo like 160-page handbook, Google describes exactly how they plan to suppress any information they deem unfit for readers. Highlighted at the bottom of page 108 Google states:

● Pages that directly contradict well established
scientific or medical consensus for queries seeking scientific or
medical information, unless the query indicates the user is seeking an alternative viewpoint.

● Pages that directly contradict well-established
historical facts (e.g., unsubstantiated conspiracy theories), unless
the query clearly indicates the user is seeking an alternative viewpoint.

These two guidelines provided by Google should set off alarm bells to anyone who has a thirst for knowledge or anyone that has the audacity to examine both sides of a topic. Imagine only being able to see and hear the corporate narrative on such important issues like vaccines, 9/11, holistic health, the Kennedy assassination, climate change, banking alternatives, and many other important matters. And that is only scratching the surface.

This information from Google’s handbook was first uncovered by Melissa Dykes at Truth Stream Media who made a great video that eloquently breaks down the importance of this complex issue. I highly recommend everyone watch it and more importantly support their work.

As bad as this news sounds there is a bright side. We have solutions people; we just have to break the habit of being slaves to the Google regime. First, we can stop using Google altogether and start using some great alternatives out there like Good Gopher, DuckDuckGo, Yandex, and The second and most important thing we can do is go old school and start bookmarking sites again (something I have been doing for years). This will cut out the middle man (Google) and enable you to see all the great information from thousands of independent journalists that Google is trying to suppress.

Below you will find a comprehensive list of great sites broken down by category that do an excellent job in their respective field. I urge everyone to bookmark this page and make it their go to when searching for news on politics, health and prepping.


Ground Zero

Caitlin Johnstone

Shane Kastler

Dr Group

Alliance For Natural Health

Juicing For Health



Hacker News

Health Ranger

Dr. John Bergman

Dr. Axe

Dr. Mercola

Dr. Eric Berg

Dr. Group

Dr. Greger



Project Veritas

Truthstream Media

Press For Truth

Mark Dice

Tim Pool

We Are Change

Chris Simpson

Paul Joseph Watson

The Still Report

Next News Network

David Icke

Frankie MacDonald

Lauren Southern

Mike Cernovich

Jason Goodman

Stefan Molyneux

Corbett Report

Steve Quayle

Gerald Celente


Rebel Media

Laughing at Liberals

George Webb


Gregory Mannarino

Dollar Vigilante

Steve Pieczenik


X22 Report

Grant Cardone

Jason A

Ron Paul Liberty Report

The Real News

Adam Kokesh

Hagmann Report

Ron Gibson

Paul Begley

SGT Report

Greg Hunter

Realist News

Clif High

Thomas Dishaw is the editor and creator of You can follow Gov’t Slaves on Twitter, Facebook and GAB or contact us by email at

This article is Creative Commons and can be republished in full with attribution. You can also view my catalog of writings at

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Gene Editing and “Genetically Modified Humans”: China’s “Golem Babies”. There Is Another Agenda

The  shocking news that a team of scientists working in China have managed to gene-edit the DNA of recently-born human twins to allegedly make them genetically immune to a HIV infection is more than bizarre and irresponsible. It suggests that certain researchers are making dangerous experiments to create ultimately the eugenics master dream—custom-designed humans. I call them Golem babies because when technology begins cutting and splicing the human DNA without certitude that the result will be stable or healthy to the human species it is not healthy.

In medieval and ancient Jewish folklore a Golem is a being that is magically created entirely from inanimate matter such as mud. Golems have no soul. Similarly, the China experiment that claims the “first successful genetically modified humans,” when we go behind the surface stories, is alarming in the extreme.

HIV Immune?

First of all the public story retailed by Chinese media and by the researcher, Chinese Professor He Jiankui, a Stanford University post-doctoral research graduate, doesn’t ring honest. He, who is professor at Southern University of Science and Technology, claimed at a Human Genome Editing conference in Hong Kong on November 28, and on YouTube, that he had successfully modified two embryos produced from the sperm of an HIV-positive donor and implanted them in a healthy mother, who gave birth to twin girls earlier this month. He used the most common “gene-editing” tool, CRISPR-cas9, to deactivate a gene called CCR5 that acts as a ‘doorway’ to allow the HIV virus to enter a cell. He basically claimed to have created the world’s first gene-edited humans, and announced that a second woman was pregnant with another of his gene-edited embryos.

Other scientists have severely criticized He for engaging in the human gene altering experiments. What He claims he did, to alter the DNA of human embryos, known as germ line gene editing, means the changes in those genes could be passed on and inherited by the next generations. Moreover, as several scientists involved in developing CRISPR have warned, He is in fact changing the human gene pool.

“We may not be able to see the impact of this until several generations later,” said Dennis Lo Yuk-ming, chairman of Chinese University’s Department of Chemical Pathology.

The scientist who first suggested developing gene drives in gene editing, Harvard biologist Kevin Esvelt, has publicly warned that development of gene editing, in conjunction with gene drive technologies, have alarming potential to go awry. He notes how often CRISPR messes up and the likelihood of mutations arising, making even benign gene drives aggressive. He stresses,

“Just a few engineered organisms could irrevocably alter an ecosystem.” 

Esvelt’s computer gene drive simulations calculated that a resulting edited gene, “can spread to 99 percent of a population in as few as 10 generations, and persist for more than 200 generations.” Esvelt was discussing gene editing of mosquitoes. Now we are moving on to gene editing of human embryos.

Adding to the drama, at the Hong Kong gene editing conference where He proudly announced his results for the first time, Professor He refused to answer questions as to who paid for his work, or why he kept his work secret until after it was done. Chinese officials claim they had no knowledge of He’s project. There has been no independent confirmation of He’s claim, nor has he yet published in any scientific peer-reviewed journal on it.

Adding to the questions around the case, Dr Michael Deem, a bio-engineering professor at the esteemed Texas Rice University, has been revealed to have worked on the gene-editing project using humans together with He. He Jiankui got his PhD at Rice in 2010 and that year began co-authoring scientific papers with Deem.

Deem also reportedly has a financial interest in two gene-editing companies that the enterprising He has set up in China. Dr. Deem, who also receives research money from the US government National Institutes of Health, did not inform Rice University of his involvement in what under current US law is illegal.

Eugenics and Unanswered Questions

He has in the meantime been ordered to stop his human experiments with gene-editing, pending a government investigation. He declared that Chinese law, which is apparently vague on the issue, does not prohibit gene-editing with human subjects.

What is clear is that, as in many areas, China sees itself in a technology race with the West. As part of the 10 development priorities of its ambitious Made in China 2025 strategy, the government lists “Biotechnology” as a priority area.

Unfortunately, the government does not exclude proven harmful biotech areas such as Genetically Manipulated Organisms or GMOs. In 2017 the state-owned ChemChina took over the Swiss-based Syngenta, the world’s largest agri-chemical producer, and third largest in GMO seed patents. In the area of toxic plant herbicide, glyphosate, designated by an WHO agency a “probable carcinogen,” Chinese companies make up far the world’s largest producers. In 2017, the global glyphosate production capacity was 1,065,000 tons. Of that was 380,000 tons by Monsanto and 685,000 tons of Chinese enterprises.

Now it appears that China is moving to become world leader in gene-editing. In January the US National Science Foundation released its annual report, Science and Engineering Indicators: 2018 report. It noted that while the USA till led in science and technology development, that “the US global share of S&T activities is declining as other nations — especially China — continue to rise.” Gene editing and Artificial Intelligence were two areas of rapid Chinese development they cited.

What is not yet clear is whether certain US Government agencies such as the National Institutes of Health which funds Deem at Rice is quietly funding the He human gene-editing projects, taking advantage of the lax regulatory regime there. Or whether the spooky Pentagon research arm, DARPA, is involved.

As I noted in a previous article, DARPA’s “Insect Allies” program “aims to disperse infectious genetically modified viruses that have been engineered to edit crop chromosomes directly in fields.” This is known as “horizontal inheritance” as opposed to the dominant vertical method of GMO alteration that make laboratory-generated modifications into target species’ chromosomes to create GMO plant varieties. The genetic alterations to the crops would be carried out by “insect-based dispersion” in free nature.

A group of European scientists strongly criticized the DARPA gene-editing Insect Allies project. They noted that no compelling reasons have been presented by DARPA for the use of insects as an uncontrolled means of dispersing synthetic viruses into the environment. Furthermore, they argue that the Insect Allies Program could be more easily used for biological warfare than for routine agricultural use.

“It is very much easier to kill or sterilize a plant using gene editing than it is to make it herbicide or insect-resistant,” according to Guy Reeves.

At this point it seems that the Chinese government is taking steps to rein in the rogue professor He and his research. What is not clear however, is whether this is cosmetic in an attempt to diffuse enormous criticism of the He human gene-editing. Earlier this year the Wall Street Journal reported that according to review of Chinese scientific journal articles, since 2015 at least 86 people have been subject of gene-editing experiments. They reported that in 2015 it began when 36 patients with kidney, lung, liver and throat cancers had cells removed that allowed were then gene-edited ad replanted in the human bodies to supposedly combat their cancer. The newspaper noted that none of the clinical trials have been formally published.

The entire field of gene-editing as with the Genome Project and GMO patented seeds, is a decades-long dream of some very influential actors such as the Rockefeller family and Bill Gates in what is called eugenics. The effort is based on fatally-flawed scientific reductionism that claims that the complexity of life can be reduced to a single gene that in turn can be modified at will.

In a recent post on the flaws of gene-editing, namely the assertion that thousands of diseases are caused by malfunction of one gene, a hypothesis yet to be proven, researcher Jon Rappoport, who sees gene-editing as “part and parcel of the trans-human agenda,” quotes Gregory Stock, former director of the program in Medicine, Technology, and Society at the UCLA School of Medicine:

Even if half the world’s species were lost [during genetic experiments], enormous diversity would still remain. When those in the distant future look back on this period of history, they will likely see it not as the era when the natural environment was impoverished, but as the age when a plethora of new forms—some biological, some technological, some a combination of the two—burst onto the scene.

Scientists, including some of the original inventors of gene-editing technologies, who call for a world moratorium on gene drives and gene-editing until the science can be conclusively proven safe, perhaps gain the ear of the world after the shocking Chinese human gene-editing reports. Something that Bill Gates and DARPA back can’t be “all good.” In the classic Golem fable, much like Dr. Frankenstein’s monster, the rabbi had to resort to trickery to deactivate it, whereupon it crumbled upon its creator and crushed him. Gene-editing of humans has eerie echoes of that Golem myth.

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Dr. Stephen Pidgeon and Victoria Lucas, will discuss GENERAL ARTIFICIAL INTELLIGENCE APPLIED, GAIA and Trans-humanism! What does the coming onslaught mean to us as believers of Yahshua and how can we over come!

Joins us in the COMPELLING AND EYE-OPENING SHOW! What is the trans-humanist agenda and how is it looming over our children’s future. Will those who don’t “Upgrade” be left in the dust physically, mentally and emotionally? Tune in as Dr. Stephen Pidgeon of and Victoria Lucas discuss this controversial topic on the latest edition of “Raising up the Remnant.”

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Slave In Secret Space Program Tells All!

Hello Patriots! My first story is one I can’t prove but this man has
a very interesting story to tell.  Tony says he was a slave
in our secret space program!   It’s a WILD ride for sure!

I do my best to bring interesting stories I enjoy also.  Some things I bring to your attention we can prove because we have the documents.  Some we can be pretty confident about because we have multiple eyewitnesses.   And some we can’t prove at all!   This story is one of those we can’t prove one way or another.  Some of you will be fascinated while some of you will run away screaming because you think Lee Harvey Oswald killed President Kennedy because the nice man on TV told you so!

20 Years a Slave In Secret Space Program! from Truth Warriors on Vimeo.

This is a story about Tony Rodrigues who says he was abducted at a young age by aliens.  He was forced by the elites into some pretty nasty jobs on Earth like being involved with drug running operations and sex slavery.  Eventually they took him to the Moon, Mars and Ceres for different jobs.   He was also on a couple of starships that went to other galaxies.  One of the most advanced bases he was on was on Ceres, a dwarf planet in the inner solar system.   Ceres was a massive underground base where it would take 40 minutes to go down into the lower levels by high speed elevators!   It was entirely run by Germans who still saluted their commander similarly to how they used to salute Hitler!   Was the Iron Sky movie based on some reality?  Some have said the Germans did have flying saucers by the end of the war and retreated to Antarctica and off planet.


We know we’ve been lied to about everything and we know they’ve hidden technology from us.

Emigrate While You Still Can! Learn More…


The FBI just released the files proving they knew Adolf Hitler never died at the end of World War II and went to Argentina!   They just quietly released it and nobody talked about it on the fake news of course.   Oh, we lied about Adolf Hitler and the true history after World War II but don’t worry about it – just take your darn flu shot!  It’s good for you!


Here’s a photo of Hitler chilling out and having a nice meal in Argentina after the war!  They lie to us about EVERYTHING!


What can be proven is Nikola Tesla had a patent on a flying saucer almost 100 years ago and he apparently built a platform he could ride around on using antigravity.  We know the US government confiscated all his equipment and blueprints as soon as he died and put the best minds on figuring out everything this genius had done.  This much can be proven absolutely.  So if you believe our official history then you must believe the best minds on the planet given unlimited funding could never figure out Tesla’s inventions and we still need rockets to get off the planet.  I know in my gut this is not true.  I would bet anything we have starships going to other galaxies right now.  Hacker Gary McKinnon hacked into NASA and saw pictures of starships in orbit.  He also saw lists of Navy ships that don’t exist on Earth as well as a list of “Non Terrestrial Officers”.


So while I can’t prove Tony Rodrigues is telling the truth here.  He has quite a bit of detail and it does match some of the information from other whistleblowers who say they were in the secret space program.  So are all these people who are blowing the whistle on the secret space program just making it all up?  What would be the point?  Just to make a buck?  None of them have made any money so far and many have been threatened according to people who know them.  Are they all pathological liars or mind controlled to put out lies?   I don’t believe this is the case.   So I present Tony’s story as something that might actually be reality for all we know.  I can’t give you the plans for the starship he was on as absolute smoking gun proof.  If I could I wouldn’t be breathing right now and I really do enjoy breathing!


It makes for a very entertaining story regardless.  It’s got some things in there like something out of movies like Iron Sky and StarShip Troopers in it.  We’ve got Germans running a lot of things in space like Iron Sky and we’ve got killer bugs like Starship Troopers!  Project Pegasus member Andrew Basiago said when I interviewed him a while back that he was told there were many things that could kill him on Mars and you needed to be armed.  He also said you could breathe there without oxygen.

One thing I found very interesting is how Tony mentioned God at the beginning and the very end of his story.  At the beginning when the alien grays were going to take him to the moon base, they asked him if he believed in God.  He said Yes, and they said, “That’s okay, we’ll fix that!”   They then mind controlled him and he doesn’t mention God until the very end.  Joe Jordan proved aliens are demonic in his Youtube video named “Unholy Communion” where he says when anybody called on Jesus for help when they were being abducted, the abduction stopped and they were saved!   But you must want it to stop and you must believe in Jesus!  I think the reason the aliens were able to abduct Tony is because he was sort of like me at that age.  He had looked into aliens and was sort of excited when he saw one and said, “I knew you were real, I’m going to tell my friends!” so they basically had his permission to take him.  He spent 20 years in slavery and then was taken back in time to 15 minutes after the point he was abducted!   This is one crazy ride at the very least!  If he’s lying, he’s a darn good liar and I want to see the movie!


See the Video about APEX and learn how a Big Pharma company planned to buy out the inventor and charge $1.1 million to each person who was given this fairly inexpensive product!   He refused the buy out because he wanted more people to be able try it! More information HERE.

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