An edited transcript of Episode 7, part 1

Introduction

TY: Welcome back to “The Truth About Vaccines.” This is our 7th and final episode. How do you feel about forced vaccinations? Are you familiar with the term homeoprophylaxis? Both of these topics and many more will be covered in tonight’s final episode. I hope you enjoy it.
We begin this episode with some valuable information on homeoprophylaxis, which is HP for short.
It’s basically the equivalent of homeopathic immunization. In homeopathy, the phrase “like to cure like” is often used. The basic theory is that any substance which can produce symptoms in a healthy person can cure similar symptoms in someone who’s sick.

Homeoprophylaxis

DR. WHATCOTT: Homeoprophylaxis has been around for over 200 years, and it’s really about the use of what we call “nosodes” in homeopathy.
And they’re made from disease products, or animal, mineral, or vegetable products as the source, and then they’re diluted and potentized so there’s no original molecules left in the substance.
But what we have is an energetic frequency of that substance. And when that’s introduced into the human system, it basically educates the immune system so that the person can recognize the disease if met in nature and build an immune response, an appropriate immune response.
So, it’s very safe. There’s no additives.
There’s no adjuvants. There’s no preservatives.
These are not grown on foreign mediums, no antibiotics. There’s never been a death from homeoprophylaxis. It’s been utilized worldwide, very, very effectively, and a number of different studies have taken place that have confirmed its effectiveness and safety.

Injection of toxic medicaments that, if you would put in a baby's bottle and had them drink it you could be arrested for attempted murder. But they inject it and say, “Oh its fine.”

DR. BELL: I've got ways to address and sensitize the immune system much safer than the injection of toxic medicaments that, if you put in a baby's bottle and had them drink it you could be arrested for attempted murder. But they inject it and say, “Oh its fine.” We utilize something called homeoprophylaxis at home. My kids have not been vaccinated and they've never even had an antibiotic because we have a different way to look at the body and support immunity.
And homeoprophylaxis uses homeopathic forms of diseases or disease processes. We call these things nosodes, and this is a safe way you can take a killed form of pathogenic material if you will, viruses, bacteria, fungal species, and safely address them via serial dilution and succussion into a homeopathic form and then administer them orally typically.
You can sensitize the immune system without devastating it, gently putting the signaling in, and in this case, you can see prevention.
There have been studies that have shown that this is efficacious as diseases drop. I think it was leptospirosis in Cuba that they’ve done the nosodes because they couldn't get the vaccine.
And it was an inadvertent study analysis that kind of put a very embarrassing mark on the vaccine belief that it takes substances at toxic levels – albeit small but still toxic in my opinion – levels in the body. They were using nosodes and found it prevented the disease much more efficiently with no adverse effects.

The Cuban study and leptospirosis

DR. WHATCOTT: Dr. Isaac Golden talked to us about the Cuban study, where in Cuba, where they have leptospirosis. It’s an endemic disease that occurs during the hurricane season, so high rain and flooding, people are able to contract leptospirosis.
So, they immunize their entire country for leptospirosis. And in 2007 and ‘08, there were multiple hurricanes that came through.
They weren’t able to immunize everyone, and they utilized homeoprophylaxis then, and had incredible results with 2.3 million people in a few different regions.
And what they found was a reduction of the incidence of leptospirosis, while in the other regions, there was an increase in the incidence of lepto. So, highly successful study at that time. And then Isaac also did a study with about 3,000 children in Australia, where he gave those children the homeoprophylaxis fo the common diseases on the recommended list: pertussis, measles, mumps.
And he studied those children for 15 years.
So, he looked at their long-term health over a period of 15 years, and found that they had fewer colds, fewer sore throats, fewer ear infections, that they had better general immunity and health, just as a process of receiving these nosodes. He compared those children to some other groups: vaccinated, unvaccinated, and found much better results with those children.

I'm not opposed to stimulating antibody production – gently, safely, but I would do it homeopathically with the nosodes.

DR. BELL: The nosodes we can use in a few ways. One of them I like is in place of, although a lot of folks get a little up in arms about saying that. But I, again, the concept of vaccination, as it’s from Jenner’s time forward, has been applied is abhorrent the way they do it.
I'm not opposed to stimulating antibody production – gently, safely, but I would do it homeopathically with the nosodes. You can also in some ways reduce the potential toxicity, for those that feel like they're trapped and they've got no way out. Prepare their body perhaps to have a lesser incidence or intensity of an adverse event.
I'm not saying that I would guarantee that, but if push came to shove, I would have you use a nosode prior to a vaccine. The other way is to detoxify from previous vaccines.
You can use nosodes or the actual vaccine material and convert it into a homeopathic form, which is not technically a nosodes in the same way, but it can sensitize the system to start throwing out some of the damage.
The initial insult and assault of the body even decades before to undo some of that damage after the fact.
I'd rather not have to undo damage that's caused, if you understand what I’m saying.
But we have a lot of people that are damaged and injured. So, that's another protocol technique to help detoxify from the adverse impact that the vaccines initially kind of unleashed.

TY: Homeopathic immunizations, or homeoprophylaxis, HP, is the use of potentized substances called nosodes in a systematic manner to prevent the development of the characteristic symptoms of disease. HP is produced from the actual disease, much like the concept of vaccines.
The difference lies in the degree of attenuation, or weakening of the original antigen. With HP, the source material is diluted until no original molecules remain. The substance is rendered harmless, and has become “energetic” as opposed to “material.” This diluted solution is then anointed onto pellets and taken orally. The energetic frequency delivers information to the recipient, familiarizing him or her with the disease pattern. When later encountered in nature, the disease is either not contracted at all, or if contracted, addressed effectively with a mature, natural immune response.
Dr. Robert Scott Bell and Cilla Whatcott both mentioned the Cuba study. In that study, where homeoprophylaxis was used on 2.3 million people, the conclusion of the authors was that “This approach was associated with a large reduction of disease incidence and control of the epidemic.” “The results suggest the use of homeoprophylaxis as a feasible tool for epidemic control. Further research is warranted.” In the Republic of India, there are several states where homeoprophylaxis is the government-approved treatment, and even preventative of many diseases.

Government approved homeopathy as a system of medicine.

DR. RAFEEQUE: Fifty years back, the government approved—the government of Kerala approved homeopathy as a system of medicine. Officially approved. Later on, they started a department of homeopathy for the treatment of people.
Through this department, free treatment is given to the people.

DR. BELL: Free treatment?

The ministers will ask what homeopathy can do. Of course, we get good support. And even many modern medical doctors support us.

DR. RAFEEQUE: Yeah, of course. Once a person comes, he will have to pay two rupees fo the registration. It’s only for the name’s sake. Then lifelong free treatment will be given, medicines and also prophylaxis will be given. Because in our department we have a special body called RAECH, Rapid Action Epidemic Control Cell Homeopathy.
Through this we give prophylaxis anytime.
Not only during epidemic, even for endemic diseases or even for all diseases that may appear. For example, tuberculosis, apoptosis, any other disease. We give on regular basis homeopathic prophylaxis.
Everywhere, the government has got different levels of treatment. For example, the state government, we have local government, local finance government, the Panchayats, the Tuluk.
So, every government sector, there will be one homeopath, who will be invited for the planning of health policies.
A homeopath will be invited, and his opinion is given great importance. So, we have the right to say what to give. They will ask.
The ministers will ask what homeopathy can do. Of course, we get good support. And even many modern medical doctors support us.

The allopathic modern medicine department, they said that “We are helpless in this particular situation.” So, the government gave an order that all allopathic network has to cooperate with homeopaths in distributing this medicine.

DR. GADUGU: In 1999, there was a very big epidemic. Very big epidemic and the efforts of the homeopaths where required in large number. Then the government, the allopathic modern medicine department, they said that “We are helpless in this particular situation.” So, the government gave an order that all allopathic network has to cooperate with homeopaths in distributing this medicine. The government brought in an order. And the health minister of that particular state was a medical doctor.
She was a gynecologist.
And the Chief Minister said, “If you want to continue as a health minister, you have to control this disease.” Then she called for a meeting of all allopaths and homeopaths and they say, “Allopaths, we have to import the vaccine from China or Korea.” “It takes a long time. Even if we import also, we can’t say whether this vaccine will be effective in controlling this particular episode of Japanese encephalitis.” Then homeopaths were asked, “Can you do anything?” That was the time I was also present in the meeting. Already, I have an experience of treating the cases. Then I have shown a particular case, how effective this particular medicine, like say evidence-based medicine.
We have a huge network of around 500 homeopathic government dispensaries; it means clinics.
All of them. Apart from that, 1,500 primary Health Centers of allopathic network. Everybody provided this particular one. That's so we could reach out to 20 million of children in a short span. Otherwise it would not have been possible.
That's how almost 20 million children were covered with homeopathic medicines. By 2000, the cases were almost one-fourth. In 2002-03 and almost cases started coming down from three digits to single digit. By 2004, there was neither mortality nor morbidity out of this particular one.
Very interesting point is only the state of Andhra Pradesh gave this treatment whereas other state, neighboring states, like Karnataka, Tamil Nadu, what’s their position? They were also equally affected by this Japanese encephalitis.
Still the mortality is very high in those states. Only in Andhra Pradesh it has come down. The government of India, now it has taken up a massive project of implementing the same strategy in other states.

TY: It’s encouraging that in the Republic of India, classically-trained medical doctors work hand-in-hand with homeopaths and natural doctors in order to ensure that the patients, mostly children, get the best possible outcome.
Another crucial piece of the overall health puzzle for infants is breastfeeding.

DR. OBUKHANYCH: For babies who are most likely to be affected by bacterial diseases, breastfeeding is what really fends off those infections.
For example, in Sweden, it has been shown that the risk of meningitis, HIB meningitis was down four-fold in exclusively breastfed babies. And the whole reason why meningitis even rose was because of the switch from breastfeeding to formula feeding that happened in the second half of the 20th century.

TY: Really?

DR. OBUKHANYCH: Yes. Instead of reversing meningitis by introducing breastfeeding o by encouraging breastfeeding, they of course, what they did they introduced a vaccine for it. So even though HIB meningitis in infancy is the problem of under-breastfeeding the solution was not really to reverse that naturally, but to get the pharmaceutical product for it.

TY: Why do you think that is?

DR. OBUKHANYCH: Why? Well I guess there is no money in encouraging everyone to breastfeed, but there's a lot of money in making vaccines.

DR. MARGULIS: If we want to practice evidence-based medicine and if we want to do what is absolutely 100 percent the best for our children, we have to support women in exclusively breastfeeding.
It is absolutely crucial that babies, that human babies drink human milk. And that's a hard thing to say and it's a hard thing for some people to hear, because there are a lot of moms who have trouble breastfeeding.
Just because it's good for you, just because it helps you doesn't mean it's easy. So, I just want to put that out there. But we have literally thousands of studies that show that breastfeeding, exclusive breastfeeding, is absolutely crucial for lifelong health

DR. THOMAS: It is so important to have a vaginal birth through a healthy birth canal that's teeming with good bacteria that then become the beginning of that child's gut flora.
You have a C-section in a sterile environment, you're in a hospital, there's hospital-acquired organisms and that becomes your flora and you get C. diff, and you're pooping blood and mucus and that's not a good start. In fact, the best way to cure those poor kids is to get good probiotics and get that going.

TY: Probiotics are essential to restore gut flora and balance the immune system. This is very important, especially if a child experienced an adverse reaction to a vaccine.
Another ancient remedy that has been used for centuries as a method of providing natural immunity is essential oils. Here is Dr. Eric Zielinski describing how essential oils were even used to combat the bubonic plague.

How essential oils were even used to combat the bubonic plague

DR. ZIELINSKI: It's an unbelievable story about taking oils like cinnamon, clove, eucalyptus, lemon, rosemary together, and combining them in such a way where the vapors actually themselves combat the volatile organic compounds from the plague, from the virus.
We actually see research. A very similar blend was researched recently, a clinical trial that actually shows it kills the flu virus, just flat out. It kills.
And again clove, cinnamon, eucalyptus, rosemary, lemon, and orange all work together. It's a synergy. It's a synergistic effect and they combat viruses.
I found this 1911 book from the Carnegie Library that started talking about essential oils with everything from pertussis, whooping cough and pneumonia and just infectious disease.
In the early twentieth century that's all that they used.
I mean that's what they used. In World Wa I, World War II they were using oregano and thyme to combat gangrene infection on the battlefield, so what happened? When we look at it, well antibiotic happened and the government and big pharma said “Look we've got a solution and its cleaner, you don't have to smell like pizza, and it's very simple and it's cheap. Take a pill.” And some people are like “Okay, makes sense.” Well, that changed the paradigm. When the antibiotics came out that changed the whole paradigm. That's the reason why we're in this situation that we're in today if you look at it historically. That was the medicine, especially European doctors. Dr. Valnais from France, that's what they used.
So, aromatherapy wasn't “invented” until the early twentieth century when René Gattefossé burned his hand in a laboratory experiment, and the story goes he was frantic looking for something to help relieve his hand and he saw a big vat of oil.
He put his hand in there, it was lavender oil, just to help relieve it. He would have put it in anything. He was surprised at how quickly it healed and how there was no scarring.
He was like, “What in the world? What was that?” They were just experimenting with lavender oil.
It really opened his eyes to look at the healing properties of lavender and other things and that's where he wrote a book called Aromatherapy and that was a French book that now that's where we know what we do today based off of his studies, now a hundred years ago.
Aromatherapy is the therapeutic use of essential oils. And there are three different ways you can use essential oils. Aromatically and that is through a diffuser. You can apply them in a nebulizer or an inhaler. You know like a steam—sort of steam sauna with eucalyptus.
Perfect.
Also, topical. You can apply essential oils topically or you can ingest them, which is a debated topic. But if done safely and wisely it's very effective. Got some stuff on pneumonia too, because essential oils have been shown—thymol, carvacrol, geraniol, citronellal. These are the chemicals in oils like lemongrass, oregano, thyme— TY: Oregano has carvacrol right? DR. ZIELINSKI: Yeah and thymol, thyme, geraniol, rose. These are oils that have been proven to kill pneumonia. What we see with whooping cough specifically, is going back to the research that we see in 1911, they were injecting a 20 percent dilution in almond oil. So, they had sweet almond oil and a 20 percent dilution of camphor and it knocked whooping cough in its pants. So, camphor also is a main chemical in rosemary.
Rosemary is a very common oil, and so what that means folks, is if your son or daughter is battling whopping cough – even using it aromatically. But again, what's in that blend we talked about? Cinnamon, clove, rosemary, eucalyptus. I mean they figured how to kill the bubonic plague. Those oils are also effective against whooping cough as well.

TY: Essential oils are most definitely time-tested medicine and they help support natural immunity and the entire immune system. Macrophages are important cells of the immune system that are formed in response to an infection o accumulating, damaged, or dead cells.
They are large, specialized cells that recognize, and engulf, and destroy target cells. Here’s Dr. Marco Ruggiero discussing GcMAF and Rerum, and how they can be used to activate macrophages, and even treat autism.

GcMAF and Rerum, and how they can be used to activate macrophages, and even treat autism

DR. RUGGIERO: GcMAF is an acronym for GC, globulin-derived microphage activating factor.
MAF stands for macrophage activating factors.
Macrophages are cells of the immune system, and I was working on these cells when I was at the NCI, National Cancer Institute, in the early 90s.
And one of my first papers on macrophages is published in PNS with many other colleagues.
So, it’s a topic that I have been studying for the past 26 years. And there are many proteins, or factors, that may activate macrophages.
Japanese researchers work—worked, because now he’s retired, in Philadelphia, identified another protein called GcMAF. Now this GcMAF activates macrophages, and therefore, we can define this protein as an immune stimulant.
And I began working with this Japanese doctor, whose name is Nobuto Yamamoto, in the late 2009-2010. And we published a paper that we presented at a World AIDS conference in India in 2010, postulating that stimulation of the immune system could eradicate HIV infection.
actually, using the same words of Professor Luke Montagne, when he says that if you have a good immune system you can get rid of the virus in weeks.
We published together this paper and we kept on working on this molecule. Then I began collaborating with a biotech company in England, and the first GcMAF conference, immunology conference, I had in Frankfurt, Germany, I had the honor and privilege to meet Dr. Jeff Bradstreet.
Now Dr. Jeff Bradstreet had a good idea in those days. He knew that at least some forms of autism are associated with viral infections, mostly latent viral infections, but he knew that there was a relationship between multiple viral infections, or in general infections, and autism. So, it was known that in autism there is a dysregulation of the immune system.
He thought that to try to rebalance the immune system of autistic children with GcMAF could have been a good idea. And so, this is what he did, and he published his first paper on this topic, I think in 2013, describing how treating the children with GcMAF improved some serological markers. But also, and this is most important, improved the symptoms.
So, he began his research on this protein.
And we kept on doing our own research in the laboratory. And the more we studied this protein and the more we published on the effects of this protein on cancer cells, on macrophages, and so on, the more we understood that the protein in itself was not the most important, or the most active part of the molecule.
By studying the molecular structure of GcMAF, we found out that the active sites were essentially four different things, four different molecules.
One is a molecule called alpha acatine galactosamine.
Now that is the molecule, by the way, removed by an enzyme that is called nagalase. And then we have vitamins of the D group, D23, a fatty acid whose healthy properties have been known for centuries, oleic acid – the basic principle of olive oil, and this was our major contribution to the field.
Glycosaminoglycan, it is a complex sugar called chondroitin sulfate. Now this chondroitin sulfate is the molecule which mediates the activation of macrophages. In other words, the GcMAF does not activate macrophages in and by itself.
It does so through the interposition of this sugar that is called chondroitin sulfate.
At that point, we were asked by Dr. Bradstreet if we could develop a molecule that was not extracted from human blood, as the old GcMAF was, that was not a protein, because protein, they have a series of difficulties to be handled, that had the same power, the same activity of GcMAF.
We began researching, we began studying, we began doing experiments in the laboratory, and we ended up with a new molecule that actually is not new at all. It is what happens in nature.
And because of this, we gave a Latin name that means about nature, Rerum.
In Latin, Rerum means “of things.” And it refers to the essay by the Roman philosophe of 2,000 years ago, Titus Lucretius, who wrote an essay entitled De Rerum Natura, which means about the nature of things. This Rerum is nothing else than the active parts of the old GcMAF without the GcMAF in itself.
It had been demonstrated that autistic children have a very, very low level of TGF-β [Transforming Growth Factor beta]. Whatever it means, it is not a good thing because control children, they had normal level, and autistic children had much lower level of TGF-β. If you treat those children with GcMAF, you do not raise the level of TGF-β.
It remains the same. You have a number of good effects, no doubt about this, in particular, on the endocannabinoid system, but not on TGF-β. With Rerum, TGF-β goes up to normal levels after only five weeks of treatment.
That’s why doctors all over the world, to name one, Dr. Nicola Antonucci, who will speak tonight, this afternoon, are reporting results of children who already had had benefits from GcMAF, but not yet 100 percent. Let’s say with GcMAF, they had gone from 20 to 60 percent.
Now they add Rerum, now they use Rerum, because GcMAF is no longer available, and they are completely in a good shape.

TY: Wow.

The best nutritional approach for autism is a so-called ketogenic diet.

DR. RUGGIERO: So, this means that it does what all the old GcMAF did plus more, just like a jet plane. It flies like the old propeller planes did, but more. Even though we are very proud of the Rerum, nevertheless, don’t think that Rerum is the miracle pill.
Rerum has to be integrated into a protocol that is a protocol that takes into account, first and foremost, nutrition. If you eat junk food, don’t expect the Rerum to do miracles. It won’t do them. So, first of all, control the nutrition.
And the best nutritional approach for autism is a so-called ketogenic diet. A diet very, very low in carbohydrates and very high in healthy anti-inflammatory fats, like olive oil or coconut oil and amino acids, crystallized amino acids that do not overload the kidneys or the liver.
So, the ketogenic diet has to be the best.
On top of that, you can reconstitute the microbiome with probiotics. We developed one that is called Bravo Probiotics, for example. And on top of that, you can add the Rerum to rebalance the immune system and to rebalance also the immune system inside the brain and protect the neurons.
What I’m saying is that do not look fo the magic pill. It doesn’t exist. If you don’t fix nutrition first, if you don’t fix your gut, your microbiome, then the Rerum or anything else will do poorly. But if you do this under the supervision of a good and competent doctor, and there are very many, let me tell you. There are very many good doctors, both in the United States and elsewhere.
Then you can expect very good results.

TY: While discussing nutrition, one of the things Dr. Ruggiero mentioned was the ketogenic diet. Here’s Dr. Toni Bark describing how a ketogenic diet can help to squelch inflammation and even reduce the symptoms of autism.

Ketosis and ketones are neuroprotective and the brain actually functions better.

DR. BARK: As you know from work you’ve done that ketosis and ketones are neuroprotective.
The brain actually functions better. You automatically see inflammatory markers dissipate when you are in ketosis. That’s just—there’s a lot of reasons. I don’t know all the reasons, all the science behind it, but I know that’s a fact. I measure them on my patients and inflammatory markers are 0.0 something on these patients.
The brain likes ketones and it can use them readily. It doesn’t have to do that much work, so it’s neuro protective and the inflammation is gone. And if you throw cannabis onboard, especially if you’ve got something like a calcium channel that’s working out of control, cannabis is a down regulator.
That’s why it’s so great. That and the fact that it promotes fat burning. It’s a down regulator. Anything that’s out of whack or out of control, it helps down regulate it. These things are very helpful for kids with autism and so many other disease processes.

TY: Right.

My autistic patients can do MCT oil or they can do lot of coconut or palm oil, but eventually really once they’re in ketosis, they just need fat. Healthy fat.

DR. BARK: I like coconut oil and I like hemp oil and olive oil. I like to get the omega-3s in with hemp. Either fish oil, hemp oil, flax, krill, chia seeds and hemp seeds.
For my cancer patients, I put them in a plant-based ketosis. My autistic patients don’t have to be plant-based, but I do want them eating organically.
I do like them getting the saturated fat, especially in the beginning to get the ketones boosted. So, they can do MCT oil or they can do lot of coconut or palm oil, but eventually really once they’re in ketosis, they just need fat. Healthy fat. Avocados. Monounsaturates and some 3s and then coconut oil’s great for many other reasons too. Those are usually the ones I rely on.

TY: Good.

DR. BARK: Lot of seeds and— TY: That’s a good solution for people that may have autistic children.

DR. BARK: It really is.

TY: The diet does matter.

DR. BARK: It does matter.

TY: Dr. Bark mentioned the importance of healthy oils in maintaining ketosis. I remember back in the 1990s when I was a competitive bodybuilder, one of the fad diets that was becoming popular at that time was the Atkins diet. This was when many of my buddies began to eat lots of fats and protein and minimize carbohydrates.
The problem was that nobody was really paying attention to the quality of the fats and oils, which is of utmost importance. But one thing that was key to the Atkins diet and also is a staple of a clean ketogenic diet is avoiding sugar.
You’re an immunologist, right? So, you understand the immune system and so you just mentioned sugar, so is that something that we should be aware of in regard to its effect on the immune system if we want to stay healthy?

Sugar, neutrophils and phagocytosis

DR. OBUKHANYCH: Absolutely. So, sugar has a very clear effect on a subset of cells called neutrophils. Neutrophils are cells that guard us from bacterial infections. They go through the body and if they detect bacteria where bacteria are not supposed to be, they engulf bacteria and this process is called phagocytosis.
Now when a sugar feed is given to people, it has been shown that that reduces phagocytosis by neutrophils by twofold and that it can last for five hours. So, if you are eating a lot of sugar every five hours, your neutrophils are not functioning properly.
You may get away with the physiological effects of that, if there is no infection going on at the moment, but if that happens while you are already sick and you keep eating sugar in the form of ice cream or whatever, you neutrophils will not be able to handle the infection.

If you keep eating sugar in the form of ice cream or whatever, you neutrophils will not be able to handle the infection.

TY: According to Dr. Tetyana Obukhanych, she’s an immunologist, sugar has a detrimental effect on neutrophils and it reduces their ability to perform phagocytosis, literally cell-eating, by 50 percent for 5 hours, every time you ingest sugar.
That’s a good reason to never eat sugar if you are sick or recovering from illness.
The medical literature is clear that diet and nutrition actually do have a big impact on your health. And as these experts are about to share, certain vitamins can have a positive effect in protecting from various infectious diseases, like measles, whooping cough, influenza, polio, and may even help prevent and/or reduce the symptoms of autism.

Vitamin A and measles

NEIL MILLER: The World Health Organization has come out and stated that they've done the research. And I summarized the studies from the World Health Organization, and from several other journals, studies that confirm that children that have complications from measles, or that die from measles, have low quantities of vitamin A.
Their nutritional status is very low for vitamin A, and vitamin A will protect babies, will protect children, from complications and death associated with measles.
And so, they went and did a study, for example, where they had, like, 200,000 kids, and they broke them up into two groups, and this was in Africa, and these kids were coming into the hospital with measles.
And they gave one group standard treatment.
They gave the other group standard treatment plus high doses of vitamin A. The group that received the standard treatment plus the high doses of vitamin A had reduction in mortality associated with the measles.
So, vitamin A is very important, and, today, if we didn't vaccinate children in the United States, the best thing that you can do to protect, not against measles—you’re still going to contract measles, measles is very contagious—you're not going to stop children that are exposed to measles from contracting that disease.
You'll never stop them from contracting the disease, and you don't want to stop them from contracting the disease, because I talked earlier that contracting the disease will offer you many benefits in later life.
It will protect you against cancer. It will protect you against coronary heart disease.
But it will protect you, if you take high doses of vitamin A, and you are exposed to measles, and you do get measles, it will protect you from complications of the disease and it will protect you from mortality.

Vitamin C

DR. HUMPHRIES: Today vitamin C is one of my primary tools as a medical doctor, and since I've discovered it, it's really been probably the best medication that I've ever used on myself or my patients. And I'm not the first to discover this, there have been many fo decades before me. And one of the first to really embrace it and write about it and use it in all kinds of different situations was Dr. Fred Klenner.
And a lot of people don't hear about Dr. Klenner because his writing is not something that circulates in conventional medical realms, because he was pretty forthright about calling the doctors of his time “quacks.” He just turned that term right around on them and showed in no uncertain terms that what they were doing was incredibly backwards and harmful.
When he was curing cases of paralytic polio, he was using antibiotics, he was using steroids, and he was also using very high doses of intravenous or intramuscular vitamin C and he outlined—there’s copious amounts of writing of his—and he outlines in great detail exactly what his protocols were and how well they worked case after case after case, and not just polio but influenza.
He used it during pregnancy in very high doses all throughout pregnancy before delivery.
Using vitamin C in infants, children, and adults who have whooping cough doesn't make the cough go away. It doesn't treat it like say you know some antibiotic could maybe treat a staph infection.
Basically, what it does is it energizes the immune system, because like I said it gives the neutrophils the energy that it needs.

There's something called “apoptosis” which is what cells that need to die do. And so, they basically involute so that they don't spill their caustic contents inside your body.

If you don't have vitamin C, those neutrophils and macrophages that are just eating these particles that are trying to infect you will just explode and cause even more inflammation.
So, vitamin C decreases inflammation in lots of ways. That's one. It's a direct antioxidant.
Whooping cough is a toxin-mediated disease.
You neutralize the toxin by putting electrons in there and you notice a difference.
It actually loosens up the secretions in the lung within 24 to 48 hours. The secretions become thinner and more watery, and it also, again, frees up the liver to do its job. So, as a toxin neutralizer an immune system enhance and it also gives tissues the strength—you can't make collagen without adequate amounts of vitamin C.
It's not a miracle and I'm very clear with parents before I get going, but so far, there's been 100 percent success rate. No babies have died. I've treated babies as young as two weeks old, and it's no picnic.
It's a nail-biting experience but when the medical system has done everything they can do and the child is still extremely sick and the parents are looking for help, they often come to me and sometimes they come to me before they go to the medical system because they're that confident in what they want.
You can read the testimonials. And when I ask parents to write testimonials I don't say to talk about me. I say, “I want you to talk about you, what your fear level was, what you expected, what the vitamin C did and how you feel now.” So, that's really what the testimonials are intended to do, is to just show other parents what vitamin C can do. It's not a miracle but it makes the baby so that they're not turning blue any more, they’re not gasping for air, the coughs become manageable, you nights become easier, they're not always easy.
There's a week where there's a lot of sleepless time during that one week.

Vitamin D

DR. OBUKHANYCH: The immune system knows how to work with what was available naturally.
It didn't have to wait until nutraceutical industry showed up in the last 50 years to make sure that the immune system works.
So, the nutrients that to we must pay attention, as far as viral diseases are concerned, are vitamin A and vitamin C. For antibacterial ones, vitamin D is very important as well as gut health, meaning probiotics, because that helps to utilize the vitamin D and they work synergistically.
Now, actually it's kind of silly to talk about each vitamin separately because once you go through the list you see that all of them are necessary one way or another. And it's not only those vitamins like the alphabetic list of vitamins, but also micro elements, minerals, phytonutrients, pretty much everything in between. The whole gamut of nutrition and lifestyle.

As far as viral diseases are concerned, are vitamin A and vitamin C. For antibacterial ones, vitamin D is very important as well as gut health, meaning probiotics, because that helps to utilize the vitamin D and they work synergistically.

DR. MARGULIS: Every parent and every doctor wants to have healthy kids. So how do you do it? Some of the ways sound so simple but they're actually really hard. So, the first thing is that we need to feed our kids real food.
Real food for babies means breast milk exclusively, and real food for kids means food that is in its recognizable form. And that's not a very exciting thing to say, feed your kids food. But the very vast majority of children are not actually eating food.
So, if you even just look at the guidelines for how many vegetables kids are supposed to have—I recently did an interview in a middle school and I talked to more than a dozen kids. Not a single child in that school had eaten a single vegetable as of 2:00 in the afternoon. And we’re supposed to be eating vegetables with every meal because we know healthy vegetables help you have a healthy microbiome, help you have a healthy brain.
So, kids need to eat real food. We need to avoid toxins. Two of those toxins, which are given like candy, are acetaminophen – the main ingredient in Tylenol – and antibiotics.
Kids need to have as much exercise and outdoor time as possible. They need sunlight. They need vitamin D. But we have kids in chairs sitting all day when our bodies want to move and be outside. We need to have kids playing in the dirt.
Let them get dirty. Let them get messy. And I'm not saying that because I think kids should wallow in mud. I’m saying that because we know that exposure to dirt helps you create a better immune system and reduces your risk of autoimmune disorders.

MIKE ADAMS: How do you save children’s lives? Well, you boost their nutrition to activate the genetic code that they all have that causes the expression of their immunology, which gives them the adaptive response to exposure to viruses in the wild.
With Vitamin D, you’re activating this huge portion of their gene code. You’re actually invoking the power of their genetics to make them able to respond in a symptomless way.
In other words, they don’t get sick, they don’t have a fever.
They don’t even know they were infected, but now they're immune, because they have that built-in immunology system. That nanotechnology of human biology. And it’s activated with things like vitamin D.

Vitamin B3 folate

DR. THOMAS: In February of 2013, I get the JAMA, Journal of American Medical Association.
I’m a member, just to keep track of what's going on. That was on my desk and I'm looking at this, and anytime I see the word autism on the study, I want to know what they're doing, because we need more studies.
So, here's a huge study out of Norway. I think it was 60,000 moms and the children followed for an average of six years. And they looked at the rate of autism in the moms who took folate while they were pregnant and the moms who didn't. It was a huge study. Prospective, long-term, comparing these two groups.
TY: What is folate?

Folate is a B vitamin, B3, and we've known that you need folate to prevent huge brain defects. Anencephaly, meningomyelocele, these sorts of things. So, it's obviously important for something to do with brain.

DR. THOMAS: Folate is a B vitamin, B3, and we've known that you need folate to prevent huge brain defects. Anencephaly, meningomyelocele, these sorts of things. So, it's obviously important for something to do with brain.
We've been giving folate for well over a decade.
Maybe two for pregnancy.
But this was a great study to show the value and the moms who took folate while they were pregnant, their autism rate was in a thousand, and the moms who didn't, it was one in 500.
So, this is 2013, and I'm thinking, I just read it's 1 in 150 here in the U.S.
What’s the difference? Why is it 1 in 1,000—because we give folate in the U.S. So why is it 1 in 1,000 there when it's 1 in 150 here? That was the a-ha, but there's no mention of that in the article.
So, I pulled up the vaccine schedule for Norway, and they don't do the Hepatitis B vaccine.
I'm not saying that's the whole reason because they do breastfeed longer and much higher breastfeeding rates there. We know breastfeeding is protective.
They have less toxins, there's no GMOs, o at least I don't think there are. I'm sure there's lots of variables.

But the exciting thing about that is just think about it, Ty, if we could do a few things here in the U.S. and get our rate from now 1 in 150 back to 1 in a thousand, how wonderful would that be?

I mean you're talking we now have over a million autistic kids. We’re creating over 100,000 a year with our current program of whatever it is we're doing that's creating this. I do believe, this is to talk about vaccines, that's a big piece of the puzzle.
But that's not the only piece. It's toxins, toxins, toxins, and it's getting your nutrients, like folate in that study. It's actually good to have methyl folate, not regular folate for most people. It's boosting the immune system. It's all about having a healthy immune system. That's what we need.

TY: That’s a recurring theme. As Dr. Paul Thomas just mentioned, the key to preventing disease is a healthy immune system. That’s actually part of the theory behind vaccinations: stimulating the immune system and helping it recognize various diseases. Dr. Thomas is a board-certified pediatrician who is also the co-author, along with Dr. Jennifer Margulis, of a book entitled The Vaccine-Friendly Plan, which is a selective and delayed vaccine schedule for those patients that do want to vaccinate, but not according to the current full CDC schedule.

The Vaccine-Friendly Plan

DR. THOMAS: I'll go back to 2008, I'm starting my new practice, and what I set up was what I’ve outlined in this book, The Vaccine-Friendly Plan. And that is a way to vaccinate that's a little gentler, way less toxic.
You don't do Hepatitis B for newborns who don't need it. And we know. Our OB-GYN colleagues have done a great job of testing women who are about to have a baby, and we know when they're delivering that they don't have Hepatitis B. So that baby does not need that vaccine.
Let's do that one when they’re pre-teen, before they're sexually active or early teens, so that one you wait. You also wait on polio.
Not because I'm against the polio vaccine.
The elder generation, I have a nurse who's retired, who lived through the polio era, and my own mom in fact, and they were both like (and she’s a nurse), “I don't know about the polio, you better do the polio.” But here's a fact, there hasn't been a case of polio acquired in the United States since 1979. There is no risk. If we want to do it we can still do it later, when the immune system is more developed, when you're not bombarding that little baby's developing immune system with so many challenges.
So, we wait on the polio. We don't do the rotavirus. The rotavirus vaccine— TY: That’s the one you were mentioning that Offit developed? DR. THOMAS: Offit developed the initial one.
You're putting a live virus that's contaminated.
These vaccines are not pure. They're contaminated with other viruses.
Both vaccines that are on the market have been proven to be contaminated. It makes no sense. So, we're skipping Hep B, polio, rotavirus, and in the Vaccine-Friendly Plan, what we are focusing on is the TDaP, mostly because of the pertussis.
At 2 months you do the HIB, which is preventing Haemophilus type B, we'll talk a little more about that, and the TDaP. So, you're protecting against tetanus, diphtheria, and pertussis.
The tetanus and the diphtheria are not an issue, really, for a kid that age. But it's the pertussis. You don't want that whooping cough and death, those five deaths per yea or whatever. And then rather than doing the Prevnar, which is the other serious bacterial disease can be caused by pneumococcus, so the Prevnar 13, it replaced the Prevnar 7.
That will prevent some meningitis and some serious infection, as well the HIB. Instead of doing them at the same time at 2 months, we move the Prevnar to 3 months. It also contains aluminum.
So, at 2 months, you're injecting HIB, which is a fairly safe vaccine, TDaP, which has too much aluminum. And then at 3 months you do the other aluminum one, the Prevnar. Then you repeat that. 4 months, 5 months, 6 months, 9 months. And then you do your final Prevna and HIB at a year. That's still a lot of vaccines, but it's half of what it would have been.

TY: What about MMR? You didn't mention MMR.

You're not at a greater risk skipping the rotavirus. And you are reducing risk by spacing out aluminum-containing vaccines and you're reducing your risk by waiting a bit on MMR.

I just decided I'm going to wait till age three. Because I had never seen a child regress into autism after age three.

DR. THOMAS: So, for on the Vaccine-Friendly Plan, I made a somewhat arbitrary decision.
That one worried me. I just decided I'm going to wait till age three. Because I had never seen a child regress into autism after age three. That was in 2008. I now have over 13,000 patients in my practice, I acquire all the patients in the area who want informed consent, who want to vaccinate differently.
I acquire a lot of families who have autism in their family because they're not getting the kind of care they need. And I have since heard one story of a child with parents who did exactly what I was thinking of doing, wait till age three then do the MMR.
And so far, in my own population, that's been fine. We haven't had any new autism in over a thousand patients who followed the Vaccine-Friendly Plan. But I did have one case where the family did that, not my recommendation, they just came later.
Got the MMR at age three and their kid regressed.
They actually had a family history of autism so that does put them at a higher risk. If you don't have family history, what I promote, if you're going to vaccinate according to the Vaccine-Friendly Plan, make sure you do not have a family history of autism or severe neurological problems and no autoimmune problems in the family.
Those two groups seem to be at highest risk for regression into autism, and perhaps if vaccines are part of the problem, I'm not saying they are but they sure look like they are.
The Vaccine-Friendly Plan is a compromise.
You're saying, “We can vaccinate slower without putting our kids at any greater risk for diseases that vaccines protect against.” So, you're not putting your baby at risk for Hep B. They're not at risk anyway. You're not putting your—at risk for polio, there's none in America. You're not at a greater risk skipping the rotavirus. And you are reducing risk by spacing out aluminum-containing vaccines and you're reducing your risk by waiting a bit on MMR.
I've studied my data. I pulled my data on February of 2015, and broke it into three groups. I got an IRB, Institutional Review Board, to look at the data retrospectively.
We weren't changing anything, we're just looking at our data. So, we were approved to do that.
And the first group, it was the children, over 1,000, who did the Vaccine-Friendly Plan or less. Because, when you do informed consent, it’s interesting. People do different things.
I think about how before I really was doing informed consent, how did we get everybody to do the CDC schedule? Well we were very, “This is the right thing to do.” End of discussion. There was no informed consent.
People just did it. You're their doctor. People trust their doctors. So, you do what they say.
If you look at my data, group 1, over 1,000 patients who followed the Vaccine-Friendly Plan. No autism, no autism spectrum. When you look at two years and up, four years and up, same. No new autism.
Group two, we had 238 unvaccinated kids. No new autism, no new autism spectrum. And group three was my more vaccinated kids, and we had 15 cases out of 900. About one in 60.

Before I really was doing informed consent, how did we get everybody to do the CDC schedule? Well we were very, “This is the right thing to do.” End of discussion. There was no informed consent.

TY: Which is about what the autism rate is.

I think if we do the good studies, let's take large groups of unvaccinated, selectively vaccinated, and CDC-vaccinated children, and just follow them over time.

DR. THOMAS: It's about what the rate is now.
This was a retrospective study, so obviously, you can tear it to shreds. But the P value for researchers who want to know, it's amazing: 0.00001. It’s like 1 in 100,000 chance that this was by accident.
I think if we do the good studies, let's take large groups of unvaccinated, selectively vaccinated, and CDC-vaccinated children, and just follow them over time.
In my own study, what I found that unvaccinated group of 238 patients by far were the least ill. I also tracked how many offices they came in for illnesses. I mean, it was like a fraction of the visits. These are healthy kids, and they're not vaccinated. So, they have a robust immune system through your natural state and probably better nutrition, maybe longer breastfeeding. I didn't have enough data to look at those factors.
But immunity is different from vaccination.
Vaccination, you're targeting that organism.
And yes, you might boost the immunity against that organism but what are you doing to the whole picture? And we're not looking at the whole picture. We need to.

These are healthy kids, and they're not vaccinated. So, they have a robust immune system through your natural state and probably better nutrition, maybe longer breastfeeding.

TY: It’s interesting that Dr. Thomas did a retrospective study of over 1,000 of his own patients and he found that the unvaccinated were the healthiest. Growing up, I was taught that vaccines were responsible for the decrease in mortality for many infectious diseases.
Was this accurate?

Then the vaccines came along and were given the credit for the death rates going down and for the life span increasing. But we've shown you with statistics that nobody argues with, and you see the death rate was going down, down, down.
In the case of measles and whooping cough, it was basically at baseline. It was basically close to zero and then the vaccine comes in.

DR. HUMPHRIES: Humanity can move in either direction, either towards health or away from health, depending on what's going on in society, what the stress levels of people, especially children, are, amount of sleep that they get, the food that they get, working conditions.
And conditions were beyond what we can actually imagine today, unless maybe you visited some of the worst parts of India, or some really poor countries that are just basically living in filth. That's what was going on back then.
So of course, any disease that came along, measles deaths were rampant. You didn't want to catch a disease back then because there was a good chance that you would die from it.
Then the vaccines came along and the medical system came along and were given the credit for the death rates going down and for the life span increasing. But we've shown you with statistics that nobody argues with, even people who don't like us don't argue with the vital statistics because all we did was graph them out.
So, what you can do is graph them out and see the death rate was going down, down, down.
In the case of measles and whooping cough, it was basically at baseline. It was basically close to zero and then the vaccine comes in.

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TY: Are you enjoying Episode 7 thus far? Have you learned some valuable information? Do you want to join our movement and support the mission to educate the world on the truth about vaccines? Then please consider owning the complete series today.

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Now, let’s get back to Episode 7.

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End of part 1

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Thank you for your attention. Let's make this world a better place together.

Love, peace and prosperity.

@Nutela

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Previous posts about vaccines:

• The Truth About Vaccines Video Docu-series - Episode 1
• transcript Ep. 1 part 1
• transcript Ep. 1 part 2
• transcript Ep. 1 part 3
• The Truth About Vaccines Video Docu-series - Episode 6
• transcript of Ep. 6 part 1
• transcript of Ep. 6 part 2
• The Truth About Vaccines Video Docu-series - Episode 7
• transcript Ep. 7 part 2