All Posts Tagged With: "ozone"

Linda comment:  We must all wake up and address the chronic infections…..I love the FIGHT protocol and have been on it for 3 years…..IT ROCKS….go to my file on Webinars and watch all six webinars on the FIGHT protocol…..

WE ALL HAVE SOME CHRONIC INFECTIONS; now there is another major breakthrough to prove this.

My Fight program clearly is meant to help us educate our patients that achieving optimal health is a lifetime challenge. With increasing sophistication of lab sciences, we will find many more challenges in every one of my FIGHT categories but with the epidemic of people with chronic fatigue, you now have even more reason to want to learn about Oxidative therapies like OZONE/UVB/SILVER.

However, a unifying approach to enhance our bodies ability to deal with the multifactorial nature of any chronic disease should increase our interest in learning more about Energy medicine. This broad topic includes Homeopathy, Accupunture, Prayer, Microelectric Current therapy, Magnetic Healing, Oxygen, Hyperthermia and much of what is now called Alternative Medicine.

The exerpt below is just one line from the great overview of viral infections and XMRV that is found in Autism and Prostate Cancer and Chronic Fatigue. This area of research is all new this year but we can expect that someone will soon find many more fungi issues or parasites issues. Of course tying impaired health to our toxin load is just beginning to be seriously considered. Do not fail to look for a moment at this article, as when you tell patients they need to deal with the chronic infection component of their current symptom complex, many feel you are off the wall.

Unless they have heard of Candida or Chlamydia, or CMV, or Herpes, or Lyme, they are not attuned to the need to lower their total body burden of pathogens. No one needs to spend the money to chase down which of these infections they have, as no one will test negative for one or more of these infections if adequately tested. So testing for most patients is impractical except to get their attention as to why they must do something about the infection component of my FIGHT program if they are to achieve optimal health.

“XMRV (xenotropic murine leukemia virus-related virus) is strongly associated with chronic fatigue syndrome/ME. The earlier study published in the journal Science was a joint study by the Cleveland Clinic, the National Cancer Institute, and the Whittemore-Peterson Institute of the University of Nevada with Drs. Vincent Lombardi and Judy Mikovits as lead authors. Here the lead author of the NIH/Harvard/FDA study, Dr. Harvey Alter, noted in a press conference that he considered his study a confirmation of the earlier WPI study, even though they had detected different MLV-related viruses (MRVs), rather than only XMRV. There does seem to be a greater variety of MRVs in chronic fatigue syndrome/ME patients than first understood. The WPI’s original study also showed some evidence of additional MRVs.”
Read more: http://www.ageofautism.com/2010/09/my-wife-my-daughter-and-xmrv.html

Sincerely,

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

September 24, 2010
My Wife, My Daughter, and XMRV
By Kent Heckenlively, Esq.

My wife has tested positive for XMRV, otherwise known as the xenotropic murine leukemia virus-related virus. 
My daughter with autism has also tested positive for XMRV, a new human retrovirus that was recently found to be highly associated with patients with Chronic Fatigue Syndrome/ME by the Whittemore-Peterson Institute.
What has been discovered and speculated about for chronic fatigue syndrome/ME and XMRV may also hold important information for autism. 
By now many of you are probably aware that in August of 2010 the National Institute of Health, Harvard University, and the Food and Drug Administration published an article in the Proceedings of the National Academy of Sciences confirming an earlier study showing that XMRV (xenotropic murine leukemia virus-related virus) is strongly associated with chronic fatigue syndrome/ME.  
The earlier study published in the journal Science was a joint study by the Cleveland Clinic, the National Cancer Institute, and the Whittemore-Peterson Institute of the University of Nevada with Drs. Vincent Lombardi and Judy Mikovits as lead authors. HERE  The lead author of the NIH/Harvard/FDA study, Dr. Harvey Alter, noted in a press conference that he considered his study a confirmation of the earlier WPI study, even though they had detected different MLV-related viruses (MRVs), rather than only XMRV.  There does seem to be a greater variety of MRVs in chronic fatigue syndrome/ME patients than first understood.  The WPI’s original study also showed some evidence of additional MRVs.  Alter is one of the true giants in the field of virology, having been a co-discoverer of the hepatitis C virus, and winning the Lasker Award for medical research, which is often compared to the Nobel Prize in Medicine in terms of its prestige.

More proof that autoimmune disease patients have chronic infections that are not widely recognized; this time we are talking about TB!

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

Full article: http://erj.ersjournals.com/cgi/content/abstract/33/3/586

Excerpt:

Screening for active tuberculosis (TB) and latent TB infection (LTBI) is mandatory prior to the initiation of tumour necrosis factor-  inhibitor therapy. However, no agreement exists on the best strategy for detecting LTBI in this population. The aim of the present study was to analyse the performance of the tuberculin skin test (TST) and QuantiFERON®-TB Gold in-tube (QFT-GIT) on LTBI detection in subjects with immunomediated inflammatory diseases (IMID).

The TST and QFT-GIT were prospectively performed in 398 consecutive IMID subjects, 310 (78%) on immunosuppressive therapy and only 16 (4%) had been bacillus Calmette–Guérin (BCG) vaccinated.

Indeterminate results to QFT-GIT were found in five (1.2%) subjects. Overall, 74 (19%) out of 393 subjects were TST-positive and 52 (13%) were QFT-GIT-positive. Concordance between TST and QFT-GIT results was good (87.7%): 13 were QFT-GIT-positive/TST-negative and 35 QFT-GIT-negative/TST-positive. By multivariate analysis both tests were significantly associated with older age. Only the TST was associated with BCG vaccination and radiological lesions of past TB. Use of immunosuppressive drugs differently modulated QFT-GIT or TST scoring.

Are you sick and tired?  My FIGHT4YOURHEALTH program can change your life even if you think LYME is your only problem. Learn more and become vibrantly healthy again.

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

Full article: http://bolenreport.com/feature_articles/feature_article072.htm

Excerpt:

Most people battling chronic Lyme disease think of the illness as an infection caused by a bacterium known commonly as Borrelia Burgdorferi, generally transmitted via the bite of an infected tick.  What many don’t recognize, however, is that recovery from chronic Lyme disease requires a recognition that the disease is truly a much more complex illness.  Recovery often challenges one to consider more than just infection as the single causative agent involved in the disease process.  It is through looking beyond the infectious component of Lyme disease and understanding the equally important aspects of damaging heavy metals and other toxic insults that a more full and lasting recovery may be realized.

Garry F. Gordon MD, DO, MD (H) co-founded the American College for Advancement in Medicine (ACAM) and serves as the President of Gordon Research Institute.  Dr. Gordon graciously spent a couple of hours with me sharing his views on chronic Lyme disease and those factors that are important in recovering from chronic illness. 

Dr. Gordon acknowledges Lyme disease as a serious infection which can lead to a wide-variety of health challenges.  He does not, however, hyperfocus on the specific tick-borne pathogens which cause the disease.  He instead believes that a multitude of infections are prevalent in anyone with chronic ill health.  In addition to these numerous infections, our state of health is closely tied to our total body burden of endogenous and exogenous toxins.  When looking at why illness is present, it is important to look at a number of factors including genetics, chronic infections, and total body burden of heavy metals and other toxins.

Peering into one’s genetic makeup can be quite helpful when establishing the proper course of action and considering what factors may have contributed to one’s state of health.  The more precisely a practitioner can understand the genetic contributors, the more accurately a treatment protocol can be outlined to fit a person’s unique needs.  As an example, a specific gene mutation can suggest an inability of the body to remove toxic heavy metals.  Thus, even tests performed to determine whether or not one is heavy metal toxic can be incorrect if the metals are not being released due to this specific genetic profile.  Where many doctors may miss a heavy metal toxicity issue in these patients, a practitioner incorporating a genetic review into their diagnostic workup is much better equipped to evaluate the potential impact of toxic metals on the overall state of health.