This Is a Very Important Message for Those Who Are Suffering From Lyme Disease
“Finally! A Proven & Highly Effective Way To Win The Battle With Lyme Disease The NATURAL Way…”
Our Non-Invasive Holistic Approach Will Get You Back
To The Abundant Health & Happiness You Deserve!
A Powerful Approach To Lyme Disease Unlike Any Other…
As you probably already know, Lyme Disease is something that can take complete control of your life…
Not only can it make you feel very ill and weak, but it can be very insidious and cause a host of other ailments in its path of destruction in your body. There are the severe aches, muscle pain, and even memory loss and so-called “brain fog”.
If you’re currently suffering from the effects of Lyme Disease, the more you know about it, and the way you approach it can make all the difference in the world when it comes to making a
COMPLETE recovery.
Many who take the wrong approach, can end up living the rest of their lives with residual effects. This can not only create a life of pain and frustration, but also depression and a very low quality of life.
Luckily for you, there IS a much more powerful and effective way to win the battle with Lyme Diseas e that takes into account your entire body and working WITH the body’s natural abilities to heal in order to get better.
But before we dive into this breakthrough approach to Lyme Disease, first things first…
Lyme Disease Is A Very Invasive (And Clever) Inflammatory Disease
This can have a tremendous impact on various symptoms in your body, and even cause painful symptoms that mimic those of other scary diseases.
Around 50% of all Lyme Disease cases begin with a “Bull’s Eye Rash”, that then progresses to flu-like symptoms, and finally, other issues like arthritis or other uncomfortable health problems.
If Lyme Disease goes untreated, things can go from BAD TO WORSE very quickly…
The symptoms may rapidly progress to create symptoms of
Encephalitis, Cardiomegaly
and even
inflammation of the Pericardium and sensory nerves in the body.
The 3 Biggest Problems of Battling Lyme Disease…
Problem #1: Most modern medicine fails to test for Lyme Disease unless you report that you’ve had a rash.
Problem #2: Most standard “solutions” to Lyme Disease are invasive and destructive on the body.
Problem #3: Most common symptoms will return at the end of most conventional treatments.
When you take a closer look at the destruction Lyme Disease can create in the body, as well as the typical approaches that modern and conventional medicine normally take, we quickly realised people were not getting properly treated in order to fully recover.
That’s when we decided to take a more holistic and natural approach to Lyme Disease recovery that looked at the entire body and the true causes of this dreadful disease.
A Much Better & More Effective Way To Beating Lyme Disease…
Our expert team has now created and carefully developed the Lyme Disease Recovery Programme, which is fully based on the transformative and healing power of Natural Medicine.
This exclusive programme is 100% customised to each patient to address their exact needs and symptoms. The focus of this programme is on identifying the ROOT CAUSE of Lyme disease, rather than merely controlling symptoms, as is the case with most conventional treatment plans.
Our expert team has successfully treated over 18,000 chronically ill patients, including 3,500 with Lyme disease, from more than 35 countries worldwide .
Our success rate is currently 90%
, thanks to our expertise and experience
in helping individuals heal from this dreaded disease.
The Lyme Disease Recovery Programme In 6 Easy Steps…
Not only is our programme
proven to be highly effective , but it’s also
very simple and straightforward to follow.
Our program consists of six steps, which include:
Step 1: RESTORATION OF GI TRACT
During this phase, we focus on restoring the gastrointestinal tract and its essential functions, which include digestion, alimentation, neurological function, defecation, immunity, and mood regulation. This phase also includes vital antibacterial treatment.
Step 2: IMMUNE SYSTEM MODULATION
The immune system is the body’s defense against infection from disease-causing pathogens such as bacteria and viruses. Immune system modulation, or immunomodulation, is a process that involves therapy to modify the immune response, often to prevent tissue damage caused by an excessive immune reaction. It is essential to maintain a finely balanced immune system.
Step 3: SYSTEMIC DETOXIFICATION
In the third phase, we focus on systemic detoxification, continuing with antibacterial treatments and introducing antiviral therapies to support your full recovery.
Step 4: IMMUNE SYSTEM MODULATION
(Repeated step)
The immune system is the body’s defense against infection from pathogens such as bacteria and viruses. Immune system modulation, or immunomodulation, involves using therapy to modify the immune response, often to prevent tissue damage caused by an excessive immune reaction. A balanced immune system is crucial for health.
Step 5: RESTORATION OF OTHER PROFILES
In this phase, we focus on restoring the metabolic, physiological, and neurological aspects of your body and healing. This comprehensive approach ensures all vital areas are addressed, restoring health where other treatments may fall short.
Step 6: PROGRAM AFTERCARE
Aftercare is an essential part of our program. Patients are entitled to one follow-up appointment each week for twelve weeks after treatment with a member of our team.
“Our Programme Is a PROVEN, MULTI-DISCIPLINARY and
EFFECTIVE Approach That’ll Help You Restore Your
Health in The Most Natural Way Possible!"
The Lyme Disease Recovery Programme
- Monthly consultations in, Natural medicine, Orthomolecular medicine, Nutrition, Herbal medicine, Homeopathy, TCM, Ayurveda
- Weekly progress reports - CoreMetrix
- Health Assessment Questionnaire
- Three telephone/Internet consultations a month
- Unlimited contact via email
- An individualised guidebook
- Emotional Freedom Technique
- Individualised recovery plan
- Individualised herbal tincture formulas
- Individualised herbal tea formulas
- Individualised balancing essential flower formulas
- Individualised restorative tissue salt formulas
- Individualised constitutional homeopathic remedies
- Measurement of 29 essential mineral elements
- Measurement of 5 toxic metals
- Description of a metabolic type and health tendencies
- Detailed food diary with recipes
- Individualised supplementation plan
- Individualised essential oil formulas
- Supply of the recommended supplements
- Supply of dietary fibre formula
- Individualised bath salts
- Supply of personalised topical creams or oils
- Individualised physical exercises
- *Additional Manual/Combined Treatments: Any additional manual/combined therapy treatments will last up to one hour.
The information that will be derived from this questionnaire alone is the equivalent of an 8-hour, comprehensive interview.
Are You Ready To Improve Your Health?
Fill In The Form Below To Get Started…
Contact us
- Babesia Bigemina
- Babesia Bovis
- Babesia Canis
- Babesia Cati
- Babesia Divergens
- Babesia Duncani
- Babesia Felis
- Babesia Gibsoni
- Babesia Herpailuri
- Babesia Jakimoni
- Babesia Major
- Babesia Microti / Theileria Microti / Babesia Vulpes
- Babesia Ovate
- Babesia Pantherae
- Bartonella Alsaticca
- Bartonella Arupensis
- Bartonella Bacilliformis
- Bartonella Berkhoffii
- Bartonella Birtlesii
- Bartonella Bovis
- Bartonella Capreoli
- Bartonella Clarridgeiae
- Bartonella Doshiae
- Bartonella Elizabethae / Rochalimaea Elizabethae
- Bartonella Grahamii
- Bartonella Henselae / Rochalimaea Henselae
- Bartonella Koehlerae
- Bartonella Melophagi
- Bartonella Muris
- Bartonella Peromyscus
- Bartonella Quintana / Rochalimaea Quintana / Rickettsia Quintana
- Bartonella Rochalimae
- Bartonella Schoenbuchii
- Bartonella Talpae
- Bartonella Taylorii
- Bartonella Tribocorum
- Bartonella Vinsonii / Rochalimaea Vinsonii
- Bartonella Washoensis
- Borrelia Afzelii
- Borrelia Berbera
- Borrelia Burgdorferi
- Borrelia Carteri
- Borrelia Caucasica
- Borrelia Duttonii
- Borrelia Garinii
- Borrelia Hermsii
- Borrelia Hispanica
- Borrelia Kochis
- Borrelia Miyamotoi
- Borrelia Morganii
- Borrelia Novyi
- Borrelia Parkeri
- Borrelia Persica
- Borrelia Recurrentis
- Borrelia Tillae
- Borrelia Turicatae
- Borrelia Valaisiana
- Borrelia Venezuelensis
- Borrelia Vincentii
- Ehrlichia Chaffeensis
- Herpes Virus HSV2 Herpes Simplex
- Herpes Virus VZV Varicella Virus
- Herpes Virus CMV
- Herpes Virus HHV6
- Herpes Virus HSV1
- Herpes Virus HHV8
- Herpes Virus VZV Zoster virus
- Herpes Virus EBV Epstein Barr Virus
- Anaplasma Phagocytophilum / Ehrlichia Phagocytophilum
- Chlamydia Pneumoniae
- Chlamydia Trachomatis
- Chlamydia Psittaci
- Mycoplasma hominis
- Mycoplasma pneumoniae
- Mycobacterium leprae
- Mycobacterium phlei
- Mycobacterium intracellulare
- Mycobacterium tuberculosis
- Mycobacterium avium
- Brucella suis
- Brucella bronchi-septica
- Brucella abortus
- Brucella melitenis
- Brucella canis
- Camplylobacter
- Staphylococci
- Pneumococinum
- Candida albicans
- Toxoplasmosis
- Meningococcinum
- Yerisenia cnterocolica
- Ureoplasma urealyticum
- Enterococcinium
- Cardiobacterium hominis
Why Is Systemic Detoxification So Crucial To
Your Success Over Lyme Disease?
The toxicological effect of one minor burden that a patient experiences can be rather significant, depending on their unique state of health with Lyme Disease. Two or more of these types of burdens can have a much greater impact.
Because of this, we test for the following trace elements: bar, boron, chrome, tin, zinc, phosphorus, germanium, iodine, cobalt, silicon, lithium, magnesium, manganese, copper, molybdenum, nickel, potassium, selenium, sulphur, sodium, strontium, vanadium, calcium, iron; and toxic elements: arsenic, aluminum, cadmium, lead, and mercury.
Our method of testing uses simple hair samples that are removed from the neck area. The hair that’s submitted for analysis should never be longer than 4cm from the scalp itself. About 200 mg (roughly 1 teaspoon) of hairs should be submitted for a thorough analysis.
Environmental sources of arsenic exposure include food, water, soil, and air. Arsenic is ubiquitous in the environment. Natural
sources are arsenic-containing mineral ores and groundwater (especially near geothermal activity). In industry, arsenic is a
by-product of the smelting process for many metal ores such as lead, gold, zinc, cobalt, and nickel. Other potential sources of arsenic exposure are:
• Commercial products: Wood preservatives, insecticides, herbicides (weed killers and defoliants), fungicides, cotton
desiccants, cattle and sheep dips, paints and pigments, antifouling paints, leaded gasoline, and fire salts (multicoloured flame).
• Food: Wine (grapes sprayed with arsenic-containing pesticides), and seafood (especially bivalves, certain cold water and
bottom-feeding finfish, and seaweed).
• Smokers may also inhale small amounts of arsenic as a result of pesticide residue on tobacco leaves.
• Industrial processes: purifying industrial gases (removal of sulfur), burning fossil fuels, burning wood treated with arsenic preservatives, electronics manufacturing (microwave devices, lasers, light-emitting diodes, photoelectric cells, and
semiconductor devices), hardening metal alloys, preserving animal hides, bronze plating, and clarifying glass and ceramics.
• Medicinals: Fowler's solution (potassium arsenite), antiparasitic drugs (carbazone), Donovan's solution, folk remedies ("Asiatic pill," kushtay, yellow root), kelp-containing health foods.
Health Effects:
• Acute arsenic toxicity may be associated with hepatic necrosis and elevated levels of liver enzymes.
• Gastrointestinal effects are seen primarily after arsenic ingestion, and less often after inhalation or dermal absorption.
• Arsenic is capable of causing acute renal failure, as well as chronic renal insufficiency.
• Long-term ingestion of arsenic in drinking water has resulted in pronounced peripheral vascular changes.
• Acute arsenic poisoning may cause both diffuse capillary leak and cardiomyopathy, resulting in shock.
• Arsenic-exposed patients develop destruction of axonal cylinders, leading to peripheral neuropathy.
• Pigment changes and palmoplantar hyperkeratosis are characteristic of chronic arsenic exposure.
• Benign arsenical keratosis may progress to malignancy.
• Inhalation of high concentrations of arsenic compounds produces irritation of the respiratory mucosa.
• Increased frequency of spontaneous abortions and congenital malformations has been linked to arsenic exposure.
• The carcinogenicity of arsenic in humans has been established, but no animal model has been developed.
• Latency for skin cancer associated with ingestion of arsenic may be 3 to 4 decades, whereas the noncarcinogenic skin
effects typically develop several years after exposure.
• In arsenic-exposed workers, there is a systematic gradient in lung cancer mortality rates, depending on the duration and intensity
of exposure.
Source: Agency for Toxic Substances and Disease Registry. 2006.
COPPER (Cu) HIGH:
This trace element is an important metalloenzyme, essential in haemoglobin synthesis. Adults absorb approximately 56% of dietary Cu, with < 50mcg/day excreted in the urine under normal and unprovoked conditions. The adult body contains
approximately 80mg copper, one third in muscle and the reminder in other tissue and body fluids. In the divalent state, copper can readily complex with many amino acids and proteins, such as metallothionein, which facilitate Cu-absorption from the stomach and the duodenum. In a large number of cuproproteins, Cu is a fixed proportion of the molecular structure, and these metalloproteins form an important group of oxidase enzymes, including ceruloplasmin (ferroxidase), SOD
(superoxide dismutase), cytochrome oxidase, lysyl oxidase, dopamine beta-hydroxylase, tyrosinase, uricase, spermine oxidase, benzylamine oxidase, diamine oxidase, and tryptophan-2,3 dioxygenase (tryptophan pyrrolase).
LABORATORY AND TESTING INFORMATION:
Urine analysis of unprovoked urine is not an adequate measure to assess copper stores or copper metabolism. Blood copper levels, SOD levels and serum ceruloplasmin are other, often more indicative measurements for copper status. Increased urinary copper levels can be caused by nutritional supplementation with copper or be the result of a high dietary intake due to copper-containing drinking water. Supplements containing high molybdenum may stimulate an increase in copper excretion because Cu and Mo are mutually antagonistic in terms of body retention.
CLINICAL SIGNS AND SYMPTOMS:
•Bacterial or other infection may cause hypercupremia, and published studies such as Vivoli, Sci Total Eniviron, 66p 55-64,
1987 have correlated increased urinary copper levels with increased blood pressure in hypertensives. Biliary obstruction or insufficiency can decrease the normal excretion of copper via the bile while increasing blood and urine levels.
•Hyperaminoacidemia, including histidinuria, can result in copper wasting since histidine is a powerful chelator of copper. Hyperaminoacidemia can be of various origins including genetic factors, chemical or elemental toxicities (high urinary copper is often seen with high mercury levels) infectious agents, hyperthyroidism, sugar intolerances, nephrotic symptoms, etc.
•In Wilson's disease, urinary copper levels may increase to above 100mcg/24hrs without provocation or chelation.
LITERATURE:
Kaplan LA; Pesce AJ. Clin Chem. Theory, analysis, correlation. 2nd ed. Mosby 1989, p535-536
LEAD (Pb) HIGH:
Occupational and environmental exposure are common causes of high urinary concentrations.
Common Sources:
Leaded gasoline, canned goods, lead paint, newsprint, tobacco smoke, air pollution, and contaminated water.
Biochemical basis of toxicity:
Only 8 to 12% of the orally ingested lead is absorbed by the small intestine, but toxic effects are severe. Lead can react with
sulfhydryl groups in enzymes, thereby inactivating important enzymes such as the aminolevulinic acid dehydratase (ALA) and
ALA synthetase, leading to haematological manifestations. Lead reduces the body's ability to utilize calcium, magnesium, zinc, iron and other important nutrients. Lead is easily absorbed by children.
Clinical Signs:
The pathological effects of Pb have been recognized for centuries. Lead affects all physiological systems including renal,
nervous, reproductive, endocrine, immune, and hemopoietic. Exposure to lead, either chronic or acute, presents a variety of
signs, symptoms, and chemical evidence. The exposed person may be asymptomatic or symptomatic.
• Mild Symptoms include tiredness, lack of energy, constipation, slight abdominal pain and discomfort, anorexia, altered sleep,
irritability, anaemia, hair loss, pallor, and less frequently diarrhoea and nausea. Formation and precipitation of lead sulfide may be
evidenced as a blue-black ‘lead line’ near the gingival margin of the teeth.
• Severe symptoms include colic, reduction of muscle power, muscle tenderness, paresthesia, and symptoms of neuropathy
and encephalopathy.
• Frequent Symptoms in children as reported by the Center for Disease control are irritability, vomiting, abdominal pain, ataxia, anorexia, behavioural changes, speech disturbances, seizures, intercurrent fever, and dehydration. Other symptoms reported
are ataxia and stupor.
Laboratory Analysis:
Two classes of persons must be considered:
1.) The occupationally exposed:
• A case of occupational lead overexposure is defined as an adult (15 years of age or older) with a BLL greater than or equal to 25 mcg/dL or 250 mcg/L.
• Childhood lead poisoning is defined by the Centers for Disease Control and Prevention as a blood lead level of 10 ug/dL or above. Long-term effects may include slow development, reduced Intelligence Quotient (IQ), learning disabilities, hearing loss, decreased height and hyperactivity. Most lead-intoxicated children do not have any symptoms. Appearing symptoms are often confused with other childhood illnesses. Very severe lead exposure (levels higher than 80 ug/dL) can cause coma, convulsions and even death.
2.) Low-level chronic exposure:
• Blood levels may or may not be significant, depending on the immediate exposure.
• Long-term exposed individuals typically show elevated hair lead.
Blood lead and urine concentrations have been reported to be about 10 to 20% higher in males than females, both in children and adults.
Literature:
American Academy of Pediatrics, Committee on Environmental Health Lead poisoning: from screening to primary prevention.
Pediatrics 1993; 92:176-183
Casey R, Wiley C, Rutstein R, Pinto-Martin J Prevalence of lead poisoning in an urban cohort of infants with high
socioeconomic status. Clin. Pediatr 1994; 33:480-484
Lead-Based Paint Hazard Reduction and Financing Task Force. Putting the Pieces Together: Controlling Lead Hazards in the
Nation's Housing. Washington, DC: US Dept of Housing and Urban Development; 1995.
National Research Council. Measuring Lead Exposure in Infants, Children and Other Sensitive Populations. Washington, DC:
National Academy Press; 1993
Med 1996; 150:609-614
Centres for Disease Control and Prevention. Blood Lead Proficiency Testing. Atlanta, GA: US Dept of Health and Human
Services, Public Health Service; 1994.
MERCURY (Hg):
Mercury compounds readily react covalently with sulfhydryl groups in proteins, resulting in inhibition of functional activity. Both
organic and inorganic mercury are potentially toxic compounds.
TOXICITY:
• Excretion levels of 100 mcg/g creatinine in random urine before chelation are representative of acute exposure, reflecting toxicity. Values equal to the Hg-Orientation Range indicate a mild exposure, values above that range and below the excretion level of 100mcg/g creatinine are representative of a past or present intoxication. Early Symptoms of Chronic overexposure may occur at much lower levels including Insomnia, dizziness, fatigue, drowsiness, weakness, depression, tremors loss of appetite, loss of memory, nervousness, headache, dermatitis, numbness, and tingling of lips and feet, emotional instability and kidney
damage.
SOURCES: Overexposure may stem from paints, bleaches, explosives, electrical apparatus, batteries, mercurial diuretics, fungicides, fluorescent lamps, cosmetics, hair dyes, amalgams in dentistry, contaminated seafood, and petroleum products.
Vaccines such as tetanus toxoid contain thimerosal, which is a mercury compound. Improper disposal of broken mercury thermometers and other apparatuses that use mercury including button cells and tube lights are additional sources of mercury exposure.
LITERATURE:
Berlin M: Mercury, In Friberg L. Nordberg GF and Vouk, VB, editors: Handbook on the toxicology of metals. Amsterdam, 1979,
Elsevier/No Holland Biomed Press.
Clarkson TW. Mercury poisoning. In Brown SS, editor: Clinical chemistry and chemical toxicology of metals. Amsterdam, 1977.
Elsevier/No Holland Biomed Press.
Kaplan LA, Pesce AJ. Clinical Chemistry, Theory, analysis, and correlation. 2nd ed. Mosby UK 1989, p 541 Thomas L. Labor
Testimonial
I had just finished college in 2016 just about to start my career in the health care field, absolutely oblivious to what was going to happen to my health and the rollercoaster ride of trying to get help.
I had such a vast array of symptoms from hormones to digestive issues to fatigue to extreme weight loss and hair that was falling out in clumps. I was always coming home from work. It was not normal for me as I never even had so much as a cold in years.
I went to a gastroenterologist, two as a matter of fact and both told me there was nothing wrong and that it was just a “classic case of IBS” and absolutely no signs of Crohn's disease as I was diagnosed with that at nine years old and it just seemed to heal by itself in the space of two years and never had any issues. I was tested for many different things, including hormones, parasites etc. and nothing was showing up. I was then admitted to the Mater Private Hospital Cork for a week, and they tested me for diabetes and all of the common diseases. I also met an Infectious disease “specialist” who even said that people in Ireland don’t get parasites, who was at Cork University Hospital.
My patience had run dry with the Irish healthcare system, so I decided to go to Germany to The University Hospital of Freiberg for a second opinion. They did a thorough examination scans and scopes, and they found that I had a split duct in my pancreas, which they thought were what matched my pain at the time. But the Professor did mention that it seemed more like a bacterial infection.
I was starting to doubt the blood tests, why nothing was showing up. I decided to go to a retired medical surgeon who practised bio-resonance in Belfast. Within an hour, he told me I had inflammation and parasites in my gut, glandular fever and Lyme disease, even though my Lyme blood test had come back negative before. I was on the fence whether to believe him, but it was the first logical explanation to what was going on. I later got another test done from a different practitioner in Leeds, which also said Lyme and other infections. I realised I needed professional help and quickly.
I went to England privately as all I was being told here in Ireland was you are depressed there is nothing wrong with you. I attended a Doctor (infectious disease) in Bristol who examined me and told me straight away it sounded like a virus. She tested me for glandular fever, and it came back positive and gave me eight weeks of antibiotics. I felt fine while I was taking antibiotics, but as soon as I finished the course, I was worse than before.
In March 2019, I came across Core Integrative Health and decided I would go for an appointment, as at this point, I had exhausted all avenues.
As I was pretty sceptical, I only told Dr Radek Lorecki that I had Crohn's disease when I was younger and that I had a glandular fever last year. After the testing, he told me what he had found, and it matched exactly to the previous tests and more, but the main issue was Lyme and some other infections.
I decided to undergo the recovery programme with Dr Lorecki, and after four months, the Lyme was no longer testing positive. I decided to cross-check this again with bio-resonance, and it showed no Lyme.
I am excited that my health is finally improving in all areas thanks to Dr Radek Lorecki.
His knowledge and patience were very much put to the test.
I cannot explain how much Dr Radek is after helping me; I am forever grateful.
If anyone is suffering from any illness, not just Lyme, I can highly recommend him.
N.B Ireland
Patient code 8579 - 2019-LYME-452
Are You Ready To Improve Your Health?
Fill In The Form Below To Get Started…
Contact us
Say Goodbay To Lyme Disease!
Get Back To Living The Healthy Life You Deserve!
Our goal is to aid patients to improve their health.
In order to succeed, we must address the underlying cause of disease, and guide patients to optimal health through effective, individualised, natural therapies that integrate the healing powers of body and mind.
In order to succeed, we must address the underlying cause of disease, and guide patients to optimal health through effective, individualised, natural therapies that integrate the healing powers of body and mind.