Fungal Infections – How to Eliminate Yeast, Candida, and Mold Infections For Good

Most, maybe all of you reading this, have Candida, even if you’re perfectly healthy. You have other fungi too. We all do. When the gut is healthy some fungus and lots of bacterial microbes live in harmony with us. Like bacteria, there will always be some fungi within us. Candida likes the human body. It’s the most common infectious fungus, typically responsible for oral thrush, skin rashes, eczema, psoriasis, athlete’s foot, vaginal yeast infections, and so much more. It’s one of our main microbes. Studies show that up to 90% of the population has Candida Albicans within them, but some (like me) suspect it’s closer to 100%.

Contents

Candida albicans is by far the most commonly known, accounting for about 50% of all cases of recognized fungal infections around the world. There is also Candida tropicalis, Candida glabrata, Candida parapsilosis, Candida krusei, Candida lusitaniae, and probably more, but let’s just call it all “Candida” for simplicity’s sake.

The most important point you should take away from this article is that Candida is not the “bad guys” any more than bacteria or other microbes are. With few exceptions, pathogens are simply responding to their environment. We understand this concept in biology well, but this concept gets ignored regarding the human body as it relates to disease. The fact is that the microbes all around our body are primarily based on the eco-system inside our gut, which is dictated primarily by the food they have to eat, i.e., the food we eat. You can take the nicest, friendliest bacteria from the gut, place it in a sanitized petri dish, introduce some sanitary junk food with simple sugars, and those bacteria are not going to look or act like our friendly little symbiotic fellows much longer. Microbes are very good at evolving to their environment, and we have a lot of different kinds. Even if you’re missing most of the beneficial bacteria that you should have, you still have a huge array of symbiotic microbes.

Candida and Bacteria

This single-cell organism, Candida, reproduces asexually and thrives on dead tissue, scar tissue, dead and decaying cells of any kind, and simple sugars from food. On that note, most all pathogens prefer to feed on simple sugars and dead or decaying cells. They are our garbage collectors. The problem is that their mere presence causes irritation (for various reasons, including gasses they release). This irritation leads to damage, so if a colony of a certain type of microbes has enough to eat in an area where they should not be, this can damage the area, giving the microbes more food, thus the vicious cycle of disease.2

Pathogens like simple sugars the best,1 but when they don’t get as much as they are used to they tend to get irritated and then turn hostile. This causes more nearby cell damage and decay which hurts us and feeds them.

When the body is in homeostasis, the microbes are balanced and the gut is healthy. When the gut is healthy, the gut doesn’t leak the wrong things into the body.

Gut Balance

When we eat foods that are best for us (like raw vegetables and herbs) the most beneficial microflora go to work. Happy with plenty of food and reproducing, they crowd out everyone else, and these guys help regulate and even produce lots of vitamins hormones as they break down protein molecules. Proteins that have not been digested thoroughly by our gut bacteria will not be digested well by us. These proteins entering the body will be looked at as “foreign proteins” which is antigenic to the body (causes immune response).3

Many of the bacteria that harm us tend to move quickly and come across as generally more agitated under a microscope. Healthy gut bacteria under a microscope look like a decent bunch of fairly slow moving microbes, just doing their thing. There are plenty of slow-moving bacteria and amoeba and other pathogens that move slowly, but looking at good bacteria, you can visually see how they can gently protect the body and crowd out or at least slow down pathogenic proliferation. Gut bacteria and mouth bacteria have a lot in common and bio-dentistry is on to this.

Check out the different behaviors of bacteria and other pathogens under a microscope. A fun experiment is to eat some raw vegetables like a salad, and then take a large saliva sample, put it under the lens in a petri dish, and find the bacteria swimming around in your mouth. See how fast they move. See how many there are. Now drink some soda or something else terrible, and get it all in your gums and everything. If you’re a smoker, do that too. In 10 minutes take another sample. The microbes are different. They’re fast and they seem angry. If you like videos, here’s a video. Note what they say about diet. I find it both wonderful and frustrating how close conventional wisdom has gotten to understanding the impact food plays on our microbes.

But we live in an antibacterial world. And while superbugs are coming to destroy us all, we’ve done a remarkable job of killing off and suppressing bacteria, for both good and bad. I had the urge to type “both good and bad bacteria,” but that’s the misnomer. Microbes are not good or bad (though for simplicity’s sake I will refer to them this way). The “bad” bacteria are just doing their job, and the beneficial bacteria that are friendly to us can mutate and become pathogenic under poor-health circumstances.

Just a quick, barely relevant fact: There are many strains of e. Coli and salmonella that we know of that often exist in our gut and cause us no harm.7 The pathogenic, virulent forms are a result of factory farming. 8 These two superbugs that kill us so often are a result of some badass e. Coli or salmonella that was actually tough enough to survive and escape the incredibly acidic and antimicrobial environment of a factory-farmed cow or chicken, respectively. It’s not only metaphoric of how our gut works. Consider the parallels between how microbes adapt and our justice system, or our drug wars, or how we fight terrorism. We as humans behave like microbes in a myriad of ways. We could learn a lot…

Also, our fruit has much more sugar in it than it used to. Even if one never eats refined foods we get more sugar from fresh fruit than we ever would have in nature before we started selectively breeding our food (hybridization). In other words, even if you’re eating the perfect modern paleo diet, you’re not eating like a paleo at all, unless your bananas look more like this:

So, as a population, we eat fruit with tons of easily absorbed sugar, we eat refined foods, and we do lots of stuff to kill our gut flora, like GMOs, antibiotics, pesticides, and herbicides, etc. But Candida is really hard to kill. We often eliminate most or all of the microbes in our gut and much around our body with antibiotics, but Candida spores cannot be killed so easily. They wait, dormant, patient, just lying around for up to 6 months.4,5 These spores will survive anything we try to do to get rid of them. As soon as they sense a hospitable environment (food, i.e. sugar) they will come to life and proliferate.6

What Causes An Overabundance of Candida?

You get the idea by now, but mostly, it’s an overall poor diet with too much sugar. At least 95% of the problem is sugar. Refined foods are sugar to the body. But there are a lot of other things we do that allow Candida to flourish and run our lives:

  • Chemical birth control
  • NSAID pain relievers
  • Steroids
  • Factory farmed meat
  • Chronic constipation
  • Alcohol
  • Recreational drugs
  • Mercury toxicity (like dental fillings)
  • Other heavy toxicity  (like from vaccines)
  • Extreme stress
  • Vitamin and mineral deficiencies

Here’s How Candida Takes Over

Candida is hanging out in the gut of a person. Said person eats a bunch of nasty food with toxins that kill our most beneficial flora, along with refined foods that quickly break down into simple sugars that do an efficient job of feeding pathogenic microbes. The person gets sick. The person takes antibiotics. The prescriptions may also kill off the Candida in the gut too, but not the spores. Said person then, hopefully feeling better by now, eats as he or she normally eats. Candida reactivates its lifecycle. They proliferate with little to no competition. Once that Candida is feeling crowded and has outgrown its home in the gut, Candida will grow out of its simple single-cell yeast form and into a filamentous, mycelial, virulent fungal form, growing root-like tentacles (hyphae) that drill deep into the mucosal lining of the gut, poking “holes” into already an irritated and inflamed, gut lining, resulting in a leaky gut.9,10 (Click here for more on mycelial fungi.) Now Candida and all kinds of other crap (excuse the pun) can leak into the bloodstream and travel throughout the body. Candida can infect every organ of the body. When it takes the fungal form, it creates a toxic biofilm that protects itself against things that would normally kill it (like antibiotics). It may or may not be Candida that is causing what ails you, but there is at least a very good chance that Candida opened the door to the pathogen at some point.

When Candida makes its escape, it proliferates into the bloodstream, and consequently, all around the body. If you smashed your elbow in a football injury 17 years ago there is still a tiny bit of scar tissue there, and that’s one of the places that Candida will set up a home outside the gut. When they don’t have sugar they will feed off of scar tissue and other “dead” cells.

Now the body is overwhelmed. The Candida will travel all over the body, but it will usually be eliminated from the blood fairly quickly. Maybe said person goes and gets a blood test, but you can read here why tests for Candida aren’t very accurate. The toxins that Candida leave behind get filtered out by the liver, eventually, hopefully, but the virulent Candida itself will be purged from the blood as the body’s immune system goes into high gear. Now the body has satellite infections of Candida all over, spread throughout. Every ache we have from an old injury is most likely hurting when there is pathogenic activity. When we wake up in the morning we are at our most achy in large part because of reduced blood flow and movement leading to more pathogenic activity. And again, this is a good thing in a balanced body, as they are taking out the garbage.

Picture that body full of Candida satellite infections. If the person eats sugars the Candida get fed, gets happy, proliferates, probably does another bloodstream ride to spread out, and that’s that. When one restricts the sugar, what do Candida eat? Us. Dead or weak cells. It kinda hurts. Feed the Candida another burst of sugar (or toxic food that damages the cells enough to feed the Candida that way), and the Candida leaves us alone for a bit. This is obviously overly simplistic, but it should show how easily and symbiotically Candida can cause poor food cravings.

There are antifungal drugs that can kill off Candida, but again, not the spores. Once those spores are all over the body, they will stay hanging around for up to six months, waiting for food.

This same sort of thing happens with other pathogens too, but Candida is the key. It literally opens the doors for other pathogens (and food particles that needed more digestion, and lots of other “crap”) by creating the holes in the gut. Other things can create this extra permeability as well, but Candida opens the gut fast and typically does it often.

Candida and Wheat

Candida causes lots of unexpected and fascinating problems that connect a lot of dots for those with chronic health issues. Take wheat for instance. A protein found in Candida called HWP-1 is identical or highly homologous (nearly identical) to two gluten proteins, alpha gliadin and gamma-gliadin. These proteins are known to stimulate immune cell responses in people with celiac disease. In other words, Candida, the yeast responsible for oral thrush and vaginal infections (and so much more), contains the same protein sequence as wheat gluten and therefore could trigger celiac disease.

It gets worse. The gluten protein is similar to protein structures in the nervous system and the thyroid tissue. The body will turn on these proteins shortly after it begins reacting to gluten. This is the essence of chronic autoimmune disease.

How To Know if You Have Candida

This is a hard one for most people to swallow, but if you’re sick, you’ve got Candida. As we’ve established, it’s not about “catching it.” If the gut is not balanced the gut has an abundance of Candida and other less-than-beneficial microbes. If any of the following pertain to you, Candida or not, it’s time to balance the gut by fixing the diet.

  • Allergies
  • Skin issues
  • White tongue
  • Floaters in vision
  • Itchy feet or hands or ears
  • Prone to any other infections

The allergies concept is especially hard for many, but it’s true. If you have food or seasonal allergies, stop blaming genetics and accept that the body’s biology is out of balance. For more on this, check out Candida Overgrowth Symptoms.

How to Prevent Candida Overgrowth

First of all, stop thinking of microbes as the bad guys. That’s not the case, not at all. Think of them more like humans. Picture yourself as you grow up in the worst war-torn part of the world you can imagine. Drone strikes, little food, toxic water, and a brain that functions half as well as yours does. How would you react to your environment? What’s the best way to fix the problem? Fix the environment. And it’s also the only way to prevent the problem in the first place.

Drink lots of water, and feed the body foods that the friendliest microbes love. Flushing the body is critical because there are lots of gasses and other toxic substances that accumulate in the body with an abundance of Candida. It slows the bodily systems, causing sluggish liver and kidney functionality.

Here are three articles on diet. The information will prevent Candida infestations in the body, as well as any other pathogen, and in most cases, with patience, this diet/lifestyle will eliminate Candida and other diseases as well.

The first one has my salad and cranberry-lemonade recipe. I suggest everyone eat and drink like that every single day.

The Best Supplements for Killing Candida, Yeast, Molds, Other Funghis

First and foremost, just pack the gut with good food. Eat a big salad. Picture the intestinal tract and imagine it being packed full of vegetables and herbs. If you’re one of those health-food hating virulent microbes, you’re at least not going to be reproducing while you’re being squeezed out by salad and salad loving microbes.

Cut out all refined foods because they feed pathogens. Cut out all toxic foods because they kill the good guys and damage the gut which feeds the pathogens. If you suffer from allergies, you eat too much sugar and/or refined foods (or drink alcohol regularly). Cut out the sugar and the allergies go away. See the above articles for more on diet. Most people don’t need supplements and can get rid of every single health issue they have with just diet. On the other hand, with the intense sugar cravings that Candida causes, supplements can not only speed up the process of getting well, they can balance a person’s body just enough to help ensure better choices are made and the supplements also compensate for the bad choices. But therein lies the rub. Most people are just looking for that one supplement that’s going to ease some of the pain their lifestyle causes. And while that one supplement should be SF722, in my opinion, the most common way someone uses such a supplement is to take enough to feel the pain relief they seek while they keep making poor food choices until more pain relief in one form or another is needed. The only difference between supplements and prescriptions in the way most people use them is that supplements don’t have the toxic side effects. But my point is that without the right diet, just consuming supplements will not create homeostasis. That said, here are the top supplements to take for Candida control:

SF722

This is my favorite for killing anything fungal. There are tons of other choices (click here), but I don’t know of anything that does a better job for the money than SF722. Candida can become fairly immune to many other antimicrobials but studies have shown that this does not happen with SF722. SF722 is antimicrobial so it can kill some of the good guys, but it doesn’t seem like it’s very good at killing bacteria compared to some other compounds. This is a benefit when dealing with Candida.

How to Take SF722

I’ve known people that take more than 60 in a day. It can acidify the body temporarily, but the acids are dispelled easily and Candida doesn’t like acidity (I wonder how many people will feel the need to check on this fact). Obviously, you want a slightly alkaline body for health, but Candida is not one of the ones that like acidic environments. The bottle says to do 15 (5×3) and I recommend moving up in dosage if need be, depending on the die-off symptoms. Take it until Candida symptoms are gone, and then have it on hand to compensate future indulgences with poor food or drink choices. I usually take 20 when I eat at a restaurant.

Berberine

Goldenseal (Hydrastis canadensis), barberry (Berberis vulgaris), Oregon grape (Berberis aquifolium), and goldthread (Coptis chinensis) contain the broad-spectrum antibiotic alkaloid berberine. Berberine is effective against pathogens including bacteria, protozoa, and fungiBerberine has been proven in some studies to be stronger than many common antibiotics.

How to Take Berberine

Take it separately from probiotics, and follow the instructions. I tend to always take twice as much as they recommend, but I also weight 220 pounds. There should not be a need for high doses while taking the other supplements.

Oil of Oregano

Oil of Oregano is one of nature’s most powerful antibiotic supplements, but I don’t think it’s all that great against Candida. Plus, it works so well that the body can’t maintain healthy bacteria. It’s a great supplement to have on hand, but it is one I reserve for the acutest cases where killing the bad guys is the primary and urgent focus.

Probiotics

Often touted as the cure everything supplement for the well-informed, probiotics are something most everyone is familiar with these days. What most do not know is that the vast majority of probiotic supplements on the market are ineffectual at best, and many actually feed yeast. How the probiotics are processed and preserved make all the difference. It’s not an easy task to produce good probiotics; our stomach acid is designed to kill it. Two of my favorite are FloraMend and Bio-K (the latter is not available in our store, but it is at most health food stores and Whole Foods). I don’t recommend taking a probiotic with antimicrobials. A really good probiotic should come out on top, but you are reducing its effectiveness when you combine it with compounds that kill. For instance, I would take SF722 all day and a probiotic at night and early morning, or vice versa, where I take the probiotic with food and the SF722 late and early. Different digestive issues can favor one over the other so try both ways and see what works for you.

How to Take Probiotics

Don’t take them with antimicrobials, and make sure they are high-quality supplements. Anyone without an appendix should take a probiotic every day with every major meal for the rest of their life. Your appendix secretes out beneficial bacteria when you don’t have enough.

One antimicrobial you can take with probiotics is Olive Leaf Extract. It’s great for maintenance but it’s not a yeast serial-killer like SF722 (otherwise it would damage the probiotic). It’s a fine supplement, but it’s not going to do much of anything all by itself.

Systemic Enzymes

I am in love with a fairly new supplement called Abzorb. It’s one of the only four I regularly take (I’ll mention the other three as well in a moment).

As we age, our pancreas produces fewer enzymes for the body. We need enzymes to survive. We need enzymes to do everything, not just break down proteins. If you are healthy, you have an abundance of healthy enzymatic activity. When enzymatic production yields are low enough, the body will break down within hours with a heart attack or a stroke.  They are the catalyst for almost anything the happens at a molecular level in the body. Without enzymes, we would not be able to do anything with our vitamins and minerals.

Enzymes break down proteins. They do this with foreign proteins (which those with Candida issue have in abundance) and fibrin, the protein that makes up scar tissue. Fibrin feeds Candida and other pathogens if you didn’t skip all that ecology knowledge up above. These enzymes also reduce toxins in the blood and help balance cholesterol. Our body produces fibrin in response to trauma and enzymes help take it away in time. Anyone working in a morgue can tell you that one of the most obvious differences between a young body and an old body is that the older person has lots of fibrin all over the inside of their body. Strokes, heart attacks, aneurysms, and other often deadly ailments can be attributed directly to this.

Inside the gut, if food is not digested, it rots and feeds pathogens (ever notice how when things rot they smell sickly-sweet?), and Candida makes it hard to digest food properly.

The more enzymes we have to break down food, the better we digest and use the nutrition. Digestive enzymes help digest food in the stomach. Systemic enzymes don’t break open until they reach the gut. So, taken on an empty stomach, the systemic enzymes will go to work to repair the body and kill some viruses while they’re at it (I forgot to mention that enzymes kill viruses).

On the other hand, if you take a systemic enzyme with food, the enzyme will go to work to digest the food inside the gut.

And this brings me to Abzorb. It’s a probiotic and systemic enzyme. If you take it with food it will help you digest the food, and it works very well for this, much better than just taking one or the other. And while the product is more affordable than some of my other favorite probiotics, I find this probiotic is just as effective at colonizing in the gut. Usually, you need to spend considerable money on probiotics and enzymes for quality, but Abzorb is affordable. It is very effective, and you get two very important and synergistic supplements in one.

How to Take Systemic Enzymes

Take them on an empty stomach as noted or with food to help digest food inside the gut. I recommend mixing it up each day, but I do recommend caution when taking systemic enzymes. Too many systemic enzymes can cause issues, they can start to eat away at the body, so I don’t just grab a big handful like I do with SF722. I personally take 4-6 a day on an empty stomach, and I take more with food as needed.

Magnesium

The byproducts of Candida albicans include ethanol, uric acid and ammonia, acetaldehyde, and about 75 other toxic gases we know of. The big one on the list is acetaldehyde.12 Acetaldehyde is also produced when you drink alcohol, smoke, or breathe in car exhaust. It’s in large part responsible for the “hungover” feeling we get after a night of debauchery.13 Magnesium is required to break down acetaldehyde. It’s unclear if magnesium deficiency can cause more Candida growth in any way, but a lack of this mineral does exacerbate the problems associated with Candida. Without enough magnesium, the body will sustain a lot more damage, which feeds the Candida overgrowth cycle. Candida causes magnesium deficiencies too, and anyone who has Candida overgrowth is low in magnesium.

How to Take Magnesium with Candida Issues

Candida causes the body to require more magnesium than the recommended daily dose of 400mg. Often a Candida cleanse can cause the magnesium levels to become dangerously low, and then the individual may suffer from sluggish bowels which just compounds the symptoms of  Candida die-off further.

Biotin

Like Magnesium, B vitamins are always low in those dealing with Candida overgrowth. Candida makes it very difficult for good bacteria to give us the b vitamins we need to make good decisions. Impulse control is severely hampered when there aren’t enough Bs. Too much fungi = not enough good bacteria = not enough b vitamins = poor food choices.

But biotin has a trick up its sleeve that causes it to make this list. Biotin is a coenzyme and a B vitamin. It is also known as vitamin H and vitamin B7. Because biotin is present in so many different kinds of foods, a serious deficiency is rare. But those who have had health issue due to Candida for a long enough period of time are likely going to be low in all Bs including B7. And B7 actually inhibits Candida from transforming into its mycelial, pathogenic form.

How to Take Biotin

With B vitamins it’s usually best to take a complex, not a single B. If one takes too much of one B vitamins it can inhibit the assimilation of other Bs and throw all the vitamins out of whack. Another option is chlorella, which has lots of B vitamins, including biotin, and it kills Candida in some other ways too.

I wanted to keep this article a bit more specific and focused. But the reality is, if you suffer from an abundance of Candida, you also suffer from many other pathogens. And the aforementioned salads can take care of the vitamin and mineral need. For people who need to heal their gut, I recommend a healthy diet void of refined and processed foods, salads every day, and the following supplements:

The first three should be plenty for most people, but for really prominent fungal issues or for impatient people with a bigger budget I’d recommend all of them. For more on diet, including salad recipes, check out:

My Supplements

Total Nutrition Formula is my multi-vitamin/mineral formula. I take it once a week, but I used took it every day with smoothies. Now I eat enough salads I don’t feel the need for it as much. It has chlorella and spirulina and lots of other good stuff. Spirulina isn’t a big Candida killer but it goes hand-in-hand with chlorella, so I figured I’d add it in. A study in 2001 found that spirulina supports our beneficial microflora which leads to less Candida,13 and an experiment from 2010 shows that spirulina enhances immune system response to Candida and other pathogens. 14 It’s said that chlorella does a similar number on Candida, and it’s rich in B vitamins including biotin, and I also read somewhere about how chlorella can break down the cell walls of fungi, but I cannot find that anywhere.

I always have SF722 on hand but I don’t take it very often. I take Abzorb in the mornings on an empty stomach, 3-4, and I take 1-2 with every cooked meal I have when I remember. I also take Liquid Light every now and then, just when I have a feeling I need a mineral boost.

When I was smoking marijuana  I constantly sipped on Mother Earth Cider. It kept me from getting sick. Now I just sip once or twice a day. Just read the ingredients and you’ll see why. This is by far my favorite supplement on the market, but it’s not here as a Candida fighter. I’m sure it does a little, but not like the aforementioned.

Conclusion

Two other big causes of Candida overgrowth that we did not touch include vaccines and amalgams. The damage these medical products cause will feed Candida indefinitely. If you have heavy metal toxicity, the only thing I would do differently in this protocol is to add the Total Nutrition Formula and take additional chlorella and spirulina daily. It’s hard to eat too much of these seaweeds, and they have tons and tons of benefits, so get them in you any way you can. I think they’re disgusting so I prefer tablets or strong smoothie concoctions to bury the taste.




Sugar Industry Has Had Evidence Linking Sugar to Heart Disease for Nearly Half a Century

Project 259 is a study that linked sucrose, a common sugar product, to heart disease and bladder cancer and would have revolutionized the way we think about sugar in regards to our health. Or at least it would have…if the sugar industry hadn’t stopped funding it halfway through the project in 1971. The project was discovered by a team of researchers at the University of California San Francisco who have been in the news for other reports on the sugar industry’s unsavory practices.

Details of the Project

Project 259 was launched by the Sugar Research Foundation in 1968. The project was in two halves, and only one of them was completed. The finished portion of the project looked at rat’s gut bacteria after rats consumed sucrose compared to starch. Early results showed that the sucrose caused gut microbes to throw off those rodent metabolisms, increasing their levels of triglycerides. Elevated triglycerides clog arteries and increase a person’s predisposition for cardiovascular disease. Project 259 also found that in a comparison to high-starch diet, a high-sugar diet boosts the activity of beta-glucuronidase, an enzyme linked to bladder cancer, when compared to a starch diet.

These discoveries were reported to Sugar Research Foundation in 1970. The results accompanied a request for 12 additional weeks of funding to finish the second half of the project, which was outlined as a deeper look at the effects of starch. Within a month, the Vice President of the Sugar Research Foundation declared these findings as nil and the additional funding never materialized. Project 259 was abandoned in 1971.

Related: Healthy Sugar Alternatives and More

Who Tells The Story

The sugar industry does not see this as a story. According to Courtney Gaine, the president and CEO of the Sugar Association, “They never called us. We would have let them look at the archives. I would let them look tomorrow. The story we have in our archives is a lot better than the story they’ve been telling,” She asserts that this study was lost in a bureaucratic shuffle, and emphasizes the industry’s ongoing interest in negative claims.

The sugar industry has a vested interest in controlling the story of sugar and health’s relationship. More than anything, Project 259 disrupts a narrative that was already being put into place.  The same researchers who found this study also uncovered a letter in the Harvard library that revealed the truth of that. Two prominent and now deceased Harvard researchers, Harvard nutritionists, Dr. Fredrick Stare and Mark Hegsted, were responsible for disproving studies that implicated sugar and concluded that there was only one dietary modification — changing fat and cholesterol intake — that could prevent coronary heart disease. Their work was published in 1967 and didn’t require disclosure of industry funds, although these newly found records state that the sugar industry trade group initiated and paid for the studies, examined drafts, and laid out a clear objective to protect sugar’s reputation in the public eye. Yes, the sugar industry wants to know about negative studies but not to offer an informed choice.

Related: Candida, Gut Flora, Allergies, and Disease

Most Frustrating “What If” Ever?

Sugar (especially the way we process and refine it) is more detrimental to the human body than anyone had previously thought, but what would our quality of life look like if this study was published? What would our sweetener options even look like?

Rates of heart disease, the number one cause of death in the world, would be far less than they currently are, and the ripple effects from consuming less sugar would be huge. Would we be facing the same level of antibiotic-resistant bacteria crises? While the majority of the blame for that coming storm can be placed at the factory farming industry’s doorstep, sugar feeds infection like no other food. Would doctors and dentists need to prescribe antibiotics at the rate they currently do?

This is all speculation. Infuriating speculation, at that, as that potential future is gone.

Related: Start Eating Like That and Start Eating Like This – Your Guide to Homeostasis Through Diet

We Should Be Angry

Not everyone who has heart disease has a history of heart disease in their family, but through the over-consumption of sugar, we have bred that predisposition into millions of people’s genetics. Anger and outrage are a daily occurrence in the current news cycles though and making this another cause for anger doesn’t send a strong enough message.

What if you stopped and said no more to products with large quantities of added sugar? Chose a different salad dressing or committed to figuring out a quick and tomato sauce recipe that kept you from reaching for the sugar-laden, jarred version on the shelf? Instead of choosing foods that create problems while willfully ignoring them, dictate your own health and choose foods that heal.

Sources:



Cell Phones and Brain Tumors Are Linked, But Will We Do Anything About It?

Have you ever wondered if your mobile phone is giving you cancer? Legally speaking, there is a link. Of course, that’s only true if you live in Italy.

Studies of the effects that cell phones have on the brain or examinations of the link between phone usage and certain cancers don’t have the same clarity. Where many studies find regular cell phone usage contributes greatly to the risk of cancer and brain tumors, other research finds the device benign. The Italian verdict is one of the first positive acknowledgments of that link. Much of that can be attributed to the Italian court’s refusal to consider studies funded by telecom industries,  but realistically there are too many variables to specifically link cellphone use to a specific condition. It is incredibly likely that cellphones are making us sick. However, they are only one aspect of a modern life designed without human health in mind.

Precedence Has Been Established

The court in the Italian town of Ivrea released an April 11th ruling ordering that a businessman receive a state-funded pension after too much phone use for work caused him to develop a benign brain tumor and resulted in the loss of his hearing. Rumors and theories surrounding the dangers of cell phone usage has swirled for years, and this is a big deal. The Italian courts had previously accepted the case of a sales manager who was on a cellphone five or six hours a day, that was subsequently rejected by a trial court. This paved the way for this ruling, as lawyers for the plaintiff, Stefano Bertone and Renato Ambrosio, pointed out “For the first time in the world, a court has recognised a causal link between inappropriate use of a mobile phone and a brain tumour…” While the court ruling is still subject to an appeal, the plaintiff in the case, Roberto Romeo, will receive 500 euros per month to be paid by INAIL, a national insurance scheme covering workplace accidents.

Recommended: How to Kill Fungal Infections

So How Much is Too Much?

Cell phones have been woven into the fabric of modern life and telling people to avoid them at all costs is not realistic. But there has to be a point at which more damage has been done that the body can recover from. In the case of the plaintiff in the Italian case, Roberto Romeo, he was required to use his company mobile phone for 3 to 4 hours of every working day for 15 years. A rat study found that rats exposed to cell phone radiation nine hours a day for a two year period were more likely to develop malignant brain tumors. Another paper found that a mere 30 minutes a day of cell phone over a ten year period increased the risk of gliomas (a malignant tumor in the brain that occurs on the side of the head) by 40 percent. Yet several other significant studies have found no causal link between cellphones and brain damage, although both the U.S. and the U.K. are in the process of conducting further long-term studies.

Recommended: Detox Cheap and Easy Without Fasting – Recipes Included

Why Don’t We Have A Definitive Answer

There are many things that modern society will ignore in the name of progress, even past the point at which something needs to be done. Cell phones are an area with lots of fingers in lots of pies, and the conflicting narratives presented by these studies reinforce that. There is also science’s inability to keep up with phone technology. Before researchers have time conduct long-term studies, phone configurations have changed enough for either side to proclaim the findings of any study out of date.

Is there a clear link between cell phones and brain tumors? After eliminating all telecom funded studies, an Italian court decided there is.

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Why the U.S. Washes and Refrigerates Eggs, & Why Other Countries Don’t

American eggs are federally required to be washed and sanitized and then refrigerated. There are a few reasons for this, but the main reason is that our factory farms are disgusting. In Europe, eggs sold in supermarkets are not legally allowed to be washed.

I live in Mexico and one of the first things I noticed at the grocery stores here is that they do not refrigerate the eggs. They’re sold on a shelf with dry goods generally, like sugar or canned milk products. There are many options from tiny spotted ones to big brown ones, but they’re unwashed and unchilled. – Lily Da Vine

The FDA states that eggs must be sterilized and chilled to reduce the likelihood of salmonella infections. Much of the world focuses on, and/or legislated to place emphasis on, producing cleaner eggs. American chicken factories, on the other hand, are legendarily filthy, and we don’t seem motivated to change that.

Abysmal factory farming conditions are what create the problematic salmonella superbug (the same is true for eColi). Eggs become contaminated with salmonella in one of two ways, by either contaminating the egg internally upon production (due to a chicken with infected ovaries), or when the egg becomes in contact with contaminated chicken manure, and salmonella sticks to the porous shell.

https://www.youtube.com/watch?v=Xbqv1SuQJ0s

So the United States, in typical fashion, has decided that instead of regulating the farms to produce healthier food, we need to wash, sanitize, and cook our eggs. If you like raw eggs, be sure they aren’t factory farmed, and especially not American factory-farmed!

So what about real farm fresh eggs from a healthy farm where the eggs have room to run around, and they all get a healthy natural diet? Those eggs should be gently cleaned off, but not washed or made wet. There is a protective coating around the eggs that you want to preserve. If the eggs do get washed they should then be refrigerated or used shortly thereafter.

If you can’t produce your own eggs try finding a local farmer who does not wash or chill their eggs, and simply leaves them on the counter when you get home. Wash them just before you use them (if you want).

Other Common Egg Questions: Shell and Yolk Color

The color of the yolks are determined by diet and the freshness of the egg. Hens that get a variety of foods including lots of plants, alfalfa, bugs, for instance, are healthier than hens that have a restricted diet.  Healthy chickens have a darker yellow-orange yolk. Factory farmed chickens in the United States typically have diets of wheat, barley, or white corn which produces pale yellow yolks.

Shells are different colors because different chickens lay different eggs.

…egg color is determined by the genetics of the hens. The breed of the hen will indicate what color eggs she will produce. For example, Leghorn chickens lay white eggs while Orpington’s lay brown eggs and Ameraucana produce blue eggs. An Olive Egger, a chicken that lays olive green eggs, is the product of a cross between a hen and rooster that are from a brown egg and a blue egg laying breed. An interesting tip is to look at the chicken’s ear lobes; typically those with white ear lobes produce white eggs.” – Michigan State

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New Pill That Can be Digitally Tracked Raises Orwellian Concerns

How much would a chocolate company pay to know exactly when you or the lady in your life is experiencing PMS symptoms in an effort to more effectively target ads? If that level of corporate involvement in your medical records upsets you, you’re not going to like the new digital ingestion tracking system approved by the Food and Drug Administration.

This new tracking system is designed to address the issue of nonadherence, where patients do not follow through on prescribed medical treatments. The treatment, in this case, is called Abilify MyCite and it’s made by Japan-based Otsuka Pharmaceuticals. The actual medication portion of the Abilify MyCite system is brand-name aripiprazole, an antipsychotic drug used for treating schizophrenia, bipolar disorder, and as an add-on treatment for depression in adults. “Being able to track ingestion of medications prescribed for mental illness may be useful for some patients,” said Mitchell Mathis, M.D., director of the Division of Psychiatry Products in the FDA’s Center for Drug Evaluation and Research. “The FDA supports the development and use of new technology in prescription drugs and is committed to working with companies to understand how technology might benefit patients and prescribers.”

How It Works

The pill part of the system is the simple part. Abilify MyCite comes with a web-based dashboard that allows a patient to track their actual drug ingestion, daily activity level and self-reported mood and sleep. The sensor that tracks that is roughly the size of a grain of sand and activates upon contact with fluid in the stomach. It detects and records the date and time the pill was taken and relays that to a patch worn by the patient. The patch then sends all of that to the patient’s smartphone. When the patient gives consent, caregivers or medical professionals are able to see all of this data, though the system does not register the ingestion in real time or emergencies. The patient is able to revoke those permissions at any time.

Is It Worth It?

The system itself does not actually increase drug compliance. Both Otsuka Pharmaceuticals and the FDA take care to note that the product does not fix nonadherence, and it remains to be seen if the patients with the first illnesses targeted by this medication will respond positively. While nonadherence is an expensive issue, schizophrenics and those with bipolar frequently skip medications because they don’t like the way they feel when on them or dislike the feeling of being controlled or manipulated. A pill that tracks their compliance is probably not going to change that.

Who Does This Product Work For?

Imagine a system where medical compliance is a condition of benefits without a way around it. Can a digital ingestion tracking system create a situation where your insurance charges you more for choosing not to take a prescription?

The more connected we become, the more difficult it is to keep information private. How secure will this data be? According to Kimberly Whitfield from Otsuka Pharmaceuticals public relations department, “the data is encrypted while it is stored in the Health Insurance Portability and Accountability Act (HIPAA)-compliant cloud environment, and the cloud service provider does not have a decryption key.” While all of these makes this information much more secure than your average social media profile, information leaks happen across every sector.

The company is clearly taking precautions, but can the information be stopped once it’s out there?

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Harvard Immunologist: Unvaccinated Children Pose Zero Risk

An open letter written by Tetyana Obukhanych, a Harvard immunologist, has has been circulating around the internet again. We thought it worth republishing. She wrote the letter back in 2015 in response to vaccine legislation. She makes a strong case for unvaccinated children not endangering the rest of the public.

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Dear Legislator:

My name is Tetyana Obukhanych. I hold a PhD in Immunology. I am writing this letter in the hope that it will correct several common misperceptions about vaccines in order to help you formulate a fair and balanced understanding that is supported by accepted vaccine theory and new scientific findings.

Do unvaccinated children pose a higher threat to the public than the vaccinated?

It is often stated that those who choose not to vaccinate their children for reasons of conscience endanger the rest of the public, and this is the rationale behind most of the legislation to end vaccine exemptions currently being considered by federal and state legislators country-wide. You should be aware that the nature of protection afforded by many modern vaccines – and that includes most of the vaccines recommended by the CDC for children – is not consistent with such a statement. I have outlined below the recommended vaccines that cannot prevent transmission of disease either because they are not designed to prevent the transmission of infection (rather, they are intended to prevent disease symptoms), or because they are for non-communicable diseases. People who have not received the vaccines mentioned below pose no higher threat to the general public than those who have, implying that discrimination against non-immunized children in a public school setting may not be warranted.

  1. IPV (inactivated poliovirus vaccine) cannot prevent transmission of poliovirus. Wild poliovirus has been non-existent in the USA for at least two decades. Even if wild poliovirus were to be re-imported by travel, vaccinating for polio with IPV cannot affect the safety of public spaces. Please note that wild poliovirus eradication is attributed to the use of a different vaccine, OPV or oral poliovirus vaccine. Despite being capable of preventing wild poliovirus transmission, use of OPV was phased out long ago in the USA and replaced with IPV due to safety concerns.
  2. Tetanus is not a contagious disease, but rather acquired from deep-puncture wounds contaminated with C. tetani spores. Vaccinating for tetanus (via the DTaP combination vaccine) cannot alter the safety of public spaces; it is intended to render personal protection only.
  3. While intended to prevent the disease-causing effects of the diphtheria toxin, the diphtheria toxoid vaccine (also contained in the DTaP vaccine) is not designed to prevent colonization and transmission of C. diphtheriae. Vaccinating for diphtheria cannot alter the safety of public spaces; it is likewise intended for personal protection only.
  4. The acellular pertussis (aP) vaccine (the final element of the DTaP combined vaccine), now in use in the USA, replaced the whole cell pertussis vaccine in the late 1990s, which was followed by an unprecedented resurgence of whooping cough. An experiment with deliberate pertussis infection in primates revealed that the aP vaccine is not capable of preventing colonization and transmission of B. pertussis. The FDA has issued a warning regarding this crucial finding.Furthermore, the 2013 meeting of the Board of Scientific Counselors at the CDC revealed additional alarming data that pertussis variants (PRN-negative strains) currently circulating in the USA acquired a selective advantage to infect those who are up-to-date for their DTaP boosters, meaning that people who are up-to-date are more likely to be infected, and thus contagious, than people who are not vaccinated.
  5. Among numerous types of H. influenzae, the Hib vaccine covers only type b. Despite its sole intention to reduce symptomatic and asymptomatic (disease-less) Hib carriage, the introduction of the Hib vaccine has inadvertently shifted strain dominance towards other types of H. influenzae (types a through f).These types have been causing invasive disease of high severity and increasing incidence in adults in the era of Hib vaccination of children. The general population is more vulnerable to the invasive disease now than it was prior to the start of the Hib vaccination campaign. Discriminating against children who are not vaccinated for Hib does not make any scientific sense in the era of non-type b H. influenzae disease.
  6. Hepatitis B is a blood-borne virus. It does not spread in a community setting, especially among children who are unlikely to engage in high-risk behaviors, such as needle sharing or sex. Vaccinating children for hepatitis B cannot significantly alter the safety of public spaces. Further, school admission is not prohibited for children who are chronic hepatitis B carriers. To prohibit school admission for those who are simply unvaccinated – and do not even carry hepatitis B – would constitute unreasonable and illogical discrimination.

In summary, a person who is not vaccinated with IPV, DTaP, HepB, and Hib vaccines due to reasons of conscience poses no extra danger to the public than a person who is. No discrimination is warranted.

How often do serious vaccine adverse events happen?

It is often stated that vaccination rarely leads to serious adverse events. Unfortunately, this statement is not supported by science. A recent study done in Ontario, Canada, established that vaccination actually leads to an emergency room visit for 1 in 168 children following their 12-month vaccination appointment and for 1 in 730 children following their 18-month vaccination appointment.

When the risk of an adverse event requiring an ER visit after well-baby vaccinations is demonstrably so high, vaccination must remain a choice for parents, who may understandably be unwilling to assume this immediate risk in order to protect their children from diseases that are generally considered mild or that their children may never be exposed to.

Can discrimination against families who oppose vaccines for reasons of conscience prevent future disease outbreaks of communicable viral diseases, such as measles?

Measles research scientists have for a long time been aware of the “measles paradox.” I quote from the article by Poland & Jacobson (1994) “Failure to Reach the Goal of Measles Elimination: Apparent Paradox of Measles Infections in Immunized Persons.” Arch Intern Med 154:1815-1820:

“The apparent paradox is that as measles immunization rates rise to high levels in a population, measles becomes a disease of immunized persons.”

Further research determined that behind the “measles paradox” is a fraction of the population called low vaccine responders. Low-responders are those who respond poorly to the first dose of the measles vaccine. These individuals then mount a weak immune response to subsequent RE-vaccination and quickly return to the pool of “susceptibles’’ within 2-5 years, despite being fully vaccinated.

Re-vaccination cannot correct low-responsiveness: it appears to be an immuno-genetic trait. The proportion of low-responders among children was estimated to be 4.7% in the USA.

Studies of measles outbreaks in Quebec, Canada, and China attest that outbreaks of measles still happen, even when vaccination compliance is in the highest bracket (95-97% or even 99%). This is because even in high vaccine responders, vaccine-induced antibodies wane over time. Vaccine immunity does not equal life-long immunity acquired after natural exposure.

It has been documented that vaccinated persons who develop breakthrough measles are contagious. In fact, two major measles outbreaks in 2011 (in Quebec, Canada, and in New York, NY) were re-imported by previously vaccinated individuals.

Taken together, these data make it apparent that elimination of vaccine exemptions, currently only utilized by a small percentage of families anyway, will neither solve the problem of disease resurgence nor prevent re-importation and outbreaks of previously eliminated diseases.

Is discrimination against conscientious vaccine objectors the only practical solution?

The majority of measles cases in recent US outbreaks (including the recent Disneyland outbreak) are adults and very young babies, whereas in the pre-vaccination era, measles occurred mainly between the ages 1 and 15. Natural exposure to measles was followed by lifelong immunity from re-infection, whereas vaccine immunity wanes over time, leaving adults unprotected by their childhood shots. Measles is more dangerous for infants and for adults than for school-aged children.

Despite high chances of exposure in the pre-vaccination era, measles practically never happened in babies much younger than one year of age due to the robust maternal immunity transfer mechanism. The vulnerability of very young babies to measles today is the direct outcome of the prolonged mass vaccination campaign of the past, during which their mothers, themselves vaccinated in their childhood, were not able to experience measles naturally at a safe school age and establish the lifelong immunity that would also be transferred to their babies and protect them from measles for the first year of life.

Luckily, a therapeutic backup exists to mimic now-eroded maternal immunity. Infants as well as other vulnerable or immunocompromised individuals, are eligible to receive immunoglobulin, a potentially life-saving measure that supplies antibodies directed against the virus to prevent or ameliorate disease upon exposure.

In summary: 1) due to the properties of modern vaccines, non-vaccinated individuals pose no greater risk of transmission of polio, diphtheria, pertussis, and numerous non-type b H. influenzae strains than vaccinated individuals do, non-vaccinated individuals pose virtually no danger of transmission of hepatitis B in a school setting, and tetanus is not transmissible at all; 2) there is a significantly elevated risk of emergency room visits after childhood vaccination appointments attesting that vaccination is not risk-free; 3) outbreaks of measles cannot be entirely prevented even if we had nearly perfect vaccination compliance; and 4) an effective method of preventing measles and other viral diseases in vaccine-ineligible infants and the immunocompromised, immunoglobulin, is available for those who may be exposed to these diseases.

Taken together, these four facts make it clear that discrimination in a public school setting against children who are not vaccinated for reasons of conscience is completely unwarranted as the vaccine status of conscientious objectors poses no undue public health risk.

Sincerely Yours,

~ Tetyana Obukhanych, PhD

Tetyana Obukhanych, PhD, is the author of the book Vaccine Illusion.  She has studied immunology in some of the world’s most prestigious medical institutions. She earned her PhD in Immunology at the Rockefeller University in New York and did postdoctoral training at Harvard Medical School, Boston, MA and Stanford University in California.

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Sulfites Kill Beneficial Bacteria According to New Study

The first scientific study to test the effects of food preservatives on beneficial bacteria has been published, and the results do not bode well for our health. Researchers from the University of Hawai‘i Maui College have found that sulfites in food preservatives, generally recognized as safe for consumption at levels of 5000 ppm (parts per million) or less, killed or inhibited the growth of beneficial bacteria at levels of 3780 ppm or less. In the words of lead researcher Dr. Sally V. Irwin,

Studies show a significant increase over the past 40 years in food allergies, obesity, and metabolic disorders that have a direct correlation to disbiosis, or changes in the microbiome…In trying to understand what in our environment may be causing this change, the use of many food preservatives and their effects on beneficial bacteria came to mind.”

What They Found

Sulfites are a food preserver found in dried fruits, wine, beer, bottled lemon and lime juices, processed meats, canned goods, and occur naturally in sauerkraut and its brine. Common sulfites include sulfur dioxide, potassium bisulfite, sodium sulfite, and sodium bisulfite. They are frequently used to stop fermentation, which is why they are most commonly associated with fermented beverages like wine.

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For this study, researchers chose four known beneficial bacteria, Lactobacillus species casei, plantarum and rhamnosus, and Streptococcus thermophilus, and tested their reactions to two different preservatives, sodium sulfite and sodium bisulfite. The sulfites were in concentrations from 10 to 3780 ppm and exposed to the bacteria for six hours. After only two hours of exposure to sulfites concentrated at 250-500 ppm, all four types of bacteria tested showed no increase or a substantial decrease in cell numbers when compared to the sulfite-free control.

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These results should not be surprising, as this is what sulfites are designed to do. They are added to stop fermentation, the development of bacteria. Many modern innovations do what they are designed to do, but there is often a resistance to believe that what they do could also be harmful. Antibiotic-resistant superbugs are on track to kill more people than cancer by 2050, a result of our indiscriminate love affair with antibiotics, that miracle of modern medicine.

The Implications

This is a preliminary study in that its subjects are lab-grown bacteria and were exposed to the sulfites for a fraction of the time that occurs during real-world digestion. Yet the damage to that beneficial bacteria was clear.

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We depend on our beneficial bacteria. Without it, we are more vulnerable to serious infections, autoimmune disease, obesity, and numerous other damaging health conditions. This study solidly links what is in our food with one of the most serious health issues we face – the decline of our gut microbe diversity. It’s also the only study directly dealing with the effect of food additives on beneficial bacteria.

But there used to be one guy talking about the damage antibiotics do. Now we have a wealth of information confirming just how much damage messing with the gut microbiome can do.

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