MAG-pie and MAG-net Alert!…
Iron Toxicity Post #61: The EYE-ronic ORIGIN of Alzheimer ’s disease (and ALL other forms of Neurodegeneration KNOWN on this Planet…)
“Discovery consists in seeing what everybody else has seen and thinking what nobody has thought.”
— Albert Szent-Gyorgyi, 1937 Nobel Laureate: “Discovery of the Vitamin ‘C’ COMPLEX”…
Trust me, I’ve wanted to write this Post since the beginning of 2017, but several KEY pieces of the puzzle were cleverly alluding me. Please know that I am FAAAAAR from done understanding all of these dynamics of neurodegeneration, but I am reasonably confident now to make several KEY ASSERTIONS, which I’ll do throughout this Post with a wrap-up at the end…
I am quite confident, many of you will NOT entirely like what this Post has to say… You will be challenged to understand the technical aspects of it – I barely have a full grasp… But the mineral & metabolic issues that are covered in this Post #61 will grow in importance, and will become a KEY cornerstone in our understanding of how best to get out of our Iron-ic shackles and regain our metabolic homeostasis.
Some notable facts about neurological conditions, in general, and neurodegenerative issues, in particular:
o 1 Billion people – worldwide – nearly 1 in 6, suffer from neurological disorders: AD, PD, M$, $troke$, Epilep$y, Migraines, brain injuries and other forms of neuroinfection…
o 37 Million people worldwide suffer with Alzheimer’s…
o 10 million people worldwide suffer with Parkinson’s…
We ALL know at least 1-2 people (family members, friends, work associates, neighbors, etc.) that are being RAVAGED by the gross IGNORANCE that surrounds these brain-related neurodegenerative conditions. It is absolutely time for this level of clinical insult & insanity to STOP. I’m doing my part today by sharing this extensive panel of research to compile the leading thinking in a way that presents what I regard as a compelling argument about a MAJOR destructive factor – THAT IS RIGHT UNDER OUR NOSES — which is contributing to the unchecked acceleration of neurodegeneration and misery on this Planet.
So what’s REALLY going on here with these neurodegenerative diseases?…
Isn’t that what you’ve come to EXPECT — to learn innovative & foundational metabolic nuggets from these “Insightful Teaching Posts” (otherwise known as Iron Toxicity Posts…)?!?
o It’s important to know that AD (Alzheimer’s) is characterized by the following mineral patterns in the brain tissue:
– HIGH Copper,
– LOW Iron,
– LOW Zinc, typically…
– LOW Ferroxidase function (aka Ceruloplasmin),
– HIGH Oxidized Serotonin, esp. in the Hippocampus
– Confusing reference(s) to MAO (as a “bad guy…”) that is meant to “turn off” neurotransmitters
– SILENCE on Melanin’s role in the Locus Coeruleus that affects the Hippocampus…
o It’s EQUALLY important to know that PD (Parkinson’s), on the OTHER hand, is characterized by these mineral patterns in the brain tissue:
– LOW Copper,
– HIGH Iron,
– LOW Zinc, typically…
– LOW Ferroxidase function, ONCE AGAIN…
– HIGH Oxidized Dopamine, esp. in the Substantia Nigra…
– Confusing reference(s) to MAO (as a “bad guy…”), again, that is “turning off” the neurotransmitters
– MORE SILENCE on Melanin’s role in the Locus Coeruleus that affects the Substantia Nigra…
Clearly, there are some notable and contrasting mineral dynamics, which adds to the mystery and clinical confusion about these two most prevalent forms of neurodegeneration on the Planet. But please understand that the fact that BOTH conditions, AND ALL NEURODEGENERATIVE CONDITIONS, COLLECTIVELY, THAT I’VE STUDIED, have a notable LACK OF FERROXIDASE FUNCTION…
Hmmmmmmm… This is a CRITICAL point to which we will return, shortly…
OK, so with that as a background, let’s begin this BLINDING Blitzkrieg Blog!…
I’ve known for quite some time that EMFs – you know those pesky little electromagnetic frequencies that EVERY CONCEIVABLE DEVICE WE USE EMITS – has an effect on our Iron status. In effect, this is a ubiquitous form or Environment Stress, and what we’ve learned is that there is ALWAYS an MBR (Mg Burn Rate) attached to ANY form of Stress. EMFs are NO different in their Mg depleting effects, and if Mg goes DOWN — trust me, the toxicity of Iron is going to be going UP!
Here are several blockbuster articles for those of you seeking to better understand this EMF dynamic to get a better handle on how this TIDAL WAVE of radio frequencies is ALTERING NOT ONLY our external environment, BUT ALSO our internal Anti-Oxidant Enzyme landscape:
Maaroufi et al, 2014, “Spatial learning, monoamines and oxidative stress in rats exposed to 900 MHz electromagnetic field in combination with iron overload”
https://pdfs.semanticscholar.org/29a3/7abf4734218e0e6276afd52ff04c59650562.pdf?_ga=2.68949969.1975053235.1498943746-1468208896.1498943746
Gherardini et al, 2013, “Searching for the Perfect Wave: The Effect of Radiofrequency Electromagnetic Fields on Cells” (The impact on Complex IV, Cytochrome c Oxidase is particularly noteworthy…)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013569/
Consales et al, 2012, “Electromagnetic Fields, Oxidative Stress, and Neurodegeneration”
https://www.hindawi.com/journals/ijcb/2012/683897/citations/
Please note that the 1st study noted ^^^^ (Maaroufi et al, 2014) is a very provocative one that chose to combine EMFs (900 MHz) with Iron loading on the experimental rodents…
The sentence that REALLY caught my “eye,” (pardon the pun…) was the following:
“A link between EMF, iron accumulation in the brain and neurodegenerative disorders including Parkinson’s and Alzheimer’s diseases has been suggested.”
Are you sitting up a bit straighter in your chair right about now?!?…
So, I’ve known about these Iron-ic properties of EMFs for quite a while, and I knew that there had to ALSO be a connection to the use of BLUE LIGHT that MANY of these devices emit, but I lacked the causal connection between that high energy spectrum of light and its impact on Iron. (Please know that there is an absolute relationship between Copper and the Copper-dependent enzymes [think Cytochrome c Oxidase…] and the other low energy end of the light spectrum where Red and Infra-red light hangs out…)
But everything changed a couple of weeks ago when my friend & colleague @Alicia Barone Stephens happened to post an article about “Blue Light” and “Alzheimer’s” that had some CRITICAL commentary & insights from UBER Brain Surgeon & Brainiac, @Jack Kruse, MD:
Jack Kruse, MD commenting on “Culprit in Plain sight in Alzheimer disease development”
https://medicalxpress.com/news/2017-06-culprit-hidden-plain-sight-alzheimer.html
Jack Kruse’s Facebook comments: https://www.facebook.com/drjackkruse/posts/1798230000241346
And I quote from Jack Kruse, MD:
“Too bad no one in this paper realize that transition metals, like Iron, draw nnEMF [non-native EMF] toward them because of the D shell electrons they contain. That is why AD is blowing up in a blue lit microwaved world. CULPRIT HIDDEN IN PLAIN SIGHT IN ALZHEIMER DISEASE DEVELOPMENT”
It doesn’t get too much clearer than that.
I’m delighted that Jack Kruse, MD elected to connect these dots so PRECISELY. What is VITAL to understand is that our EYES are rich sources of Iron to support the high metabolic demands of our eyes, and yet this pesky Heavy Metal ACCUMULATES as we age. Again, this is NOT my conjecture, it is addressed in almost EVERY article that I’ve read about Eye Disorders and Disease over the last two years.
Here’s one of ~35 that I’ve read on this EYE-ron-ic dynamic:
Loh A et al, 2009, “Iron homeostasis and Eye Disease”
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2718721/pdf/nihms-125393.pdf
OK, so what do we know thus far?…
o The incidence of Neurodegeneration is EXPLODING — ALL OVER this Planet…
o We know that the two most prevalent forms, AD & PD, have notable mineral differences, YET notable overlaps in KEY enzyme dynamics that CAUSE these so-called “conditions”…
o We know that our contemporary & “constantly-connected” environment is TEEMING with technology that is causing BOTH Oxidative Stress, and has known connections to THE very Heavy Metal that FUELS the relentless Oxidative Stress that ails us…
o And while we’ve talked about this “Iron-induced Oxidative Stress” MANY TIMES before, the spin has always been around our “food & dietary” intake of Enriched Iron – NOT our Eyes!…
What I want to emphasize in THIS Iron Toxicity Post #61, is that there are added nuances to this crisis that even I was unaware of until forcing myself to sit down and PIECE THIS PUZZLE together. And I’m HARDLY done, despite ALL the hours, and hours of effort to read, synthesize and now write this unsettling piece… And as it turns out, our daily “intake” of our popular & dependent technology is ONLY adding to our growing metabolic woes, esp. as we age…
Trust me, I would MUCH RATHER be outside enjoying this beautiful Saturday (July 1, 2017) than be ZAPPPPPPING my Eyes, my Thyroid (thank you @Jack Kruse for THAT keen nuance that I missed!), as well as my Brain, with this nnEMF/Blue Light emitting, Oxidative Stress-creating Computer Screen!… 😉 But I figure you all are worth it!!!
Alright, if there is ANYONE In the MAG FB Group — at this point — that doubts that the foundational FLAW in the conventional understanding of the meteoric rise in the prevalence of AD or PD has nothing to do with a LACK of Ferroxidase enzyme function to keep Oxidative Stress in the Brain at bay, please note the following studies…
A “Sampling” of Proof that Alzheimer’s & Parkinson’s are connected to Copper<>Iron Dysregulation:
Kristinsson et al, 2012, “Ceruloplasmin and iron in Alzheimer’s disease and Parkinson’s disease: a synopsis of recent studies”
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493298/
Torrsdottir et al, 2011, “Ceruloplasmin and Iron Proteins in the Serum of Patients with Alzheimer’s Disease”
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3243634/
Montes et al, 2014, “Copper and Copper Proteins in Parkinson’s Disease”
https://www.hindawi.com/journals/omcl/2014/147251/
Again, not to beat my weary chest, but these are merely THREE of ~50+ articles that I’ve read and analyzed — ad nauseum — to get to the ROOT CAUSE of this maddening & frightening neuro-crisis… And up to this point, I was quite clear & confident that the Liver was the single greatest producer of Ferroxidase enzyme (aka FOX, or Ceruloplasmin Oxidase, or Cp), and that the Brain was #2. That hierarchy had been noted in dozens of recognized & repeatedly referenced articles. (It is worth noting that FOX is ALSO made in the Endocrine Glands, the Kidney, the Uterus, the genitals, the breasts, etc. – anywhere there is HIGH metabolic activity to address the potential toxicity of Iron found in Oxygen-rich Hemoglobin…)
But please understand, EVERYTHING CHANGED when I read this MIND-NUMBING study by Lin Chen, and colleagues at the University of Pennsylvania, at the start of this year…
Chen et al, 2003, “Increased Expression of Ceruloplasmin in the Retina following Photic Injury”
Abstract: http://iovs.arvojournals.org/article.aspx?articleid=2416930
Full Article: http://www.molvis.org/molvis/v9/a22/v9a22-chen.pdf
Please take a moment to familiarize yourself with these finding and let the significance of this study ^^^^ sink in, in light of ALL that we’ve covered, esp. these past two years…
What Dr. Chen & colleagues discovered is that the EYES make 8 X MORE Ferroxidase enzyme (Ceruloplasmin) than the Brain. Yes, you read that correctly — EIGHT TIMES!…
Do you understand the MAG-NITUDE of these findings?!?…
That it is our EYES that are NOT ONLY taking it “on the chin” with the INCREASED Oxidative Stress, but that they are supposed to be making EIGHT TIMES MORE FERROXIDASE THAN OUR BRAINS in a nutritional/medical environment that has gone out of its way in the past 50+ years to DESTROY the body’s & the eye’s ability to MAKE FERROXIDASE ENZYME, and then add insult to injury by going on to NOT even bother to measure it… (Thus, the infamous “not known, and not looked for” medical mantra…)
Do you FINALLY UNDERSTAND WHY I “D”espise Hormone-D SOOOOOO MUCH?!? (That obnoxious, synthetic, toxic supplemental Hormone – that is COMPLETELY misunderstood by scientists, clinicians and the Masses — KILLS Retinol, the very metabolic BACKBONE for making this VITAL Ferroxidase enzyme…)
And isn’t it interesting that we are chided for using Retinol, even though it is ESSENTIAL for the very function and metabolic activity of the Retina… Get it?… Retinol for the Retina?!?… (Good heavens, why do we need to work THIS HARD to connect these most obvious metabolic dots that have been expunged from the medical record and clinical training?!?)
And do you NOW FINALLY UNDERSTAND my OBSESSION with the Root Cause Protocol, that is inspired by MTHR NATURE, and is designed to ENHANCE the viability and function of the Ferroxidase enzyme (again, aka FOX, Ceruloplasmin Oxidase, and Cp…)?!? Think it might be a GOOD IDEA right about now to adopt that protocol?…
And lest you think that that “Retina<>Cp” was a “one-and-done-study,” here’s what that provocative team based at U Penn went onto discover, in addition to their blockbuster revelations about FOX:
Hahn, Chen, et al, 2004, “Disruption of Ceruloplasmin and Hephaestin in mice causes retinal iron overload and retinal degeneration with features of age-related macular degeneration”
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC518844/pdf/10113850.pdf
So, here we have PROOF that the very “disruption” of Ferroxidase function, as expressed in both Ceruloplasmin and Hephaestin (an enzyme “cousin” of Cp…), CAUSES Iron to build, which then goes on to CREATE even MORE Oxidative Stress.
Hmmmmmmmm… This is sounding pretty darn important, wouldn’t you agree?!?…
So, has anyone been wondering WHY I chose the Graphics for this particular Post?!?…
What we’re “seeing” in those pictures is the UNIQUE Structure and Placement of the Eye, it’s Optical Nerve and the AMAZING “Optic Chiasm” [Greek for “criss-cross”] that creates an “X” in a particularly important and vulnerable part of the Brain:
o The Pituitary & Thyroid are BELOW that Chiasm…
o The Limbic Region of the Brain (think MASTER Regulatory regions, like the Hypothalamus, etc.) is directly ABOVE that Chiasm…
Do you think that there just might be building, wandering, and destructive Iron-induced Oxidative Stress that’s ASSOCIATED with the Retina(s), and subsequently the Optic Nerve(s), that is COMPROMISED in its ability to make the VERY ANTI-OXIDANT ENZYME that must be VITALLY important for our optimal health, or WHY would our Maker have enabled us to make soooooo much of this Anti-Oxidant enzyme, and in that particularly SENSITIVE area of our body?!?…
And yes, I know you’re started to get tuckered out with this EYE-Popping Post… I am, as well, because I’m getting a bit tired WRITING IT, but we’re NOT QUITE DONE YET!…
It would be reasonable to think that the systemic & progressive LACK of this “Ferroxidase thingy” is the SOLE reason for all this chaos, but as Mark Twain might say: “It just AIN’T so!”… There are OTHER Anti-oxidants involved, as well… There are Brain chemicals known as “Prion Proteins,” and it was JUST TODAY that I learned that they are Copper dependent. I had NOT learned that in my prior readings. And these key proteins play VERY important roles as an Anti-oxidant, but they get functionally TWEAKED, esp. when they’re in the presence of Iron-laden Macrophages, that are called Micro-glia and Astro-glia, which are found in the Brain region.
Here are some compelling studies that support the role of Prion Proteins, but also how they are being accused – WRONGLY, imho – for being a “source” of the problem, when they are seeking to come to the aid of the oxidizing tissue. Nothing like blaming a KEY component that is being affected by Iron-toxic Macrophages that alter the optimal function & physiology of these Copper-driven chemicals.
Price et al, 1993, “Alzheimers Amyloid Plague and Prion Diseases”
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC46935/pdf/pnas01471-0012.pdf
Kercher et al, 2007, “Prion Protein Expression Differences in Microglia and Astroglia [Macrophages] Influence Scrapie-Induced Neurodegeneration in the Retina and Brain of Transgenic Mice”
http://jvi.asm.org/content/81/19/10340.full.pdf+html
Zhang et al, 2014, “Role and mechanism of microglial activation in iron-induced selective and progressive dopaminergic neurodegeneration”
https://www.ncbi.nlm.nih.gov/pubmed/24277523
And it doesn’t STOP there, unfortunately…
Anyone who has loved ones suffering from these neurological conditions, esp. Alzheimer’s, is aware of Amyloid Protein Precursor (APP) that, as it turns out, ACTUALLY has Ferroxidase enzyme function. (You might want to re-read that AGAIN…) APP is seeking to QUELL the rising Oxidative Stress that is coming from the daily INTAKE of Iron-enriched FOOD and our never far-from-us Iron-enriching ELECTRONICS!
Duce, 2010, “An iron-export ferroxidase activity of β-amyloid protein precursor is inhibited by Zinc in Alzheimer’s Disease”
http://www.sciencedirect.com/science/article/pii/S0092867410009384
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2943017/
Please take stock of the added significance of this study ^^^^ by NOTING that ZINC INHIBITS THE FERROXIDASE ACTIVITY of this critical Brain Tissue Anti-Oxidant. This is consistent with OTHER studies that have PROVEN that Zinc ZAAPPPS Ferroxidase function, which we have examined in prior Posts. Please, do NOT use Zinc supplements — under ANY circumstances — if your ultimate objective is to INCREASE THE LEVEL & FUNCTIONALITY of your Ferroxidase enzyme… You get Zinc from your diet, NOT from a bottle!
LET’S KEEP IT SIMPLE, SEEKERS… Let me quote the LAST sentence of the Abstract of this ILLUMINATING study by Duce et al, 2010:
“Iron causes selective and progressive dopaminergic neurodegeneration, and microglial NOX2 activation potentiates the neurotoxicity. PKC-σ, P38, ERK1/2, JNK, and NF-КBP65 are the potential molecules relevant to microglial NOX2 activation.”
Is that CLEAR ENOUGH?!?… Yes, I get that there is INSTANT “Brain Fog” with all that blah-blah-blah, but hopefully you get the START of it: “Iron CAUSES…” And it would be WONDERFUL if MORE practitioners, pundits and FB Posters would be THIS DIRECT about all this clinical chaos occurring inside the brains of their patients and readers!
As I’ve said TIME, and TIME, and TIME again… the three MOST DANGEROUS MINERALs – in a supplemental form — that are the MAINSTAYS of Allopathic practitioners – are Calcium, Iron & Zinc. They are ABSOLUTELY NOT THE ANSWER!… They NEVER have been, and they NEVER WILL BE. I only hope that more & more MAG-pies will have fresh eyes to “see” the MINERAL TRUTHS in this Post #61!…
Now to make it EVEN SIMPLER, let me state my FOUNDATIONAL IRON-ic HYPOTHESIS:
“IRON & IRON DYSREGULATION, due to a Systemic LACK of Bioavailable Copper, CAUSES NEURODEGENERATION. PERIOD!”
And as I’ve noted above ^^^^ what is rarely, if ever addressed, are the many KEY Brain & Neural tissue Anti-Oxidants that are being underproduced and/or compromised time, and time, and time again, throughout the brain stem and the brain cortex tissue. And now we come to learn that it STARTS in our EYES!… The BULK of Conventional neurodegeneration research blows ENTIRELY past the CENTRAL role of Ferroxidase enzyme, and prion proteins as KEY anti-oxidants, and APP as yet ANOTHER key anti-oxidant enzyme, and what I’m now discovering is that there is a GRAND-DADDY Anti-Oxidant of them all, it’s called: MELANIN!…
HUH?!?…
Did you say “Melanin,” that “Pigmentation thingy” that is found in my hair, skin and I think, my eyes?!?… Am I remembering that correctly?… Oh no, MY EYES?!? There’s Melanin in my Eyes, but that’s just for “color,” right?!?…
And if you think that Melanin is “just for color,” then you must STILL believe in the Tooth Fairy… 😉
And NO, I’m NOT talking about Melatonin… I’m ZEROING IN on MELANIN, a key chemical that plays a central role in MANY areas of the brain, not the least of which is the Locus Coeruleus [which means “Black Dot, btw!”], which is a MAJOR source of making Dopamine to influence the functionality and balance of MANY, MANY sections of the Brain.
OK, MAG-pies & MAG-nets, this would be a REALLY GOOD time for you to take yet another tug on your seatbelts!… The ride is about to hit some turbulence…
Now, let me completely BLOW YOUR MIND…
Arias-Esparza et al, 2011, “The Unexpected Capability of Melanin to Split the Water Molecule and the Alzheimer’s Disease”
http://file.scirp.org/pdf/NM20110300006_69226653.pdf
I realize that I’ve thrown practically EVERYTHING, including the Kitchen Sink, at you in this MONSTER Post, but this study ^^^^ is an ABSOLUTE MUST READ… This study breaks CRITICAL NEW GROUND, and shatters the very foundation of our known knowledge of cellular energy, electrical transmission around the body, as well as KEY anti-rusting factors, to name but a few functions, that have been shielded from us… I know NOT why, but I have a few theories… 😉
NO, Melanin is NOT just “skin, & hair pigment…” That is the equivalent of saying that your Mom is just a “maid…” I mean REALLY?!?… Please, before you jump ahead, please re-read that sentence AGAIN so you’re ready for the PENETRATING PUNCH LINE!
If I were to fully go into the TRUE roles & functions of this DARK MATTER, you all would truly think me MAD, and no longer think me such a MAG-nificent guy… 😉 But for those that want to FULLY delve deeper into this DARK & MAG-ical world, I would STRONGLY encourage you to read the following:
Richard D. King, MD, 2001, “Melanin: A Key to Freedom”: https://www.amazon.com/Melanin-Key-Freedom-Richard-King/dp/1602810958/ref=sr_1_12?s=books&ie=UTF8&qid=1498928462&sr=1-12&keywords=melanin
Edward Bruce Bynum, PhD & Richard D. King, MD, 2014, “WHY DARKNESS MATTERS: (New and Improved): The Power of Melanin in the Brain”: https://www.amazon.com/WHY-DARKNESS-MATTERS-Improved-Melanin/dp/1502411172/ref=sr_1_5?s=books&ie=UTF8&qid=1498928462&sr=1-5&keywords=melanin
Please know that I plan to write MUCH, MUCH MORE about Melanin in future Posts, but suffice it to say we have been COMPLETELY BAMBOOZLED about:
o It’s role as a SOURCE OF MITOCHONDRIAL ENERGY,
o It’s role as a SUPER CONDUCTOR of Electricity – it is prevalent in KEY areas of the CNS…
o It’s role as an Iron-trapping agent, which is WHY it’s prevalence BUILDS in lock-step with the rising Iron in the Eyes…
o It’s role as a MASTER ABSORBER of the complete visible Light Spectrum…
o It’s role as a MASTER ABSORBER of Sound in the Inner Ear…
o It’s role as a CRITICAL facilitator of Pineal health & function…
o Trust me, I could go on…
What is particularly POIGNANT to understand is that Melanin, imho, has been HIJACKED and relegated to this lowly status as a “pigment,” and has also been methodically corralled into a MASTER IRON-TRAPPING AGENT, which has COMPLETELY diverted its ability to fulfill its MAJESTIC roles in the human body, as briefly and incompletely noted above…
In effect, Melanin has become the “Iron Police Force” responding to the TIDAL WAVE INCREASE of Iron in our bodies. Please know, Melanin is MOST effective at LOCKING UP that “toxic” Heavy Metal Iron, and keeping it out of harm’s way… And here’s a clever twist, what’s a popular nickname for Policemen?!?… Yup, they’re called COPPERS!… So we’ve got “Coppers!” putting this toxic metal “behind bars!” Clever, eh?!?…
And for those that are UNFAMILIAR with HOW you make Melanin…
The synthesis of Melanin is ENTIRELY dependent on ANOTHER KEY COPPER ENZYME: Tyrosinase!…
And where is THAT enzyme found in MTHR NATURE?!?
Why none other than Wholefood Vitamin-C that Albert Szent-Gyorgyi, PhD discovered in the 1930’s studying Peppers from his hometown of Budapest, Hungary!…
And what’s SOOOO SPECIAL about all of this?!?…
The MOST EFFECTIVE WAY to BIND UP Melanin is with absurd levels of Iron Fortification in the food…
The MOST EFFECTIVE WAY to PREVENT Melanin production is to “D”rown the Masses with Ascorbic Acid (devoid of ANY Tyrosinase enzyme…) and synthetic Hormone-D that drives Iron storage “D”eeper and “D”eeper into the tissue, which also CAUSES Renal Potassium Wasting (Ferris et al, 1962), thereby making the cells and the tissue MORE attractive to Iron storage, and Iron-induced Oxidative Stress!…
And the MOST EFFECTIVE WAY to “D”ISTRACT or to “D”ETRACT Melanin ENTIRELY from the scene, and GUARANTEE Global Neurodegeneration, is to do JUST WHAT THE SYSTEM HAS DONE… And as @Jack Kruse, MD so aptly states, it’s been done RIGHT UNDER OUR NOSES and we NEVER EVEN “SAW” IT!!!
Well, I’ll just speak for myself… I NEVER saw this FULL COURT PRESS OF MULTIPLE IRON-ic FACTORS TO ENSURE NEURODEGENERATION coming, despite my years, and years, and years of meticulous, minerals-based research… But you can NO LONGER ignore these conclusions…
So, what have we NOW learned, additionally?!?…
We have complete and UTTER chaos from a conventional medical system that HONORS the following aphorism:
“Not known, because NOT looked for…”
(Your favorite M.ineral D.enialist IS, in fact, the infamous “drunk” in that joke, looking for their keys under the Street lamp down the street — because the light’s BETTER there — even though s/he LOST them FAAAAR from >>> there!…)
OK, so what to do?…
o STOP beLIEving ANYTHING your doctor has to say about Neurodegeneration being a Medical Disease. (this is complete & UTTER fantasy on their part, and clearly a lack of awareness of the literature…)
o START to focus on understanding that excess, unbound Iron, and the dysregulation that Iron CREATES, is the VERY EPICENTER of this destructive metabolic dynamic…
o STOP thinking or beLIEving that this is a “genetic” condition or a “familial” condition – that is simply NOT SO… It is ENTIRELY an EPI-genetic one, or said another way, an ENVIRONMENTAL condition…
o START understanding the SCOPE & REACH of Iron-induced Oxidative Stress in ALL aspects of conditions and syndromes that you might be aware of or battling… They are TRULY ALL CONNECTED and riding on that “Ferrous Wheel” that runs your Symptoms…
o STOP, for the love of God, STOP beLIEving that you are “ANEMIC!” (NOTHING COULD BE FARTHER FROM THE TRUTH!…)
o And finally, please START the Root Cause Protocol to REVERSE this relentless pattern of mineral dysregulation – triggered by IRON — that has CAUSED the metabolic dysfunction with which your mind is now IMPRISONED…
I do apologize for the length of this particular Post… It has been building for 6+ months, and I have wanted to share these important insights & discoveries for that entire time, but I also wanted to wait for just the right moment, when I felt more complete, and thus more confident, in my observations and conclusions.
This is our time, MAG-pies and MAG-nets!
We absolutely need to pursue our Health Freedom, if for no other reason than to gain our MEDICAL INDEPENDENCE from this kind of twisted, chaotic, demonic and myth-guided clinical thinking that STILL BELIEVES NEURODEGENERATION IS A MEDICAL DISEASE – despite the countless articles that I’ve cited!…
I trust that those of you who have labored and hung with me throughout this ENTIRE Post would agree that that kind of clinical belief is SERIOUSLY FLAWED, at best, and GROSSLY IRRESPONSIBLE, at worst…
I bid you a wonderful holiday weekend (at least hear in the States with the 4th of July just days away…) and I hope that this extended Iron Toxicity Post #61 helps you gain your freedom and your health!… In subsequent Posts and on-line chats, we will explore the important steps & options that we can ALL take to CURB this Iron-ic INFLUX of toxicity in our GUT, and NOW as we’ve learned, our EYES…
A votre sante!
Morley Robbins
