Better Health begins with VIDACELL®

VIDACELL  is an incredible cell food that has laid the foundation for a life-changing opportunity!

VIDACELL is an all natural cell food that provides your body’s cells with vital and essential nutrients they can use to fight the “cellular aging process” and promote better health.

Better Health begins at the “Cellular Level”

In today’s modern lifestyle, our body’s cells tend to degenerate much faster than they normally would due to constant exposure to toxins, poisons, stress and environmental impurities.

These ongoing negative exposures create free radicals within our bodies that attack our cells and literally steal our lives away!

Free radicals…

  • Are cellular killers
  • Damage our DNA structure
  • Alter and destroy our body’s cells and ultimately affect our overall health
“The average person’s diet bombards their cells with over 200 lbs of chemicals per year.”
– Dr. Theodore J. Cole


VIDACELL Cell FoodDid you know…

  • Your body is made up of over 73 trillion cells
  • Your body’s overall health can be measured by the health of your cells
  • Healthy cells produce more cellular energy (ATP) than unhealthy cells
  • You’re only as healthy as your cells!
“When it’s really broken down, every single health issue, no matter the name, comes to cellular health.”
-Dr. Mark Smith, N.D., Ph.D.

The Solution to Better Health is…VIDACELL

VIDACELL is an all natural cell food that provides your body’s cells with vital and essential nutrients they can use to fight the “cellular aging process” and promote better health.

As a Result VIDACELL effectively:

  • Enhances cellular energy (ATP) production up to 54%
  • Assists in fighting free radical damage
  • Promotes cellular detoxification
  • Enhances the immune system
  • Supports cellular regeneration
  • Promotes oxygen in the blood
  • Supports DNA repair
  • Promotes antioxidant production
  • Enhances the digestive system
  • Enhances mental clarity

Bottom line… Healthy Cells equal a Healthy Life!

* These statements have not been evaluated by the Food & Drug Administration. This cell food is not intended to diagnose, treat, cure or prevent any disease.

Development

VIDACELL contains a complete amino acid profile, complex carbohydrates, Polysaccharides Peptides, and cofactors necessary for life, all in a bio-available form for complete and immediate utilization by the body.

VIDACELL contains NO dairy, wheat, gluten, sugar, chemicals, fillers, binders, artificial colors, artificial flavors, additives, preservatives or genetically modified organisms (non-GMO).

VIDACELL is made from all native strains of specially selected fractions of rice grains grown in the Siam Valley of Thailand. This is a region of the world that has some of the most fertile and mineral rich soils due to thousands of years of natural organic mineral accumulation.

After harvesting, the select rice grains are then put through a proprietary process known as Alphaglycanology. This process extracts vital nutrients and reduces the particle size for enhanced absorption to obtain the most bio-available essential nutrients necessary for the cellular energy production process.

Proprietary Process recognized as a Top Innovation

In March of 2007 VIDACELL received Thailand’s first award ever presented by Thailand’s Department of Intellectual Property (DIP) and Thailand’s National Innovation Agency (NIA) for being recognized as a Top Product of Innovation.

Award group photo

* These statements have not been evaluated by the Food & Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

History

How was VIDACELL Discovered?

ScientistIn the early 1990’s a group of scientists, food technologists and doctors in Thailand were doing some research on instant cereal formulas that they were producing as baby foods. The scientists were experimenting with the idea of adding unique native strains of select fractions of rice grains to the cereals, using a proprietary nanotechnology and mechanical hydrolysis process.

Not long after the scientists made the formula modifications, they began receiving regular feedback. The feedback the scientists received was very unusual, but incredible! Not only was the cereal nourishing the babies, but in many cases, a multitude of immediate health benefits were being reported. In some cases, even babies that had been diagnosed as chronically ill, were reporting positive results.

This constant feedback prompted the scientists to undertake further research projects to investigate the different health benefits in both the babies and adults that were now on the formula.


The research work involved the use of:

  • Ancient Thai Folk Medicine and Bio-Food Engineering techniques and theories
  • A proprietary nanotechnology and mechanical hydrolysis process resulting in high bioavailable nutrients preserved in a powder form
  • Specially selected native rice grains harvested at the right age, cultivated in areas with natural alkaline soils, continuously enriched with natural organic matter and enhanced micronutrients.

ScientistUltimately, this ongoing research led to the development of a unique and innovative “functional food” that we now know today as VIDACELL – Cell Food. As a result of this incredible discovery, VIDACELL – Cell Food has literally opened the eyes of many leading scientists, physicians and biochemists to a new way of supplementing the body at a cellular level.

The ongoing research as to the benefits of VIDACELL – Cell Food has now come under the sponsorship of Thailand’s National Innovation Agency (NIA), a department under the Ministry of Science and Technology, as a Product of Innovation in the “functional food” sector of Thailand. This prestigious relationship has provided GreatLife International with the ability to have access to the Thai government-owned research facilities for further research into the additional benefits of VIDACELL – Cell Food.

* These statements have not been evaluated by the Food & Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

Science

VIDACELL is the trademark of ingredients containing a unique functional and cell food formulation of nutrients that are essential for bodily functions. VIDACELL contains all of these naturally derived nutrients in a bioavailable form:

  • Polysaccharide – Available as biological fuel for cellular energy (Also know as Polysaccharides Peptides )
  • Polypeptide – Amino Acids available in the right quantity and ratios to be used as raw materials to the cells to perform their functions effectively and promote cellular renewal
  • Natural Vitamins and Minerals – As raw materials for cellular enzyme production and overall function
  • Phytonutrients – provide cofactors for cellular processes

VIDACELL – Cell Food Ultra-Structure

Ultra Structure

Studies by: Solid State Cross Polarization Magnetic Angle Spinning (CP/MAS) C-NMR (Nuclear Magnetic Resonance) Spectroscopy.

Mechanically Hydrolyzed Polysaccharides Peptides

VIDACELL is a biologic phytocompound. It can be classified as a non-dialyzable high molecular weight polysaccharide with low molecular weight poly-peptides.

The molecular weights of the different compounds range from 150 to 300kDa. A major chemical feature of these Polysaccharides and Peptides is the presence of linkage of D-glucose units in the main chain.

VIDACELL Under Scanning Electron Microscopy (SEM)

Scanning Electron MicroscopyFig. 1 Atypical Molecular Pyramid-like
Structure, average size 200-300 microns with one-sided fiber-like surface

Safety Report

VIDACELL is hypoallergenic Polysaccharides Peptides and has no known side effects. It contains no dairy, wheat, sugar, chemicals, fillers, binders, artificial colors, artificial flavors, additives, or preservatives and it contains no genetically modified organisms (non-GMO).

In-Vitro Study

In-Vitro Alzheimer Model Study with Neuroblastoma Cells (Sawatsri et al.)

Conclusions and Discussion: In-Vitro studies of neuroblastoma (neuron cells) showed 100% cell death and severe damage of dendrites when neurotoxins were induced. However, when the neuroblastoma (neuron cells) were pretreated with the VIDACELL, in-vitro studies showed different levels of cell survival and apparent recovery of dendrites from the neurotoxin injuries within 48 hours.

Invitro Study

Figure: Serving dependent of VIDACELL against glutamate-induced toxicity to cells and dendrites, A. LA-N-5 under control conditions appear healthy (cytoplasm and neuronal processes). B. LA-N-5 exposed to 0.2 mM Glutamate after 24 h. display shrunken cell bodies and degeneration of neuronal process. C. LA-N-5 grow in the presence of 0.066 mg/ml VIDACELL for 2 days prior to exposure to 0.2 mM Glutamate after 24 h display exhibit clear features of neuronal viability for cell bodies and clearly defined neuronal process similar to those of control neurons not treated with 0.2 mM Glutamate. D. similar C but if increased serving VIDACELL to 6.66 mg/ml, showed neuronal viability and neuronal process obviously similar with control (Ccompare B, D compare B). X 400

Conducted By:

Royal Thai Army Medical Center, PMK Research Center and, Emory University School of Medicine, Atlanta, Georgia; USA

Medical Doctors and Scientific Advisors:

Researcher: Col. Sayan Sawatsri, M.D.; Clinical Associate Professor of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA, USA. Director of the Div. of Family Planning OB-GYN Dept.; Pharamongkutklao Hospital and College of Medicine, Bangkok, Thailand

Advisors: Wanphen Yumkhunthong, M.Sc. Prof. Neil Sidell, Ph.D., Somchai Boonchuen, DVM, Dipl. Functional Medicine, Col. Chalermporn Boonsiri, M.D. and Col. Nirundorn Pidet, M.D.

In-Vitro Study

In-Vitro Mitochondria Cellular Viability/Energy Study (Sawatsri et al.)

Conclusions and Discussion: VIDACELL showed dose dependent for neuroprotective effect in AD model and 1:100 VIDACELL demonstrated the optimal effect with a significant increase of ATP in mitochondria metabolism of about 54% when compared with control.

Conducted By:

Royal Thai Army Medical Center, PMK Research Center and, Emory University School of Medicine, Atlanta, Georgia; USA

Medical Doctors and Scientific Advisors:

Researcher: Col. Sayan Sawatsri, M.D.; Clinical Associate Professor of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA, USA. Director of the Div. of Family Planning OB-GYN Dept.; Pharamongkutklao Hospital and College of Medicine, Bangkok, Thailand

Advisors: Wanphen Yumkhunthong, M.Sc. Prof. Neil Sidell, Ph.D., Somchai Boonchuen, DVM, Dipl. Functional Medicine, Col. Chalermporn Boonsiri, M.D. and Col. Nirundorn Pidet, M.D.

Full Research In-Vitro Study:

Neuroprotective Effect of PSP02 in Cell Line Models of Alzheimer’s disease

(In particular the ATP production in mitochondria metabolism)

Cell Line MachineColorimetric MTT (Tetrazolium) Assay

Bar Chart

* p < 0.05 Figure 1.

Neuroprotective effect of 0.033, 0.066, and 0.33 mg/ml a-PSP02 (1:1000, 1:500, 1:100x) on LA-N5 that was induced by a 20 min. exposure to 30 µM H2O2 (hydrogen peroxide-induced toxicity). The highest percentage of cells viability was 54.5% as estimated by colorimetric MTT (Tetrazolium) Assay. The values represent mean + SEM of at least three separate experiments, each performed in triplicate, p < 0.05 compared with control group.

Statistical analysis: Data was analyzed using Student’s t-test for measuring the cells viability of experimental groups compared with control groups.

Discussion: The percentage of cells viability of neuroblastoma cell at 0.33 mg/ml of a-PSP02 increased 54% as shown in Figure 1. A Student’s t-test (two-tailed) was used to determine p-value of the experiment and showed that p-value was less than 0.05 (p < 0.05). It was found that the percentage of cells viability at 0.33 mg/ml a-PSP02 (experimental group) and a control group were significantly different. From the result it was shown that 0.33 mg/ml a-PSP02 can significantly survive from hydrogen peroxide-induced toxicity when compared with control group.

Conclusion: a-PSP02 showed dose dependent for neuroprotective effect in AD model and 1:100 PSP02 demonstrated the optimal effect with a significant increase of ATP in mitochondria metabolism of about 54% when compared with control.

References:

  • Brinton RD, Chen S, Montoya M, Hsish D, Minaya J. The estrogen replacement therapy of the woman’s health initiative promotes the cellular mechanisms of memory and neuronal survival in neurons vulnerable to Alzheimer’s disease. Maturitas 2000; 34: S35-52.
  • Mattson MP, Furukawa K, Bruce AJ, Mark RJ, Blanc E. Calcium homeostasis and free radical metabolism as convergence points in the pathophysiology of dementia. In: Wasco W. and Tanzi RE., editor. Molecular Mechanisms of Dementia. New Jersey: Humana Press. 1997; 103-43.
  • Roth Adrian, Schaffner W, Hertel C. Phytoestrogen kaempferol (3,4′,5,7-tetrahydroxyflavone) protects PC12 and T47D cells from b-amyloid-induced toxicity. J Neurosci Res 1999; 57: 399-404.
  • Calderon F, et al. PC12 and neuro 2a cells have different susceptibilities to acetylcholinesterase-amyloid complexes, amyloid25-35 fragment, glutamate, and hydrogen peroxide. J Neurosci Res 1999; 56: 620-31.
  • Munch G, et al. Microglial activation induces cell death, inhibits neurite outgrowth and causes neurite retraction of differentiated neuroblastoma cells. Exp Brain Res 2003; 150: 1-8.
  • Fabrizi C, Businaro R, Lauro GM, Starace G, Fumagalli L. Activated a2 macroglobulin increase b-amyloid (25-35) induced toxicity in LAN5 human neuroblastoma cells. Experimental Neurol 1999; 155: 252-9.
  • Behl C, Davis JB, Lesley R, Schubert D. Hydrogen peroxide mediates amyloid beta protein toxicity. Cell 1994; 77: 817-27.
  • Schubert D, Behl C, Lely R, Brack A, Dargusch R, Sagra Y, et al. Amyloid peptide are toxic via a common oxidative mechanism. Proc Natl Acad Sci USA 1995; 92: 1989-93.
  • Olivieri G, et al. Mercury induces cell cytotoxicity and oxidative stress and increases beta-amyloid secretion and tau phosphorylation in SHSY5Y neuroblastoma cells. J Neurochem 2000 Jan; 74 (1): 231-6.
  • Hansen MB, Nielsen SE, Berg K. Re-examination and further development of a precise and rapid dye method for measuring cell growth/cell kill. J. Immunol Meth 1989; 119: 203-10.

* These statements have not been evaluated by the Food & Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

Holistic Microscopy: Live & Dry

Holistic Microscopy is the study of Live and Dry Blood samples using a high-powered microscope to view a drop of blood for the purpose of determining the life force of the blood cell. The Live Blood Analysis demonstrates what has been happening in your blood for the last 120 days. The Dry Blood Analysis can demonstrate what the strengths and weaknesses are of the different organs and systems in the body.

The Live Blood Analysis (left image) demonstrates what has been happening in your blood for the last 120 days. A few qualities we look for are…

  • Perfectly round cells
  • Plump cells with no fermentation in the center Scientist with microscope
  • Free flowing cells that are not sticky

The Dry Blood Analysis (right image) can demonstrate what the strengths and weaknesses are of the different organs and systems in the body. A few qualities we look for are…

  • Blood that looks red without white puddles (acidic fermentation)
  • Blood that is coagulated; not broken up
  • Blood that is vibrant (not washed out)

Demonstration #1

  • Client: Female
  • Age: 57
  • Lifestyle: Vegetarian
  • Test Time: 21 Days (3 weeks)
  • Amount of VIDACELL – Cell Food : 2 to 3 packets per day

Participant’s best Live & Dry Blood Samples taken Saturday January 5, 2008.

Live and Dry Blood Cell Sample

Participant’s best Live & Dry Blood Samples taken Saturday January 28, 2008.

Live and Dry Blood Cell Sample

Demonstration #2

  • Client: Female
  • Age: 45
  • Lifestyle: Standard North American Diet
  • Test Time: 21 Days (3 weeks)
  • Amount of VIDACELL – Cell Food: 3 packets per day

Participant’s best Live & Dry Blood Samples taken Saturday January 5, 2008.

Live and Dry Blood Cell Sample

Participant’s best Live & Dry Blood Samples taken Saturday January 28, 2008.

Live and Dry Blood Cell Sample

Summary: Demonstrations show that VIDACELL – Cell Food has the ability to support and enhance the overall condition, environment, and function of blood cells.

Performed by Fred Shadian – Holistic Microscopist

* These statements have not been evaluated by the Food & Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

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Healing The Symptoms Known As Autism

 https://www.facebook.com/HealingTheSymptomsKnownAsAutism/posts/956275311114555

From Dr. Marco Ruggiero:

Shortly after the AutismOne meeting in Chicago on May 18-25, 2015, Dr. Jeff Bradstreet, myself and my wife, Dr. Stefania Pacini, begun working on a scientific project that, in our opinion, could have elucidated the underlying cause of autism and opened the way for a definitive cure of the disease. As a matter of fact, in his last lecture at AutismOne, Dr. Bradstreet explicitly stated, using a rhetorical question, how close we were to a cure for autism.

We begun working at this project very intensively and our goal was to identify the pathogenesis of autism and then to merge our respective protocols into a single one that addressed such ultimate pathogenesis of autism.

About one year earlier, we had observed that the brains of autistic children showed peculiar lesions that could be identified and classified using transcranial ultrasonography. These observations were published in a peer-reviewed journal, Frontiers in Human Neuroscience that can be retrieved in PubMed.

It is worth noticing that Frontiers in Human Neuroscience, is a Journal that is associated with the Nature Publishing Group, the most prestigious in the world. Frontiers in Human Neuroscience has become the #1 most-cited journal in psychology, the #1 most-cited open access journal dedicated to neuroscience and the 10th most-cited journal in all of neuroscience. It is also the 2nd and 3rd largest journal in all of psychology and neuroscience, respectively.

The presence of these lesions has been confirmed, using other methods of imaging such as MRI, by other research groups, and there is almost unanimous consensus that there are anatomical alterations in the brains of autistic children. It is also generally accepted that such anatomical alterations are correlated with the severity of the symptoms.

The key missing point, however, was the cause of such anatomical alterations and, without knowing such a cause, any type of therapeutic approach was, at best, empirical.

In the first two weeks of June, we had been able to hypothesize the cause of these brain alterations in autism and we worked day and night to write a scientific paper reporting the results of our observations. We worked so frantically because we knew that such a paper would have been a milestone in autism research because it solved the most basic question regarding autism that, in lay term, is: “what is the cause of autism?”

As soon as the paper was ready, Dr. Bradstreet submitted it to the same prestigious journal where we had published one year earlier, that is Frontiers in Human Neuroscience.

Fortunately, considering what happened immediately thereafter, the publisher is located in Switzerland, notoriously a neutral country.

A few days after the submission of the paper, Dr. Bradstreet tragically died.

The paper, however, had already been submitted and, therefore, I was able to revise it and to make all the changes that were necessary for its publication. It took about 5 months of intense work to complete the paper and to render our hypothesis acceptable by the mainstream medical scientific community.

This fundamental paper can be considered a posthumous homage to the scientific figure of Dr. Bradstreet and it is now published in Frontiers in Human Neuroscience from where it can be freely downloaded.

http://journal.frontiersin.org/…/10.…/fnins.2015.00485/full…

In this paper we write that infection or inflammation of the deep cervical nodes that drain lymph from the brain and from the mouth and throat may lead to impaired lymph drainage with consequent accumulation of extra-axial fluid in the brain that leads to disruption of the connections between neurons and glial cells.

Therefore, impaired lymphatic drainage would result in the accumulation of metabolites (toxins) in the brain and in constant inflammation of the brain and the meninges with consequent alterations of brain development and function.

Although the following speculation is not included in the paper, it can be hypothesized that impaired lymphatic drainage would decrease the immunological defenses of the brain and its capability to fight pathogenic microbes that penetrate into the brain, mainly from the intestine.

In fact, it was recently demonstrated that in the brain there are microbes that are commonly found in soil and water and the cells of the immune system (macrophages) carry these microbes to the brain (PLoS One. 2013;8(1):e54673. doi: 10.1371/journal.pone.0054673).

After the publication of our paper, we hypothesize that the brain lymphatic system, as described in our paper, through which the immune cells travel, is instrumental in carrying the good or the bad microbes to the brain and influence its function.

Although the interconnections between gut microbes, the immune system and brain development and function were well known, following the publication of our paper, we are now confronting a radical paradigm shift.

Microbes in the gut DO NOT INFLUENCE the development and the function of the brain: THEY ARE CELLS of the brain just like neurons and glial cells. Microbes are AS IMPORTANT as neurons and glial cells for brain function and the microbes that you have in the intestine are the microbes that you have in the brain.

Now that the pathogenesis of autism is clearly hypothesized in this paper of ours, it is foreseeable that it will open the way for a definitive and successful therapeutic approach.

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Cancer’s Sweet Tooth – We can live on fats, cancer cannot!!

Simply put, I have always found that not eating sugar made a significant difference in my health.  I have also found that it is not easy!
Today I am reading about cancer research from Warburg.
  • In 1931, Dr. Otto Warburg won the Nobel Prize Physiology or Medicine for his discovery that cancer cells have a fundamentally different energy metabolism compared to healthy cells.
  • Most experts consider him to be the greatest biochemist of the 20th century. His lab staff also included Hans Krebs, Ph. D., after whom the Krebs cycle was named.
  • The Krebs cycle refers to the oxidative reduction pathways that occur in the mitochondria. So just how does the metabolic inflexibility of cancer cells differ from healthy cells?
  • A cell can produce energy in two ways: aerobically, in the mitochondria, or anaerobically, in the cytoplasm, the latter of which generates lactic acid — a toxic byproduct. Warburg discovered that in the presence of oxygen, cancer cells overproduce lactic acid. This is known as The Warburg Effect.
It has been straightforward for me.  If the body is too acidic, lower it by eating more dark green vegetables, help the digestion by eating clean protein and making sure you have digestion power to convert your food ALL THE WAY to amino acids.  This requires that we eat no sugars, carbs or alcohol that turn into sugar.  No three lumps every time you have coffee.  No more “crack sugar”.
Warburg’s work is what the PET scan is based on.  It finds areas that are up-taking excess glucose.  Get it?  Not all cells are in this boat but the ones that are, NEED YOUR ATTENTION and CARE.
What has worked for me is simply abstain from sugar cravings.
This does a few things for me.
1.  My cells don’t have a massive reservoir of energy to remove sugar from my body.  After I eat too much, the insulin and cortisol start to overproduce.  It will take weeks to remove the flood of sugar I had because I cheated.
2. I want to empower myself by starving the collection of microbial cells that have disturbed metabolism.  At this time, I go to burning oils which burn slow and clean vs. carbs which burns hot and dirty.
3.  Sugars feed retro-viruses.  A very dark virus that produces proteins that re-coded our cellular DNA to the frequency of the virus rather than my frequency.  My immune system can’t reach or repair them to my body’s healthy tissues and function.
I have always starved myself of excess sugar in order to be healthy.
Not because I want to be thin, but because glucose feeds aberrant cells. And starving them of “crack sugar” really, really helps.
Helping Others
Lots of people can’t see their way to even conceive of this method of abstinence.  It seems too much, unnecessary and they quickly dismiss it.  If there is cancer and if it has a “hold”, the reaction has a common theme.   Quick dismissal!  The aberrant cells are winning.
I see the solution as a way that I can empower myself but it has taken years for me to get a moderate grip on it!  I started 15 years ago!
But now, I am getting much more organized.
The strongest factor for me of staying straight is emotional stress.  It’s hard to stay straight if I am doing too much or otherwise stressed.  That is the new thing that I track.  Why am I stressing myself and what am I avoiding by doing that.
When I am not stressed, it works much better.  I have built my life on being able to digest my food, my life’s events, and all the mental and emotional issues around me.  When I do that, including not going to bed with food I haven’t digested, I do great.
I now watch the growth to health, not the downfall.  It lets me focus positively and not “pick on myself” because the cells are not responding to my immune system.
Here is what helps:
works to encode the cell’s hijacked DNA frequency back online to my body
  • Cistus tea
  • Origin-22M
  • Rerum/imuno
I wish all this health and discipline for you too!
Put up a chart on your fridge.  (Your relationship  with food)
Count the times you are overwhelmed by the need to stress eat and try to win over that craving!  (PS if you are eating things like sugar and wheat, you are stress eating)
Simply by empowering your health and sticking up for your body, we can get ourselves up and out of a big mess.  How much mess you want to be rid of will dictate how much you support and empower your health.

https://www.ludwigcancerresearch.org/news/targeting-cancers-sweet-tooth

🙂
Mimi
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NOURISHING HOPE FOR AUTISM SUMMIT

Join Julie Matthews, Dr. Raphael Kellman and many autism specialists at the FREE online event:
NOURISHING HOPE FOR AUTISM SUMMIT
July 30th – August 3rd, 2018

This breakthrough online event is FREE
Click here for more information and to register

 Children can improve and even recover from autism. 
I’m excited to be one of the country’s top autism experts interviewed for the Nourishing Hope for Autism Summit. This summit is going to share life-changing information for families affected by autism.

For 16 years, Julie Matthews, nutritionist and founder of Nourishing Hope, has provided scientifically based nutrition strategies that heal the symptoms and behaviors associated with autism. As the co-author of the “gold standard” 12-month research study that definitively substantiates the approach, she has gathered twenty five leading experts to share proven, effective solutions.

The summit presents the science, clinical results, and steps parents and practitioners can take to help children with autism, including:

  • Methylation Genes: What You Need to Know About Methylation in Autism with Ben Lynch, ND
  • The Profound Effects of Bacteria and the Microbiome in Autism with Raphael Kellman, MD, Founder of “Microbiome Medicine”
  • Understanding Lyme, Infections, Mold, and Heavy Metals and The Affects of Autism with Dietrich Klinghardt, MD
  • How to Calm Anxiety, and Eliminate Aggression and Obsessive Compulsive Disorder with Trudy Scott, CN
  • The Immune System and Autism: Autism as a Neuroimmune Condition with Elisa Song, MD
  • Food is Medicine: Inspiration from a Chef with Pete Evans
  • How Gluten May Be Harming Your Brain, Body and Autoimmunity (Even if You’re Gluten-Free) with Tom O’Bryan
  • How to Dramatically Improve Behavior Through Nutrition with Nicole Beurkens, PdD

I look forward to seeing you at this informative event!

Yours in total health,
Raphael Kellman, MD
Kellman Center for Integrative and Functional Medicine
www.kellmancenter.com

Kellman Center for Integrative and Functional Medicine
7 West 45th Street, Suite 301
New York, NY 10036

(212) 717-1118

Click here to learn about Dr. Raphael Kellman’s newest book,
THE WHOLE BRAIN

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Dr. Ruggiero – Alzheimers and Brain Aging

https://www.youtube.com/watch?v=cq_-b77Dkzs

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Dr. Ruggiero – Rerum

https://www.youtube.com/watch?v=YIWNgxipvzY

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Dr. Ruggiero – Autism One 2016

https://www.youtube.com/watch?v=yYIbLWnkTAY

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Dr. Ruggiero on Vimeo – The Truth About Vaccines

https://vimeo.com/214773414

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Dr. Ruggiero Lecture #3 The Microbiome

https://www.youtube.com/watch?v=5DKgT5Go6sU

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Dr. Ruggiero – RAADfest

http://raadfest.com/ruggiero/

 

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