At Earth Med Research, we endeavor to change the way people think about medicine. Science is waking us up to the reality that many chronic diseases today have complex environmental causes that may require intervention on many fronts. Leveraging this understanding, many forward-thinking physicians and patients have apparently already witnessed dramatic reversals or remissions of chronic diseases that – according to published science – have scarcely or sometimes even never been documented within the context of a controlled trial. It is our vision to investigate through controlled clinical trials whether or not such results can be reliably reproduced. To this end, we intend to pilot a model of decision-making which we term Robust Empirical Treatment. In this model, all (or many) possible contributing environmental causes of a chronic disease are simultaneously or sequentially targeted using a multi-interventional natural medicine protocol, even in the absence of proven etiology.
- Environmental Medicine – Identifying Upstream Causes
- Five Classes of Environmental Causes
- Complexity, Overlap, and Entanglement
- Natural Medicine – Targeting Environmental Causes
- Responding to Critics
- Evolutionary Tolerance and Therapeutic Versatility
- The Corruption of Evidence – It’s Worse than Most Realize
- Corruption Is Not One-Sided
- Fix, Don’t Reject
- Empiric Therapy – Questioning the Dogma of Proof
- Information Is Always Incomplete
- Balancing Overage and Underage Costs
- Proof Is Needed – Is That a Fact or a Belief?
- Keeping Pace with Disease
- Our Research Objectives
- EMR Newsletter
- Manufacturing Supplements
- Multi-interventional Clinical Trials
- Other Proposed Clinical Trials
Environmental Medicine – Identifying Upstream Causes
We believe it is largely correct to say that many of the chronic diseases we face today are not truly distinct, but are rather different flavors of one overarching environmental disease complex. Environmental medicine looks at the upstream root environmental causes of chronic disease. We define it as follows:
Environmental medicine is the subset of medicine concerned with any etiological factor that primarily originates externally to the human body and which can be targeted within or without the human body for the prevention and/or treatment of disease.
Our view of chronic disease today is that it is caused predominantly by the environment, and that other explanations such as longer lifespan, increased diagnosis, and genetic inheritance have become exaggerated in the medical mind. Moreover, such a disease-causing environment has come into existence largely due to the adverse activities of mankind. We believe all of these views are well-substantiated by published science.
Five Classes of Environmental Causes
We identify five major classes of environmental etiologies of chronic disease today. These are:
- Nutritional deficiency and poor diet
- Stress, trauma, and lifestyle
- Food allergies and sensitivities
- Chronic infection
As we progress through our article series, we will see that these etiological classifications almost uniformly fit every major chronic disease today. Although noninherited food allergies tend to be a complication of prior environmental factors, we mention it as an exception, owing to it being an important front of intervention.
We could loosely equate the use of our term “environmental” with the term “largely nonhereditary”.
Complexity, Overlap, and Entanglement
Throughout our article series we will be substantiating a 19-point environmental hypothesis of chronic disease. In it, we will discuss three important relationships between chronic diseases and their environmental etiologies:
- Complexity – Virtually every major chronic disease is associated with multiple members of each and every one of the five classes of environmental etiologies.
- Overlap – Individual members of a given class of environmental etiologies (such as a particular toxicant, particular dietary habit, particular infection etc.) are frequently linked to many chronic diseases, and not just one.
- Entanglement – Each of these five classes of environmental etiologies are not distinct but are rather interdependent. Members within a given class can cause or exacerbate members of a different class. For example, chronic infection could lead to food allergies, which in turn could lead to more inflammation, malabsorption, and nutritional deficiency, which could in turn weaken immunity and worsen infection, which could all make someone severely stressed, etc.
These are some of the reasons why our organization will be emphasizing multi-interventional clinical trials. In fact, failure to account for such complexity and entanglement could theoretically make the difference between interventions appearing worthless or even harmful when tested in isolation, and those same interventions becoming beneficial when tested in combination. For example, removing a knife from a wound without stopping the bleeding will not save a patient. Neither will stopping the bleeding without ever removing the knife. And even if you do both, you may still need to treat an infection that set in during the interim. Clinical trials could well conclude that all three of these are useless interventions if tested individually, and yet this would be a completely wrong conclusion as they could be curative when used together. We believe these phenomena of complexity and entanglement explain some of the discrepancy between the sometimes dramatic disease reversals environmentally-oriented clinicians are seeing in practice, and the relative lack of such dramatic disease reversals being documented in clinical trials. In other words, complementariness and perhaps at times even synergy of environmentally-oriented therapies are real things, and people haven’t fully realized it yet. The very way we have been looking at clinical research has not adequately reflected the realities of clinical practice where multiple interventions can be used, and where frequent reevaluation of treatment direction can occur. If a bucket has many holes, the more holes you plug, the better the results.
Natural Medicine – Targeting Environmental Causes
We define another abstraction called “natural medicine”. This describes medicines that are naturally occurring, without any molecular modifications not found in nature. Examples of natural medicines are vitamins, minerals, fatty acids, phospholipids, herbal products, amino acids, probiotics, and endogenously occurring chemicals like coq10, glutathione, alpha-lipoic acid, etc. Intravenous therapies like high-dose vitamin C or ozone autohemotherapy also count. Also included are activities such as exercise, meditation, sun exposure, sauna therapy, food allergy elimination, dietary changes, fasting, lifestyle changes, hygiene changes, grounding, EMF remediation, mold remediation, and toxicant remediation.
Take notice of the relationship between environmental medicine and natural medicine. Incidentally, the kinds of interventions that are needed to target environmental etiologies of chronic diseases are predominantly natural. Nothing can correct a magnesium deficiency except magnesium. No FDA-approved therapy can fix a horrible diet. Nothing can correct a lack of exercise and sunlight except exercise and sunlight. No drug can remove a food allergen from ones diet or prevent a chronic toxic exposure. And the list goes on. In fact, with the exceptions of anti-infective drugs and vaccines, there are very few pharmaceutical therapies that have even the potential to target the environmental causes of chronic disease. With distorted financial incentives, much of modern medicine has condemned itself to looking in a terminally mediocre direction that does largely deserve the term “symptom management”. Once realized, this forebodes both a perpetual failure to truly prevent and reverse most chronic diseases, as well as an eventual financial collapse. This is not to say that physicians don’t practice prevention with the tools that they have. But if our approach to prevention was really good enough, then why is the overall burden of chronic disease on the rise? We say it is because we have not been adequately looking at the environment, and that claims to the contrary are naive.
Responding to Critics
Some critics do not believe the drug industry lacks incentive to take natural medicines through to FDA-approval. This is largely untrue. Firstly, many natural medicines are activities rather than drugs. Secondly, natural medicines cannot be patented because chemical isolates are viewed as “discoveries” rather than “inventions”. The US Patent Office has explicit policies against granting patents for chemical isolates. Simple isolates are also less likely to require complicated manufacturing processes that mystify the layman. Thus often lacking the factors necessary to justify high prices and prevent competition, natural medicines are not on even footing with nonnatural analogues or entirely novel chemicals. While it is true that methods of purification or synthesis can be patented, this may not be uniformly sufficient to prevent competition from finding other ways to manufacture a given natural medicine. Furthermore, many of the natural medicines we are searching for as a society are already commercially available as low-cost dietary supplements. Many of them have enough research to have led to very positive systematic reviews and meta-analyses. The only way the drug industry could highly profit from them would be through a nonnatural modification. Distorted motive is even evidenced by the fact the industry is scarcely developing antibiotics, even though they could be patented. Antibiotics are taken short-term and don’t maximize profit.
Testing combinations of natural chemicals is also eschewed by profit motive. We isolate plant chemicals and try to determine their effects. But what if the best efficacy can be achieved by a combination of unpatentable chemicals? This is especially of concern with regards to cancer and infection, and avoiding drug resistance. Combination therapies may also allow for diversification of toxicity (i.e. low doses of a combination of chemicals, versus a large dose of a single chemical), potentially making therapies safer. Yet industry would be hard-pressed to find a way to patent and manufacture every chemical in such a combination in a way that is still maximally profitable.
Some would still argue that analogues of natural medicines are made for the sake of increasing efficacy and/or decreasing toxicity. Yes this happens, but only incidentally to a process of greed. Is it uniformly the case that such chemicals outperform their natural counterparts? Cherry-picking a few examples would not count as proof. Proof would require at minimum a systematic review of animal studies of analogue drugs (that were either hoping for approval or received approval) that shows the analogues by and large have superior chronic toxicity profiles than does their natural counterparts, perhaps expressed as percentages of their respective equivalently efficacious doses. To the best of our knowledge, no such review exists. And even if it did, it would not count as a replacement for a systematic review of a nonexistent body of head-to-head clinical trials that test natural medicines versus their respective patentable analogues. If such research were to exist, we believe that natural molecules would do as well or better than their FDA-approved counterparts a substantial percent of the time. Consider that there already exists a sizable body of head-to-head trials where such allegedly inadequate dietary supplements match or outperform FDA-approved drugs that aren’t in any way structurally related. And it turns out that adjustments for bias in these trials would even further favor the natural medicines. Where then are the FDA-approved analogues of these supplements? We will review this topic in the future. We will also be presenting a general review of the safety of dietary supplements, which will include some examples of analogues that become more toxic than their natural counterparts . The data suggests that overall, natural medicines do have a tendency to be safer than nonnatural pharmaceutical drugs. The view that such an apparent safety is only due to testing irrelevant doses that are too low to be effective is contradicted by a large body of clinical trials and epidemiological studies.
Evolutionary Tolerance and Therapeutic Versatility
We posit two properties of many natural medicines that tend to make them functionally different from nonnatural drugs:
- Evolutionary tolerance – Materials we are exposed to either through our diet or through endogenous synthesis have been with us a long time. And such materials describe a large portion of our abstraction called natural medicine. It is reasonable to conjecture we have evolved to better tolerate several such materials.
- Therapeutic versatility – Many natural medicines have demonstrated efficacy in randomized controlled trials against not just one, but multiple chronic diseases. Many natural medicines are also associated with reductions in all-cause mortality. Some of these reductions are quite large. Nutrients and endogenous chemicals have myriad purposes – sometimes hundreds. Nature has rarely evolved anything relevant to us that has only a single narrow beneficial biological activity. This is fundamentally different from nonnatural drugs which are typically designed to have narrow targets. Unlike having to worry about balancing the benefits versus the risks of a drug, many natural medicines may provide benefit in a given disease while simultaneously reducing the risks of several other diseases.
In addition, natural medicines are as a whole dramatically cheaper than patentable drugs, potentially making them far more cost-effective. Hence, for all the reasons discussed, we reject the view put forth by some skeptics that creating a rough abstraction between natural and nonnatural medicines is not a substantial point of discussion. We are not proposing a dichotomy – just an abstraction that describes functional and economic tendencies.
The Corruption of Evidence – It’s Worse than Most Realize
There are many problems with the genesis of so-called “evidence” in medicine, which will be a major theme of our article series. In our opinion, peer-reviewed research has shown that industry fraud is the norm and not the exception. Drug companies hide trials they don’t like. They willfully use placebos that aren’t actually placebos. They willfully bias the selection of patients. They claim their trials are blinded when they know the blinding has been broken. They choose trial durations that they know will give them the best results. They only report the select outcome measures they like. They present negative or tiny effects with flowery wording and relative measures that make them sound very positive. They underreport adverse events or else rename them as something more flattering. They flatly omit bits of data they don’t like, falsely claiming they are inconsequential. Thus they succeed in presenting the FDA with studies carefully engineered to show benefit, regardless of reality. And even so, they may still only succeed in showing a marginal benefit. Then they bias the FDA officials and advisory committees who have serious conflicts of interest in deciding whether or not to approve a drug. The FDA may even approve a drug that lacks even this much distorted evidence, instead asking for postmarketing research. But once a drug is approved, you know the chances of its approval ever being revoked in a timely fashion are slim. Then drug companies market the drugs to physicians and present them narratives that don’t match what the FDA has authorized them to say. Then they advocate off-label prescribing, using drugs for situations they have never been approved for. They fund ghostwritten studies to give the illusion of independent research. Then journals funded by ads publish drug recommendations that are less critical than journals funded by subscriptions. Then we find out years later about the long-term increased risks of other diseases from taking a drug – risks that are never tested for in relatively short-term studies prior to FDA-approval. And even once that happens, the FDA drags its heels in warning consumers about the risks. And when it does, it is through tiny letters on a label that no one will ever read. Then to top it off, such drugs of questionable safety are used in cocktails that have scarcely been studied as such. The overall impact of taking combinations of toxic drugs has not been adequately assessed, and a growing body of evidence suggests that there is reason to be concerned. All of these problems – and more – have in our opinion been clearly demonstrated in peer-reviewed research, and we will discuss these issues at length.
Though there is growing awareness about all of the abovementioned problems, we believe there is still grossly inadequate appreciation for how severely the value of scientific research is compromised when it is considered that all of these issues are compounding one another simultaneously. We go so far as to say that there is not a new FDA-approved drug for chronic disease today that is truly “proven” – at least not at the moment of its FDA-approval. We believe that many presently approved drugs are going to ultimately be rejected for causing more long-term harm than good.
Corruption Is Not One-Sided
Though many may feel disillusioned with the questionable evidence behind many pharmaceutical drugs, it must also be admitted that many problems plague the dietary supplement industry as well. Companies hide their cheap ingredients behind pseudoscientific marketing terms, allowing them to mark up the price. This is the natural medicine substitute for patenting a drug. Or people rely too heavily on anecdotal evidence, cherry-picked studies, misleading relative risks, studies of poor design, etc. In other words, the problems in medicine exist on all sides of an imagined fence, and not just one of them. Though we will say that the dietary supplement industry is not nearly as practiced in these arts of deception as is its larger pharma counterpart. Their products are generally also not nearly as risky.
Fix, Don’t Reject
The solution is not to reject the present medical system, but to fix it. In theory, legislation could fix many of the problems of corruption we are facing. We should not be cynical and believe such changes could never happen. And even in the absence of corrective legislation, a piece of bad science can only harm us if we fail to exercise adequate skepticism. And we must also realize that the very fact we know about all the various facets of scientific corruption is precisely because there are aspects of academic science that are working reasonably well.
Empiric Therapy – Questioning the Dogma of Proof
The terms empiric therapy or empirical treatment refer to medical treatment that is undertaken in the absence of complete or perfect information. This information can be incomplete either in the sense of not being certain of the cause of a disease, or in the sense of not being certain of the effect of a treatment. We argue that empirical treatment that simultaneously targets multiple potential environmental etiologies of chronic disease using low-risk natural therapies is actually a sensible approach.
Information Is Always Incomplete
The first thing we need to realize is that information is always incomplete. Many drugs are prescribed based on averages. A drug might have a Number-Needed-To-Treat (NNT) of 10 or even 50. That means you might have to prescribe a drug to 50 people just to result in only 1 person actually being benefited. The other 49 people would only experience risks. On average, such a therapy may be viewed as doing more good than harm. But if you look at just the subset of nonresponders, that therapy may on average yield harm without benefit. And yet this can very well pass as a “proven” therapy in evidence-based medicine (EBM). But does this really deviate much from the definition of “empiric therapy”? After all, within a given individual, you do not have complete information as to whether or not that patient will experience more help than harm. Furthermore, for all the realities of corruption which we have already discussed, the reliability of much of published medical science is not nearly what many may still believe it to be. It is for these reasons that we insist that medical “proof” is something that exists by degrees, and that it is rarely a strictly binary descriptor.
Balancing Overage and Underage Costs
A key concept in decision analysis is the effort to balance overage and underage costs. A classic illustration of this concept is called the “newsvendor model”. A newsvendor is faced with deciding how many newspapers to print on a given day in the face of uncertain demand, and knowing that unsold copies will be worthless the next day. The underage cost is the cost of a lost sale due to not stocking enough papers. The overage cost is the cost of wasting an unsold paper. Depending on these parameters, mathematical analysis can be used to recommend an optimal number of papers to print. If for example, the cost of printing a newspaper is only a fraction of a cent, and a newspaper sells for a dollar, the optimal decision would be to print way more papers than you expect to sell.
How can this concept be better applied in medicine? Say a physician has a patient with a chronic disease. He has identified 10 natural therapies that either exhibit therapeutic versatility or else target one of several potential contributing environmental causes of the disease. He decides to use all 10 natural therapies simultaneously. If we assume that all of these hypothetical therapies have no overage costs, and that each has an independent 10% chance of benefiting (NNT= (1/0.1)=10), then the probability of this patient benefiting from at least one intervention is 65% (1-(0.910)=0.65). Thus the overall treatment has a Number-Needed-To-Treat (NNT) of only 1.5. In other words, it is theoretically possible to use relatively unproven therapies in combination or in sequence, and yet have the overall therapy be highly likely to benefit, having been based on a reasonable science of decision-making. Natural medicines lend themselves to such a scenario owing to low overage costs and therapeutic versatility. We argue that this line of thinking may be further merited by phenomena of complementariness and synergy, which we have already mentioned.
Proof Is Needed – Is That a Fact or a Belief?
There is a widespread mentality that using only proven therapies is what will optimize outcomes. But this approach is by definition only a heuristic. How can we actually know one heuristic is better than another within a specific context? The ideal way would be to formulate medical decisions as a definite mathematical model, and test competing heuristics . But the real world is far too complex to reduce it to such a model.
The next best approach is to track outcomes under multiple competing heuristics, and then compare. We intend to do exactly this. We propose a decision-making paradigm called Robust Empirical Treatment (RET). In RET, all (or many) potential environmental etiologies of a chronic disease are simultaneously or sequentially targeted using multiple low-risk natural therapies, even in absence of proven etiology. Our proposed head-to-head clinical trials could form the beginning of such a comparison between two different decision-making paradigms. We believe that the results of such trials might very well bring a central dogma of EBM into serious question. These trials may ultimately substantiate an approach that complements EBM, helping us to function better in clinical practice in areas where science is relatively incomplete, or might never be complete.
Keeping Pace with Disease
Overall, chronic disease is on the rise. We must face the possibility that the present paradigm of evidence-based medicine that aims to make decisions by emphasizing a high level of evidence for each and every isolated treatment and etiology may simply not be able to keep pace with the evolution of chronic disease. By the time environmental associations with disease have been solidly proven to be causal, the disease we seek to treat might no longer exist. Its complex environmental etiologies might have already evolved into something else. Completely new diseases will also surface. Furthermore, testing isolated interventions may be unable to adequately account for the aforementioned issues of complexity and entanglement. Interventions tested individually may appear ineffective, and yet be effective when tested in combination. Hence, investigating other more adaptive paradigms of research and treatment decision-making not only makes sense, but may in the long run be the only chance we have of avoiding a crippled society that failed to generate science fast enough.
A New Strain of Physician
A widespread movement of nonconforming physicians is growing. Terms such as “alternative”, “natural”, “integrative”, “holistic”, “environmental”, and “functional” medicine are becoming more common. And yet these terms don’t actually have any clear definitions. We will be the first to admit that a lot goes on in the names of these kinds of medicine that really doesn’t make sense. But what happens after all such negative elements are pushed aside? Is there any substance left to this movement? We believe that there is, and at its core, we identify three primary shortcomings of EBM for which many of these physicians feel compelled to distinguish themselves. We have already alluded to these:
- A bias towards drugs and away from addressing environmental etiologies – A literacy deficit truly exists. Most physicians are simply not aware of a lot of material that they need to be reading. Except in situations where immediate stabilization is needed, it is sensible to always address upstream environmental etiologies of chronic disease prior to embarking on indefinite drug therapies that have narrow downstream biological targets and give no chance of cure. The need for drugs can be reduced or completely eliminated more often than people realize.
- Inadequate appreciation of fraud and fallacy – Again, a literacy deficit truly exists regarding the true extent of harm, fraud, bias, and fallacy in industry-funded medicine. Even many well-read medical skeptics somehow fail pick up on quite a lot of literature that would enhance their skepticism of many FDA-approved therapies. As we will argue, many drugs are actually doing more harm than good. Thus the imperative to “first do no harm” is a major factor in what drives a physician to rebrand himself and place greater emphasis on generally safer natural therapies.
- Inadequate appreciation of empiric therapy – As we have argued, using multiple low-risk therapies that have varying degrees of evidence in order to empirically treat likely environmental etiologies of chronic disease is exactly what needs to happen. Yet physicians have been trained to think otherwise.
Hence, despite its defects, we view this growing movement among physicians to have at its core a set of necessary adjustments that need to be made to EBM.
Our Research Objectives
At Earth Med Research, we intend to contribute towards these needed corrections in the following ways:
We have identified approximately 125 topics we wish to review through our online article series. These articles will serve as a basis for demonstrating the sensibility of our proposed clinical trials. They will review environmental associations with major chronic diseases. They will also review clinical trials that have occurred with natural medicines in those diseases. Among other things, this will enable us to identify the natural medicines that exhibit the most therapeutic versatility, as well as the environmental etiologies that exhibit the most overlap between diseases. Our article series will also give us a chance to dialogue with the public and refine our hypotheses and research agenda. We will also be taking a skeptical look at many purportedly evidence-based therapies. Insensibilities within the world of alternative medicine will also be examined. We will attempt to offer an environmentally-oriented look at medicine today that avoids inflammatory narratives present in many websites.
In advance of conducting our clinical trials, it will be necessary to formulate and manufacture a line of dietary supplements to be used in those trials. In practice, we are not satisfied with the materials presently available on the market. Some of the reasons we have this view are as follows:
- Overpricing – We are confident we can do a lot better than much of what is presently available. Some ingredients may be dirt cheap to buy in bulk, yet be sold for high prices for no other reason than its being in vogue.
- Failure to formulate as a system – There are many considerations that need to be made regarding how supplements interact with each other. And when supplements do attempt to account for this, they do not always correctly interpret what the evidence indicates should be done.
- Physical inconvenience – Many supplements that would be important in the context of our clinical trials are sold individually. With commercially available options, a patient might well be asked to swallow 30 or more capsules in a day. To overcome this, we will be emphasizing liquid supplements, which avoid fillers, and allow for many ingredients to be delivered in a compact manner.
- Nonsensical doses – Sometimes, dosing just makes no sense in light of published science. Sometimes the absence, presence, amount, and ratios of ingredients are incidental to where the material is cheaply sourced from, rather than being an intentional formulation from scratch.
- Safety – It turns out that one of the most serious risks of dietary supplements is actually choking. This is a reason we will be formulating liquids. Some important supplements are also known to be reactogenic. We advocate liberal use of ramping in order to control the severity of potential Jarisch-Herxheimer and detoxification reactions. Liquids facilitate this. In other instances, products may simply have unsafe doses of certain ingredients.
- Inadequate delivery vehicles – Some materials are poorly absorbed or are damaged by stomach acid. Even if not, some materials are simply made more effective when delivered properly. Examples of useful delivery vehicles are liposomal encapsulation, mineral chelation, and acid-resistant capsules.
- Incorrect forms of nutrients – A formula may simply fail to include the form(s) of nutrients that have been clinically substantiated.
- Patient-to-patient variability – There is also significant patient-to-patient variability in absorption and/or retention with respect to a number of materials. In fact, there might be ample research to substantiate a particular widespread nutritional deficiency, and yet at the same time there may be no good science on how to reliably correct that deficiency. Aside from leveraging delivery vehicles, we will be diversifying the forms of nutrients in order to hedge against these uncertainties.
Tentatively, we intend to make commercially available a total of 6 dietary supplements. These are:
- A liposomal formula including vitamins (A, B-complex, C, D, full spectrum E, full spectrum K), phytochemicals (green tea extract, curcumin, resveratrol, astaxanthin, ecklonia cava extract), and endogenous chemicals (glutathione, alpha-lipoic acid, acetyl-L-carnitine, CoQ10).
- A complete liquid mineral supplement which includes generally neglected minerals (such as silica, lithium, boron, molybdenum, rubidium, iodine, indium, vanadium, chromium, etc.), and which diversifies the forms of minerals by chelating a portion of each to the amino acid glycine.
- An amino acid and MSM supplement, formulated in ratios shown to cause the amino acids to almost entirely follow the anabolic pathway.
- A poly-herbal formula. Herbal polypharmacy is discussed more on our research page.
- Electrically isolated silver (a.k.a. colloidal silver). EIS is also discussed more on our research page.
- Probiotics with as many strains as possible (tentatively 25), and delivered in a capsule that survives the stomach acid, and which can also be used as a starter to make a novel probiotic drink.
Our article series will give us ample opportunity to discuss and refine the formulation of these supplements. Sales of these supplements will support our organization and help us fund our proposed clinical trials. We wish to build a small line of products that people can trust, and that simplifies the bewildering experience many may have of exploring the endless world of dietary supplements. Our formulations will always be completely transparent. We will also disclose the true cost of materials of all of our products. In fact, we will encourage others to replicate our formulas and will even be willing to certify other products as being functionally equivalent. In the event our clinical trials have positive results, we definitely want to make sure these materials are cheaply available to all. We really have no interest in getting into the supplement business. It is just that we view it as necessary. Also, having a relatively standardized line of supplements may be important in the event others wish to reproduce our clinical results.
Multi-interventional Clinical Trials
As we have mentioned, our ultimate aim is to empirically treat multiple chronic diseases with a robust multi-interventional natural medicine protocol that targets many likely environmental etiologies simultaneously or sequentially, and that further incorporates multiple natural medicines that exhibit therapeutic versatility. We term this heuristic as Robust Empirical Treatment. On our research page we have described 14 tentative types of interventions we wish to uniformly apply in most of today’s major chronic diseases. In addition to the above-mentioned 6 dietary supplements, we also wish to include dietary changes, food allergy elimination, exercise and sun exposure, meditation, oral hygiene modifications, possible mold avoidance, and a number of energy oriented therapies including grounding, EMF remediation, and blue-light remediation. As needed, other individualized therapies may also be used. This multi-interventional natural medicine protocol will be tested against each disease’s respective standard treatments. Placebo-controlled trials are infeasible due to the impossibility of avoiding unblinding with so many simultaneous interventions. Subjective outcome measures will be eschewed as far as possible in favor of objective tests and “hard” outcomes. Where unavoidable, the test protocol may include standard drugs and other treatments as adjuncts, with a view to tapering drugs if health improves sufficiently. We will attempt to enroll patients who have been recently diagnosed. Primary outcomes will be specific to each disease, but there will also be a standardized secondary set of outcomes. Most trial durations are tentatively 1 year. Participants will be required to enroll an advocate to help understand and comply with this complex protocol. Online forums will be established to enable group dialogue between trial participants as well as investigators. We will consider testing this protocol (or modifications thereof) in all of the following chronic diseases, disorders, and scenarios:
Type 2 diabetes and diabetic neuropathy, fibromyalgia, rheumatoid arthritis, osteoporosis, COPD, chronic fatigue syndrome, hypertension, heart disease, Alzheimer’s disease, Parkinson’s disease, Crohn’s disease, kidney disease, multiple sclerosis, obesity, schizophrenia, autism, chronic Lyme disease, congestive heart failure, multiple cancers, mold illness.
We may also consider tailoring multi-interventional treatments for the following diseases and scenarios:
Stroke recovery, chronic spinal cord injury, vaccine-injury recovery, antidepressant discontinuation, and opiod discontinuation.
We hypothesize that the results of such trials will overall be very positive, with instances of either dramatic reversal or complete remission being documented in several trials.
We may also at some point consider doing a large prospective long-term study of our protocol that looks at all-cause mortality as the primary outcome. We hypothesize a large reduction would be evident.
Other Proposed Clinical Trials
We have other trials planned related to Lyme disease and Rife machines, electrically isolated silver, herbal polypharmacy, specific infectious diseases, sepsis, hair quality, and hair loss. Read our research page for more discussion of these.
How You Can Support Earth Med Research
What we have described is an ambitious long-term vision. And of course, if results don’t pan out, entire lines of research would have to be discarded. In any case, we feel our research agenda is in line with the kind of research that at least several million Americans would like to see happen. We don’t know how far we will get towards our goal of conducting these trials, but we are daring to dream big. One thing that is certain is that we will not be able to accomplish these goals without the support of a large community. Here’s how you can help:
- Subscribe to our newsletter
- Leave constructive comments on our articles. Balanced criticism is more helpful than praise.
- Share and dispassionately discuss our articles on social media.
- If you are an MD or scientist who may be a match for our Board of Advisors, feel free to reach out to us.
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Let’s work together for a better medical system.