Eximius Miracle Oil Marketing

What is Eximius Miracle Oil as explained by a Medical Doctor

FINALLY: A COMPLEMENTING PROTOCOL THAT CAN REVERSE HIV, DIABETES, CANCER, RENAL FAILURE AND OTHERS, IN A MATTER OF FEW DAYS, WEEK, WEEKS! A SUPPLEMENT THAT HAS BEEN PREVENTED FROM BEING IN THE MARKET FOR YEARS!

EXPOSE MOLECULES:
ARE SINGLE MOLECULES COMPLETELY EXPOSED (DISPERSED) TO THE MEDIA, IN WHICH THEY RESIDE, ARE DISSOLVED AND ABSORBED FASTER WHETHER THEY ARE SOLUBLE OR NOT.

Advantages of Expose Molecules:
It has the ability to penetrate and rapidly absorb in lipid coated and envelope viruses;
It is considered better that that of nanotechnology (nanosized molecules) due to its excellent penetration in the Blood Brain Barriers without utilizing bile salts that result in absolute energy;
It is known to be a medical food specifically for people who undergoes a medical procedure and chemotherapy;
It is the secret to reverse medical condition such as HIV, Diabetes, Renal Failure, Cardiovascular Problems, Cancer and Immune System deficiencies.

HOW?
Enveloped viruses are hard to penetrate that even Anti-RetroViral (ARV) drugs, or even nanotechnology medicines or supplements are having problems in penetration and absorption.

A product with EXPOSE MOLECULES can penetrate and be absorbed rapidly in ANY lipid coated membranes and Enveloped Viruses.

This new technology oil with Expose Molecules Medium Chain Triglycerides with Lauric Acid can penetrate and rapidly absorb in the Blood Brain Barrier without bile salts. Lauric acid has been scientifically proven to be effective in fighting bacterial and viral infections, which gives stronger immune system because of the immunity-boosting qualities of Lauric Acid that helps to protect from viral and bacterial propagation. Combine this protocol with 2 other modalities, you can unlock the real secret to perfect health and restore your way of life.

Blood Brain Barrier: a filtering mechanism of the capillaries that carry blood to the brain and spinal cord tissue, blocking the passage of certain substances.

It is a highly selective permeability barrier that separates the circulating blood from the brain extracellular fluid (BECF) in the central nervous system (CNS). The blood–brain barrier is formed by brain endothelial cells, which are connected by tight junctions with an extremely high electrical resistivity
It occurs along all capillaries and consists of tight junctions around the capillaries that do not exist in normal circulation.
It acts very effectively to protect the brain from many common bacterial infections. Thus,
infections of the brain are very rare.
Infections of the brain that do occur are often very
serious and difficult to treat. Antibodies are too large to cross the blood–brain barrier, and only
certain antibiotics are able to pass. In some cases a drug has to be administered directly into the cerebrospinal fluid (CSF). However, drugs delivered directly to the CSF do not effectively penetrate into the brain tissue itself, possibly due to the tortuous nature of the interstitial space in the brain.[13] The blood–brain barrier becomes more permeable during inflammation. This allows some antibiotics and phagocytes to move across the BBB. However, this also allows bacteria and viruses to infiltrate the BBB.

What Clinical Significance can an Exposed Molecules do to Cerebrovascular Diseases?

Meningitis is an inflammation of the membranes that surround the brain and spinal cord (these membranes are known as meninges). Meningitis is most commonly caused by infections with various pathogens, examples of which are Streptococcus pneumoniae and Haemophilus influenzae. When the meninges are inflamed, the blood–brain barrier may be disrupted.[13] This disruption may increase the penetration of various substances (including either toxins or antibiotics) into the brain. Antibiotics used to treat meningitis may aggravate the inflammatory response of the central nervous system by releasing neurotoxins from the cell walls of bacteria - like lipopolysaccharide (LPS). Depending on the causative pathogen, whether it is bacterial, fungal, or protozoan, treatment with third-generation or fourth-generation cephalosporin or amphotericin B is usually prescribed.

Brain abscess
A brain or cerebral abscess, like other abscesses, is caused by inflammation and collection of lymphatic cells and infected material originating from a local or remote infection. Brain abscess is a rare, life-threatening condition. Local sources may include infections of the ear, the oral cavity and teeth, the paranasal sinuses, or epidural abscess. Remote sources may include infections in the lung, heart or kidney.

A brain abscess may also be caused by head trauma or as a complication of surgery. In children cerebral abscesses are usually linked to congenital heart disease. In most cases, 8–12 weeks of antibacterial therapy is required.

Epilepsy
Epilepsy is a common neurological disease that is characterized by recurrent and sometimes untreatable seizures. Several clinical and experimental data have implicated the failure of blood–brain barrier function in triggering chronic or acute seizures. Some studies implicate the interactions between a common blood protein (albumin) and astrocytes. These findings suggest that acute seizures are a predictable consequence of disruption of the BBB by either artificial or inflammatory mechanisms. In addition, expression of drug resistance molecules and transporters at the BBB are a significant mechanism of resistance to commonly used anti-epileptic drugs.

Multiple sclerosis
Multiple sclerosis (MS) is considered to be an auto-immune and neurodegenerative disorder in which the immune system attacks the myelin that protects and electrically insulates the neurons of the central and peripheral nervous systems. Normally, a person's nervous system would be inaccessible to the white blood cells due to the blood–brain barrier. However, magnetic resonance imaging has shown that when a person is undergoing an MS "attack," the blood–brain barrier has broken down in a section of the brain or spinal cord, allowing white blood cells called T lymphocytes to cross over and attack the myelin. It has sometimes been suggested that, rather than being a disease of the immune system, MS is a disease of the blood–brain barrier. The weakening of the blood–brain barrier may be a result of a disturbance in the endothelial cells on the inside of the blood vessel, due to which the production of the protein P-glycoprotein is not working well. There are currently active investigations into treatments for a compromised blood–brain barrier. It is believed that oxidative stress plays an important role into the breakdown of the barrier. Anti-oxidants such as lipoic acid may be able to stabilize a weakening blood–brain barrier.

Neuromyelitis optica
Neuromyelitis optica, also known as Devic's disease, is similar to and is often confused with multiple sclerosis. Among other differences from MS, a different target of the autoimmune response has been identified. Patients with neuromyelitis optica have high levels of antibodies against a protein called aquaporin 4 (a component of the astrocytic foot processes in the blood–brain barrier).

Late-stage neurological trypanosomiasis (sleeping sickness)
Late-stage neurological trypanosomiasis, or sleeping sickness, is a condition in which trypanosoma protozoa are found in brain tissue. It is not yet known how the parasites infect the brain from the blood, but it is suspected that they cross through the choroid plexus, a circumventricular organ.

Progressive Multifocal Leukoencephalopathy (PML)
Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease of the central nervous system that is caused by reactivation of a latent papovavirus (the JC polyomavirus) infection that can cross the BBB. It affects immune-compromised patients and it is usually seen with patients suffering from AIDS.

De Vivo disease
De Vivo disease (also known as GLUT1 deficiency syndrome) is a rare condition caused by inadequate transportation of the sugar glucose across the blood–brain barrier, resulting in developmental delays and other neurological problems. Genetic defects in glucose transporter type 1 (GLUT1) appears to be the primary cause of De Vivo disease.

Alzheimer's disease
Some evidence indicates that disruption of the blood–brain barrier in Alzheimer's disease patients allows blood plasma containing amyloid beta (Aβ) to enter the brain where the Aβ adheres preferentially to the surface of astrocytes. These findings have led to the hypotheses that (1) breakdown of the blood–brain barrier allows access of neuron-binding autoantibodies and soluble exogenous Aβ42 to brain neurons and (2) binding of these auto-antibodies to neurons triggers and/or facilitates the internalization and accumulation of cell surface-bound Aβ42 in vulnerable neurons through their natural tendency to clear surface-bound autoantibodies via endocytosis. Eventually the astrocyte is overwhelmed, dies, ruptures, and disintegrates, leaving behind the insoluble Aβ42 plaque. Thus, in some patients, Alzheimer's disease may be caused (or more likely, aggravated) by a breakdown in the blood–brain barrier.

Cerebral edema
Cerebral edema is the accumulation of excess water in the extracellular space of the brain, which can result when hypoxia causes the blood–brain barrier to open.

Prion and prion-like diseases
Many neurodegenerative diseases including alpha-synucleinopathies (Parkinson's, PSP, DLBP) and tauopathies (Alzheimer's) are thought to result from seeded misfolding from pathological extracellular protein variants. This prion-like hypothesis is gaining support in numerous studies in vitro and involving in vivo intracerebral injection of brain lysates, extracted protein (tau, alpha-synuclein) and synthetically generated fibers (PFFs in alpha-synucleinopathies).

These proteins are also detectable in increasing amounts in the plasma of patients suffering from these conditions (particularly total alpha-synuclein in Parkinson's disease patients). The extent to which and the mechanisms by which these prion-like proteins can penetrate the blood–brain barrier is currently unknown.

HIV encephalitis
It is believed that latent HIV can cross the blood–brain barrier inside circulating monocytes in the bloodstream ("Trojan horse theory") within the first 14 days of infection. Once inside, these monocytes become activated and are transformed into macrophages. Activated macrophages release virions into the brain tissue proximate to brain microvessels. These viral particles likely attract the attention of sentinel brain microglia and perivascular macrophages initiating an inflammatory cascade that may cause a series of intracellular signaling in brain microvascular endothelial cells and damage the functional and structural integrity of the BBB. This inflammation is HIV encephalitis (HIVE). Instances of HIVE probably occur throughout the course of AIDS and are a precursor for HIV-associated dementia (HAD). The premier model for studying HIV and HIVE is the simian model.

Rabies
During lethal rabies infection of mice, the blood–brain barrier (BBB) does not allow anti-viral immune cells to enter the brain, the primary site of rabies virus replication. This aspect contributes to the pathogenicity of the virus and artificially increasing BBB permeability promotes viral clearance. Opening the BBB during rabies infection has been suggested as a possible novel approach to treating the disease, even though no attempts have yet been made to determine whether or not this treatment could be successful

EXPOSE MOLECULE TECHNOLOGY aids AntiRetroViral drugs and other suppements achieve significant penetration and absorption in Envelope Viruses of HIV, HEPATITIS, CANCER CELLS, BRAIN BARRIER and other Auto Immune and Metobolic Diseases.

EXIMIUS is a combination of more than 5 kinds of Fatty Acids (OIL) and contains 21 Essential Exposing Fatty Acids (Amino Acids, Lauric Acid, Oleic Acid, Caprilic Acid, Alpha Aliphalic Acid). These are EXPOSE MOLECULES that will PENETRATE RAPIDLY & KILLS ENVELOPE VIRUSES INCLUDING CANCER CELLS

PRODUCT DESCRIPTION:

Medium Chain Triglycerides (MCT’s) are fatty acids (oil) that do not require bile salts in digestive system and can absorb intact to be taken to the Liver, where they are used directly for absolute energy. MCT’s are found naturally occurring in virgin coconut oil and palm kernel oil. It is considered 5x better than that of VCO in terms of penetrability, energy, and considered a medical food specifically made for people who undergoes medical operation and chemotherapy.

EXPOSED MOLECULES and NANOSIZED PARTICLES
EXPOSED MOLECULES is the result of the surface tension evaporation to eliminate the oil film attached to the molecules. The evaporation produces molecular dissociation resulting in the opening of essential molecules.
NANOSIZED PARTICLES in nanotechnology, a particle is defined as small object that behaves as a whole unit with respect to its transportation and digestion properties. Its ultra-fine particles produces excellent penetration and absorption in the lymphatic system.

GENERAL INFORMATION:
AntiRetroViral kill cancers and promote DNA Repair (Powerful than stem cells) and NEUTRALIZES Metastasis. It also balances in, Kills the bad (rogue) cells and strengthens and retains good cells. Expose Molecules aiding coupling reaction of your drug to prevent waste and provide rapid absorption and penetration. Lastly, exposing the molecules of Essential Fatty Acid – The Principle of Absorption and Penetration, Elimination of waste stage and Perfect Balancing.

A virus that has an outer wrapping or envelope comes from the infected cell, or host, in a process called “budding off.” During the budding process, newly formed virus particles become “enveloped” or wrapped in an outer coat that is made from a small piece of cell’s plasma membrane. The envelope may play a role in helping virus survive and infect other cells.

ANTIRETROVIRAL DRUGS ACHIEVES SIGNIFICANT PENETRATION & ABSORPTION IN ENVELOPE VIRUSES OF:

1. Human Immunodeficiency Virus (HIV)
2. Hepatitis & C-Viral Infections
3. Blood Brain Barriers
4. Cancer Cells
5. Liver Infections
6. Brain Diseases
7. Other Health Problems such as:
Stroke and High Cholesterol
Gastric Problems / Acidity / Acid Reflux
High Blood Pressure
High Sugar Level
Fights Pneumonia, Dengue Virus
Staphylococci Infections (Boils)
8. Aids the body in
Increase Body Resistance / Energy Booster
Immune System Defense
Attack/Neutralizes Blood solids
Revitalizes Skin, Body and hair
Regulates / Balances Body Hormones
Controlling Allergic Reaction
Relieves muscle spasm / Cramps / Rheumatism / Arthritis and Gout
Heals burned skin fast.

IF YOU OR ANYONE YOU KNOW IS SUFFERING FROM ANY MALADY OR FIGHTING A DREADFUL DISEASE, THE ODDS OF HEALING THEM IS NOW BETTER THAN EVER. THEIR DISEASES ARE REVERSIBLE.

International orders are welcome.

** For orders or inquiry, Contact Us at **
Email Address:  LuckyCowShop@gmail.com
Mobile Number: +63917-838-1337

 

Let Us Save Lives.
Please help share this product to your family and friends.