Excerpted
From the Writings of Dietrich Klinghardt, MD, Ph.D., edited
by Eve Greenberg, LPC, CN, Explore Staff Reporter and
Director of the Klinghardt Academy of Neurobiology
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
client’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 what else?
The new kid on the block is Borrelia burgdorferi (Bb)
and some of us have looked at it for a long time as
possibly being the bug that opens the door for all the
other infections to enter the system. Another one is
Lyme disease, which 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 you get, the more foreign DNA is attached to your
own DNA. Somewhere along the line, pathogenic microbes
invade the host’s DNA and become a permanent part of it.
Since you use only 2 percent of your DNA, it may not be
a problem. In fact, it may make you who you 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 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 and have been with us
for a long time, maybe centuries or much longer than
that.
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 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) Regular lab parameters affected by Lyme:
- Abnormal lipid profile (moderate cholesterol
elevation with significant LDL elevation)
-
Insulin resistance
-
Borderline low white blood cells, normal SED
rate and CRP
- Normal thyroid 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)
- Complex changes in cytokines, interferones,
NK cells, white blood cell indicators, etc.
Bb tends to infect the B-lymphocytes and other
components of the immune system that 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 percent of stinging flies and mosquitoes (2, 8, 9,
and 10) are carriers of Bb and co-infections. In South
East Germany and Eastern Europe 12 percent of mosquitoes
have been shown to be infected.
In addition, 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 that 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.
Many Bb symptoms are mistaken for problems of natural
or premature aging.
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.
Common Co-Infections
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.
What Influences the
Severity of Your Symptoms?
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 major 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 is 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).
The severity of symptoms is not related to the number
of spirochetes in your system but rather to your
individual immune response.
Taking all of the above into account, we do not
distinguish between people who have the Bb infection and
those who don’t. Instead, we distinguish between people
who have Lyme disease and those who do not.
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 is 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 (ASD),
seizure disorder and others. Detoxifying these kids with
transdermal DMPS and treating the chronic infections is
often curative.
The Three Components
of Lyme disease
Lyme disease has three 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 your 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 “co-infection”.
For treatment options, see below.
Component #2: the illness producing
effect of microbial exo- and endotoxins and toxins
produced by the host in response to microbial trigger
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 toxin
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 (14), 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 your liver, be processed, and enter your
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 -- 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.
The KMT microcurrent frequencies dramatically
increase the speed of toxin mobilization and access body
compartments the biochemical compounds cannot .
Psychotherapeutic intervention 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.
Lymph drainage in combination with colon hydrotherapy
accesses toxins stored in the lymphatic
body-compartment.
German practitioners have pioneered
the combination of oral cilantro and the “Toxaway”
microcurrent footbath.
Component #3: The immune
reactions provoked by the presence of both
toxins and microbes (there are three sub-possibilities,
which have to be recognized and addressed).
Your immune reactions are largely depending on
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.
A multitude of biochemical serum markers is used
today to determine the status of the infection (see
below). A subset of NK killer cells, CD 57+ is emerging
as a valid marker for activity of the illness (lower
counts indicate worsening).
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 hyper coagulation. The microbes
tend to live in your endothelium where the food is
most abundant. There they trigger the coagulation
mechanism to lay down a layer of fibrin on top of
them to evade recognition by your immune system,
etc. For this aspect we use three 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 and
frequently leads to rapid subjective improvement.
Lumbrokinase is far more effective than
Nattokinase,but both appear weak when compared to
Rechtsregulat.
We also work on recognizing and eliminating those
factors that block the 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
2: Allergy -- appropriate or
exaggerated immune reactions (both cellular
TH1-reaction and TH2-cytokine activation).
In Lyme disease oftentimes (but not always), TH-1
is overly active early in the illness and can easily
be downregulated by fluconazole. Later TH2 becomes
overly active.
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 psycho kinesiology
(muscle-biofeedback psychotherapy).
A very effective and yet simple technique to
re-regulate TH1 and TH2 back 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
micro pore filter and injecting it intra-muscularly,
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.
3: Autoimmunity -- the toxins
and microbes often act as haptens -- marking the
cell, cell wall or tissue in which they are hiding
as foreign and therefore for destruction. This
happens especially against a backdrop 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 your immune
cells to mount a specific and targeted attack on the
invaders, sparing your 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). Some surface antigens in the spirochete
are identical to myelin. This explains why
anti-myelin antibodies are often present.
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).
But
instead 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 that simultaneously address the
three 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 use of
herbs alone or in combination with antibiotics has
emerged as the most important core strategy.
The Importance of
Minerals
To feed, fuel and perk up the cells of the immune
system (especially NK cells and macrophages) numerous
interventions have been attempted, 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 should medical drugs 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. Your immune
system uses those two metals in the process of phagocytosis. They are the main constituent of the
enzymes (or “bullets”) your 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 your hair and skin as that’s your body’s most
efficient way of excreting toxins without damaging your
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 leads 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 your CNS structures from
neurotoxin damage.
Patients also almost always benefit clinically from
frequent treatment with parenteral magnesium. It is most
meaningfully given in a modified Meyer’s cocktail. We
also use a 5:2 ratio of folic acid (not folinic) and
hydroxycobolamine (not methyl- or cyano-) sublingually
several times/day.
In addition methyl-cobolamine is
givenintra-muscularly twice weekly and is important in
the methylation/restoration of reduced glutathione.
Hydroxy-B12 protects your brain from nitric oxide
induced damage.
Many Lyme patients 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 Vitamin
Diagnostics in New Jersey. 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 most critical element in the Lyme patient,
however, is iodine. A two inch square of Lugol’s iodine
is painted on the patient’s 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 your 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 of
Effective 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.
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 best, most of
my patients learn how to manage their illness with very
little help.
Klinghardt Lyme
Disease Protocol
Biological treatment of Lyme disease and chronic
infections: (based on over 900 successful treatment
cases)
The treatment of Lyme disease requires 4
distinctive steps:
- Decreasing toxic body burden/unloading the
system
- Improving disturbed physiology
- Decreasing microbial count
- Immune modulation
Decreasing toxic body burden/unloading the
system
- Proper sleep
- Low EMF (turn off all fuses, sleep sanctuary,
turquoise light/photon wave to increase melatonin
and non-rem Delta sleep)
- Non-toxic/allergenic bedding material (cave:
flame retardants/PBDEs)
- Avoid light/noise pollution at night
1. Short form of toxin elimination and
antimicrobial treatment: “Le Cocktail”
Freeze dried garlic (against microbes, toxins,
sulfur), chlorella (viruses, bacteria, toxins,
nutrients), cilantro (bacteria, viruses, toxins) and
fish oil (for microcirculation and cell wall
flexibility)
The Long Form of Healing
Toxin elimination:
- Remove intestinal biofilm: 1 tsp clay followed
by 1 tbsp fiber laxative for 6 weeks, prior to do
anything else
- Address genetic glitches (methylation,
sulfation, acetylation – B12, B2, Folic acid, SAM-e,
Methionine, Taurine, MSM)
- Mercury and metal detox -- Phospholipid Exchange
(EDTA, phospholipids, alpha lipoic, magnesium,
energy), Matrix Metals, CVE and CGF, DMEP(ORS),
sound cracked chlorella, nanonized chlorella and
cilantro, EDTA, DMSA, DMPS
- Solvent and carbon based detox: glycine,
laser-or homeopathy aided detox
- Consider the UNDA remedies (243 is best)
Self Help:
- Colon hydrotherapy and lymphatic drainage,
rhythmic cranial and liver compression
- Dry skin brushing and warm/cold showers
- Swedish sauna and Toxaway ionic foot bath
Detect and resolve interference fields:
- Scars
- Jaw infections and devitalized teeth
- Chronic localized infections (tonsils, appendix,
sinuses, etc)
- Dysfunctional autonomic ganglia (superior
cervical, sphenopalatine, pelvic ganglia, etc.)
Remove “allergenic triggers” from your environment
- Food allergies
- Volatile organic compounds from carpets,
furniture and paints
- New car smell (phthalates)
- Newspaper and office printing ink
- Work/profession related compounds
Removing psychological toxins
- 20 minute writing exercise to overcome past
trauma
- Family constellation work to resolve
trans-generational issues
- Applied Psycho-Neurobiology to resolve conflicts
and severe trauma
- Regular time spent in healthy nature
- Regular massage
- Qi Gong, Tai Chi or Meditation
Removing structural blockages
- Optimize the dental occlusion to restore cranial
lymphatic pump
- Craniosacral therapy to improve fluid dynamics
in CNS
- Visceral manipulation to improve organ function
2. Improving disturbed physiology and
biochemistry (vitality, detox, immune
responses, tissue repair)
Biochemistry
- Always start with KPU urine test and address it!
- Assessment via lab work or ART -- correct what
is missing and what is too much (hormones, minerals
and electrolytes, glutathione, sulfur, etc.)
- Genetic testing: find minimal bypass nutrition
to correct for SNPs or gene deletions/mutations
- Diet: gluten and casein free diet, Specific
carbohydrate diet, Metabolic typing, blood group
diet or ART based diet
- Common deficiencies in Lyme: magnesium: has to
be given transdermal or via injection. Oral
Magnesium feeds spirochetes
- Copper, zinc and iron are spent by macrophages
and appear in oxidized form in hair and serum,
giving the wrong appearance of excess
Improving disturbed biochemistry and
physiology: KPU/HPU
- Over 80 percent of our Lyme patients have
developed HPU (hemo-pyrrol-lactam-uria). The term
falsely used in most US literature is KPU
(krypto-pyrrol-uria)
- HPU disarms the immune system by catastrophic
depletion of zinc, manganese, arachidonic acid,
histamin, taurine.
- These losses are hard to detect with any current
technology (only bone and CNS biopsies are reliable.
- Labs to consider:
KPU urine test (Vitamin Diagnostics)
- alkaline phosphatase low normal
- copper: zinc ration greater than 1 in hair and
urine
- low Omega 6 in red cell membrane fatty acid test
- white blood cell zinc, red cell copper level
If KPU is treated first and the system is
restored to normal levels (4-8 months),
Borrelia, Bartonella-like organisms and Babesia respond
to much milder interventions without
significant Herxes or problems
Neurophysiology
- Gives your brain healthy rhythms: KMT technology
- Listen to Lyme entrainment CDs
- Spend time in nature
- Avoid EMF’s (cordless phones, cell phones,
wireless technology, home near airport (radar),
computer
Exercise
- Stretching
- Weight lifting
- Movement (dance, Tai Chi, Qi Gong, etc.)
- Aerobic exercise -- avoid post exercise fatigue
and pain
3. Rizols (ozonated castor oil
treated with high voltage electrolysis) decrease
microbial count. Rizols have
strong and specific anti-microbial
properties, no known adverse long
term effects, are relatively inexpensive and are
pleasant to take.
They have been used successfully
since 1905. (You’ll find the recipes
below.)
1: treat parasites, mold and anaerobes
Rizol Gamma (effective dose: 15-20 drops tid)
2: treat both RNA (Borna, etc.) and DNA (HHV-6,
EBV, etc.) viruses: Rizol Zeta (20
drops tid)
3: when on full dose of Gamma and Zeta, treat
Babesia:
After 2 months on full treatment: stop or reduce
Rizol Gamma and treat Bartonella:
Rizol My (20 drops tid).
After 2 months reduce dose of rizols Zeta and My
to 10 drops tid and treat spirochetes:
add Rizol Epsilon and Jota, 10 drops tid each.
Always follow rizol with adsorbent (biosorption):
chlorella (20 tbl), chitosan (1-2 caps), zeolite (1
tsp) or charcoal (2 caps)
Rizol-Gamma
70 percent Rizol-raw material (ozonated castor
oil treated with high voltage electrolysis)
10 percent clove oil
10 percent oil of artemesia
10 percent black walnut oil
Rizol-Zeta
69.3 percent Rizol-raw material
10.0 percent oil of artemesia annua
10.0 percent clove oil
5.0 percent black cumin oil
3.0 percent moxa oil
1.8 percent walnut oil
0.9 percent oil of majoram
Biological effects, according to the Steidl/Carstens
studies:
- The ozonides transfer oxygen and change the
environment in which anaerobic pathogenic germs
live, making it aerobic
- This prevents anaerobic germs, such as
Clostridia, from multiplying
- The oil is surface-active and, with its active
substances, moistens your intestinal mucous membrane
where nests of fungi and bacteria and parasites
might be located
- Rizol constituents have been found
intracellularly and in the matrix (indicating
anti-microbial activity both intra-and
extracellularly)
Cell toxicology studies:
- Mitochondria are not damaged,
- OECD test for mutagenicity produced the result:
not mutagenic.
- Normal human cells are guided into apoptosis
(beneficial and genetically pre-programmed cell
death)
- Previously damaged and tumor cells are destroyed
- No adverse pharmacological effects were found in
numerous cell culture tests
4. Immune modulation
- Use the CD 57 test (Labcorp – Stricker panel) to
monitor immune status
- Enderlein remedies: treat immune responses to
mold: Pleo Nig, Not, Muc, Fort, Pef, Ut and UT-S,
Lat
- Auto-hemotherapy or auto-urine therapy (2 ml
biw)
- Buhner herbs (Quintessence from BioPure) 8-10
dropperfull in 1 liter water
- Adjunctive physics based immune modulation
tools:
- KMT frequency-based biofield treatment
- Health Light super LED treatment of focal areas
- Valkion: singlet oxygen energy delivery via
inhaled air or drinking water
- Photon Wave or Jae Laser immune modulation
Medical drugs: Occasionally the use of medical
antimicrobials is beneficial in addition to this program
(ILADS recommendations). Top of the list:
- anti-virals (Valtrex and Valcyte)
- anti-fungals (itra- and voriconazole)
- anti-parasitics (Alinia and Biltricide)
- antibiotics (with above program, minocycline,
and anti-Malarials work again!)
Lyme Disease as a
Messenger
In the course of conquering this illness there has
been a lot of personal growth and a lot of learning.
There has been much speculation as to 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 percent 150 years ago to 19
percent 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 is 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 as 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 that 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, we
may be on the endangered species list someday not too
far from now.