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 host'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 Enderlein'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 book ''Lab 257'' 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 than 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 - 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 ``Lab 257'': 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, Parkinson'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

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:
� Abnormal lipid profile (moderate cholesterol elevation with significant LDL elevation)
� insulin resistance
� borderline low wbc, normal SED rate and CRP
� normal thryroid hormone tests but positive Barnes test and excellent response to giving T3
� type 2 (high cortisol, low DHEA) or type 3 adrenal failure (low cortisol and DHEA)
� low testosterone and DHEA
� 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 ``typical''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 ``Lyme cognizant'', 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 don't. We distinguish between people who have Lyme disease and those who don't

a) Patients who are infected with any type of Borrelia and are symptomatic have ``Lyme''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 ``disease''. Most often several of the ``co-infections'' 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:

Component #1:
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 22simultaneously occurring ``co-infection''.

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 than 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 (``Phospholipid Exchange'') 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.

Component #3:
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 host'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 (``right rotatory fluid'') 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 work on recognizing and eliminating those client'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 than 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 patient's urine concentrates the antigens (disposed cell walls and cell fragments of offending microbes which the immune system has successfully eliminated). By passing the client'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 - the toxins and microbes often act as haptens - 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 body'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 ``for good'', 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 host'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 ``bullets'') 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 body'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 Meyer'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 patient'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 careful 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 Lugol'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 Lugol's is available under the name Iodoral (Optimox, Torrance, Ca).
Filling up the body'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.

Sequencing

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 1/2 tsp of sea salt first thing am in a glass of water.

Sometimes we enhance the program by using the ``Arise-and-Shine'' 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 (``tonsillar tags''), 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 ``regenerative cryotherapy'' ( 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 1/2 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 ``Pro Boost'' (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 ``Matrix Flora'' ( 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 ``diet therapy software'' (21) for a rapid and profound diet evaluation and recommendation. Most successful is the ART food sensitivity test for every single item in the client'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 cat'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 -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.

Outlook

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 ``Lab 257''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 institutioenns discover Lyme disease as a far more important factor in chronic illness than 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 ``alternative'' 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 don't change, someday not too far from now we may be on the endangered species list.

Helpful References

1. Borrelia burgdorferi group: in-vitro antibiotic sensitivity: Orv Hetil, 2002 May 26; 143(21): 1195-8 (article in Hungarian), JP Henneberg, U Neubert -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)
4. www.BradfordResearchInst.org
5. www.Bowen.org
6. www.neuraltherapy.com
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
10. www.Lymenet.org
11. Borrelia Burgdorferi infection may be the cause of sarcoidosis
Hua B, Li QD: Chin Med J (Engl) 1992 Jul; 105(7): 560-3
12. www.vorsoft.com/medical/niacin/index.htm
13. www.chronicneurotoxins.com
14. www.biopureUS.com also: [email protected]
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
18. [email protected]
19. www.lymephotos.com
20. www.kryopraxis.com
21. [email protected]
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

Wow, this is a keeper!

I also saw the first mention of Taurox 6X I have seen outside of the study done by it's manufacturers. This stuff works.

I am printing this one out for future reference. These are the very protocols which have pulled me back into life.

You cannot get well until you help your body fight this from within.

------------------
C O L O R A D O * S U P P O R T * S Y S T E M
[email protected]

I was having severe cognitive problems for over a year before getting my first neuromuscular symptoms that I considered to be the onset of my lyme (no tick bite around the time of sx onset). The neuromuscular sx came on 3 weeks after a major trauma.

6 months prior to that trauma I'd been to the Pfeiffer Center myself and was diagnosed with a metallothionein disorder and moderately elevated kryptopyrroles. They also said that I was harboring some sort of infection, though I was not aware of one.

So, it looks like I've had lyme for possibly much longer than I think, and it "poked through" after my immune system cratered in response to a trauma.

Thanks, as always, GiGi!

In one section, it says "In Lyme disease often (not always) the TH2 (humoral portion of the immune system) is overly active, TH1 is asleep (the cellular immune system)."

In another place it says, "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)"

The problem is that both of these cannot be true. Why? The first case says Th1 is "asleep" which means that Th1 function is downregulated. The second case (Marshall protocol) is based on the notion that Th1 is OVERproducing (upregulated).

A Lyme patient's (or anyone for that matter) Th1 cytokines cannot both be underproduced and overproduced. Of course, the notion that Th1 is upregulated as assumed by the MP may be incorrect, but to have both notions in the same overview is concerning. The inconsistency hit me when reading this over...

Very interesting info. Thank you. ping

Thanks for this article. Does Dr. K. recommend people use the KMT even if they are not his patients? Does he sell them? And does he sell the Rechtsregulat enzyme he mentions in the article? Thanks!

Yes, he recommends the KMT because it addresses so many situations besides the thousands of infections. He is the brain child behind it and since he has been treating chronically ill for so many years, every aspect is covered in that little device. When one of my kids get the flu/a viral infection, they use it. Where can you get a quick lymph drainage or a treatment for cell regeneration? ATP production? Healing currents? Frequencies that inhibit unwanted microbial reproduction?
(for info, call Nancy/AANT at 541-488-6770).

b) Rechtsregulat (``right rotatory fluid'') 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 work on recognizing and eliminating those client'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).

Excellent Article. There is so much information in there. Just out of curiousity, What does Dr. K do for Colortherapy ? This is something I might want to explore.

Thanks again,

All Dr. Valletta used to cure RA, ulcerative colitis and invasive bowel cancer was Mg pyrophosphate and sublingual B6.

("Magnesium for AUTOIMMUNE" - U.S. Patent)

All the Romanian cancer doctors used to cure lyme was Mg and antibiotics.

And Mg, we now know, inactivates an enzyme to put the brakes on the cholesterol pathway which is the pathway Bb uses.

(Above documented in For My Friends post.)

And...(Bb is PFK dependent):

"We hypothesize that extracellular Mg2+ regulates PFK and glycolysis in these neoplastic cells not by entering the cytosol but by a specific interaction with the plasma membrane."
PMID: 1832860

And:

E. Required by immunological process. Magnesium, immunity, and allergy: Mg is required for several steps of immunological reactions

1. Lymphoblastic transformation, a prerequisite of secretion of antibodies by lymphoblasts, requires Ca2+ and Mg2+

2. Mg is required for synthesis of proteins, immunoglobulins included

3. Antibody-induced complement activation is Mg dependent

4. The antigen-immunoglobulin-complement reaction induces degranulation of the mastocyte
http://www.mdschoice.com/elements/elements/major_minerals/magnesium.htm

And...

It seems Mg chloride can increase the killing power of our own WBCs (Dr. Delbet's research many years ago)
www.mgwater.com/rod04.shtml

But most important, perhaps:

4. The physical integrity of the DNA helix appears to be dependent on Mg2+

a. Mg2+ ion decreases the number DNA replication errors

b. Mg2+ ion stimulates DNA repair
http://www.mdschoice.com/elements/elements/major_minerals/magnesium.htm

That blew me away.

P.S. When was the TH1 pathway turned off?! Lyme patients are stuck in this default pathway.

The first sign of a copper deficiency is the reduction of neutrophils. Stress requires extra copper...maybe why we are all low ;-) Cortisol depresses metallothionein and copper storage protein. Bile salts remove copper. They come from cholesterol being broken down. I could go on...

have been ordering the Rechtsregulat at my home town pharmacy in Germany. We have been taking it for years and we consider taking it forever unless something better comes around. We hardly take any other supplements besides some minerals, because all problems often start with the lack of enzymes as we get older, and especially when we fight infections. Thick dark blood is a poor nutrient/med transporter. Any of the international pharmacies can get it. E-mail me if you need help.

Do you need a prescription for it? Can your doc supply it to non patients? I live in the U.K which pharmacy would you suggest?

Healing thoughts,

Most of us take supplemental magnesium.

You might also consider the first point of landing in Germany. Call a pharmacy there and see if they can order it for you, cost, etc. Mine ships within a day or so. You need to advice your credit card company that this is an okay transaction through a foreign based pharmacy. They make sure no stolen cards, etc. I order six bottles at a time (350 ml each), but both my husband and I are taking it. It is not exported. Sadly.

Oral doses don't cut it.

I'm trying to keep this from spiraling further downward and leading to many other problems...hormones shot, enzymes shot, diabetes developing, even cancer (lymphomas).

Duramater, I'm with you. I find many inconsistencies...and, well, you know.

P.S. Niacin lowers cholesterol. And here's some other info. you may find helpful:

Excess Vitamin C May Worsen Osteoarthritis

By Jennifer Warner
WebMD Medical News Reviewed By Brunilda Nazario, MD
on Thursday, June 03, 2004

June 3, 2004 -- It may be possible to get too much of a good thing when it comes to vitamin C and your health.

And...

o TH1 / TH2 - are two arms of the immune system. They need to be in balance. TH1 fights bacteria, virus, fungi. TH2 fights cancer, allergies and antibody responses.
o Vaccines seem to cause in ASD kids TH2 goes up and TH1 goes down - causing an immune system imbalance. Many of these kids cannot fight basic things like viruses, bacteria, fungi.
o ASD kids then seem to become allergic to the world due the imbalance and autoimmune nightmares.
o This is documented in ASD kids / medical journals.

http://216.239.53.100/search?q=cache:zLNMfNllHaIC:laurynhb.tripod.com/seminarnotes.html+cytokines+Th1+magnesium&hl=en&ie=UTF-8

Stuck in the TH1 pathway to fight this bacteria...less likely to make antibodies, fight cancer and allergies develop. Know why? Read my updated nutshell post.

quote:

---

Originally posted by Marnie:
Oral doses don't cut it.

---

Could you please be more careful about these statements?

You're then suggesting high doses of IV Mag, right?

If this is true, then noone would get cured of Lyme disease.

...because almost noone does IV Mag, perhaps except you and a few others.

Maybe high doses of IV Mag helped for you, or whatever you did with Mag.

Maybe you're convinced that that is what "did it" for you. And maybe it did.

But it sure ain't true for everybody.

Because, by far, most people get cured of Lyme disease WITHOUT resorting to IV Mag.

I accept that you're exited about Mag, and that you're convinced about it's importance, but as everything else in Lyme there's no golden answer to anything.

Second: This is the same Dr. Klinghardt who has a website http://www.neuraltherapy.com/
which is really Dr. Klinghardt - and all Dr. Klinghardt. He sells phamplets etc for $50.00 a pop.

I remember him from a few years ago when he was advocating bee venom as the answer to Lyme treatment. He still has his articles about that at his site. I know that was some years ago, but it is still there as new information - not dated in any way.
http://www.neuraltherapy.com/a_lime_disease.asp

In the article on that he states:
quote:
"Multiple antibiotic regimes have been tried with varying successes. The cystic stage responds only to one antibiotic: metronidazole (Flagyl). This drug should be given intravenously."
(and later in the same article)
"My preferred treatment is a combination of enzymes, herbs, specific transfer factors and the injection of honeybee venom."

If you click on "products" at his site, you will be amazed at the scope and range of stuff for sale.

He still has so many things in his protocol that a person would never be able to tell what is working and what isn't.

One needs to order it from Germany I gather. Some French, no German. Thanks for the kind offer I will consider it in a few months.

When he writes:

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

I interpret that as saying that uses the MP protocol only for Sarc patients.

Congratulations on your improving health.

Healing thoughts,

If magnesium is the cure, then prove it. Find me somebody cured by magnesium, in the last few years that you've been touting it.

We all know magnesium drops in chronic illnesses of various kinds and that supplementation is useful. Many of us get IV or IM, as well as oral. Its important but not a cure and adding it onto Gigi's thread is just off topic.

Both Marnie and Gigi have helped me a lot. I am getting well.

Please do not harrass those who are trying to help us......I mean really both of them have no obligation to give the countless hours to this site that they do.

If you don't like the info, then don't follow it.....but please be kind to all trying to help......... there are others ( like me) that really appreciat the info they provide.

It's ok to disagree but please do so in a kind way.....

"oxygenbabe: Marnie, there is such a thing as evidence-based medicine.
If magnesium is the cure, then prove it. Find me somebody cured by magnesium, in the last few years that you've been touting it."

Oxygenbabe:If you are only going to accept proven treamants for lyme ..... you are gonna be ill for a long time. There ae many paths.....I am sure you are treating with what you belive in..... I hope you get well....truly....I hope we all do......but there is no proof to any of the tratment I know of.

I have also had many iv MAG infusions to clear out the system when I ART tested positive for the combined ingredients of the infusion. If there is only one substance in it that my body at this point does not want, it will not be a beneficial infusion for me.

Once you understand that medicine is neither black nor white, you have come a long way. I am not like any of you and thank God you are not like me. What gets you up that mountain to the cure cannot be repeated in the next person. I infected my husband with the same bug and co-infections, yet his symptoms where totally different, the co-infections had not the same strong or weak damaging effect, and his treatment followed a totally different method. He never had a sweaty night because of Babesia, though he defiinitely had it and was successfully treated for it; while I died a thousand deaths from sweating because of Babesia. His body does not react like mine, and mine does not react like his.

We did not drink nor swim nor spend a month in a hospital for mag infusions. Two results out of Romania do not make the case. We do not know what happened to these patients before, nor after. Anytime I got mag at a high amount, I ended up with the runs for weeks. We cannot live without mag, but it can also kill us the same as anything else excessive, such as drinking too much water, can eventually wipe you out.

Balance is the name of the game, and timing is even more important. When your body is not ready to be treated with a strong med for worms, the time is wrong and the treatment most likely not effective. It happens all the time. ART testing for all these different approaches seems to be the perfect tool. If, for instance, an organ tests weak or is blocked, that's where the treatment needs to go. If the liver is blocked and dysfunctional to begin with, adding insult to injury by adding more drugs, makes matters worse.

Yes, I would love to hear from someone that has gotten well with mag. But please tell me all the stuff they did before, during and after. I have met with hundreds of patients and I have yet to meet the person. I appreciate Marnie's research, though I do not understand it and am not really trying to understand it. I am better off feeding my soul at this point in time with what it really needs. It's definitely not biochemistry. We have too many of these guys running around as it is, many of whom do not know what they are talking about or the problems they are getting people into.

I know people that have used mag as part of a tool to balance the minerals that have gotten well and/or are well on the road. But it never amounted to just mag or a large amount of mag, IV, IM or otherwise. This disease, with all the ones that it brings along, takes a minimum of years (5, more like 7) to clear out. Our system simply is not capable of doing it any faster.

But if a total approach is taken, addressing all the side infections and overgrowths (that includes TB in most Lyme patients today; yes, most of Dr. K's patients now need treatment for TB also), total wellness can be achieved.

Both my husband and I did it. I am not just improving: I am well. So is my husband.

I really do not want to waste a word on the sad comments made about our doctor on this thread. Nasty comments are not appreciated. I would like to think whether you wanted to or not, many have learned from what I have posted here, all at the generosity of a successful doctor; whether you like him or not. And to clear things up: He is teaching his treatment methods, including ART, Neural Therapy, APN, all over the world. Has done so for years. In Germany there are at least 6000 physicians/practitioners who practice his methods very successfully. He has been kind enough to answer questions that I have brought to him. No, he doesn't need patients; he can't accommodate the ones he has right now, because it takes a long time to see one patient from start to finish.

So shut your mouth before you get into bad-mouthing. It is not becoming and it is not a mode to live by when you want to achieve health again. This same doctor also is not rich and never will be. He runs the oldest little car you have ever seen and wears the same pair of pants and shirt a lot! He is only a doctor - a doctor with the desire to heal and has found a way to do it successfully in many cases.

Our 13 year old Sumi (black standard poodle) got run over by a car recently; Dr. K. was sweet enough to come by our house after the last patient at 9 PM that night )having seen patients from early morning on)and treated Sumi with Neural Therapy. Then she was barely moving with a lame behind, a bump on her head; Two days ago, she jumped on the high bed for the first time again successfully, and has regained four pounds that she lost. She is one happy girl again!

There are some real human beings in this world that do not cheat or deceive or swindle people - but if you carry hate and disgust in your heart, you will not notice them.

Not one method works in the same way for everyone and not one size fits all.

Take care.

Ann-Oh

this article you are questioning is a copy of Dr. Klinghardt's notes. He was an invited guest speaker at the Linus Pauling Institute (OHM) in San Francisco, at which several LLMD's (Dr. Jones, Dr. Stricker, Dr. Harris/Lab) ) etc. were present. In other words, he gave me a copy of his notes. I think this similar article will also appear
in Explore and/or the Townsend Letter - I forget which. No, I didn't make it up. The lecture weekend was planned for 300 - approx. 500 showed up - . It was extremely well received.

Some of the people from Lymenet went to the lecture, but I have yet to hear one word of what they learned or any of the comments to the various speakers. It's been dead silence on their part.

The product list on his outdated website is for doctors who wish to purchase some of the equipment that is needed if they want to treat their patients with ART and similar methods as taught by Dr. Klinghardt. It is not meant for you or me. Neither are the articles or protocols. They go back years - lots is still being treated in the same way; while other methods have changed for even better ones. He is a busy man traveling from one end of the world to the other, while in the meantime also seeing patients and he does not have time to spend on a website. It's great, I think that we have at least what's on it. I have always posted it as a "neglected" website.

Really, I do not understand why I even respond to your comments, Ann.

Abxme:

Dr. K. uses different colored eye-glasses in combination with ART. He also uses the Photron (comes out of Holland, I think).
Color is usually applied to bring some Unresolved Emotional Conflict to the surface or to treat the conflict once it has been brought to the surface with APN (Applied Psychokinesiology). I really do not understand it fully, since I needed very little treatment on that basis. Many people do benefit immensely and all of a sudden turn toward wellness. Our emotional make-up play a big role. Most people do not believe that. So be it. It's part of the "Five levels of Healing". If you are living within a sick family framework and are trying to bury it, chances for wellness are very limited. It's all part of being a healthy human being.

This kind of treatment usually takes minutes, rather than hours. It's possible that you walk around with a certain coloar eye-glasses for a few hours a day for a while. But once in a while, why not rose-colored glasses or whatever it takes?

He has had great results with dyslexic children and color therapy for a number of years.

You have done an amazing job in printing this. Thank you.

I loved the ending in particular:

There has been much speculation, why Lyme disease seems to be increasingly common. The book ``Lab 257''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 than 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 ``alternative'' 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 don't change, someday not too far from now we may be on the endangered species list.

Healing thoughts,

Wallace

quote:

---

Originally posted by zipzip:
the 3 components of lyme disease :

1. sifting through lies, deceit, ignorance and b.s.
2. bad luck.
3. good luck.

---

Good one zip.

Don't need to be a scientist to understand that one.

Btw, we need to optimize #3.

I took T3 at the lowest possible strength for a short time and wound up having a complete heart evaluation because of all the side effects.

Just the tiniest exertion and my heart would pound out of my chest.

With my severly dimished mental capacity I forgot to tell the docs about the T3 untill after all the expensive tests. DUH!!!

Stopped T3 and my heart was back to normal.

T3, like anything else that you really dont need can cause you a lot more harm than good.

I do take levoxyl every morning even tho my tsh was always normal. I had alll the thyroid symptoms except weight gain. I was wearing a coat in July and my skin was so sensative that I couldnt wear pants because they molested my skin too much.

Smallest dose of levoxyl fixed it just fine.

I have improved by:

1. Abx combo of Zithromax/Minocin.
2. ART testing to determine that that was a good combo (other, it turned out were not).
3. Meyers cocktails (IV magnesium, calcium and vitamins).
4. Lots of exercise.
5. Not getting any new tick bites!

Thanks to both GIGI and Marnie; I appreciate all the good research and information you post!

The hormones in particular: Years ago, I have had the experience of having taken a natural hormone supplement from the health food store and one from the pharmacist - basically I don't care where it comes from - the informed doctor or pharmacist - and started to take it for a period of time. I started to dive into one of the severest depressions I have ever heard of; I was ready literally to run over the cliff! until my husband finally figured out what brought it on. It took weeks to get the substances out of my system and the depression ended.

I hear many of you on hormone replacements of one sort or another, and I hear at the same time that you need anti-depressants!
Watch what you are putting into your mouth - onto your skin as dermals - some of the stuff can be perfect for one and be an absolute killer for the next person. Have yourself tested on it. Sometimes the body tolerates it well for a week and then all of a sudden it turns against it. The symptoms of the rejection can vary widely.

I just want to warn you here that a lot of what we are doing and what I used to do has nothing to do with Lyme Disease - is not a Lyme Disease symtpom, but is really that your body is not fit to tolerate a certain substance. The actual hormone in my case may have been fine, but the filler or agents used to use it dermally may arouse your autonomics in a way that stresses your system every second it is on or in your body. Just read or ask your pharmacist about all the artificial colorings and flavorings you take in with this agent that is intented basically to help you.

So be alert. If you do not have access to a practitioner that does ART, find someone that does good kinesiology (always only upon first unblocking the autonomic nervous system; otherwise no kinesiology works; the blocked body cannot give a true answer in muscle testing and has to be unblocked before. Dr. K. calls this type of testing
"department store muscle testing". It is worthless and the response given by the body is incorrect. All meridicans have to be open and working - then muscle testing works great. A sick body is usually blocked almost all the time. The MFT method that I used to offer here for someone to learn to open oneself is easy to learn. Even EFT does a good job to unblock your body and let it be in a healing mode. A blocked body does not have much chance at healing. Any time you take a substance that your body does not want, you put yourself into stress. IIt could be the best and most expensive organic food. There are many people around the world who do good kinesiology.

I have over time learned to unblock myself and also learned to muscle test everything, even food, before I put it in my mouth. All takes effort - I know - but that's Lyme Disease.

I realize that is all woodoo for many of you.
But so is a lot of what I say, and that does not bother me. The guy who told me all about it turns out to be right over and over again. The proof is in the pudding. There are a few that have picked up on it and I do appreciate the notes that I get from people who are grateful because they are getting well. I do pass on these positive notes to Dr. K. - because that's where I learned every bit of what I have posted for five years - of course along with a bit of the common sense that my Mom and Dad taught me early on in life.

Thank you for all the time and trouble you consistently go to in putting all this information out here. It is especially kind of you since you are out of this hell hole called Lyme and could just forget all of us.

Gigi, thank you so much for all the time and effort you put into these posts, and for all the others who contributed. I am so glad to hear you got well with Dr. K and all the work you did on your own. I am liking the sound of his approach the more I read, and Gigi, I think we share a similar philosophy of healing.

Your comment about healing possibly taking 5-7 years does not thrill me, but I've been at it longer than that already (pre-lyme-dx) and I have not given up yet. I found out that my healing path is also my spiritual path, and the life-enrichments this journey has provided are too numerous to count.

Has anyone else seen Dr. Klinghardt? If you have already posted your experiences, please let me know and I will search for your posts.

I began abx with an LLMD, but I keep feeling this is just the beginning medically. I feel drawn to ART, but there is a long waithing list for Dr K. I was wondering if someone would email me woth a doctor's name on someone who trained extensively with Dr K, but is more accessible both geographically and appointment-wise. I am in Southern Louisiana, but I can travel. Thank you for this and I will also post in the doctor's referral section.

Thank you for these articles and recommendations and urls to what has worked for you.