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The number of chronically ill individuals continues to steadily increase.

Chronic “Mystery” Illness- is it an Injured Limbic System?

SOME CHRONIC ILLNESS SYMPTOMS CAUSED BY FAULTY BRAIN SIGNALS

The number of chronically ill individuals continues to steadily increase.

The number of chronically ill individuals continues to steadily increase.

Some absolutely amazing findings coming from recent neurobehavioral and psychology research are unraveling a fabric of mystery which is demonstrating that a number of symptoms of “mystery Illnesses” like chronic fatigue syndrome, fibromyalgia, multiple chemical sensitivity and electromagnetic frequency sensitivity may be significantly generated by faulty brain messages being generated from a Limbic System that has been injured by a variety of toxic insults including mold toxins, Lyme and associated persistent infections, toxic chemicals in air, food and water, psychological trauma and physical head injury.

NeuroPlasticity is able to completely eliminate Limbic System False Signals!

The amazingly wonderful associated discovery is that our brains are quite capable to “rewire” and recover using the principle of NeuroPlasticity.  This literally means that the brain can learn to reroute and reprogram the damaged areas allowing the associated symptoms to lessen and in many cases disappear.  This is not really different from the mechanism that allows the victim of a stroke to relearn to walk or talk.

Since the limbic system (which is made up of the cingulate gyrus, the amygdala, the hippocampus and the hypothalamus) acts as a control center for the autonomic nervous system, the immune system, the endocrine system and the digestive system, many physical signs, symptoms and abnormal lab findings may be directly caused by false or inappropriate limbic system messages to the rest of the body.

At Texas Integrative Medicine our goal is to identify the environmental toxic triggers that have led to limbic system disorder sometimes referred to as a Limbic System Trauma Loop.  First priority is to stop further exposure to the toxins.  For example, we might find that there is toxic indoor mold in a person’s home, school or workplace and we would make every attempt to stop further exposure.  Perhaps a person’s drinking water is tainted with lead or pesticides.  Again we try to eliminate these exposures.  Next, it is necessary to use the body’s natural means of toxin elimination (kidneys, liver, sweat glands, bowel elimination, immune system) to clear the body’s stored toxins and harmful germs as best we can.

We are learning that even once toxins have been significantly reduced, the limbic system may still remain “stuck in a rut”.  A good analogy would be when a circuit breaker breaks from too much current demand.  You can unplug the excessive appliances, but the system doesn’t work until the circuit breaker is RESET.

Removal of Toxins Helps but Limbic System Reset Often Needed

There are two successful ways to reset or reprogram the damaged limbic system that we have been working with at Texas Integrative Medicine.

Annie Hopper from Victoria, Canada has developed a system of behavioral training which she has named the Dynamic Neural Retraining System.  You can find out more about it at her website- www.retrainingthebrain.com.  Her system has helped many people recover from complex “mystery” illness.  Please check out some of the Success Stories on her webpage.

Neurobiofeedback scientists and clinicians are perfecting modalities that combine monitoring brain electromagnetic waves (EEG) with reward systems such as using brain signals to alter the color and sound loudness of a movie DVD.  In Austin, Lynda Kirk and associates at Austin Biofeedback and EEG Neurofeedback Center offer the most advanced devices and protocols to retrain the limbic system in a way that leads to resolution of symptoms and improvement in brain function.  You can learn more about their approach at  https://www.austinbiofeedback.com

SHINING SOME LIGHT ON LYME DISEASE

Do rays of light offer hope to individuals suffering from conditions like Lyme disease?

Thor phototherapy device being used to treat lower back inflammation and pain.

Thor phototherapy device being used to treat lower back inflammation and pain.

As a doctor who sees patients with chronic, complex disease on a daily basis, I see regularly patients who have been told that they have Lyme disease.  I must start by saying that I believe the term Lyme disease is a poor term.  First of all as I am sure most of the citizens of the quaint Connecticut town of Lyme would agree, Lyme is merely the name of the town where in the early 1970’s an epidemic of arthritis, body aches, fever and skin rash was determined to be due to infection with a strain of spirochete later named Borrelia burgdorferi.  Today we know that chronic disease symptoms caused by many different strains of spirochetes (screw-shaped bacteria) and other germs occur all over the world and have for decades if not centuries.  I prefer to use the term stealth infection to describe generally the condition whereby a difficult to diagnose (and eradicate) persistent microbe is contributing to the existence of chronic symptoms of disease in the patients that I treat.

New tests are identifying the unique DNA and RNA of infection-causing microbes that were difficult to diagnose in the past.

Thanks to the development of new microbiology diagnostic tests (such as PCR testing), we are now better able to demonstrate the presence of DNA or RNA strands that are unique to specific strains of harmful microbes also known as pathogens.  These tests are only now just beginning to make their way in to clinical practice in order to make the diagnosis of stealth infection.  Stealth pathogens may include bacteria, viruses, yeasts, molds, and even parasites.  Many stealth infection pathogens are very difficult, if not impossible to culture in a lab and have therefore been able to elude diagnosis.  Up until now these infections have sometime been identified by using various immune system tests also referred to as serologic tests.  There are problems with serologic tests when the infection is not caused by the exact strain of pathogen as the test is made for (serologic type) or if the patient’s immune system is incapable of reacting normally to the pathogen.  This may occur more often than widely believed.  This can result in false negative results.

So what does this all have to do with the title of my post?  It actually has a double meaning.  Clearly I want to “shine light on Lyme disease” to make the general condition of stealth infection better understood by my readers, but the main reason for the article is to introduce the concept of using light as a therapy to treat stealth infection.  Light, as from the sun, actually has an extremely important role to play in the beneficial treatment of many different stealth infections.  Light is made up of light waves containing photons.  Different light waves have different frequencies of vibration which we know as color.  Sunlight contains all the wavelengths of light including both those visible and invisible to our eyes.

Man-made antibiotics have their limitations.

Man-made antibiotics have a number of drawbacks when used to treat stealth infections.  Light therapy has several advantages over the use of antibiotics in a number of circumstances.  There appears to be much less damage to our normal intestinal bacteria known as the microbiome.  Light does not put foreign chemicals into the body which must be eliminated by our body’s mechanisms of detoxification.  Light is generally less expensive to produce than antibiotics.  Light seems to have a much less likely tendency to cause allergic or toxic effects when used in appropriate dosage.  Stealth pathogens do not develop resistance to light in the same way that they develop resistance to antibiotics.  Antibiotic resistance is a big problem nowadays leading to the development of “superbugs” such as MRSA.

Light therapy also known as PhotoBioModulation therapy or PBMT has been extensively researched and used for decades to treat a wide range of disease.

Various wavelengths of light have been studied in the treatment of various medical conditions since the 1800’s if not before.  In fact the beneficial effects of the sun on health has been known since ancient times.  One of the early pioneers of light treatment, Niels Ryberg Finsen, was awarded the Nobel Prize in Medicine in 1903 for his work “in recognition of his contribution to the treatment of diseases, especially lupus vulgaris, with concentrated light radiation, whereby he has opened a new avenue for medical science”.  (Quote from the Nobel Foundation)   Lupus vulgaris has been shown to be caused by a persistent infection by the tuberculosis pathogen.

Various light devices have been used especially in the 1930’s, 40’s, and 50’s to treat a number of conditions including a number of cancers and infections even in the United States.  With the advent of antibiotics and vaccines in the 1940’s and 50’s in the United States and Canada, light therapy quickly fell out of favor although it continued to be actively used in Eastern Europe and Russia.  Today light therapy also known as PhotoBioModulation therapy is making a comeback.

Several colors of light have demonstrated beneficial effects in the treatment of injury and disease.

Ultraviolet light (UVL) is capable of damaging the DNA of stealth pathogens like viruses and bacteria.  In fact UVL is used to sterilize or sanitize operating rooms and hot tubs.  Although UVL can also result in damage to the cells of the human body, our cells are much more capable of repairing damage caused by UVL than the pathogens are which is the reason that it can be effective as a form of treatment.  This is similar to the ability of cancer chemotherapy to kill cancer cells more readily than the body’s normal cells.

Other wavelengths/colors of light interact with receptors in our cells to induce beneficial changes much in the way that light is absorbed by plant leaves to produce sugars in a process known as photosynthesis.  The mitochondria, the powerhouses of the cells, have proteins known as cytochromes that absorb photons of red or near infrared light causing activation.  This process leads to a number of direct and indirect effects that result in production of mitochondrial energy (ATP), cellular recovery and repair, increase in the number of circulating stem cells, reduction of harmful free radicals, reduction of harmful inflammation, and beneficial modulation of the immune system.  The role of red and near infrared light in the treatment of sports injuries and other forms of tissue injury has been extensively studied.  New evidence is emerging that is showing that these same wavelengths of light can assist in the recovery of inflammation and tissue injury caused by stealth infection.

Other wavelengths of light have other beneficial effects on our cells and tissues.  Green light has been shown to have an anti-oxidant effect and a beneficial effect on red blood cell flow in our microcirculation.

At Texas Integrative Medicine I have recently introduced treatments with the Thor Low Level Laser device (www.thorlaser.com).  This device which is FDA approved for use in humans was developed in the United Kingdom and has been studied for use in multiple conditions in humans and animals.  It is used often in veterinary medicine as well as orthopedic and sports medicine.  A number of studies have been performed by researchers at Harvard.  In my clinic we are using it for its known beneficial effects to restore cellular energy, modulate inflammation, reduce pain, and to speed up tissue repair and regeneration from a wide assortment of injuries including those caused by stealth pathogens.  If you would like to learn more about the Thor LLLT treatments, please call and speak to one of our phototherapists at 512-803-6790 or make an appointment to be evaluated at our clinic by calling 512-420-9300.

The FDA has not approved light therapy including the Thor device for the treatment of any infectious disease including Lyme.

Aboutdr_tyler Wally Taylor MD

Dr. Taylor practices integrative medicine at Texas Integrative ENT and Allergy in Austin, Texas.  After obtaining a general medical doctorate degree from University of Texas Southwestern Medical School in Dallas he completed a general medical internship and residency training in head and neck surgery ENT and allergy.  After 20 years service in the US Army Medical Corps and practice in Colorado and Texas he founded Texas Integrative where he now offers a functional holistic approach to disease which treats the entire individual instead of each separate symptom.  He has found more satisfying results using this Systems BioIndividualized approach.  His motto is Health and Wellness from Head to Toe”.   www.texasintegrative.com     office phone-512-420-9300  

NAVIGATING COMPLEX ILLNESS

FORUM FOR INTEGRATIVE MEDICINE CONFERENCE ON     NAVIGATING CHRONIC COMPLEX ILLNESS PROVIDED OPPORTUNITY TO INTERACT WITH NATION’S LEADERS TREATING THE CHRONICALLY SICK PATIENT

The number of chronically ill individuals continues to steadily increase.

The number of chronically ill individuals continues to steadily increase.

Last week I had the privilege to attend a gathering of a select group of the nation’s best health care providers who have accepted the challenge to treat the sickest of the sick.

The conference which took place in San Diego, California was organized by the Forum for Integrative Medicine and the topic was “Navigating Complex Chronic Illness”.

The atmosphere of the conference was one of compassion for the suffering and passion for the understanding of the best ways to identify the root causes of chronic, complex illness and to allow and facilitate the body to heal itself.

Participants were treated to very stimulating presentations of the latest clinical  pearls for treatment of a group of devastating diseases including autoimmunity, illness due to mold exposure, rheumatoid arthritis, migraine headaches, Hashimoto’s thyroiditis, Morgellon’s disease, dementia and other degenerative brain disorders,  a host of hormone disorders, depression and anxiety, insomnia, cancer, PANDAS, autism, and many other conditions.  Presenters included a “Who’s Who” of the nation’s best practitioners in this field.  Those in attendance were treated with the most recent understanding of how chronic inflammation-based disease is caused by the harmful effects of toxins (poisonous substances that we get from the germs in our bodies) and toxicants (damaging substances that man has polluted into the environment (80,000 different chemical substances with 2,500 new ones being added every year).  We discussed how our inherited genetic traits along with the factors that determine how those traits are expressed (a process known as epigenetics) dictates how each individual has a different predisposition to manifest illness when we encounter the various toxins and toxicants in our world.

Our environment is rapidly becoming polluted with harmful man-made toxicants.

Our environment is rapidly becoming polluted with harmful man-made toxicants.

CONFERENCE FOCUSED ON THE ROLE THAT PERSISTENT INFECTION BY “STEALTH PATHOGENS” IN CONTRIBUTING TO CHRONIC COMPLEX ILLNESS

The experts presented the role that numerous “stealth germs” play in setting up persistent infections in our tissues.  In the past it was accepted dogma that one germ caused one disease and that our bodies were for the most part sterile.  Our current paradigm which is becoming more completely understood day by day indicates that we all literally have a “zoo” of microbes in our bodies.  Some subsist peacefully with us and in fact provide necessary support (the healthy intestinal “microbiome” for example) while many others contribute to disease (think HIV virus, the Borrelia spirochete causing Lyme disease, mycoplasma causing chronic lung disease, Strep bacteria causing PANDAS as examples).  These stealth pathogens (harmful microbes) include viruses, bacteria, rickettsia, yeasts, fungi, protozoans (single-cell parasites), and helminths (parasitic worms) cause symptoms by complicated mechanisms.  Many of them can make proteins and other molecules that break down our tissues, weaken our immune systems, imbalance our hormones, and rob us of vital nutrients.

At the same time that the biotoxins made by the germs are causing damage, our body’s own immune system tries its best to halt the infection by creating inflammation to thwart the damage.  Unfortunately in the process of doing so, the immune system creates its own set of harmful proteins and small molecules that also have a harmful, toxic effect on our cells and tissues.  In this way our immune system is really a two edged sword.  Seems as though we can’t live with it and we can’t live without it so to speak.

LATEST TECHNIQUES FOR ASSISTING THE BODY TO SELF-HEAL FROM THE EFFECTS OF CHRONIC INFECTION AND EXPOSURE TO ENVIRONMENTAL TOXINS WAS EMPHASIZED

We learned about exciting techniques (many just becoming available to our clinics now) that can be used to accurately identify and characterize these many lurking germs that up until now have been next to impossible to identify.  The experts presented an impressive armamentarium of tools and techniques useful to provide natural measures to “remove, restore, replace and regenerate” the body.  We discussed the role of plant-based botanical agents, energy techniques, proper adjustment of diet and lifestyle, replacement of healing nutrients, and healing hands-techniques including applied kinesiology (muscle testing).

I always feel fulfilled after returning from a medical conference if I can institute one or two new techniques to better care for my patients.  In San Diego after the 20 hours of formal lectures, case presentations, and lively question and answer sessions I came away with 54 pages of clinical pearls and a very long list of new protocols and modalities to better assist my complex, chronically ill patients to navigate their way back to restoration of true health and wellness.

I want to thank Scott Forsgren, the Better Health Guy, and Susan McAmish  and her team at Beyond Balance for organizing the event.  I also want to acknowledge the generous contributions of the stimulating presenters who included Dietrich Klinghardt MD, Kristine Gedroich MD, Ann Corson MD, Ginger Savely DNP, Steve Harris MD, Raj Patel MD, Sunja Schweig MD, Michael Lebowitz DC, Todd Thoring ND, Kelly McCann MD, Amy Joy Smith NP, and Christabelle Yeoh MD.  I came away with the sensation that I had spent three days “drinking from a fire hose” of knowledge.  What a blessing!

 

 

STEALTH INFECTION IN CHRONIC DISEASE-PART 2

In my last blog post, Part 1 of this series, I introduced the concept of stealth infection as a cause of chronic disease.  I explained that many persistent illnesses with many different symptoms-diseases like autoimmune disease, diabetes, thyroid disorder, adrenal fatigue, heart disease, and even cancer- may in fact  be manifestations of the presence of harmful microscopic organisms called pathogens within the body.  Since stealth germs are often very difficult to identify and recover in the body, the concept of stealth infection has been underappreciated by many health care providers.  I explained how diseases such as HIV/AIDS, chronic viral hepatitis, chronic neuroborreliosis (Lyme Disease) and others are explained by this phenomenon.  I discussed how symptoms like chronic fatigue, chronic pain, arthritis, depression, brain fog, irritable bowel are common symptoms associated with stealth infections.Germs

In Part 2 I will dive a little deeper into this subject and attempt to answer some common questions about stealth infection.

Why are stealth infections sometimes difficult to diagnose?

The answer to this question requires a brief explanation of how infection is generally diagnosed.  Infection is first suspected clinically based on symptoms and signs that the patient exhibits.  Often symptoms of infection are caused by the immune system’s response to infection that is sometimes referred to as inflammation.  If the immune system does not recognize or respond to infection, symptoms of disease are often absent or diminished.  This may not be a good thing since the pathogen proceeds unchecked.  When there are symptoms of inflammation-classically fever or warmth, local or generalized pain, swelling or induration, and redness-infection is likely at fault.  Infection may be diagnosed by growing the pathogen in appropriate culture conditions from a specimen (urine, blood, sputum, etc.) of the sick person.  In the case of a Strep throat or a bacterial urinary tract infection this is straight forward.  In many other infectious diseases it if very difficult if not impossible to culture the disease-causing germ.  Viruses are especially resistant to culture.

Infection is sometimes diagnosed by seeing the pathogen usually under a microscope since they are very tiny.  Again this can be routine as when the germ causing tuberculosis is seen under the microscope in a sample of a sick patient’s sputum.  Many germs that cause stealth infection are difficult to see.  Viruses because they are extremely tiny are not typically seen under the light microscope but may be seen under an electron microscope.  Many germs that cause stealth infection have adapted the ability to enter our human cells and may be more difficult to see even under the microscope.  Special staining techniques can assist in seeing these pathogens within cells.  Stealth germs may reside in nests of sticky material known as biofilms and not be readily visible.  When stealth germs are present in specimens in small numbers, which is often the case, they may be overlooked with microscopic visualization techniques.  Techniques are sometimes employed to try to increase the numbers of pathogens in a specimen using tricks to concentrate their numbers in order to make it more likely that they may be seen.

What are some of the tests use to diagnose stealth infection?

Very commonly infection is inferred by indirect tests that depend on measuring factors from the patient that are specific for infection.  These tests are sometimes referred to as serologic tests (present in the patient’s serum/blood) or antibody titer tests.  Often, but not always, when a stealth pathogen is present it will trigger the immune system to form antibodies which are proteins produced by specialized cells of the immune system.  Of course this requires that the patient’s immune system is capable of making enough antibody to measure.  Sometimes the amount of antibody is measured at the onset of suspected infection and again later to see if the quantity of antibody rises (acute and convalescent titers).

Are some germs that cause stealth infection able to defeat our immune system?

Some stealth pathogens have developed the capability of preventing the patient’s immune system from making antibodies that would normally assist in the control or elimination of the disease.  These stealth pathogens have “learned” to become immune system disruptors in order to give them a survival advantage in evading immune system attempts to control or eliminate them.  Some stealth pathogens make enzymes that break down or digest elements of our immune systems rendering it ineffective in combating disease.  In other cases antibodies that are produced by the body may not be specific for the germ that is causing the stealth infection and the infection may be wrongly diagnosed.  These types of antibodies are said to be cross-reactive.

More recently molecular diagnostic techniques are emerging that attempt to identify molecules within the patient that are unique to a specific stealth infection-causing germ.  Often the DNA or RNA molecules of the stealth pathogen are the targets for this type of testing which sometimes goes by the name PCR testing.  DNA and RNA, of course are the unique instruction-containing “molecules of life” that differentiate one living being from another.  They are “fingerprints” so to speak that identify each creature.  Testing techniques which attempt to identify DNA or RNA of a stealth pathogen are rapidly being developed.  One drawback is that there must be enough DNA or RNA to pass the threshold of detection within the specimen being evaluated.  The exact sequence or makeup of the DNA or RNA of the stealth germ must have been previously determined in order to diagnose a specific infection much in the same way that to catch a criminal with a fingerprint, the fingerprint of that criminal must have been determined previously.  Even though the DNA or RNA of a specific stealth germ is identified in a patient’s specimen, there is no guarantee that the presence of the germ in question is directly causing the patient’s chronic disease.

Later we will explore how stealth germs actually cause disease once they enter the body.

Aboutdr_tyler Wally Taylor MD

Dr. Taylor practices integrative medicine at Texas Integrative ENT and Allergy in Austin, Texas.  After obtaining a general medical doctorate degree from University of Texas Southwestern Medical School in Dallas he completed a general medical internship and residency training in head and neck surgery ENT and allergy.  After 20 years service in the US Army Medical Corps and practice in Colorado and Texas he founded Texas Integrative where he now offers a functional holistic approach to disease which treats the entire individual instead of each separate symptom.  He has found more satisfying results using this Systems BioIndividualized approach.  His motto is Health and Wellness from Head to Toe”.   www.texasintegrative.com     office phone-512-420-9300