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AT AutismOne in 2015 Dr. Marco Ruggiero describes the protocol for taking Bravo Yogurt in this video at minute 40.https://www.youtube.com/watch?v=TPsVpuYw11c&feature=youtu.beSee made the Rubia Cordifolia product for you! Please login to see it.
Is it okay to have powders outside the fridge? Yes, store long term in the fridge
Is the yogurt okay if I left my jar out overnight? It’s okay but not for days
What if I am on antibiotics? It will kill everything and it takes a long time to rebuild
Noted as an anti-aging remedy:
Bravo Yogurt is Recognized by Anti-Aging Authority
You may know, Dr. David A. Sinclair, PhD, Professor at Harvard Medical School. He is the world’s authority in the field of anti-aging medicine. He authored seminal articles in major scientific journals as well as a New York Times Best Selling book.
Well, it turns out that he is one of us!! He enjoys his Bravo Yogurt every morning!
Without any solicitation from us, as Dr Ruggiero has never met him, Dr Sinclair told the world that he uses Bravo Yogurt every morning as part of his anti-aging/wellness protocol. The excerpt of his interview is here.
Dr. Ruggiero is the inventor of Bravo Yogurt and is deeply interested in studying anti-aging. He believes that we as people should have more capacity to endure. He has studied lobsters who don’t die of old age and cancer which can stay alive in a petri dish for 60 years. He thinks that we can change our fates and has put his ideas to work in a product of longevity.
I am quite sure that this book by Dr. David A. Sinclair, PhD, Professor at Harvard Medical School is a book worth reading and practices worth noting. For example, use your Bravo yogurt every morning. Make it a daily part of your very long life! www.bravocoop.com
Zach Bush: Glyphosate has interrupted and interfered with the essential amino acids plants were providing to humans.
How did it do this? It did it thru blocking an enzyme pathway called the shikimate pathway.
Wikipedia:
The shikimate pathway (shikimic acid pathway) is a seven step metabolic route used by bacteria, archaea, fungi, algae, some protozoans, and plants for the biosynthesis of folates and aromatic amino acids (phenylalanine, tyrosine, and tryptophan).
This pathway is not found in animals and humans. Animals and humans require these amino acids. Hence the products of this pathway represent essential amino acids. They must be obtained from organisms which are not animals; or, from animals whose diet includes lower organisms who do have the shikimate pathway and can make these amino acids.
Monsanto claims Roudup is safe because it interferes with an enzyme pathway only present in bacteria, archaea, fungi, algae, some protozoans, and plants .
So Gly kills the pathway in plants that makes teh essential amino acids humans need.
He details the snowballing effects on infants of loss of healthy bacterial biome.
He says if you go 100% organic, in three weeks, some chronic symptoms begin backing off.
The brain has traditionally been considered an immune privileged organ, in part due to the lack of evidence for lymphatic vasculature (Galea et al., 2007). Two centuries ago, the existence of lymphatic vessels on the surface of the human brain was proposed but it has since been widely dismissed (Lukic et al., 2003). Therefore, while T cells leave all other organs via the lymphatic system to reach nearby lymph nodes, the prevailing view has been that infiltrated T cells exit the brain via venous blood circulation, circumventing the lymph nodes (Ransohoff and Engelhardt, 2012). The recent evidence for the existence of a lymphatic vascular system in the brain’s meninges provided independently by two labs, first by the Kipnis lab (Louveau et al., 2015) and then by the Alitalo lab (Aspelund et al., 2015), challenges this view and raises the intriguing possibility of an alternative gateway for T cells to egress the brain.
The key for identifying these meningeal lymphatic vessels by both labs was the use of a whole-mount preparation where the meninges were fixed while still attached to the skull, thus enabling the preservation of fine meningeal vessels. Kipnis’ lab identified a rather simple network of narrow vessels with a distinct lumen that ran along the blood vessels in the superior sagittal and transverse sinuses on the top of the brain and importantly, expressed multiple molecular hallmarks of lymphatic endothelial cells including lymphatic vessel endothelial hyaluronan receptor 1 (Lyve-1) and vascular endothelial growth factor receptor 3 (VEGFR3). Alitalo’s lab additionally described that this lymphatic network becomes more extensive at the base of the brain, where it contains lymphatic valves, and exits the skull alongside the cranial nerves. The anatomical and cellular classification of these meningeal vessels was strengthened by complimentary experiments from both labs demonstrating functional implications of VEGFR3. Injections of a VEGFR3 ligand, VEGF-c, into the cerebrospinal fluid (CSF) resulted in an increased diameter of the meningeal lymphatic vessels. Conversely, mice with impaired VEGFR3-VEGF-c signaling showed a complete absence of meningeal lymphatic vessels indicating that these vessels, like peripheral lymphatic vessels, are functionally regulated by VEGFR3.
An essential functional characteristic of lymphatic vasculature is permissiveness to fluid and drainage to lymph nodes. In line with this, dyes injected into the CSF were detected both in the lumen of Lyve-1-expressing vessels and in the deep cervical lymph nodes (dcLN), whereas dyes administered in the blood were not. Ligation of the lymphatic vessels above the dcLN completely abolished drainage of dye to these lymph nodes and additionally, increased the diameter of the meningeal lymphatic vessels, indicating that these vessels drain to the dcLN. The Alitalo lab further demonstrated that dye injected into the brain parenchyma was absorbed by lymphatic vessels and preferentially drained into the ipsilateral dcLN from the base of the brain. Surprisingly, Kipnis’ lab excluded the best-known route of drainage into the dcLN, via the nasal cavity’s cribriform plate and the nasal mucosa (Kida et al., 1995), as they failed to see dcLN drainage of dye injected into the nasal mucosa. In contrast, the Alitalo lab’s elaborate imaging studies indicated that lymphatic vessels indeed pass through the skull in the meningeal lining of the cribriform plate and into the nasal mucosa, corroborating the nasal drainage route as one of many possible passages to the dcLN. Hence, future research will be required to map out the extent of this newly discovered lymphatic system and its relationship to the rest of the lymphatic circuitry in the body. This may be particularly important given that disrupting drainage of excess fluids in the peripheral lymphatic system leads to peripheral lymphedema which affects millions of people worldwide. Interestingly, blocking drainage to the dcLN has been shown to exacerbate ischemic-evoked edema in rats (Si et al., 2006), raising the question whether the meningeal lymphatic system plays a critical role in reducing brain edema. This possibility should be considered in future scientific discussions both in basic and clinical sciences.
One intriguing question that remains is whether the lymphatic vessels act as a cellular afferent route out of the brain, allowing T cells to circulate through the meninges and to the dcLN. In their study, Kipnis’ lab observed a ten-fold higher density of T cells that aligned within the lumen of Lyve-1-expressing vessels compared to that of blood vessels. Importantly, removal of the dcLN increased the density of T cells in the meninges, indicating that drainage to the dcLN might be crucial for T cells to egress. While these data suggest that meningeal lymphatic vessels contain T cells, more experiments are necessary to demonstrate whether T cells indeed are circulating via these vessels. Interestingly, metastasis from primary brain tumors (e.g., gliomas) has been found in the dcLN (Mondin et al., 2010), supporting the notion of a direct cellular route. It would be very interesting to investigate the flow of T cells in meningeal lymphatic vessels during infection and inflammation and to determine fluctuation in number of T cells drawn to (and out of) the brain parenchyma which potentially would change our understanding of T cell circulation in the brain.
The functional implications of this newly discovered lymphatic network in both health and disease are broad and raise many exciting questions. Of particular interest would be how this newly discovered meningeal lymphatic system relates to the recently described glymphatic system, which potentiates waste clearance from the brain by facilitating the flux of CSF across the brain parenchyma (Iliff et al., 2012). It will be interesting to investigate if and how pathological agents, such as amyloid β are transported between the glymphatic and lymphatic systems. For example, would removal of amyloid β and other misfolded proteins from the brain parenchyma be reduced in mice with an impaired meningeal lymphatic system (e.g., following removal of the dcLN or in VEGFR3-deficient mice)? Do meningeal lymphatic defects correlate with or cause enhanced risk of patients developing neurodegenerative diseases such as Alzheimer’s and Parkinson’s disease?
Arguably the most appealing aspect of the existence of meningeal lymphatic vessels is the insight it provides about the circulation of T cells in the brain. Immune cells and immune-related molecules are increasingly recognized to play crucial roles in brain wiring in both development and disease. Interestingly, Kipnis’ lab has previously shown that removal of dcLN can induce learning and memory impairments in mice (Radjavi et al., 2014), suggesting that disrupting T cell circulation has gross behavioral consequences. Mapping the cellular lymphatic route and understanding its potential role in behavioral paradigms such as learning and memory, sleep, and stress will advance our understanding of communication between the central nervous system and the immune system. Furthermore, elucidating a potential path for T cell circulation could potentially unveil new therapeutic targets for interventions in neurodegenerative diseases and neurological disorders, including those considered to be triggered by inflammatory responses, such as multiple sclerosis.
These exciting new findings have reopened the discussion about to what degree the brain is immune privileged by revealing a potential lymphatic gateway for T cells to egress the brain.
Aspelund A., Antila S., Proulx S.T., Karlsen T.V., Karaman S., Detmar M., Wiig H., Alitalo K. A dural lymphatic vascular system that drains brain interstitial fluid and macromolecules. J. Exp. Med. 2015;212:991–999.[PubMed]
Black Cumin: The Magical Egyptian Herb for Allergies, Asthma, and Immune Disorders by Peter Schleicher, M.D. and Mohamed Saleh, MD
This remarkable “black seed” has had a very rich traditional history over the centuries, containing over 100 compounds, including vitamins, trace elements, antioxidants, and essential fatty acids. It has a spicy, pungent, nutty flavor and aroma with notes of black peppercorns.
I started with Black Seed oil and dabbed a drop of oil onto each of my endocrines each day. I don’t always take everything when I travel, however, my body “let me know” right away how important my black cumin oil was! I now use it as a daily supplement as dabs to each of the endocrines. It keeps me very balanced and my mood buoyant.
This is not a free copy. Please email me that you are taking a copy and I will send money in for your book. send your email to mimi@healthyenergetics.com
Hi, this is Mimi from Bravo Coop sending you a PDF copy of Dr. Ruggiero’s book and my notes. I hope you enjoy it.Please feel free to stop by the Bravocoop Teleconference on Tuesday nights to learn more about Bravo Products. Tuesdays 6:30 PM EST to 8:30 PM EST. Dial into 1-302-202-1106 Then enter Conf Code: 466134
See us, get more info and purchase products at our website www.bravocoop.com
🙂
Mimi
Pearls from the Your Third Brain: The Revolutionary Discovery to Achieve Optimum Health
The key difference in survival (cancer) is nutrition and the immune system.Pg 38. In the US and Europe, most people are malnourished Malnutrition is described as the improper balance of three out of four macronutrients: carbs, sugars, proteins, lipids
Microbial strains may hold the key to who we are. Pg 150 Different microbial strains give us different behaviors aspects such as courage or honesty. You can positively influence your behavior by discovering microbes that give you qualities.
You are what you eat is no joke! Page 151. Food is essentially genetic information which our genes interpret and pass on. We will suffer if our food is genetic info that is corrupted or incomplete (depleted)
The team worked for months on this premise: Pg217 The most negatively charged molecule in the organic universe was associated with the hydrophobic liquids. Just as if oil and water could uniformly and spontaneously mix.
Then the team worked for years on this premise: (also a paradigm shift) Pg 218-9. That heparin actually directly inhibited the proliferation of cancer cells in vitro (does not imply a “cure”). Heprin seems to perform a novel type of anticancer surveillance on our bodies and then internalized from cell wall. This info was not accepted prior to their work. Binding of heparin disturbed the function of DNA of cancer cells in such a way that they couldn’t replicate. Vitamin D, more like a hormone, than a vitamin was studied.
More secrets revealed Pg 223 Learning about intercellular receptor and Vit D binding protein (Gc) The team showed that the brain is directly connected to the immune system through lymphatic vessels (new science) Pg 229 Autism, Alzheimer, multiple sclerosis to amyotrophic lateral sclerosis are connected to disorders with this connection
This is the practice of using 21st-century medical tech along with boosting the body’s own internal combative systems. Stimulating the immune system kicks it into high gear and in many cases is able to use that infection to fight cancer. This kind of boost gives the body something it can fight and it begins to fight all the fights.
Dr. William Coley was the father of immunotherapy.He found references from the used 13th century upon which he built his cancer research.This research went dormant for 50 years.Dr. Ruggiero revitalized it and much of his work is based upon it.
From Mimi and all of us that are impacted by this work.
Dr. Ruggiero: Our thanks to you and your team for endless hours of study and keeping yourselves open to the information as it impinges upon you with new revelations. Then there is the dedication to hold the whole picture and the mechanics on so many levels of how it all fits together. There is also the strength to express it into a world that at times resists change. To you and your team… OUR THANKS, SUPPORT, and GRATITUDE!
