Dietrich K.Klinghardt, MD, PhD
Bellevue WA email@example.com 1/7/05
In the last decade the majority of outcome-oriented physicians observed a major shift: we realized that it was neither the lack of vitamins or growth hormone that made our patients ill. We discovered that toxicity and chronic infections were most often at the core of the clientâ€™s suffering. We watched the discussion, which infection may be the primary one: mycoplasma, stealth viruses, HHV-6, trichomonas, Chlamydia pneumoniae, leptospirosis, mutated strep, or whatelse?.
The new kid on the block is Borrelia Burgdorferi (Bb) and some of us have looked at it for a long time as possibly the bug that opens the door for all the other infections to enter the system.
Lyme disease has become a buzzword in the alternative medical field. Since none of the recommended treatments are specific to either one of the microbes, we can never assume that we really know what we treated once a patient has recovered. Microbiologist Gitte Jensen, PhD had shown, that the older we get, the more foreign DNA is attached to our own DNA. Somewhere along the line pathogenic microbes invade the hostâ€™s DNA and become a permanent part of it. Since we use only 2% of our DNA, it may not be a problem. In fact, it may make us who we finally become. It may also cause a number of symptoms and chronic illness. Genius Guenther Enderleinâ€™s discoveries take us off the hook: if one microbe can change into another given the right environment, why bother to find out, who we are infected with? . The bookâ€Lab 257â€ suggests that Bb is a an escaped man- made US military bio-warfare organism (just like myoplasma incognitus and HHV 6).
Other authors suggest that different subtypes of Borrelia which cause illness in humans, such as B. afzelii and B.garinii have probably existed longer then B.burgdorferi and occur naturally (1, 2) and have been with us for a long time, maybe centuries or more. Neurologist Prof. J.Faust MD, PhD of the Albert-Ludwig University in Freiburg, Germany (3) related many neurological and psychiatric illnesses to spirochete infections as early as the 1960s. He was so skilled in his clinical knowledge that he could â€“ only based on clinical neurological symptoms – accurately predict which valley in the Black Forest the infected patient was from! This clearly was a time before Bb – showing that non-syphilis spirochete infections were around earlier then the famous Bb outbreak in Connecticut in the mid seventies. It also makes a strong statement to the fact how easily these creatures may mutate and adapt to local conditions. It may however validate the findings published in â€œLab 257â€: Tuebingen, the place where German/US warfare spirochete expert Traub was continuing his spirochete experiments in the early 50s, is situated in the Black Forest also. Were these spirochetes genuine or have they escaped from a university laboratory?
Making the diagnosis
It appears, that many patients with MS, ALS, Parkinsonâ€™s disease, autism, joint arthritis, chronic fatigue, sarcoidosis and even cancer are infected with Borrelia burgdorferi. But is the infection causing the illness or is it an opportunistic infection simply occurring in people weakened by other illnesses.
My experience is based on
a) using direct microscopic proof of the presence of Borrelia burgdoferi (Bb) and other spirochetes (4, 5)
b) the information many affected clients have brought to me
c) my own clinical training and experience ( 30 years in Medical practice, 15 years Bb cognizant)
d) ART testing (autonomic response testing), which is the most advanced and scientifically validated method of muscle testing (6)
e) lab parameters affected by Lyme:
â€¢ Abnormal lipid profile (moderate cholesterol elevation with significant LDL elevation)
â€¢ insulin resistance
â€¢ borderline low wbc, normal SED rate and CRP
â€¢ normal thryroid hormone tests but positive Barnes test and excellent response to giving T3
â€¢ type 2 (high cortisol, low DHEA) or type 3 adrenal failure (low cortisol and DHEA)
â€¢ low testosterone and DHEA
â€¢ decreased urine concentration (low specific gravity)
Bb tends to infect the B-lymphocytes and other components of the immune system which are responsible for creating the antibodies, which are then measured by an ELISA test or Western Blot test. Since antibody production is greatly compromised in infected individuals, it makes no sense to use these tests as the gold standard or benchmark for the presence of Bb (7). We also are aware that in endemic areas in the US up to 22% of stinging flies and mosquitoes (2, 8, 9,10) are carriers of Bb and co-infections. In South East Germany and Eastern Europe 12 % of mosquitoes have been shown to be infected. Also many spiders, flees, lice and other stinging insects carry spirochetes and co-infections.
Making the history of a tick bite a condition for a physician to be willing to even consider the possibility of a Bb infection seems cynical and cruel.
To use conventional diagnostic tests such as the Western Blot, one has to think in paradoxes: the patient has to be treated with an effective treatment modality first before the patient recovers enough to produce the antibodies, which then are looked for in the test. A positive Western Blot proves that the treatment given worked to some degree.
A negative Western Blot does not and cannot prove the absence of the infection.
Having taken another route altogether, we have recognized the following:
Today many if not most Americans are carriers of the infection. Most infected people are symptomatic, but the severity and type of the symptoms varies greatly. The microbes often invade tissues that had been injured: your chronic neck pain or sciatica really may be a Bb infection. The same may be true for your chronic TMJ problem, your adrenal fatigue, your thyroid dysfunction, your GERD and many other seemingly unrelated symptoms.
In most places the diagnosis of an active Bb infection is made only, if the symptoms are severe, persistent, obvious and many non-specific and fruitless avenues of treatment have been exhausted. Acute new â€œtypicalâ€cases of Bb infection are rare in my practice. Symptoms tend to get stranger and more obscure every year.
Frequently, if the patient is fortunate enough to see a practitioner who is â€œLyme cognizantâ€, the diagnosis of a supposedly fresh case of symptomatic Lyme disease is made when a significant tissue toxin level has been reached (threshold phenomenon) or when a new co-infection has occurred recently. The symptoms can mimic any other existing medical, psychological or psychiatric condition. The list of significant co-infections is limited: roundworms, tapeworms, threadworms, toxoplasmosis, giardia and amoebas, clostridia, the herpes virus family, parvovirus B 19, active measles (in the small intestine), leptospirosis, chronic strep infections and their mutations, Babesia, Brucella, Ehrlichiosis, Bartonella, mycoplasma, Rickettsia, Bartonella and a few others. Molds and fungi are always part of the picture. The pattern of co-infections and the other preexisting conditions such as mercury toxicity determine the symptom-picture but not the severity.
The severity of symptoms correlates most closely with the overall summation or body burden of coexisting conditions and with the genetically determined ability to excrete neurotoxins. The genes coding for the glutathione S-transferase and for the different alleles of apolipoprotein E (E2, E3 and E4) play a mojor role. E2 can carry twice as much sulfhydryl-affinitive toxins (such as mercury and lead) out of the cell as the E3 subtype, E4 carries out none. Trouble in the methylation, acetylation and sulfation pathways are also common. Other factors, such as diet and food allergies, past toxic and electromagnetic exposures, emotional factors and unhealed ancestral trauma, scar interference fields and occlusal jaw and bite problems are also important (6).
Taken all of the above into account, we do not distinguish between people who have the Bb infection and those who donâ€™t. We distinguish between people who have Lyme disease and those who donâ€™t.
a) patients who are infected with any type of Borrelia and are symptomatic have â€œLymeâ€disease
b) healthy people who are not symptomatic often already have a spirochete infection as well. They may or may not be disasters waiting to happen. But they do not (yet) have Lyme â€œdiseaseâ€. Most often several of the â€œco-infectionsâ€ are already present prior to the infection with Bb or other spirochetes.
In treatment we focus on exploring the difference between symptomatic and asymptomatic carriers. We treat what the symptomatic person is missing (such as enough magnesium in the diet) or has extra (such as mercury) compared to the asymptomatic one. The group suffering most are newborn babies and young children, who rarely are diagnosed correctly and therefore are not treated appropriately. They often carry the labels ADHD, autistic spectrum disorder, seizure disorder and others. Detoxifying these kids with transdermal DMPS and treating the chronic infections is often curative.
The 3 Components of Lyme disease
Lyme disease has 3 components, which should be recognized and addressed with treatment:
The presence of spirochete infection and co-infections
The co-infections are bacterial, viral, fungal and parasitic. Since the spirochetes paralyze multiple aspects of the immune system, the organism is without defenses against many microbes. Many – if not most – of the co-infections are really a consequence of the spirochete infection and not truly a simultaneously occurring â€œco-infectionâ€.
For this aspect of treatment we use pulsed electromagnetic fields (KMT-microbial inhibition frequencies), niacin in high doses (12)herbs, minerals, bee venom (6) and – sometimes – antiparasitic medication and antibiotics.
The KMT microcurrent technology is new and revolutionary(17). The instruments are FDA approved for pain control. Designed by Japanese engineers they use 4 different – but simultaneously applied – high frequency superimposed biological waveforms. The interference pattern is creating thousands of harmonics which are then manipulated into the specific published microbial inhibition frequencies ( against Bb, mycoplasma etc.). This stealthy microcurrent travels freely through the body reaching every tissue. The instrument measures the skin conductance over a 100 times/second adjusting the amperage constantly (so that the body never creates habituation/resistance against it). The microbes are inhibited in their metabolic and sexual activity and gradually die out or disappear from the body. The instrument looks not much different then a TENS unit and is applied via 4 electrodes to the skin or used by translating the electric field into a vector force field using signal enhancer technology. The KMT frequencies are designed to not only interfere with the reproductive mechanism of the microbes and parasites, but also to awaken the immune system, entrain the white cells to recognize the invaders and at the same time help to absorb and shuttle the effective medication to the body compartment, where the infection actually is. Otherwise, most treatment substances given never reach the target in sufficient concentration.
Component #2: the illness producing effect of microbial exo- and endotoxins
Most of these are neurotoxins, some appear to be carcinogenic as well, others block the T3 receptor on the cell wall, etc. Decreased hormonal output of the gonads and adrenals is a commonly observed neurotoxin mediated problem in Lyme patients. Central inhibition of the pineal gland, hypothalamus and pituitary gland is almost always an issue that has to be resolved somewhat independently from treating the infection. Furthermore, biotoxins from the infectious agents have a synergistic effect with heavy metals, xenobiotics and thioethers from cavitations and NICO lesions in the jaw and from root filled teeth. My published neurotoxin elimination protocol can be downloaded for free (6).
We use toxin binding agents such as fiber rich ground up raw vegetables, chlorella, cholestyramine ( 13 ), beta-Sitosterol, propolis powder, apple pectin and mucuna bean powder ( 14 ). A solid heavy metal detoxification program should be used simultaneously with the first phases of the Lyme treatment. Safe toxic metal elimination is an art unto itself. However, the information is widely available now( 15 ).
The more difficult objective is to choose agents and methods to trigger the release of neurotoxins from their respective binding sites. Only then can they be transported to the liver, processed and enter the small intestine from where they can be carried out by the binding agents. The toxins occupying the T3 receptor are competitively displaced by oral T3 – cycled with the Wilson protocol (available at most compounding pharmacies). The toxins blocking the cortisol receptor are mobilized with the herb forskolin. CGF chlorella – a sophisticated mix of chlorella and chlorella growth factor (14) – and cilantro given together with a non-irradiated mucuna bean powder mobilize most everything else. I also use alternate day dosing of an energetically enhanced phospholipid/EDTA/Alpha-Lipoic acid mix (â€œPhospholipid Exchangeâ€) which is currently the most tolerated and effective form of phospholipids for the Lyme patient (14).
The KMT microcurrent frequencies dramatically increase the speed of toxin mobilization and access body compartments the biochemical compounds cannot (17). Psychotherapeutic intervention (15) to uncover and treat old trauma is most profoundly effective in triggering a neurotoxin release when none of the other methods appear to work anymore. After each APN session we pre-medicate the patient with CGF-chlorella. Sometimes the extraction of a devitalized tooth or the injection of one of the facial/cervical ganglia with glutathione or another detox agent can trigger a major neurotoxin release (16). Lymph drainage in combination with colon hydrotherapy accesses toxins stored in the lymphatic body-compartment.
The immune reactions provoked by the presence of both toxins and microbes (there are 3 sub-possibilities, which have to be recognized and addressed)
The immune reactions are largely depending on host factors, such as genetics, prior illnesses, mental-emotional baggage, early childhood traumatization, current exposure to electromagnetic fields (sleeping location, use of cell phones, poor wiring in car or home, etc), food allergies and diet, socio-economic background, marital stress etc.
1: Anergy – the absence of reaction due to the successful evasion of the host-defenses . One of the more known mechanisms the microbes use to create anergy is hypercoagulation. The microbes tend to live in the endothelium, where the food is most abundant. They trigger the hostâ€™s coagulation mechanism to lay down a layer of fibrin on top of them to evade recognition by the immune system. etc. For this aspect we use 3 techniques: a) the KMT-microcurrent technology and homeopathics to wake up and entrain the immune system
b) Rechtsregulat (â€œright rotatory fluidâ€) which is an enzyme rich extract of fermented fruits and vegetables (14). It has outperformed the s.c. injection of heparin in our own trials. Lumbrokinase is far more effective then Nattokinase. Both appear weak when compared to Rechtsregulat. We also clientâ€™s system (geopathic stress, EM stress, food allergies, emotional factors, interference fields such as scars and disturbed ganglia and we substitute vitamins and minerals based on ART testing).
c) the Enderlein remedies (especially the haptens) from Pleomorphic-Sanum
B: Allergy – appropriate or exaggerated immune reactions (both cellular TH1-reaction and TH2-cytokine activation). In Lyme disease often (not always) the TH2 (humoral portion of the immune system) is overly active, TH1 is asleep (the cellular immune system). Nothing works better then the APN-desensitization procedure (15): while the patient is exposed to the allergen ( we use a glass-carrier fixated culture of the offending microbes) the ANS is kept in a state of equilibrium, using tapping of acupuncture-points, hypnotherapeutic trauma-recall and intervention techniques and our proprietary psychokinesiology (muscle-biofeedback psychotherapy). A very effective and yet simple technique to turn TH1 back on is auto-urine therapy. The patientâ€™s urine concentrates the antigens (disposed cell walls and cell fragments of offending microbes which the immune system has successfully eliminated). By passing the clientâ€™s urine through a micropore filter and injecting it i.m, the lymphocytes on patrol in the connective tissue are brought in contact with the antigen and quickly mount a specific and appropriate immune response. We use 2 ml of filtered urine once weekly for 12 weeks. All other similar approaches (autohemotherapy, homeopathic autonosodes, manipulating the immune system with supplements) are far less effective.
C: Autoimmunity â€“ the toxins and microbes often act as haptens â€“ marking the cell, cellwall or tissue in which they are hiding as foreign and therefore for destruction . This happens especially against a back drop of pre existing heavy metal toxicity, which has to be addressed aggressively and prior to treating the microbes themselves. We use the MELISA test (memory lymphocyte immune-stimulation assay) to establish which metals the patient is reactive to. The same lab in Bremen, Germany also offers the most sensitive Bb test. The KMT microcurrent technology is very effective in recognition entrainment, helping the immune cells to mount a specific and targeted attack on the invaders, sparing the bodyâ€™s own tissues. It breaks through one of the prime mechanisms the offending germs are using: molecular mimicry (the pathogens present antigens on their surface that are indistinguishable from a normal body tissue).
The technique also breaks another trick the spirochetes have developed: the molecular interaction that occurs between a specific Lyme virulence factor (OspE) and a host protein fH (factor H).
The novice in the field tends to treat component #1 only. We have only rarely observed lasting improvement when course after course of antibiotics was given. Because of the defense mechanisms inherent in the Bb and co-infections, current wisdom suggests that 18 months of antibiotics would be curative in many cases (25). We have observed severe, lasting and unacceptable side effects from this approach (such as tinnitus, kidney failure, intractable immune system breakdown and others). By using the synergistic effect between treatment-modalities which simultaneously address the 3 issues outlined above, lasting improvements are the norm rather than the exception. By using the synergy principle and abandoning the arrogant idea of being able to eradicate all of the microbes in the system â€œfor goodâ€, chronic Lyme patients can often live a normal healthy life again.
The Mineral Issue
To feed, fuel and perk up the cells of the immune system (especially NK cells and macrophages) numerous interventions have been tried, mostly based on orthomolecular and herbal medicine principles. We found that amongst those approaches, abundant mineral substitution based on the red cell mineral analysis is most rewarding. Rarely medical drugs should be used.
Amazingly, the most depleted minerals in our Lyme patients are often copper, magnesium, manganese ( in Lyme) and iron (in Babesiosis). Bb and Bartonella need magnesium to duplicate and deplete the hostâ€™s body rapidly. Copper and iron have all but disappeared from most of our supplements based on faulty interpretation of hair analysis. The immune system uses those 2 metals in the process of phagocytosis. They are the main constituent of the enzymes (or â€œbulletsâ€) the immune cells use in the battle against the invaders. Oxidized used-up iron and copper get displaced into the extracellular compartment and body fluids and appears in the hair and skin, as the bodyâ€™s most efficient way of excreting toxins without hurting the kidneys. This has led to the dangerous and in its consequence catastrophic assumption, that these metals are the enemy and need to be restricted. It is true, that oxidized metals pose a danger and have to be reduced (=substitution of electrons) or eliminated. However, when copper and iron are needed and substituted appropriately, major improvements have been observed. Appropriate antioxidant treatment can reduce these metals. Homeopathic copper and iron will lead to beneficial redistribution of these metals and makes them bio-available again.
Lithium-orotate or aspartate in low doses (15 mg/day) has been shown to protect CNS structures from neurotoxin damage. Patients almost always benefit clinically from frequent treatment with parenteral magnesium. It is most meaningfully given in a modified Meyerâ€™s cocktail, where we use a 5:2 ratio of folic acid (not folinic) and hydroxycobolamine (not methyl- or cyano-). Hydroxycobolamine is given i.m at the same time as the i.v.injection of the cocktail.
Many Lyme patientâ€™s suffer from Pyrroluria, a metabolic illness where abnormal porphyrins carry out significant amounts of needed zinc and vitamin B6. Diagnosis is made with the appropriate test at the Pfeiffer institute in Chicago. Even though it is assumed that this illness is hereditary I have my doubts, since most Lyme sufferers have a degree of it. I suspect that the appearance of kryptopyrroles in the urine is induced by the illness. However, I am carefull with excessive substitution of zinc. Zinc has a synergistic effect with mercury in the brain and also promotes the growth of the herpes viruses.
If clients show abnormal high losses of sex steroid hormones in the urine, the patient may be cobalt deficient. The urine hormone test and cobalt drops are available at the Tahoma clinic Renton, Wa. For a while selenium should be given in high doses to suppress viral replication and render bioavailable mercury non-reactive.
The element most critical in the Lyme patient however is iodine. A 2 inch square of Lugolâ€™s iodine is painted on the patients skin and should remain visible for 24 hours. The sooner it is absorbed the more deficient the patient. An oral form of Lugolâ€™s is available under the name Iodoral (Optimox, Torrance, Ca).
Filling up the bodyâ€™s mineral reserves has always been the most essential part of our heavy metal detox program. It is also the most essential part of our Lyme treatment.
There is an inherent order in which the microbes should be treated. If the order is correct, gentle methods work. Treatment should always combine electromagnetic interventions, using specific microbial inhibition frequencies (KMT technology) with the appropriate herb, antibiotic or other antimicrobial strategy. It should also always be combined with a toxin elimination program, good psychotherapy and general life style hygiene (all the stuff, that alternative Medicine stands for).
The Lyme ABC
A. We start with deworming our clients. We often use a simple yet agressive seasalt/Vit C protocol (19) which has an independent effect aginst the spirochetes also. The high salt conmcentration kills large parasites by osmotically induced dehydration (osmotic shock). High salt levels also increase the enzyme elastase which has a strong antimicrobial/anti-spirochete effect (4)
Protocol: 1.5 grams of seasalt per 20 lbs of body weight in 4 divided doses per day for 3 weeks. With each dose also give 1-4 gms of Vit C (dose has to be just below bowel tolerance). Three 3-6-week cycles with a 2 week break inbetween. The BP should be monitored and not elevate outside acceptable levels. 5 % of the population are salt sensitive and react with a significantly increased blood pressure. In the off weeks we give Â½ tsp of sea salt first thing am in a glass of water. Sometimes we enhance the program by using the â€œArise-and-Shineâ€ herbal program. Often I will add in a course of Albendazole or Biltricide. We developed antiparasitic CDs for entrainment of the immune system. The frequencies were obtained by German physicists by taping the sounds of microbes in their respective live activity in an underground lab which was soundproof and electromagnetically completely shielded (6).
B. the next step is the treatment of giardia, entamoeba histolytica and trichomonas, which most often are overlooked. Lab detection of large parasites in most US labs is hopeless. Amoeba and giardia trophozoites can only be detected in a fresh stool for about 20 minutes. None of the labs available to us comply with this necessity. The detection rate is so substandard that only ART testing, a therapeutic trial or abdominal palpation by an experienced practitioner are capable of establishing the diagnosis. Protocol: organic freeze dried garlic ( 14 ) treats all of the above astoundingly successfully. Sometimes we add Tinidazole 500 mg bid for 10 days always followed by long term garlic therapy (3 caps tid after meals).
C. Next we attend to the chronic strep infections, which often coexist with the herpes viruses. No other treatment has been as successful as Pleo Not (penicillum notatum) from Pleomorphic-Sanum followed by a 6 month course of Pleo Sancom (antidotes for aspergillus niger and mucor racemosus). We always look at the tonsils: if they are scarred with crypts, or lymph tissue has regrown since the tonsillectomy (â€œtonsillar tagsâ€), surgical intervention is needed. Otherwise these patients (which are most of them) never get well. We recommend a procedure developed by Dr. Sergej Dorochov, MD, PhD called â€œregenerative cryotherapyâ€ ( 20 ). It involves freezing the surfaces of all lymphatic tissue of the head/neck region which creates a barrage of growth factor and cytokine responses, that often lead to dramatic improvements in our Lyme patients. Lymph drainage using the KMT technology has been superb in speeding the healing of the sinus/head/neck/region.
D. the next step is the treatment of Babesia . There are now at least 17 subtypes of this intracellular Malaria-like organism. Eye, brain and dental symptoms are most often caused by this mean microbe.
Protocol: Frequency #2 in the KMT 22 TENS unit inhibits the metabolic activity of Babesia and is used 3 times weekly.
I also use Artemisinin, 2 cap 2times/day. 3 weeks on, 1 week off. Always with Â½ glass of grapefruit juice. 3 cycles. Watch iron levels! Artemisinin provokes the intestinal wall to secrete an enzyme which destroys the medication before it can be absorbed. This process builds up over 3 weeks. After a one week pause the enzyme has disappeared and takes another 3 weeks to reemerge. Grapefruit juice prevents formation of this enzyme. Alternatives are the Swiss Malaria drug Riamet (1 course) which is very well tolerated and Mepron, which is forbiddingly expensive.
Taurox 6X, a sophisticated designer compound marketed as a homeopathic remedy, is very effective in treating the associated fatigue, eye symptoms and erratic emotional behaviour. It has an independent immune system regulating effect.
E. The next step is to start the client on a systemic antiviral treatment. I use the ayurvedic herb cocktail – Indian Gooseberry, Chebulic and Beleric myrobalan ( 14 ) , which has given the most profound and lasting effect on the viruses of the herpes family, which flourish in the immune suppressed Lyme patient. The Japanese mushroom extracts have also been helpful. . I also like the North American product â€œPro Boostâ€ (thymus extract) to help awaken the cellular immune system.
Olive leaf, virox and other chaparral- derivatives have been disappointing. The insomnia of Lyme disease is often herpes viral in nature (EBV, VZ or HSV 1, HSV II). As a diagnostic trial I often use 1000 mg of the medical antiviral drug Valtrex at bedtime. If there is a dramatic improvement, herbal antiviral treatment has to be considered for a long time. We have designed an antiviral program for the KMT instruments (frequency #4) and an anti viral CD, which s played through a walk man or regular sound system at low volume 3 times/week. This has been extremely effective. Zinc fosters the growth of HSV I and II, copper and selenium inhibit it.
F. Simultaneously I address the fungal/yeast component which is most often present, especially if clients had prior antibiotic treatment. Fungi and viruses seem to support each other in yet unknown ways. I use both the antifungal CD and the KMT TENS-frequencies in program #4 which contains all known anti-yeast and anti-mold frequencies ( 6 ). With ART technology we could show that the most successful and well tolerated antifungal is either the drug amphotericin B (250 mg bid) or the combination of organic freeze dried garlic and oil of oregano. Substitution with effective microbes is important. We use â€œMatrix Floraâ€ ( 14 ) which contains over 80 lesser known beneficial microbes. Every patient is also on a more traditional acidophilus/bifidus/FOS product. Eating a low carb diet is often a must. We monitor the fasting insulin level. If it is low, we are ok. If it is high, we restrict the carbs. Do not restrict the carbs if it is not necessary. We have seen dangerous mistakes in this field. Metabolic typing is a safeguard, but time consuming to do at home, especially if you are very ill. I use the â€œdiet therapy softwareâ€ (21) for a rapid and profound diet evaluation and recommendation. Most successful is the ART food sensitivity test for every single item in the clientâ€™s diet (6). It may take 15 minutes, is more sensitive then the ELISA, MELISA and other lab tests – and it does not incur lab fees (6). The rotation diet by Sally Rockwell prevents relapses.
G. Mycoplasma responds well to enzymes, when it is treated in sequence with the other microbes as outlined here. The most effective strategy is the German product Rechtsregulat (14). This simple drink has been extremely effective in eradicating mycoplasma and other cell wall deficient microbes. It also has a heparin like anti-fibrin effect that surpasses injected heparin by far. It has just like heparin, a strong biological effect against Babesia as well. Dosage: 1 tbs/2 times per day. The KMT program #4 is designed for treatment of mycoplasma (6).
H. The spirochetes and their close relatives ( Bartonella, Rickettsia, Ehrlichiosis, Brucella abortis) are best treated last – with antimicrobial herbs or antibiotics., 1 tsp bid. We use an alternating course of teasel root tincture (15 drops 3 times per day) for 6 weeks and then TOS free catâ€™s claw tincture (10 drops tid). We also use Echinacea root tincture , 2 dropperfull 3 times/day. Organic freeze dried garlic sometimes has a profound effect on the spirochetes. Many other herbs have enormous potential in the treatment of chronic Lyme disease.
Frequency #1 in the KMT TENS unit inhibits the microbial growth of spirochetes and Bartonella, simultaneously activates specific immune responses and aids the uptake of antimicrobial herbs.
Injected bee venom has long been my favorite during this phase of the treatment (22, 23). The peptide mellitin has strong antibiotic activity against all spirochetes (24). Bee venom also contains nerve growth factor, the very substance needed for healing, when everything else has been attended to.
For the psychiatric presentations of Lyme disease I use large doses of Niacin. Niacinamide and no-flush Niacin do not work. 3-6 gms in 3-4 divided doses often show amazing results. It appears that Niacin has tremendous antibiotic potential against all types of Borrelia (12). I suspect that our mentor and genius in orthomolecular psychiatry, Abraham Hoffer, MD discovered a treatment for Bb long before Lyme-disease was known.
The current antibiotic protocols are discussed and listed elsewhere (10). My favorites include Zithromax and Minocycline (both work symbiotically by binding to separate regions of the bacterial 50s ribosomal nucleic acid and both inhibit the microbes from taking part in protein transcription). I also use Rifampin.
Often patients develop sarcoidosis, which is rarely recognized (11). The Lyme infected lymph nodes produce abnormal amounts of 1.25 di-hydroxy vitamin D. The client often develops marked osteoporosis (most often in the spine) along with other more typical Lyme symptoms. The blood test (1.25 di-OH vit D) will usually reveal the pathology (levels over 45), necessitating therapy with the Trevor Marshall protocol (18). It uses antibiotics together with the angiotensin II receptor blocker olmesartan â€“medoxomil. By adding the KMT lymphdrainage technology twice/week results are often rapid and miraculous. We hope to find alternatives to the antibiotic regimen in the near future.
When the sequence outlined here is observed, few people have severe Herxheimer reactions, which are the rule in other approaches.
Most clients will need some support for several years, before they have found and adapted to a new life style in which the symptoms are absent. Lyme disease is marked by cyclic rhythms and unexpected returns of the symptom from time to time. Once a patient has figured out what works for him or her best, most of my patients learn how to manage the illness with very little help – on their own, living normal healthy lives worth living. In the course of conquering the illness there has been a lot of personal growth and a lot of learning. Many treatment modalities have been surprisingly ineffective: ozone, hyperbaric oxygen, ICHT (intracellular hyperthermia) and many others. Some treatments have been unexpectedly effective: dental splints, colortherapy, Tomatis therapy and neurosensory stimulation, elevating the body temperature with T3 supplementation, regular bee venom injections, tonsillectomies and cryotherapy and many others. After 15 years of dealing consciously with this illness, Lyme disease is still a mystery to me. Currently its impact outweighs other important issues like heavy metal toxicity, unresolved psychological issues and nutritional deficiencies.
There has been much speculation, why Lyme disease seems to be increasingly common. The book â€œLab 257â€is an investigative report on the issues involved. The insects which are the vectors for these microbes thrive in warmer climates. I have no doubt, that to a large degree the greenhouse effect is responsible and will be confronting us with the onslaught of more and more aggressive microbes. The partial pressure of oxygen on the earth at sea level has decreased from 30% 150 years ago to 19% today. The oxygen producing algae in the oceans are dying.
The response of the public health system so far has been denial and anger towards those who try to uncover the puzzle and help the afflicted patients. This will certainly change in the near future. I expect that by the time the institutions discover Lyme disease as a far more important factor in chronic illness then currently acknowledged, we will be confronted with new, far more dangerous microbes. Antibiotics have disappointed in the treatment of Lyme disease as a single modality. Antibiotics alone will not help us to cope with the coming plagues.
All of us â€œalternativeâ€ practitioners have to start looking beyond antibiotics for help and for hope. The microbes have always been with us. They are not the enemy. It is us who have altered the environment so severely and in a way which facilitates the growth of lower evolved species like cell wall deficient microbes and viruses – and ends the life for many more evolved species. Extinction may be forever.
Lyme disease is a messenger. If we donâ€™t change, someday not too far from now we may be on the endangered species list.
1. Borrelia burgdorferi group: in-vitro antibiotic sensitivity: Orv Hetil, 2002 May 26; 143(21): 1195-8 (article in Hungarian), JP Henneberg, U Neubert â€“department of dermatology, Ludwig-Maximillian University, Munich, Germany
2. Erythema chronicum migrans (Afzelii) associated with mosquito bite: acta Derm Venereol (Stockholm) 46, 473-476
3. Personal experience while doing a residency rotation in neurology at the Albert Ludwig-University, Freiburg, Germany under Prof.Faust (1976)
7. www.vcu.edu/ Journal of Immunology Dec 2004
8. The etiologic agent of Lyme disease in deer flies, horse flies and mosquitoes
J Infect Dis 154 (1986), 355-358, LA Magnarelli, JF Anderson, AG Barbour
9. Klinik der Lyme-Borreliose: Hans Huber Verlag, Bern, CH (2002).
39-40, Norbert Satz
11. Borrelia Burgdorferi infection may be the cause of sarcoidosis
Hua B, Li QD: Chin Med J (Engl) 1992 Jul; 105(7): 560-3
14. www.biopureUS.com also: firstname.lastname@example.org
15. www.neuraltherapy.com applied neurobiology (APN) manual/video
16. www.neuraltherapy.com neuraltherapy papers
17.www.neuraltherapy.com Klinghardt Matrix Therapy (KMT) manual/video
22. Bee Venom Therapy for Chronic Pain: D Klinghardt, J. of Neurol and Orthop. Med and Surg., Vol. 11, Issue 9, Oct 1990, pp. 195-197
23. www.mercola.com : The Treatment of Lyme Disease with Bee Venom: D Klinghardt, M.D., Ph.D., 1999
24. Bee Stings as Lyme Inhibitor: L. L. Lubke and C. F. Garon, J. Clin. Infect. Diseases, July 1997, 25 Suppl. 1, pp. 48-51
25. Lyme disease, potential plague of the 21st century: R Bradford and H Allen, Townsend Letter for Doctors and Patients, Jan 2005, 70-79
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