Thursday, December 4, 2014

You may not be stuck with your genetic mutations (MTHFR, CBS, NOS...)


Okay, you have done the DNA tests and found out you have mutations on many different SNPs, such as MTHFR, CBS, and several others. You are freaking out that you are permanently sick now...but are you really? Are you really stuck with the genetic mutations that you have inherited or have acquired in your lifetime from microbial interference, radiation, and toxins from your environment?

There is much disagreement among clinical doctors who are in practice, and bench scientists who like to represent that genetic problems such as MTHFR and CBS are unchangeable conditions. Finally there is research from the bench scientists that seems to support the idea that you may not be stuck with the illness from these mutations!

Clinical doctors, such as those at the Hansa Center for Optimum Health, are using this newly released science in new ways and often see dramatic improvements in people who according to bench science and mainstream medicine say should never improve due to genetic mutations.

While happy patients does not qualify as scientific fact, there may be an explanation for these improvements found in our doctor's utilization of the latest knowledge of how genes can be turned on and off, and even repaired, by treatments that seek to restore the body's regulation of the 4 million gene switches that were identified by scientists in what is called the ENCODE Project. 

Okay stay with me and read to the end of the article. If may seem a little technical, but push through, because the more you know, the better you can understand what is possible.

—Pamela Scherer McLeod, writing for "Clinical Laboratory and Pathology News and Trends" states, "The big news is that researchers participating in the ENCODE Project have identified up to 4 million critical “gene switches.” The switches reside on the 80% of human DNA that has long been considered “junk.” (emphasis added) 

"On September 5, 2013, prestigious scientific journals published a coordinated set of multiple papers and reviews announcing the discoveries, according to a National Human Genome Research Institute (NHGRI) press release. Almost 40 papers associated with the ENCODE research appeared in print, almost simultaneously. That unusual event is, in itself, a sign of the importance of these new scientific findings.

The published papers included one main integrative paper, plus five related papers in the journal Nature. The journal, Genome Research published 18 papers. The journal, Genome Biology published 6. Additionally, six review articles are being published in the Journal of Biological Chemistry, as well as two related papers in Science and one in the scientific journal Cell.

The findings are the outcome of a mammoth federal research project called ENCODE, an acronym of the Encyclopedia of DNA Elements. NHGRI, part of the National Institutes of Health (NIH), launched the project in 2003. The concerted effort involved 440 scientists from 32 laboratories around the world.

The ENCODE findings surprised researchers in two ways. First, they were surprised to find that at least 80% of the DNA is in fact active and needed. Second, they did not expect that a large proportion of this “junk” DNA is gene switches. “[Before ENCODE,] if you had said half of the genome—and probably more—has instructions for turning genes on and off, I don’t think people would have believed you,” observed John Stamatoyannopoulos, M.D., Associate Professor of Genome Sciences and Medicine at the University of Washington, in a story published in The New York Times. Stamatoyannopoulos participated in the ENCODE project.

The scientific community already considers the ENCODE discoveries a major medical and scientific breakthrough with enormous implications, the Times reported. The data showed that many complex diseases appear to be caused by minute changes in hundreds of gene switches. 

“Most of the changes that affect disease don’t lie in the genes themselves,” explained Michael Snyder, Ph. D., Professor and Chair of Genetics at Stanford University, in the Times story. “[T]hey lie in the switches.” Snyder is Director of the Stanford Center for Genomics and Personalized Medicine and worked on the ENCODE project." (emphasis added)

Once again, happy, apparently healthy patients, who had chronic problems from gene expression problems and gene mutations do not qualify as true scientific proof that gene expression has changed. The only valid proof is to repeat the set of genetic tests post-treatment and see the problems no longer present. 

Of course, no doctor normally would ever repeat a genetic test since the now outdated knowledge has been so deeply ingrained with the idea that your genetic mutations are permanent. Now possibly, once you have been treated and seem to have sustained improvement, it might be worth doing a followup DNA test to see if the mutations have changed!

The doctors at the Hansa Center are presently working with genetic laboratories to determine if the treatments can be documented scientifically through treatment and repeat analysis of the classical genetic testing methods. The idea is to affect the structure and function of the body's SNPs by targeting know mutations, such as MTHFR, through bioenergetically modifying the signals being transmitted biophotonically from the heart to these genetic switches. Some doctors will say, "All you have to do is treat the whole person, think nice thoughts, take this or that protocol of supplements, just do their version of energy medicine or machine." I guarantee you, none of these holistic approaches have resulted in one change to the actual SNP mutations. Others will say, I am only treating the SNPs and missing the whole person. Hear me now...if a mutation is to be repaired at all it will require a new and fundamental shift in how the entire person is treated.

No one knows yet how long this takes to get the switches to flip, or exactly how to affect the structure and function of the body in a consistent way, since everyone comes with their own unique "software" and their own and family history of traumas, and illness.

The only way to effect the whole of the body is to treat with the idea of correcting everything we can find that has gone wrong from head to toe, from the inside out, and the outside in. That is why our doctors are working fast and furious for at least an hour everyday for two weeks to address and facilitate the restoration of the most optimum structure and function of every possible problem we can find.

What is clear is that if we can document and reproduce ways to flip the right gene switches, the lights will turn on and health will follow, which is good news to all of those people who thought they were just stuck with their condition.

There is hope!

*Note: I recommend the Nutrigenomic Methylation Pathway Analysis to test for mutations in your metabolic and detox pathways. (The following link is the test I recommend: http://www.holisticheal.com/health-tests/nutrigenomic-testing The results of this report will come with more detailed health information with your DNA test than the 23&me test.




For over 20 years the Hansa Center for Optimum Health, in Wichita, Kansas has specialized in the restoration of health for people with previously unresponsive and chronic illnesses of virtually all types. Over 85% of people come from other states and countries. If you have done everything you and your doctor know to do and are still struggling, contact our wonderful Patient Care Coordinator, Kara, at patientcare@hansacenter.com, for information on the exciting new treatments we have developed at the Hansa Center for Optimum Health. For additional info, visit our website at www.HansaCenter.com.

This article is for educational purposes. Before implementing any supplements/remedies always consult with your healthcare professional. Due to the complexity of the human condition there remains the possibility of symptoms getting worse. Again, discuss the ideas presented here with your health care professional before beginning, and stop, or get support, if your condition worsens. This information is not intended to treat, cure, diagnose, or mitigate any disease or illness, and has not been evaluated by the FDA. The Hansa Center does not treat named diseases, but seeks to restore the body's optimum structural and functional integrity so that the body can rapidly heal itself. 

*Due to the exhaustive time spent per day with each patient, and poor repayment history of insurance companies, we unfortunately cannot accept insurance assignment. We do participate in Care Credit, and accept all major credit cards. We will gladly accept insurance when our elected officials revamp the health insurance industry to cover all results-based care. We encourage you to vote with this in mind. Please call 316-686-5900 ext. 1, for current pricing for our economically-priced, All-inclusive 2-3 weeks intensive packages of care.
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2 comments:

Robin said...

Wow. Of course you're not stuck with your genetics. Most patients on the lyme and ME/CFS forums know this, that it's an issue of genetic expression, and not some sort of defect.

Anonymous said...

Agree wholeheartedly with Robin here. With the gift and hope that Epigenetics offers, the switch is being flipped for many with a change in lifestyle as a whole. No one thing can help in isolation. It took a lot of damage for us all to get to where we are so it will take a while to reverse this damage. Be aware that the 23andMe test furnishes people with 600,000 SNPs in their results for just $99 while the one you mention only gives results for on 40 of those SNPs for $400 AND recommendations to buy thousands MORE dollars in supplements WITHOUT a consult with a Dr!

Addressing these issues will cost thousands no doubt. Why would I start spending it without the guarantee that a Dr will supervise my treatment? Right now, the test you suggest offers a chat group for $400 while 23andMe does exactly the same for $99. Now that I know you consider genetics as a factor, I'd really like to see someone at your center Dr Hansa so this post was very encouraging.