food allergies – F.I.G.H.T for your health! http://lymebook.com/fight Linda Heming describes her Lyme disease healing journey Wed, 06 Nov 2013 05:54:37 +0000 en-US hourly 1 https://wordpress.org/?v=4.9.25 Dr. Gordon’s Comments – germline variants & sialic acid in autoimmunity http://lymebook.com/fight/dr-gordons-comments-germline-variants-sialic-acid-in-autoimmunity/ http://lymebook.com/fight/dr-gordons-comments-germline-variants-sialic-acid-in-autoimmunity/#respond Tue, 19 Oct 2010 04:39:52 +0000 http://lymebook.com/fight/?p=1771 A relatively common defect involving Sialic acid –sets the stage for patients to develop autoimmune related illnesses! I continue to discuss my FIGHT program, as the best way to approach any autoimmune related condition.www.gordonresearch.com

Possibly, in the future, with evidence this strong, genetic testing for this variant could lead to patients being advised to go on my FIGHT program before they have the symptoms of one of the over 100 different autoimmune related conditions. The best statistics today indicate that over 40% of us have difficulty with either dairy or gluten. So, before we start seeing auto-antibodies to our tissues, those with this variant might want to eliminate those foods and do the rest of the FIGHT program too.

Garry F. Gordon MD,DO,MD(H)
President, Gordon Research Institute

Full article: http://www.ncbi.nlm.nih.gov/sites/entrez/20555325?dopt=Abstract&holding=f1000,f1000m,isrctn

Excerpt:

Functionally defective germline variants of sialic acid acetylesterase in autoimmunity.
Surolia I, Pirnie SP, Chellappa V, Taylor KN, Cariappa A, Moya J, Liu H, Bell DW, Driscoll DR, Diederichs S, Haider K, Netravali I, Le S, Elia R, Dow E, Lee A, Freudenberg J, De Jager PL, Chretien Y, Varki A, Macdonald ME, Gillis T, Behrens TW, Bloch D, Collier D, Korzenik J, Podolsky DK, Hafler D, Murali M, Sands B, Stone JH, Gregersen PK, Pillai S.
Cancer Center, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, USA.

Abstract
Sialic acid acetylesterase (SIAE) is an enzyme that negatively regulates B lymphocyte antigen receptor signalling and is required for the maintenance of immunological tolerance in mice. Heterozygous loss-of-function germline rare variants and a homozygous defective polymorphic variant of SIAE were identified in 24/923 subjects of European origin with relatively common autoimmune disorders and in 2/648 controls of European origin. All heterozygous loss-of-function SIAE mutations tested were capable of functioning in a dominant negative manner. A homozygous secretion-defective polymorphic variant of SIAE was catalytically active, lacked the ability to function in a dominant negative manner, and was seen in eight autoimmune subjects but in no control subjects. The odds ratio for inheriting defective SIAE alleles was 8.6 in all autoimmune subjects, 8.3 in subjects with rheumatoid arthritis, and 7.9 in subjects with type I diabetes. Functionally defective SIAE rare and polymorphic variants represent a strong genetic link to susceptibility in relatively common human autoimmune disorders.

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Alert of the Week: We Need Labels on GM Foods Now http://lymebook.com/fight/alert-of-the-week-we-need-labels-on-gm-foods-now/ http://lymebook.com/fight/alert-of-the-week-we-need-labels-on-gm-foods-now/#respond Sat, 17 Jul 2010 21:34:15 +0000 http://lymebook.com/fight/?p=1359 Full article: http://www.organicconsumers.org/bytes/ob229.htm#SEC2

Excerpt:

Gen-M, the first Monsanto Generation of humans force-fed genetically modified foods hasn’t reached reproductive age yet (they were born in the late 1990s). But, if a critical mass of animal feeding studies are any indication, the millennial generation, reared on Food Inc.’s unlabeled “Frankenfoods” can look forward to a long-term epidemic of cancer, food allergies, learning disabilities, sterility, and birth defects.

Corn (85% of U.S. production is GM), soy (91% GM), cotton (88% GM), canola (85% GM) and sugar beets (95% GM) are all genetically engineered by Monsanto to withstand massive doses of the company’s glyphosate herbicide RoundUp, or else to exude their own pesticide, Bacillus Thuriengensis (Bt). RoundUp, the favorite weedkiller poison of non-organic farmers and gardeners, causes brain, intestinal and heart defects in fetuses. And scientists warn that RoundUp, the most extensively used herbicide in the history of agriculture, “may have dire consequences for agriculture such as rendering soils infertile, crops non-productive, and plants less nutritious.” In addition, hundreds of thousands of US dairy cows are injected with genetically engineered Bovine Growth Hormone (developed by Monsanto) in spite of studies linking BGH with cancer, and longstanding bans on the drug in the EU, Japan, Canada, and most industrialized nations.

With genetically modified foods and crops threatening public health and the environment, not to mention the next generation’s reproductive capacity, why isn’t there a massive consumer outcry to restrain Monsanto’s biotech bullying and ban genetically engineered foods and agriculture?

The answer is disturbingly simple. Collusion between Monsanto and elected public officials (including the current Obama Administration) has obscured the fact that almost all non-organic foods in the US contain GMOs. Despite poll after poll indicating that 85-95% of US consumers want mandatory labels on foods containing GMOs, Congress has heretofore listened to Monsanto and corporate agribusiness, rather than their own constituents. In the European Union, Japan, or South Korea, where GM foods must be labeled, there are no GM foods on grocery story shelves (and little or none served in restaurants), since most consumers would not buy them and a significant number would complain if they saw GMO labels on products. Consequently there are very few GM crops being cultivated in the EU (mainly a small amount of corn in Spain for animal feed).

Most Americans simply do not understand that 80% of non-organic supermarket processed foods (basically every product containing soy, corn, canola, cottonseed oil, or sugar beet derivatives) are contaminated with GMOs. While nearly everyone in North America has eaten genetically modified foods, only 26% believe that they have.

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Dairy and wheat http://lymebook.com/fight/1151/ http://lymebook.com/fight/1151/#respond Mon, 31 May 2010 05:32:58 +0000 http://lymebook.com/fight/1151/ Linda’s comment’s:  Don’t you just love reporters who don’t have a clue??!!  This Gina Kolata has obviously NOT done her homework, but then again we have to look at who she works for.  Her comment that there are “Many who think they have food allergies actually do not”…. she doesn’t mention anything about “food sensitivities”?? My question IS?  Who paid for this article??  Would you think that the food industry had anything to do with this BS article?  I don’t know about you, but I take it as a grain of salt and investigate further what the NY Times puts in print. 
Eliminating dairy and wheat makes a proven difference in many illnesses so NY Times headline by Gina Kolata suggesting food allergies are rare will confuse our patients. Maybe we all need to clean up our language and tell people we are concerned about possible food intolerances.

People will only see this headline and their compliance with restricting foods will plummet. You need to know your patients will not have time to read the entire article where food intolerances are explained and where the technical fact that food allergy involves IMMUNE mediated reactions.

This is a disservice to our efforts to help our patient’s health using my FIGHT program. I repeat that patients can do everything, drink best food, raise organic food picked ripe from balanced soil, exercise, detox, etc, and yet sabotage their results by ignoring the need to avoid certain foods. I admit that it is difficult to identify all food intolerances and no test is perfect. But, irresponsible reporting to sell newspapers where the full story is not told does serious disservice to the millions whose health is being adversely impacted by a food they lack the enzymes to metabolize, like lactose intolerance, which admittedly is not a food allergy but clearly is adversely affected the health of millions.

Garry F. Gordon MD,DO,MD(H)
President, Gordon Research Institute
www.gordonresearch.com

http://www.nytimes.com/2010/05/12/health/research/12allergies

May 11, 2010
Doubt Is Cast on Many Reports of Food Allergies
By GINA KOLATA

Many who think they have food allergies actually do not.

A new report, commissioned by the federal government, finds the field is rife with poorly done studies, misdiagnoses and tests that can give misleading results.

While there is no doubt that people can be allergic to certain foods, with reproducible responses ranging from a rash to a severe life-threatening reaction, the true incidence of food allergies is only about 8 percent for children and less than 5 percent for adults, said Dr. Marc Riedl, an author of the new paper and an allergist and immunologist at the University of California, Los Angeles.

Yet about 30 percent of the population believe they have food allergies. And, Dr. Riedl said, about half the patients coming to his clinic because they had been told they had a food allergy did not really have one.

Dr. Riedl does not dismiss the seriousness of some people’s responses to foods. But, he says, “That accounts for a small percentage of what people term ‘food allergies.’ ”
Even people who had food allergies as children may not have them as adults. People often shed allergies, though no one knows why. And sometimes people develop food allergies as adults, again for unknown reasons.

For their report, Dr. Riedl and his colleagues reviewed all the papers they could find on food allergies published between January 1988 and September 2009 — more than 12,000 articles. In the end, only 72 met their criteria, which included having sufficient data for analysis and using more rigorous tests for allergic responses.

“Everyone has a different definition” of a food allergy, said Dr. Jennifer J. Schneider Chafen of the Department of Veterans Affairs’ Palo Alto Health Care System in California and Stanford’s Center for Center for Primary Care and Outcomes Research, who was the lead author of the new report. People who receive a diagnosis after one of the two tests most often used — pricking the skin and injecting a tiny amount of the suspect food and looking in blood for IgE antibodies, the type associated with allergies — have less than a 50 percent chance of actually having a food allergy, the investigators found.

One way to see such a reaction is with what is called a food challenge, giving people a suspect food disguised so they do not know if they are eating it or a placebo food. If the disguised food causes a reaction, the person has an allergy.

But in practice, most doctors are reluctant to use food challenges, Dr. Riedl said. They believe the test to be time consuming, and worry about asking people to consume a food, like peanuts, that can elicit a frightening response.

The paper, to be published Wednesday in The Journal of the American Medical Association, is part of a large project organized by the National Institute of Allergy and Infectious Diseases to try to impose order on the chaos of food allergy testing. An expert panel will provide guidelines defining food allergies and giving criteria to diagnose and manage patients. They hope to have a final draft by the end of June.

“We were approached as in a sense the honest broker who could get parties together to look at this question,” said Dr. Matthew J. Fenton, who oversees the guidelines project for the allergy institute.

Authors of the new report — and experts on the guidelines panel — say even accepted dogma, like the idea that breast-fed babies have fewer allergies or that babies should not eat certain foods like eggs for the first year of life, have little evidence behind them.
Part of the confusion is over what is a food allergy and what is a food intolerance, Dr. Fenton said. Allergies involve the immune system, while intolerances generally do not. For example, a headache from sulfites in wine is not a food allergy. It is an intolerance. The same is true for lactose intolerance, caused by the lack of an enzyme needed to digest sugar in milk.

And other medical conditions can make people think they have food allergies, Dr. Fenton said. For example, people sometimes interpret acid reflux symptoms after eating a particular food as an allergy.

The chairman of the guidelines project, Dr. Joshua Boyce, an associate professor of medicine at Harvard and an allergist and pediatric pulmonologist, said one of the biggest misconceptions some doctors and patients have is that a positive test for IgE antibodies to a food means a person is allergic to that food. It is not necessarily so, he said.

During development, he said, the immune system tends to react to certain food proteins, producing IgE antibodies. But, Dr. Boyce said, “these antibodies can be transient and even inconsequential.”

“There are plenty of individuals with IgE antibodies to various foods who don’t react to those foods at all,” Dr. Boyce said.

The higher the levels of IgE antibodies to a particular food, the greater the likelihood the person will react in an allergic way. But even then, the antibodies do not necessarily portend a severe reaction, Dr. Boyce said. Antibodies to some foods, like peanuts, are much more likely to produce a reaction than ones to other foods, like wheat or corn or rice. No one understands why.

The guidelines panel hopes its report will lead to new research as well as clarify the definition and testing for food allergies.

But for now, Dr. Fenton said, doctors should not use either the skin-prick test or the antibody test as the sole reason for thinking their patients have a food allergy.
“By themselves they are not sufficient,” Dr. Fenton said.

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Lyme and Infection Control with ACS 200 http://lymebook.com/fight/lyme-and-infection-control-with-acs-200/ http://lymebook.com/fight/lyme-and-infection-control-with-acs-200/#comments Thu, 08 Oct 2009 22:18:54 +0000 http://lymebook.com/fight/?p=260 [Originally posted to FACT forum on Wed May 27, 2009 11:51 am]

Lyme seems suddenly to be everywhere and now we learn that most of us have Cytomegalic Virus too. This new research helps explain the sudden increase in Lyme world wide!

This information combined with the CMV research should be enough that, when considered altogether, leads me to believe that soon infections might overtake all other challenges including toxins, heavy metals, food sensitivities etcetera, as the key missing culprit that must be dealt with in all chronic disease patients if you are to see real lasting results!

INFECTION CONTROL- with ACS 200

ACS 200 becomes increasingly important since not too many will follow for any length of time the other suggestions for controlling chronic infections that I have made such as higher doses of BIOE’NR-G’Y C, which virtually anyone can handle in 8 gm a day or higher levels. Use C Stix to involve patients in the benefits of Vitamin C rich urine, as proof of ongoing detoxification effects. Also recommended are Immuni-T 2 or Vit D or Kyolic or short term use of high dose Vitamin A.

Most U.S. based patients have difficulty locating doctors offering IV UVB and Ozone. That is sad since it provides a great way to start any treatment to lower total body burden of all Pathogens. As an alternative, patients can use ACS very aggressively for a time. Start with 1 ounce and then use 1-2 ounces a day of ACS 200, as a part of their infection control program until results are being seen, usually 2-4 weeks minimum. Then lower the ACS dose to save money, BUT DO NOT STOP TAKING ACS 200, using at least doses of 30 sprays tid-qid for several months or even years along with my other suggestions.

Then follow my FIGHT program so that their own body over time can help control their total body burden of these newly recognized pathogens that clearly none of us can avoid. Read Plague Times by Ewald and get the full story on infections!

Garry F. Gordon MD,DO,MD(H)
President, Gordon Research Institute
www.gordonresearch.com

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Discovery Of Lyme Disease Bug Clone May Explain Disease Spread
ScienceDaily (June 29, 2008)
http://www.sciencedaily.com/releases/2008/06/080626145806.htm

Benjamin Luft, M.D., Professor of Medicine, Stony Brook University Medical Center, and colleagues discovered that a certain clone of Borrelia burgdorferi, the spirochete that causes Lyme disease, appears to be the most common strain causing Lyme disease in North America and Europe, and may account for the increase in cases for the past 20 years.
According to Dr. Luft, Lyme disease is the most common vector-borne disease in the United States with more than 20,000 cases reported annually. While B. burgdorferi is the primary pathogen in the United States, clones of the pathogen are known to cause major disease. The ospC-A clone was one of the first strains ever identified.
In a new article, Dr. Luft and colleagues detail various methods of genetic testing of 68 B. burgdorferi isolates from Europe and North America. Based on the findings of their tests, the researchers concluded that the ospC-A clone dispersed rapidly and widely in the recent past and in both regions of the world.
“I believe this discovery will make an important contribution since it identifies an identical and high virulence clone of Borrelia in both Europe and North America,” said Dr. Luft. “This may explain the recent spread of Lyme disease in North America.”
The researchers report that the isolates of the clone were prevalent on both continents and uniform in DNA sequences, which suggests a recent trans-oceanic migration. More specifically, they explained: “The European and North American Populations of B. burgdorferi sensu stricto have diverged significantly because of genetic drift. Plasmid genes evolved independently and showed various effects of adaptive divergence and diversifying selection…genetic variation within the two continents contributed to most of the total sequence diversity, which suggests recent common ancestry, migration, or both, between the European and North American populations.”
The research was funded partly by the Lyme Disease Association and the National Institutes of Health. Dr. Luft’s colleagues include: Wei-Gang Qui, Ph.D., and William D. McCaig, Hunter College of the City University of New York; John F. Bruno and Yun Xu of Stony Brook University; Ian Livey, Baxter Vaccine AG, Orth/Donau, Austria, and Martin M. Schriefer, of the Centers of Disease Control and Prevention, Fort Collins, Colorado.
________________________________________
Journal reference:
1. . Wide Distribution of a High-Virulence Borrelia burgdorferi Clone in Europe and North America. Emerging Infectious Diseases, July 2008
Adapted from materials provided by Stony Brook University Medical Center.

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We Are All ‘Living In A Sea Of Toxins’ http://lymebook.com/fight/we-are-all-living-in-a-sea-of-toxins/ http://lymebook.com/fight/we-are-all-living-in-a-sea-of-toxins/#respond Wed, 01 Jul 2009 16:57:31 +0000 http://lymebook.com/fight/?p=117 Mark Hyman MD has done an excellent job at the 13th Annual Functional Medicine Conference of organizing thoughts about the EFFECTS of environmental and exogenous chemicals on our health, and why blood testing underestimates the extent of the problem.

I draw your attention to a few paragraphs from his extensive presentation, which discusses some of the impact of chemicals and toxins on our health. Click the link to view the entire 13th annual conference proceedings ‘Managing Biotransformation: The Metabolic, Genomic, and Detoxification Balance Points’.

Garry F. Gordon MD,DO,MD(H)
President, Gordon Research Institute
www.gordonresearch.com

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The Proceedings From the 13th International Symposium of The Institute for Functional Medicine
http://www.alternative-therapies.com/at/web_pdfs/ifm_proceedings_low.pdf

(Excerpt from presentation article by Mark Hyman, MD entitled ‘Systems Biology, Toxins, Obesity, and Functional Medicine’)

LIVING IN A SEA OF TOXINS: THE PROBLEM

Why should we worry about toxins unless we work with toxic chemicals or spray pesticides for a living? Isn’t exposure minimal? Unfortunately, risks of exposure are substantial, pose significant public health risks, and can no longer be ignored. We live in a sea of toxins. Every single person and animal on the planet contains residues of toxic chemicals or metals in their tissues. Eighty thousand new chemicals have been introduced since the turn of the 20th century and most have never been tested for safety or for synergistic actions. The Centers for Disease Control issued a report on human exposure to environmental chemicals. They assessed human blood or urine levels for 116 chemicals (and there were thousands more for which tests were not conducted) as part of the National Health and Nutrition Examination Survey.1 While they found high levels of toxins in some, and low levels in many more, the study, in isolation, may not tell the whole story. Why? Because these chemical toxins move quickly from the blood into storage sites-mostly fat tissue, organs, and bones-so the blood or urine levels underestimate the total toxic load. Both weight gain (because of stored toxins) and the total toxic load can frustrate attempts at weight loss by impairing two key metabolic organs-the liver and the thyroid, by damaging the mitochondria- the site of energy metabolism, by affecting neuroendocrine signaling, and by increasing inflammation and oxidative stress.

FAT AS A STORAGE DEPOT FOR FAT SOLUBLE TOXINS

The Environmental Protection Agency has monitored human exposure to toxic environmental chemicals since 1972 when they began the National Human Adipose Tissue Survey. This study evaluates the levels of various toxins in the fat tissue from cadavers and elective surgeries. Five of what are known to be the most toxic chemicals were found in 100% of all samples (OCDD or octachlorodibenzo-p-dioxin, styrene, 1,4- dichlorobenzene, xylene, and ethylphenol-toxic chemicals from industrial pollution that damage the liver, heart, lungs, and nervous system). Nine more chemicals were found in 91-98% of samples: benzene, toluene, ethylbenzene, DDE (a breakdown product of DDT, the pesticide banned in the US since 1972), three dioxins, and one furan. Polychlorinated biphenyls (PCBs) were found in 83% of the population. A Michigan study found DDT in over 70% of 4 years olds, probably received through breast milk. With the global economy, we may be eating food that was picked a day before in Guatemala, Indonesia, or Asia, where there are not the same restrictions on the use of pesticides as there are in the United States. Many of these chemicals are stored in fat tissue, making animal products concentrated sources. One hundred percent of beef is contaminated with DDT, as is 93% of processed cheese, hot dogs, bologna, turkey, and ice cream.

WHERE DO TOXINS COME FROM?
Exposure to toxins comes from two main sources: the environment (external toxins) and the gut (breakdown products of our metabolism, or internal toxins). Both can overload endogenous detoxification mechanisms.

External Toxins: The Dangers from Without
The external toxins include chemical toxins and heavy metals. The heavy metals that cause the most ill health are lead, mercury, cadmium, arsenic, nickel, and aluminum. Chemical toxins include volatile organic compounds (VOCs), solvents (cleaning materials, formaldehyde, toluene, benzene), medications, alcohol, pesticides, herbicides, and food additives. Infections (hepatitis C virus) and mold toxins (sick building syndrome) are other common sources of toxins. Our modern refined diet can be considered toxic because it places an exta burden o detoxification systems through excessive consumption of sugar, high-fructose corn syrup (the two most important causes of elevated liver function tests), trans fatty acids, alcohol, cafeine, aspartame, foods made with genetically modified organisms (GMOs), and the various plastics, pathogens, hormones, and antibiotics found in our food supply.

Testing for Toxins and Detoxification Function
* Genetic testing of detoxification pathways for phase I and phase II SNPs
* Detoxification challenge test (provocations with caffeine, aspirin,
acetaminophen)
* Measurement of detoxification enzymes
– Reduced glutathione
– Glutathione peroxidase
– super oxide dismutase (SOD)
* Heavy metals
– RBC or whole blood
– Hair analysis
– Chelation challenge with DMPS or DMSA
* Urinary organic acids
– Specific compounds measured, including sulfates, pyroglutamate,
orotate, and others, can give clues to problems with detoxification
pathways.
* Chemical antibodies to various toxins and metals (can occasionally be useful)
* Organophosphates: identified through a 24-hour urine collection test
* Mold and mycotoxin antibodies
* IgG food sensitivity testing
* Celiac testing (IgG and IgA anti-gliadin antibodies, tTG IgA)
* Digestive stool analysis for dysbiosis
* Tests for hidden infections (Lyme, H. pylori, etc.)

Practical Suggestions for Patients
Remove Toxins
* Eat organic food and animal products to avoid petrochemical pesticides, herbicides, hormones, and antibiotics.
* Drink filtered water (reverse osmosis or carbon filter).
* HEPA/ULPA filters and ionizers can be helpful in reducing dust, molds,
volatile organic compounds, and other sources of indoor air pollution.
* Clean and monitor heating systems for release of carbon monoxide, the most common cause of death by poisoning in America.
* Have houseplants that help filter the air.
* Air out your dry cleaning before wearing it.
* Avoid excess exposure to environmental petrochemicals (garden
chemicals, dry cleaning, car exhaust, second-hand smoke).
* Reduce or eliminate the use of toxic household and personal care products (aluminium-containing underarm deodorant, antacids, and pots and pans).
* Remove allergens and dust from your home as much as possible.
* Minimize electromagnetic radiation (EMR) from radios, TVs, and
microwave ovens.
* Reduce ionizing radiation (from sun exposure or medical tests such as X-rays).
* Reduce heavy metal exposure (predatory and river fish, water, lead paint, thimerosal-containing products, etc.).

Improve Elimination of Toxins
* Have 1-2 bowel movements a day.
* Drink 6-8 glasses of water a day.
* Sweat regularly.
– Use exercise to help you sweat regularly.
– Use steam baths or saunas – infrared saunas may be even more beneficial.
* Regular exercise, yoga, or lymphatic massage can improve lymph flow and help flush toxins out of your tissues into your circulation so they can be detoxified.

To read the rest of this article, see page 136 of The Proceedings From the 13th International Symposium of The Institute for Functional Medicine at http://www.alternative-therapies.com/at/web_pdfs/ifm_proceedings_low.pdf.

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F.I.G.H.T. Environmental Toxins and Epigenetic Changes for Optimum Healing and Anti-aging in Every Patient http://lymebook.com/fight/fight-environmental-toxins-and-epigenetic-changes-for-optimum-healing-and-anti-aging-in-every-patient/ http://lymebook.com/fight/fight-environmental-toxins-and-epigenetic-changes-for-optimum-healing-and-anti-aging-in-every-patient/#comments Wed, 10 Jun 2009 23:14:40 +0000 http://lymebook.com/fight/?p=39 These are my thoughts on how to more effectively help EVERY patient better by using my F.I.G.H.T. for Health Program. F.I.G.H.T. is an acronym that stands for: Food allergies/sensitivities and leaky gut syndrome, Infections and pathogens, Genetics and epigenetics, and methylation issues needed for detoxing, Heavy Metals and Hormones, and Toxins that every person is exposed to everyday, everywhere. Regardless of the condition or disease your patient is suffering from, you will have better results by addressing each of these categories in every patient.

I also want to help move us into a new preventative medicine and anti-aging testing system developed by I-M Heath. This unique program measures up to 37 different biomarkers in a patient, resulting in an overall personal biological score that is presented ‘visually’ on a body-map. This helps the patient to “see” their current condition (how slowly or quickly they are aging) and allows the doctor and patient to work together on a holistic program that is supported by published clinical science. visualisations-female

FOOD

With Food it is hard to identify all sensitivity reactions so, at minimum, serious rotation is advised but building a healthy gut flora is vital or we become sensitive to other foods anyway. Since few want to be told to eliminate foods, we can encourage them to eat foods that are in the books by Peter D’Adamo ND, author of Eat Right For You Blood Type and Live Right For Your Blood Type.er4yt
For example, if you are blood type A, you want to eat a largely vegetarian diet, and if you are blood type O you’ll do better with meat-based diet like Atkins; if you are B or AB you are more in the middle of these. The food issue is never resolved adequately with any one test available, so some will rely on strict avoidance of known foods like corn, soy, wheat, and dairy.

Others can learn to eliminate some foods by counting their pulse before and after eating single foods, as described by Dr. Arthur F. Coca, the Chief of Allergy at Columbia, in his book The Pulse Test (available through Amazon.com for about $ 15).

We could do some food sensitivity testing using methods like ALCAT or Elisa testing for food reactions, as usually there will be some food sensitivity blunting the healing response we need.  But since leaky gut is unavoidable with the GMO soy and corn in everyone’s diet providing a pesticide effect in our intestines and altering our flora. I place anyone hoping to have high health on a daily probiotic for life but this will not work optimally without Inuflora, a food derived from the Jerusalem artichoke that is in  Beyond Fiber™ which provides the ultimate PREBIOTIC. This is NOT FOS. This is a huge molecule that alone lowers Candida counts over just a few months time, ensuring healthy flora to flourish while harmful pathogens are choked out.

Beyond Fiber™ is part of my POWER DRINK which I create by adding the following FOUR main ingredients to juices:

1) Beyond Fiber™
2) MACA powder™
3) Dr Gordon’s Advanced Green Powder™
4) BioE’nR-G’y C™

Amounts required are around 1 tsp of each ingredient at least once a day; but some will do better with bid building up slowly. Start with an even ½ tsp of these once a day, as we MUST rebuild the flora for all this to work optimally.

The Power Drink is best sipped over 2 hours ideally bid so you need well tolerated, neutral PH forms of Vitamin C with methylation support like TMG AND MSM, as found in BioEn’R-G’y C™ (or Vitality C). BioE’nR-G’y C™ is key to recovery of all patients; I like about 4 tsp a day giving 16 gms of ascorbic acid. But this must be taken with a quality acidophilus, ideally for life. I am using Kyodophilus or UAS Probioplex DDS caps.

INFECTIONS

Infections are hard to adequately handle unless you routinely offer a short series of 3-6 UVB and OZONE treatments over a couple of days or 2 weeks.  The alternative is to use 50-80+ gm IV ascorbic acid drips ideally followed the same day with HBO treatments.  This goes to H202.

Also, there are reasons to look on my website www.gordonresearch.com under INFECTIONS, and learn how to use natural things like ACS 200 and Immune support and short courses of antibiotics like Azithromycin, or even a week or so of oral Alinia. All of this is needed, as we try to lower the total pathogen load. I do that without spending a fortune trying to identify all the pathogens, as literature shows we all carry them.  Chlamydia is just the tip of the iceberg and we all will have to deal with some CMV and Mycoplasma etc.

We know there is infection and generally we do not need to spend $5k plus with Garth Nicolson’s lab in Huntington Beach or others to attach some name to this pathogen burden. We can safely assume that some stealth organisms are present and the body is not adequately handling them. I have heard of patients using 1 ounce of ACS 200 a day (150 sprays in divided doses) for over a year. Although slowly improving, the infections are still not being hit hard enough so we may need more aggressive oxidative therapies like 100 GM IV ascorbic acid or UVB/Ozone. We just know we need something oxidative, even HBO with high dose IV Ascorbic Acid followed by HBO almost at the same time, which is another way to lower total body burden of pathogens.

Also, look at things such as high-dose Garlic like Kyolic (which some can take and others will not touch) and help the immune system with short-term high dose Vit A, 5-8 days of ½ million units a day. Nutrisorb-A is a liquid form providing 10,000 units per drop.

I find that most patients are not holding their pathogens under adequate control so I help support their immune function. My program uses Longevity Plus© products that are truly comprehensive and a bargain since no immune support product provides the comprehensive coverage found in their Immuni-T™ products. The Immuni-T2™ is primarily for acute infections and the Immuni-T3™ is designed more for chronic issues including cancer. I recommend taking both for 1-3 months starting with 2 tid of each for 2 to 3 weeks then 2 bid for a couple months or longer.  This will help your patients deal with the infection aspect of F.I.G.H.T.

GENETICS

Many labs offer gene testing today and the price will come down and accuracy will increase. But I am confident there will be issues around things like MTHFR and METHYLATION so that helps explain why some patients cannot get optimal response without addressing the need for methylation support.

So I advise all 3 forms of Folic Acid and sublingual B12. Preferably both adult males and females will receive H.R.T Plus (Herbal Remedy from Thailand), which provides Estrogen receptor treatment with the amazing herb Pueraria mirifica. This does many things like protecting against bone loss. Combined with my total program for osteoporosis including Beyond Bone Defense™ and Beyond Chelation Improved™, this is a vital step in allowing us to live long and still have soft arteries and hard bones, even when you are 90.

Ideally, we need to move into anti-aging medicine and select some patient to use as a test case, for learning how to use International Anti-aging Systems (IAS) new program that Phil Mican helped develop with the help of Ward Dean. So go to the I-M Health website and ask for a test sample to learn how to analyze your patients BIOLOGICAL AGE. That is a great way to show over the next 6-12 months that we are getting real benefits. The program will show your patient who complies with all of this getting younger, as the red dots it uses to highlight problem areas will start to become green over time. This is a great way to increase compliance, as the report highlights areas of concern that over the coming years we will see improve!

If we stick to my F.I.G.H.T. concept we can to this without using genetic testing because, for example, the Agouti mice research shows we have Epigenetic changes due to environmental toxins. This research by Randy Jirtle at Duke helps explains today’s epidemic of Obesity and Diabetes due to things like BISPHENOL A. You can safely assume most people have been exposed to BISPHENOL A and that has caused some of these epigenetic changes like methylation defects.

So using the BioE’nR-G’y C™ with TMG AND MSM, at least 1 slightly heaping tsp 2-4 times a day i.e.  taking 8-16 gm a day, preferably with all the other three ingredients found in my Power Drink for optimal results. Nothing beats the Beyond Fiber formula for lowering toxins particularly when taken along with ACZ Nano. It seems that the Zeolite formula is helping move some of the toxins that even Beyond Chelation Improved™ and Heavy Detox™, and hi-dose vitamin C with Fiber, and sweating are moving around, but we need lots of assistance to usher all of these toxins out of the body!

HEAVY METALS
HORMONES

F.I.G.H.T. means lots of detoxing is MANDATORY and that means more than a year of intensive work, which can never be discontinued, as we continue to eat, drink and breathe in toxins. This detox can be helped with homeopathics for drainage. Consider, for example, HEEL has their DETOX kit and I often add 10 gtts of each of the three bottles to each glass of my Power Drink.

For heavy metals the goal is get them as low as possible. Lead is in the bones of everyone, and it is at 1000+ times greater quantities than was present 400 years ago. Bones take 15 years to remodel, so I recommend some of my ‘short’ or push Calcium EDTA IV’s weekly to start and following ideally with IV MYERS.. After 20 or so, switch to perhaps monthly for another 20-30 or more. But always with the full Oral Chelation Program which includes my Beyond Chelation Improved™ plus Power Drink.

For more in-depth information on the causes of universal toxicity and affordable, natural solutions to ‘getting the lead out’, check out my latest book ‘Detox with Oral Chelation: Protecting Yourself from Lead, Mercury & Other Environmental Toxins’.doc-cover-small1

And, of course, ideally patients can join a gym and sweat in the sauna or steam room, or get their own FIR sauna. They now have the new portable versions (that you sit in with head out) costing less than $500. Sweating frequently is crucial as this is an ideal way for Mercury and many other toxins to get out.

For Hormones, I use topical Testosterone – Progesterone Chrysin 150-5-200 per cc, the full 15 years.

TOXINS

So we still must deal with the T for toxins. To prove to patients that they need this you might use US BIOTEK lab and get their urine test for 5 toxins and have the interpretation of their $120- $140 urine stick test interpreted by Mark Schauss. They will test for Phthalates, styrene, benzene, toluene, etc. This is useful so that patients know they are not wasting their time and money on all this detoxing.

For those patients who can afford the expense, it is beneficial to spend the $4900 and send the 20 vials of blood to Mt Sinai School of Medicine to get all 240 toxins measured.  See the excellent Environmental Working Group web site to learn more about that blood test for toxins. Bill Moyers tested and it revealed that in spite of eating and living organically, he too is loaded with endocrine disruptors, carcinogens and neurotoxins and he has lived all organic for years.

I hope what I have written here will prove useful in your practices. If we can broaden our approach to every patient by utilizing the F.I.G.H.T. concept and covering even more issues, you will be getting better results in all patients.

Dr. Garry F. Gordon, MD, DO, MD(H)
Gordon Research Institute
www.gordonresearch.com

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