All Posts Tagged With: "National Institutes of Health"

Beyond Fiber with comments by Linda, Dr. Gordon

Linda’s comments:  The Beyond Fiber in Dr Gordon’s drink is one of the best fibers I have every used.  I have tried many fibers, but the Beyond Fiber wins over all fibers on the market.   I will have to admit, his Power Drink is POWERFUL….in the beginning you will be visiting your bathroom, but trust me you will feel wonderful afterwards…..YESSSSSs, you will need to mix it with your favorite juice….I like mixing it with Mango, Peach or Pear…..Dr G is right, when you begin to feel what the MACA does for you, you will learn to drink it…..I have been on the FIGHT protocol for 2 years now and can tell you, IT WORKS….Those with chronic illness, the FIGHT protocol is a must…..I tell folks….just do it for 90 days, and stick to it.  You might find yourself pleasantly surprised.

My talk for IFIM in Chicago in June will be on “Advanced Detoxification for Infinite Health and Wellness”. I cannot achieve that goal without all forms of fiber but enhanced, as I make them with my “Power Drink”: Organic Greens, MACA, Beyond Fiber, and the one and only BioEn’R-G’y C, one slightly heaping tsp of each supplement in 10+ ounces of any
fluid. I like it with Pellegrino but tap water works fine too. Some of you will want to flavor their Power Drink with anything from mango, as seen in Vemma, or pomegranate juice. Most will not like the glucosinolate based MACA, as it is from the turnip family. But, if you learn what it does, you will do whatever is needed to make it palatable enough to use once or twice a day.

This is my way of preventing enterohepatic reuptake of toxins that start to move with oral or parenteral chelation or even zeolite but need to be ushered out of the body! I take this twice a day but I have to look healthy at 76 in order to lecture on advanced detoxification around the world. And now that I see what PEMF and Magnetico sleep does to raise my ATP levels so I my cells have the energy to assimilate nutrients and pour out toxins, I can tell you I am really getting younger and all of you can too.

Fiber is just the tip of the iceberg but it alone is reducing the risk of death from all causes. Imagine how healthy you can get if you amplify it with my Power Drink and the energy the body needs to push out intracellular toxins and assimilate the nutrient supplements we all take but may be seeing less and less results.  Then you too can start to feel, as fantastic as I feel all the time. Imagine what can be done when you amplify this detoxification effect!

Dr Yikyung Park, of the National Cancer Institute (NCI) in Rockville, Maryland, USA, and colleagues from NCI and AARP also found that dietary fiber was linked to a reduced risk of death from any cause over a nine-year period. 

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

Link: http://www.medicalnewstoday.com/articles/216469.php

Excerpt:

A diet rich in fiber, particularly from whole grains, may cut risk of death from cardiovascular, infectious and respiratory diseases, according to a report that was published online in the Archives of Internal Medicine this week.

Dr Yikyung Park, of the National Cancer Institute (NCI) in Rockville, Maryland, in the US, and colleagues from NCI and AARP also found that dietary fiber was linked to a reduced risk of death from any cause over a nine-year period.

Plasmid systems in Lyme

Link: http://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=21193609&retmode=ref&cmd=prlinks

Excerpt:

The restriction-modification (R-M) systems of many bacteria present a
barrier to the stable introduction of foreign DNA. The Lyme disease
spirochete Borrelia burgdorferi has two plasmid-encoded putative R-M genes,
bbe02 and bbq67, whose presence limits transformation by shuttle vector DNA
from E. coli. We show that both the bbe02 and bbq67 loci in recipient B.
burgdorferi limit transformation with shuttle vector DNA from E. coli,
irrespective of its dam, dcm, or hsd methylation status. However, plasmid
DNA purified from B. burgdorferi transformed naive B. burgdorferi much more
efficiently than plasmid DNA from E.
coli, particularly when the bbe02 and bbq67 genotypes of the B. burgdorferi
DNA source matched that of the recipient. We detected adenine methylation of
plasmid DNA prepared from B. burgdorferi that carried bbe02 and bbq67. These
results indicate that the bbe02 and bbq67 loci of B. burgdorferi encode
distinct R-M enzymes that methylate endogenous DNA and cleave foreign DNA
lacking the same sequence-specific modification. Our findings have basic
implications for horizontal gene transfer among B. burgdorferi strains with
distinct plasmid contents. Further characterization and identification of
the nucleotide sequences recognized by BBE02 and BBQ67 will facilitate
efficient genetic manipulation of this pathogenic spirochete.

Rapid, Simple, Quantitative, Sensitive Lyme Test — Yes, For Real!

Full Article: http://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=20392886&retmode=ref&cmd=prlinks

Excerpt:

Neurobiology and Pain Therapeutics Section, Laboratory of Sensory
Biology, National Institute of Dental and Craniofacial Research,
Laboratory of Clinical Infectious Diseases, National Institute of
Allergy and Infectious Disease, National Institutes of Health,
Bethesda, MD 20892.

There is currently a need for improved serological tests for the
diagnosis and monitoring of Lyme disease, an infection caused by
Borrelia burgdorferi (Bb).
Here, we evaluated Luciferase Immunoprecipitation Systems (LIPS)
for profiling antibody responses to a panel of Bb proteins for
diagnosis of Lyme disease.
Initially, a training serum cohort of patients and controls
(n=46) was profiled using 15 different Bb antigen constructs. In
the patient sera, antibody responses to several Bb antigens
including VlsE, Flagellin (FlaB), BmpA, DbpA, and DbpB, showed
high levels of immunoreactivity. However, the best diagnostic
performance was achieved with a synthetic protein, designated as
VOVO, consisting of a repeated antigenic VlsE-OspC-VlsE-OspC
peptide sequence.