Heart Disease, Diabetes, High Cholesterol.. Successfully Treated by Integrative & Holistic Treatment
NAME:
Adrian See
PLACE:
Singapore
WORK:
Real Estate
TREATMENT CASE SUMMARY
PRE-TREATMENT
Disease Symptoms
- Chest pain
- Breathlessness
- Tiredness & fatigue
- Cold hands & feet
- Bloating
Medical Conditions
- Ishemic heart disease (3 arteries blocked)
- Congestive Heart Failure
- Diabetes
- High Cholesterol
- Gastritis
Medications
- Heart failure med
- Anti-platlet med
- Diabetes med
- Cholesterol med
- Gastritis med
POST-TREATMENT
Disease Symptoms
- Chest pain - Resolved.
- Breathlessness - Resolved.
- Tiredness & fatigue - Resolved.
- Cold hands & feet - Resolved.
- Bloating - Resolved.
Medical Conditions
- Ishemic heart disease - Resolved 80%.
- Congestive Heart Failure - Resolved 80%.
- Diabetes - Improved 90%.
- High Cholesterol - Resolved 90%.
- Gastritis - Resolved.
Medications
- Heart failure med - Weaned off.
- Anti-platlet med - Weaned off 50%.
- Diabetes med - Weaned off 70%.
- Cholesterol med - Weaned off.
- Gastritis med - Weaned off.
PATIENT TESTIMONY
TREATMENT EFFECTIVENESS
SERVICE QUALITY
DOCTOR
STAFF
PRICE
RECOMMENDED
DOCTOR
STAFF
PRICE
RECOMMENDED
My wife and I researched for weeks. Most Western doctors, even those who offer natural therapies, eventually revert to medication — because that is all they are trained to do. They treat the condition in front of them. They never ask: why did this condition appear in the first place? That was the question I needed answered.
At Heal Within®, Dr. Lee Cheng Lok asked exactly that question -- his entire treatment is based upon finding and treating the underlying root causes. This approach is what is called Integrative & Holistic Treatment — and it is what sets Heal Within® apart from every other doctor and clinic we had looked at.
At Heal Within®, Dr. Lee Cheng Lok asked exactly that question -- his entire treatment is based upon finding and treating the underlying root causes. The diagnostic process was unlike anything I had experienced — blood tests, saliva tests, live blood analysis. When I first saw my own blood cells, I was taken aback: dark, clumped, barely flowing. Dr. Lee discovered high heavy metal levels traced to mercury from old dental amalgam fillings, gut dysbiosis, hormonal imbalance, and several other root causes that had been silently driving my heart disease and diabetes for years. No conventional doctor had ever gone this deep. They had been treating my clogged pipes — but nobody had looked for what caused the clogs.
Once the root causes were identified, treatment followed logically: IV Chelation to clear the heavy metals, IV Nutrition, oral detoxification, targeted supplementation, FIR Sauna Detoxification following my amalgam removal. Alongside the clinical treatment, I made five lifestyle changes — quitting smoking and alcohol, restructuring my sleep, cleaning up my diet, and exercising daily.
The results speak for themselves. Blood cells bright red, separated, and freely flowing. Blood sugar down from a diabetic 6–7 to a healthy 4–5. Cholesterol under control. All gastric symptoms gone. Energy dramatically higher. More productive and more alive than before my heart attack.
You were not born to take medications every day. There is another way — but it requires the willingness to find the real cause, not just manage the symptoms. If you are ready for that, Heal Within® is where that journey begins.
DOCTOR'S CASE PRESENTATION
PATIENT CASE DETAILS
PRE-DISEASE LIFESTYLE
Food
Standard Asian-style meals, with a heavy preference for carbohydrates
Nutrition
No dedicated supplementation. Standard pharmacy multivitamins.
Exercise
No regular exercise routine prior to treatment.
Environment
Typical busy urban city environment.
Rest
Irregular sleep schedule. Late nights were habitual.
Mind & Emotions
High-functioning professional under the habitual pressures.
Periodic Detoxification
None.
Periodic Medical Screening
Standard hospital and clinic health check-ups
MEDICAL HISTORY
(Prior to treatment in Heal Within®)
🗓 — Prior to April 2025.
Conditions present: Diabetes, High Cholesterol, Gastritis.
Sought treatment at: General practitioners and specialist clinics in Singapore.
Treatment administered: Diabetes medication, cholesterol medication, gastric medication.
Result: Conditions managed and kept within tolerable levels with medication, but without resolution. No investigation into underlying root causes.
🗓 — April 2025.
Symptoms: Chest pain upon waking, cold sweats, difficulty walking normally.
Sought treatment at: Local outpatient clinic, then A&E at hospital, Singapore.
Diagnosis: Acute myocardial infarction (heart attack). One coronary artery found to be 100% blocked; two further arteries functioning at approximately 35% capacity. Congestive heart failure confirmed.
Treatment administered: Emergency coronary stent procedure. Post-procedure: cholesterol medication, anti-platelet medication, heart failure medication, diabetes medication, gastric medication. Advised by attending cardiologist that he would be on medication for life.
Result: Acute event stabilised. Discharged from hospital on multiple medications. Root causes not investigated.
🗓 — April – August 2025.
Symptoms: Residual tiredness, breathlessness, cold hands and feet, bloating.
Sought treatment at: Cardiologist follow-up appointments, Singapore. Initially fortnightly, then monthly.
Treatment administered: Continued medications as prescribed. Cholesterol-lowering injections recommended by cardiologist.
Result: Cholesterol levels reduced by approximately 50% through patient’s own lifestyle efforts. Despite this improvement, cardiologist continued to push for cholesterol-lowering injections. No acknowledgment of lifestyle progress. No root cause investigation. Patient increasingly motivated to seek an alternative approach.
🗓 — September 2025.
Symptoms: Breathlessness, tiredness, chest discomfort, cold hands and feet, bloating persisting.
Sought treatment at: Heal Within®.
Diagnosis: Read in full case details below.
Treatment administered: Read in full case details below.
Result: Read in full case details below.
TREATMENT IN HEAL WITHIN®
PHASE 1: DIAGNOSIS
1. Vitality Factors
*100% represents optimal level for patients’s genetics, gender & age.
2. Disease Symptoms
- Chest pain
- Breathlessness
- Tiredness & fatigue
- Cold hands & feet
- Bloating
3. Medical Conditions (Diseases)
- Ishemic heart disease (3 arteries blocked)
- Congestive Heart Failure
- Diabetes
- High Cholesterol
- Gstritis
4. Causes & Root-causes to Medical Conditions
◉ Gut disbiosys & acidosis
What it is:
‘Gut Dysbiosis’ is a disruption to the gut microbiome resulting in an imbalance of gut microbiota, abnormalities in their metabolic activities and functions, and a shift in their local distribution throughout the digestive tract. ‘Gut Acidosis’ is an over-acidification of the fluids within the gut environment. Together, these two conditions compromise the integrity of the intestinal lining, impair nutrient absorption, dysregulate immune responses, and generate systemic inflammation that extends far beyond the digestive system into every organ and tissue in the body.
Root-causes / Sources:
High carbohydrate and sugar-heavy diet, low vegetable and fibre intake, absence of probiotic or nutritional supplementation, chronic stress, irregular sleep patterns, prolonged use of pharmaceutical medications.
Mechanism:
When gut dysbiosis and acidosis are present, the gut barrier becomes permeable and the microbial environment becomes pathological. Bacterial toxins and undigested particles enter systemic circulation, triggering chronic inflammation, hormonal disruption, and immune dysfunction throughout the body. In Adrian’s case, this compromised gut environment was a significant underlying driver of his cardiac, metabolic, and gastrointestinal conditions.
Ischemic Heart Disease & Congestive Heart Failure:
- Gut dysbiosis produces inflammatory bacterial metabolites that enter the bloodstream
- These compounds promote systemic inflammation, accelerating arterial plaque formation
- Increased intestinal permeability allows endotoxins to circulate, elevating cardiovascular inflammatory markers
- Chronic gut inflammation dysregulates lipid metabolism, worsening cholesterol profiles
- Impaired absorption of heart-protective nutrients — magnesium, CoQ10, omega-3 — weakens cardiac muscle function
- Systemic inflammatory burden increases cardiac workload, progressively impairing heart function
Diabetes:
- Gut dysbiosis disrupts the microbial regulation of blood glucose and insulin sensitivity
- Inflammatory bacterial by-products impair insulin receptor signalling in cells
- Compromised gut barrier allows endotoxins to trigger chronic low-grade inflammation
- This inflammation directly promotes insulin resistance at the cellular level
- Acidic gut environment impairs absorption of chromium, magnesium, and B-vitamins essential for glucose metabolism
- Dysbiotic microbiome reduces production of short-chain fatty acids that regulate blood sugar balance
High Cholesterol:
- Gut microbiome imbalance disrupts bile acid metabolism, impairing cholesterol regulation
- Dysbiotic bacteria produce compounds that increase hepatic cholesterol synthesis
- Impaired absorption of plant sterols and fibre reduces the gut’s natural cholesterol-lowering capacity
- Systemic inflammation from gut dysbiosis elevates LDL oxidation and triglyceride levels
- Acidic environment impairs liver detoxification pathways responsible for cholesterol clearance
- Compromised gut barrier allows inflammatory mediators to dysregulate lipid metabolism in the liver
Gastritis:
- Gut dysbiosis directly disrupts the mucosal lining of the stomach and upper gastrointestinal tract
- Imbalanced microbiota allows pathogenic bacteria to proliferate, increasing gastric inflammation
- Acidic gut environment erodes the protective mucous layer lining the stomach wall
- Compromised intestinal integrity allows digestive acids and toxins to irritate gastric tissue
- Dysbiosis impairs the production of digestive enzymes, causing food fermentation, bloating, and gastric discomfort
- Chronic gut inflammation triggers hypersensitivity of the gastric lining, perpetuating symptoms
◉ Toxins & Heavy-metals
What it is:
Toxicity refers to the accumulation of harmful chemical compounds, environmental pollutants, and metabolic waste products within the body’s tissues and bloodstream at levels that exceed the body’s natural capacity to eliminate them. Heavy metal accumulation specifically refers to the build-up of toxic metallic elements — in Adrian’s case, mercury — within body tissues and the circulatory system. Mercury is a potent cardiovascular toxin that disrupts cellular function, promotes oxidative stress, and triggers chronic systemic inflammation.
Root-causes / Sources:
Long-term presence of dental amalgam fillings containing mercury, environmental pollutant exposure typical of urban living, accumulation of dietary toxins, impaired natural detoxification capacity due to poor diet and absence of periodic detoxification.
Mechanism:
Heavy metals and accumulated toxins interfere with cellular biochemistry at a fundamental level. They bind to and inactivate critical enzymes, generate excessive free radicals that damage cell membranes and DNA, trigger persistent immune activation, and impair the function of every organ system they infiltrate. In the cardiovascular system, mercury and other heavy metals are particularly destructive — they promote arterial inflammation, accelerate atherosclerotic plaque formation, impair the electrical signalling of the heart, and compromise the integrity of the vascular endothelium. In Adrian’s case, chronic heavy metal burden was a key underlying driver of his ischemic heart disease and congestive heart failure.
Ischemic Heart Disease & Congestive Heart Failure:
- Mercury and heavy metals directly damage the vascular endothelium, initiating arterial inflammation
- Toxic metals promote oxidative stress within arterial walls, accelerating atherosclerotic plaque formation and coronary artery narrowing
- Heavy metal accumulation impairs mitochondrial energy production in cardiac muscle cells, weakening heart contractility
- Toxic burden activates chronic immune responses that sustain arterial inflammation and progressive blockage
- Mercury disrupts the autonomic regulation of heart rate and cardiac electrical signalling
- Impaired liver detoxification from toxic overload elevates circulating inflammatory markers that further damage coronary vessels
Diabetes:
- Heavy metals interfere with pancreatic beta cell function, impairing insulin production and secretion
- Mercury induces oxidative stress in insulin-sensitive tissues, reducing cellular glucose uptake
- Toxic accumulation impairs mitochondrial function in liver and muscle cells, disrupting glucose metabolism
- Heavy metals displace essential minerals — zinc, chromium, magnesium — from enzyme binding sites critical to insulin signalling
- Chronic toxic burden triggers systemic inflammation that promotes insulin resistance at the cellular level
- Impaired detoxification allows glucose-dysregulating compounds to circulate and accumulate in metabolic tissues
High Cholesterol:
- Heavy metal toxicity impairs liver enzyme function, disrupting the liver’s regulation of cholesterol synthesis and clearance
- Mercury-induced oxidative stress increases LDL oxidation, making cholesterol particles more atherogenic and dangerous
- Toxic burden disrupts bile acid production and recycling, impairing the body’s natural mechanism for cholesterol elimination
- Heavy metals impair the function of lipid-metabolising enzymes throughout the hepatic system
- Chronic inflammation driven by toxicity dysregulates lipid metabolism, elevating triglycerides and unfavourable cholesterol fractions
- Detoxification pathway impairment reduces the liver’s capacity to process and excrete excess cholesterol effectively
◉ Essential-nutrients deficiency
What it is:
Essential Nutrient Deficiency is a deficiency of one or more critical nutrients — proteins, vitamins, minerals, essential fats, or trace elements — in the blood or organ tissues. These nutrients are not optional extras; they are the biochemical building blocks that every cell, enzyme system, and organ in the body depends upon to function correctly. Without adequate levels, cellular repair slows, immune defences weaken, metabolic processes break down, and the conditions for chronic disease are quietly but steadily established.
Root-causes / Sources:
High carbohydrate, low vegetable diet providing insufficient vitamins, minerals, and phytonutrients. Low fibre intake. Absence of targeted nutritional supplementation. Impaired nutrient absorption secondary to gut dysbiosis. Prolonged use of pharmaceutical medications known to deplete key micronutrients.
Mechanism:
When essential nutrients are chronically deficient, the body’s repair and maintenance systems begin to fail silently. Enzyme reactions that regulate inflammation, energy production, hormonal balance, and immune function all become compromised. Tissues that depend on continuous renewal — the arterial walls, the cardiac muscle, the pancreatic cells, the gastric lining — progressively deteriorate. Over time, this silent deterioration manifests as diagnosable chronic disease. In Adrian’s case, nutrient deficiency was a pervasive background condition amplifying every other root cause present in his body.
Ischemic Heart Disease & Congestive Heart Failure:
- Magnesium deficiency impairs vascular smooth muscle relaxation, increasing arterial tension and cardiovascular strain
- CoQ10 deficiency — worsened by statin use — severely reduces mitochondrial energy production in cardiac muscle cells
- Omega-3 fatty acid deficiency increases systemic inflammation and promotes platelet aggregation, accelerating arterial plaque formation
- Vitamin D deficiency dysregulates immune function and promotes vascular inflammation
- B-vitamin deficiencies elevate homocysteine levels, a well-established independent risk factor for coronary artery disease
- Antioxidant deficiency — vitamins C and E, selenium — allows unchecked oxidative damage to arterial walls and cardiac tissue
Diabetes:
- Chromium deficiency directly impairs insulin receptor sensitivity and glucose uptake in cells
- Magnesium deficiency disrupts insulin signalling pathways and glucose transporter function
- B-vitamin deficiencies impair cellular energy metabolism and mitochondrial glucose utilisation
- Vitamin D deficiency reduces pancreatic beta cell function and insulin secretion capacity
- Zinc deficiency impairs insulin synthesis, storage, and secretion in the pancreas
- Antioxidant deficiency allows oxidative damage to pancreatic cells, progressively impairing insulin production
High Cholesterol:
- Omega-3 fatty acid deficiency removes a key natural regulator of triglyceride levels and LDL particle size
- Magnesium deficiency impairs the enzyme systems responsible for cholesterol synthesis regulation in the liver
- Vitamin C deficiency compromises the conversion of cholesterol into bile acids for elimination
- Niacin (B3) deficiency removes a natural mechanism for raising HDL and reducing LDL cholesterol levels
- Antioxidant deficiency allows LDL particles to become oxidised, making them significantly more atherogenic
- Fibre and plant nutrient deficiency reduces the gut’s capacity to bind and excrete dietary cholesterol
◉ Metabolic acidosis
What it is:
Metabolic Acidosis is a systemic condition in which the body’s pH balance shifts toward excess acidity, disrupting the optimal biochemical environment required for normal cellular function. The human body is designed to operate within a tightly regulated, slightly alkaline pH range. When this balance is compromised — through an acidic diet, impaired acid elimination, or excessive metabolic acid production — cellular processes slow, enzyme systems malfunction, inflammation escalates, and tissue degeneration accelerates.
Root-causes / Sources:
High intake of refined carbohydrates, sugar, and processed foods. Low consumption of alkalising foods such as vegetables and fruits. Inadequate intake of alkalising minerals. Impaired kidney and liver acid elimination capacity. Chronic stress generating excess metabolic acids. Prolonged pharmaceutical medication use impairing acid-base regulation.
Mechanism:
When the body becomes chronically acidic, the consequences cascade through every organ system. Inflammatory enzyme activity increases. Tissue repair and cellular regeneration slow significantly. The body is forced to buffer excess acidity by leaching alkalising minerals — calcium, magnesium, potassium — from bones, muscles, and organ tissues, progressively depleting these critical reserves. Blood vessel walls, cardiac muscle, pancreatic cells, and the gastric lining are all highly sensitive to pH shifts, and all suffer measurable functional deterioration under sustained acidic conditions. In Adrian’s case, chronic metabolic acidosis created the permissive internal environment in which his heart disease, diabetes, high cholesterol, and gastritis were able to develop and progress.
Ischemic Heart Disease & Congestive Heart Failure:
- Acidic conditions directly damage the vascular endothelium, initiating and sustaining arterial wall inflammation
- Inflammatory enzyme activity increases significantly in an acidic vascular environment, accelerating plaque formation
- Acidosis impairs mitochondrial energy production in cardiac muscle cells, reducing heart contractility and efficiency
- The body buffers excess acidity by depleting magnesium and calcium, critically weakening cardiac muscle function
- Acidic blood environment promotes platelet aggregation and blood viscosity, increasing clotting and coronary blockage risk
- Chronic acidosis activates systemic stress responses that elevate blood pressure and increase cardiovascular strain
Diabetes:
- Acidic cellular environment impairs insulin receptor function and reduces cellular sensitivity to insulin
- Metabolic acidosis disrupts pancreatic beta cell activity, impairing insulin secretion
- Acidosis impairs glucose transporter function in muscle and liver cells, reducing glucose uptake and utilisation
- The body’s buffering response depletes chromium and magnesium — both essential for glucose metabolism and insulin signalling
- Acidic conditions increase cortisol production, which directly elevates blood glucose levels
- Chronic acidosis promotes systemic inflammation that further entrenches insulin resistance at the cellular level
High Cholesterol:
- Acidic conditions impair liver enzyme function, disrupting the normal regulation of cholesterol synthesis
- Acidosis promotes LDL oxidation, increasing the proportion of dangerous, atherogenic cholesterol particles in circulation
- The body produces more cholesterol as a protective buffer against acidic cellular damage — paradoxically worsening lipid profiles
- Acidic environment impairs bile acid production and recycling, reducing cholesterol excretion capacity
- Mineral depletion caused by acid buffering impairs the enzyme systems that regulate healthy lipid metabolism
- Chronic low-grade inflammation from acidosis dysregulates hepatic lipid processing, elevating triglycerides and unfavourable cholesterol fractions
* Learn more about the 10 Root Causes to Diseases.
PHASE 2: TREATMENT
The primary objectives of the treatment:
- Clear (or reduce to the minimal) accumulated plaque from coronary arteries; and, open-up new collateral capillaries to restore normal blood-flow to the heart.
- Treat all the root causes to plaque-formation, and thereby stop the on-going formation & accumulation of new plaque.
- Optimise the condition and function of all organs.
No one therapy or treatment modality can achieve these objectives alone. An integration — a strategic combination — of various therapies is necessary. This is what is called an Integrated & Holistic Treatment — and one of its most powerful characteristics is that all of Adrian’s conditions were treated simultaneously, inducing healing across the whole body rather than addressing each disease in isolation.
The following therapies were strategically integrated and administered to the patient:
✙ Oral Detoxification Therapy
What it is:
Oral Detoxification Therapy is a structured therapeutic protocol combining natural bioactive compounds — medicinal herbs, essential nutrients, therapeutic fats, mineral salts, antioxidant compounds, probiotic strains, digestive enzymes, and specialised detoxifying agents — administered in precisely timed oral doses over structured treatment cycles. This multi-agent approach works systematically to enhance the body’s natural detoxification pathways, restore gut microbiome balance, alkalise body tissues, and safely bind and eliminate accumulated toxins and metabolic waste products through the digestive and urinary systems.
Used for:
- Restoring healthy gut microbiome balance to correct the gut dysbiosis identified as a key root cause of Adrian’s conditions
- Alkalising body tissues to counteract the chronic metabolic acidosis driving systemic inflammation across his cardiovascular, metabolic, and digestive systems
- Enhancing liver phase I and II detoxification pathways to support the safe processing and elimination of toxins mobilised during IV Chelation sessions
- Strengthening intestinal barrier integrity to prevent ongoing toxin reabsorption and leaky gut
- Supporting kidney filtration capacity for efficient elimination of waste products and mobilised heavy metals
- Providing essential cofactors and nutrients that sustain the body’s detoxification enzyme systems between intravenous treatment sessions
Effects:
- Progressively corrected the gut dysbiosis and metabolic acidosis that had been sustaining systemic inflammation across Adrian’s heart, metabolic, and digestive conditions
- Supported the complete resolution of gastritis symptoms — bloating, gastric discomfort, and digestive irregularity — which Adrian reported as fully resolved over the course of treatment
- Enhanced the effectiveness of IV Chelation Therapy by maintaining active detoxification pathways between intravenous sessions
- Contributed to the alkalisation of Adrian’s internal environment, creating the biochemical conditions necessary for tissue repair and disease resolution
- Supported the overall reduction in systemic inflammatory burden, benefiting all of Adrian’s conditions simultaneously
- Improved digestive enzyme function and gut motility, directly contributing to better nutrient absorption and thereby amplifying the benefits of both IV and oral nutritional therapies administered concurrently
✙ IV Chelation therapy
What it is:
IV Chelation Therapy is a medically administered intravenous treatment in which a chelating agent — delivered as a clear fluid drip directly into the bloodstream — binds to heavy metals and toxic mineral deposits circulating in the blood and lodged in body tissues. These bound complexes are then safely eliminated from the body through the kidneys and urinary system. It is one of the most effective clinical tools available for systematically clearing heavy metal accumulation, and carries well-documented cardiovascular benefits through its ability to reduce toxic arterial burden and restore healthy vascular function.
Used for:
- Binding and safely eliminating the elevated mercury and heavy metal levels identified in Adrian’s live blood analysis at first consultation
- Reducing the toxic arterial burden that was a key root cause driver of his ischemic heart disease and congestive heart failure
- Decreasing systemic oxidative stress generated by years of heavy metal accumulation in his tissues
- Improving vascular endothelial function and blood flow by clearing toxic deposits from vessel walls
- Reducing the overall inflammatory load on the cardiovascular system
- Supporting the liver and kidneys in safely processing and excreting the mobilised toxins
Effects:
- Directly addressed the elevated heavy metal levels found in Adrian’s bloodstream, removing a primary root cause of his cardiac disease
- Progressive improvement in blood cell appearance — from dark, clumped, and sluggish to bright red, separated, and freely flowing — observed across successive live blood examinations
- Reduction in systemic inflammatory burden, producing measurable benefits across his heart, metabolic, and digestive conditions simultaneously
- Contributed to the significant improvement in energy levels and overall vitality reported by Adrian as treatment progressed
- Supported the progressive reduction of anti-platelet and heart failure medications as cardiac function improved over the course of treatment
✙ Oral Nutrition therapy
What it is:
Oral Nutrition Therapy is a structured, physician-prescribed programme of targeted nutritional supplementation — comprising full-spectrum vitamins, minerals, essential fatty acids, therapeutic oils, amino acids, and specialised nutraceutical compounds — taken orally in precisely determined doses and timing protocols. While IV Nutrition Therapy delivers nutrients directly into the bloodstream for immediate cellular uptake, Oral Nutrition Therapy provides sustained, continuous nutritional support between clinical sessions — ensuring that the body maintains the nutrient levels required for ongoing repair, immune regulation, hormonal balance, and organ optimisation throughout the full course of treatment.
Used for:
- Providing sustained daily nutritional support to maintain and build upon the therapeutic nutrient levels established through IV Nutrition Therapy sessions
- Correcting specific deficiencies critical to Adrian’s cardiovascular health — including omega-3 fatty acids, CoQ10, magnesium, and antioxidant vitamins — on a continuous daily basis
- Supporting healthy cholesterol metabolism through targeted lipid-regulating nutrients including omega-3 fatty acids and plant-based compounds
- Improving blood viscosity and platelet function through omega-3 and essential fatty acid supplementation to support healthier blood flow
- Providing chromium, zinc, B-vitamins, and other insulin-sensitising nutrients to support the normalisation of blood sugar levels
- Supporting gastric mucosal repair and digestive function through targeted gut-supportive nutrients and enzymes
Effects:
- Delivered continuous day-to-day nutritional reinforcement that sustained and compounded the benefits achieved through IV therapy sessions
- Directly supported the improvement in blood cell quality observed in Adrian’s live blood examinations — with cells progressively transitioning from clumped and sluggish to separated and freely flowing
- Contributed to the sustained reduction in blood sugar levels from a diabetic range of 6–7 to a healthy 4–5, supporting the progressive reduction of diabetes medication
- Supported the normalisation of Adrian’s cholesterol profile — with the LDL/HDL margin brought within an acceptable range — without the need for the cholesterol-lowering injections his Singapore cardiologist had been recommending
- Improved Adrian’s energy levels, mental alertness, and daily productivity as nutritional reserves were progressively restored across the body
- Enabled Adrian to manage his supplement regimen independently as part of his daily routine, embedding nutritional discipline as a lasting lifestyle practice
✙ IV Nutrition therapy
What it is:
IV Nutrition Therapy is the intravenous administration of a precisely formulated combination of essential vitamins, minerals, antioxidants, and therapeutic nutrients delivered directly into the bloodstream, bypassing the digestive system entirely. This direct delivery method achieves tissue and cellular concentrations far beyond what is possible through oral supplementation alone — making it a powerful tool for rapidly correcting deep nutritional deficiencies, restoring cellular energy production, and supporting the body’s natural healing and repair processes at the organ level.
Used for:
- Rapidly correcting the severe and longstanding essential nutrient deficiencies underlying Adrian’s cardiovascular and metabolic conditions
- Restoring critical cardiac nutrients — CoQ10, magnesium, B-vitamins, vitamin C, and antioxidants — to levels sufficient to support cardiac muscle function and energy production
- Supporting mitochondrial repair and cellular energy restoration in cardiac, metabolic, and gastrointestinal tissues
- Providing the nutritional cofactors required for effective liver detoxification during and between chelation sessions
- Reducing systemic oxidative stress and supporting vascular endothelial repair throughout the treatment programme
- Strengthening immune function and overall organ resilience to support recovery across all of Adrian’s conditions simultaneously
Effects:
- Addressed the chronic nutritional deficiencies that had been silently undermining cardiac muscle function, insulin regulation, cholesterol metabolism, and gastric mucosal integrity
- Supported the marked recovery in energy levels Adrian reported — from moderate pre-treatment vitality to significantly higher energy, alertness, and work productivity
- Provided the essential biochemical building blocks required for the body’s ongoing repair of arterial, metabolic, and digestive tissues throughout treatment
- Complemented IV Chelation Therapy by ensuring the body had adequate nutritional resources to heal and regenerate effectively following each detoxification session
- Contributed to the normalisation of blood sugar levels from a diabetic range of 6–7 down to a sustainable 4–5 over the course of treatment
✙ Bio-identical Hormone therapy
What it is:
Bio-identical Hormone Therapy is the clinical administration of hormones that are molecularly identical to those naturally produced by the human body. Unlike synthetic pharmaceutical hormones, bio-identical hormones match the body’s own hormonal structures precisely — allowing them to bind to receptors and perform their biological functions exactly as endogenous hormones do. Under conditions of chronic disease, chronic stress, poor nutrition, and toxic burden, hormonal production declines and balance becomes disrupted — impairing the regulation of metabolism, cardiovascular function, immune response, energy production, and tissue repair. Bio-identical Hormone Therapy restores hormonal levels to their optimal range, reactivating the body’s own regulatory and healing systems from within.
Used for:
- Correcting the hormonal imbalances identified in Adrian’s diagnostic assessment as a contributing root cause of his cardiovascular and metabolic conditions
- Restoring optimal hormonal support for cardiac muscle function, vascular tone, and cardiovascular regulation
- Reactivating insulin sensitivity and metabolic hormone regulation to support blood sugar normalisation
- Supporting healthy lipid metabolism through the restoration of hormones that regulate cholesterol synthesis and clearance
- Optimising mitochondrial energy production in cardiac and metabolic tissues through hormonal rebalancing
- Restoring the body’s natural anti-inflammatory hormonal regulation to reduce the systemic inflammatory burden driving Adrian’s conditions
- Supporting the repair and regeneration of gastric mucosal tissue through hormonal optimisation of digestive system function
Effects:
- Addressed the hormonal imbalances that had been impairing cardiovascular regulation, metabolic function, and digestive health — complementing and amplifying the benefits of the detoxification and nutritional therapies administered concurrently
- Supported the progressive improvement in cardiac function and reduction of heart failure symptoms as hormonal regulation of vascular tone and cardiac muscle performance was restored
- Contributed to the normalisation of blood sugar levels by restoring insulin sensitivity and the hormonal regulation of glucose metabolism
- Supported healthy cholesterol profile improvement by reactivating the hormonal mechanisms governing lipid synthesis and clearance in the liver
- Produced marked improvement in Adrian’s energy levels, mental clarity, and daily vitality as mitochondrial function and metabolic hormone balance were restored
- Reinforced the body’s systemic anti-inflammatory capacity, reducing the hormonal drivers of chronic inflammation across all of Adrian’s conditions
✙ Far-Infra-Red therapy
What it is:
Far Infrared (FIR) Sauna Detoxification Therapy uses far infrared radiant heat to penetrate deep into the body’s tissues — beyond what conventional sauna heat can achieve — gently raising core body temperature and inducing a deep, sustained therapeutic sweat. Unlike surface-level perspiration, FIR-induced sweating mobilises and eliminates toxins, heavy metals, and metabolic waste products stored deep within fat cells and body tissues. At Heal Within®, FIR Sauna Detoxification is administered as part of a structured protocol — combined with an IV drip and salted water intake prior to and during the session — to maximise toxin mobilisation and safe elimination while maintaining the body’s electrolyte balance throughout.
Used for:
- Providing deep tissue detoxification to eliminate heavy metals and toxins mobilised during and between IV Chelation sessions
- Administered as a critical post-amalgam-removal detoxification protocol — following Adrian’s dental mercury amalgam removal — to safely clear any mercury released into the body during the removal process
- Enhancing systemic toxin elimination through therapeutic sweating, complementing the kidney and urinary elimination pathways activated by IV Chelation
- Improving peripheral circulation and blood flow to cold and poorly perfused tissues — directly addressing Adrian’s cold hands and feet
- Supporting cardiovascular function through the vasodilatory and circulatory benefits of deep infrared heat therapy
- Reducing the overall toxic burden in Adrian’s body tissues, lowering the systemic inflammatory load driving his cardiac and metabolic conditions
Effects:
- Played a critical role in the safe clearance of mercury following Adrian’s dental amalgam removal, preventing reabsorption of released mercury into the bloodstream and tissues
- Contributed to the progressive reduction in heavy metal burden alongside IV Chelation Therapy, compounding the detoxification benefit across both elimination pathways
- Supported the improvement in peripheral circulation, with Adrian’s cold hands and feet symptoms fully resolving over the course of treatment
- Enhanced the overall detoxification process, accelerating the reduction of the systemic toxic and inflammatory burden across Adrian’s cardiovascular, metabolic, and digestive conditions
- Contributed to the progressive improvement in blood cell quality and flow observed in successive live blood examinations
- Provided a deeply therapeutic and restorative experience that Adrian found genuinely pleasant — supporting his motivation and commitment to continue through the full treatment programme
✙ Wholesome Food therapy
What it is:
Wholesome Food Therapy is a physician-guided dietary restructuring programme in which the patient’s daily food intake is systematically assessed, educated upon, and progressively transformed. It is not a rigid elimination diet, but a purposeful shift in food awareness and dietary habit — replacing inflammatory, nutrient-poor food choices with whole, natural, nutrient-dense foods that support detoxification, reduce inflammation, stabilise blood sugar, and optimise organ function. At Heal Within®, Wholesome Food Therapy is regarded as a foundational pillar of treatment — and sits alongside six other essential foundations that the body requires for genuine healing. To understand all seven, read: The Healing Essentials: 7 Non-Negotiable Foundations Your Body Needs for Healing.
Used for:
- Educating Adrian on the direct relationship between food choices and the root causes driving his heart disease, diabetes, high cholesterol, and gastritis
- Progressively reducing his high carbohydrate intake — a primary driver of his hyperglycaemia, gut dysbiosis, and metabolic acidosis — through a structured, gradual reduction approach rather than a sudden overhaul
- Increasing vegetable and fibre intake to support gut microbiome restoration, alkalisation of body tissues, and natural cholesterol regulation
- Guiding Adrian on the quality of dietary fats — distinguishing between harmful and therapeutic oils — to support healthy lipid metabolism and cardiovascular function
- Educating on the role of natural mineral salts versus refined salt, and their differing effects on cardiovascular and metabolic health
- Replacing inflammatory processed and sugar-laden foods with whole, natural food choices that support blood sugar stability, monitored actively through Adrian’s Continuous Glucose Monitor (CGM)
Effects:
- Directly supported the normalisation of blood sugar levels — Adrian progressively reduced his blood glucose from a diabetic range of 6–7 to a sustainable 4–5 through the combination of dietary restructuring and clinical treatment
- Contributed to the improvement in cholesterol profile by increasing the intake of therapeutic fats, fibre, and plant nutrients that naturally regulate lipid metabolism
- Supported the resolution of gastritis and bloating symptoms by removing inflammatory dietary triggers and replacing them with gut-supportive whole foods
- Empowered Adrian with lasting nutritional awareness — understanding which foods spike his blood sugar, which oils are therapeutic, and how to make informed daily food choices independently
- Established a sustainable dietary foundation that reinforces the benefits of all clinical therapies and reduces the risk of disease recurrence long term
- Transformed Adrian’s relationship with food from one of habitual, taste-driven consumption to one of informed, health-conscious daily practice — a shift he has maintained and continued to build upon beyond active treatment
PHASE 3: POST-TREATMENT TESTS & RESULTS
1. Vitality Factors
*100% represents highest optimal level for patients’s genetics, gender & age.
2. Disease Symptoms
- Chest pain | Resolved.
- Breathlessness | Resolved.
- Tiredness & fatigue | Resolved.
- Cold hands & feet | Resolved.
- Bloating | Resolved.
3. Medical Conditions (Diseases)
- Ishemic heart disease (3 arteries blocked) | Resolved 80%.
- Chronic fatigue syndrome | Resolved.
- Insomnia | Resolved.
- Subclinical hypothyroidism | Resolved.
- Anxiety disorder | Resolved.
- Leaky gut syndrome | Resolved.
- Ishemic heart disease (3 arteries blocked) | Resolved 80%.
- Congestive Heart Failure | Resolved 80%.
- Diabetes | Improved 90%.
- High Cholesterol | Resolved 90%.
- Gstritis | Resolved.
4. Medications
(Prescribed by other doctors Prior to Heal Within®)
- Heart failure medicationWeaned-off.
- Anti-platlet medWeaned-off 50%.
- Diabetes medication Weaned-off 70%.
- Cholesterol med Weaned-off.
- Gastric medication Weaned-off.
MEDICAL TEST REPORTS
*Click/Tap each image to enlarge-view”.
Dr Lee's
Integrated & Holistic
HEART DISEASE
TREATMENT PROGRAM
Holistic
Healing
Recurrence Prevention
Long-term
Wellbeing
Angina (chest pain) | Coronary artery disease | Heart attack | Heart failure | Palpitations | Congenital heart disease | Arrhythmia | Cardiomegaly (enlarged heart) | Cardiomyopathy | Mitral regurgitation, Mitral valve prolapse (heart valve diseases) | Pulmonary stenosis | and more…
