-Periodically do chelation therapy (which to some extend maintains the Zeta Potential)
-Make sure you've properly healed any old injuries.
-Do something that regularly moves the fluids in your body (large trampollene is best, daily walking also works)
-Be on top of catching issues that emerge in your body before they progress to something more serious (ie. a hip going out of allignment).
-Do regular Tai Chi or something equivalnt.
-Periodically water fast.
-Avoid processed foods.
A lot of the people I know who have done this successfully (ie I know a highly active 88 year old who everyone thinks is in their 50s) also believe regular sunlight exposure is important but I am not sure how important that one is.
One of the very first things I noticed with Covid was that it had all the clinical signs of destroying zeta potential within the body, which is something you almost never see (and many other clinicians have observed the same things I have although very few of them are aware of this and a potential concept and hands do not have an explanation for what they are observing). Since that time, I have also noticed the vaccines will often do the same thing. Some of the signs are very hard to pick up on (and may make me sound a little weird once you go into fluids besides the blood), but one of the key ones is that the blood starts to clump together and becomes significantly more viscous. For example, all of you have seen the microscope slides of vaccinated blood being clamped together, and I have started hearing stories of vaccinated patients where is not possible to do blood draws on them even through their external jugular vein (because the black keeps clotting), which is something most of us had never run into. Who is one of these people, it took about six weeks of them being on proteolytic enzymes before it was actually possible to do a large vein blood draw, which is extremely concerning put it mildly.
That is unheard of! Are you talking about living patients actually??? Do the unjabed patients with Covid have identical symptoms of that severe clamping or it is 'just' the jabbed? Thank you very much for sharing all this... Actually I wrote many posts with the genetic analysis of the Spike code, which has pieces of everything, including every single clotting factor out there, as if the Spike sequence was made for hemophiliacs, to keep their blood running properly...
Oh that's crazy, I had no idea that spike protein had clotting factors in it. Could you like me to that post? That is really interesting.
Regarding your question, I have seen patients with Covid who had a very thick blood, and blood that was very dark and look different (which I know from having done a lot of blood draws correlates with low zeta potential), and I have friends who have had Covid whose body filled with major clots (to the point they needed blood transfusions once the clots were removed).... but the blood clotting being described here has only occurred in alive and vaccinated patients.
That is really interesting. As you probably know, one of the major issues with Covid blood clots and vaccine damage is that they don't really respond to anticoagulants. Each of the anticoagulants on the market (the main ones are heparin and Xarelto and Plavix) don't really workтАж Plavix is the only one that seems to stop the blood clots. This will probably make more sense if you look at it yourself, but it's very likely one of the things that's happening is that the spike protein is messing with the coagulation cascade in a way that are not designed to address. I do not have a good enough background in hematology to say anything definitive on this, but I suspect that there's some extent, the spike protein coagulation factors are able to activate sequential parts of the coagulation cascade. Would you be open to taking a deep dive on this and seeing if the structure of any of the coagulation factor like domains could cause a subsequent part of the coagulation cascade to activate? This might require some In Silico modeling or docking analysis. If that's beyond your ability to do, I might know someone who could figure this out. Overall, I do not think this is that complicated and disco potentially be a really big deal for what all the clinicians are working with in the field.
do you know that FActor IX is also called Christmas Factor? Named after the first AIDS patient who needed lot of blood transfusions and subsequently died? Guess when the biggest HIV specialist has his birthday: 24 Dec, on Christmas. I'm talking Dr. Fauci.
I also wonder if one of the reasons why you periodically see clotting disorders and severe hemorrhages after exposure to the spike protein is because they are having antibodies to the clotting factor form within the body (I am the most familiar with this occurring in hemophiliacs from foreign factor VIII).
if you know the part sequence of those anti-bodies just check it with the known Spike sequence. Once you chop it down, you end up with all these pieces! There is a good paper about the epitopes within the spike, every single segment of it is an epitope, wrote abut it in the last few posts all the time...
if you are performing the 'official medicine' then yes, normal drugs won't help, you need new drugs, more drugs.. Was just listening to Dr. Klinghard on acu2020 hearing:
He is using 3ple combo, of which heparin is just one component, which won't work on its own. He adds hydroxychloroquine and zinc, with antibiotic. I think they will translate his 1 hour interview so you can listen to it yourself and get the formula.
I used to do macromolecular modeling years back, but no more for the last quite few years, do not have the software for that. Just do the open source support in the bioinformatics area, but can check out if online support is available. Also I must say, people need HELP NOW, FAST. The NATURAL remedies for anticoaglation are out there, just have the guts to use it, against your board of .... Last but not least, the ANTI-venom remedy is equally worth to try out. Even I, as NON-MD, know what to use to help myslef...
I would argue that the clotting found in Covid infections and vaccine injuries been caused by the spike protein rather than graphene oxide is actually Occam's razor here, and I am relatively sure at least 95% of people would agree with that assessment.
My problem with the spike protein narrative is that, as far as I understand, the hydrogel-embedded mRNA starts up a chain reaction that cannot be controlled.
The number of people echoing the same thing doesn't make it true...
Hydrogels are supposedly degraded by EDTA, the strongest metal chelator out there. To destroy the toxic synthetic genetic material should be known too, at least by those criminals who produce it.... Even the synthetics needs to be 'protected' by the lipids and nanos, thus something should be able to get rid of it, enzymes which can cut it down. Well, once you have the wrong building blocks I don't know how the body gets rid of that 1-methy-pseudouridine....
one could find that out, maybe even done already.. Get the commercial Spike powder and rGO. Concentrate both to appropriate level in physiological solutions and mix up with blood under microscope while filming what is happening. The difference between what is happening while having the jabs is, that the Spike or its parts (S1 or S2 ) is actually embedded in the cell membranes which bind ACE2, which is in all blood vessels and on surface of many organs.... The pathological findings from Prof. BRurkhardt showed that the SPike is also freely floating in cells, thus that suggested experiment would give the proper answer at least in part. Reduced Grahene Oxide (rGP) is a FLAT, electrically and thermally conductive surface capable to cut proteins/DNA via the edges, get into brain directly^1, etc. but it would be hard to imagine it is capable of stacking the entire red blood cells regularly or clumping them entirely, like what is known to be done by wi-fi radiation, interacting with iron dipole moments of the hemoglobin molecules. While cutting comepletely randomly in blood rGO would create a mass of byproducts seen as a big clump, but not as a regular organized entity.
I'm looking for papers on the graphene influenced blood stacking, so far nothing out there. Thus the suggested experiment could be useful.
1. PEGylation of reduced graphene oxide induces toxicity in cells of the blood-brain barrier: an in vitro and in vivo study. 06 Oct 2016 Molecular Pharmaceutics.
I just want to note that even though we have a little bit of a disagreement over the vaccine terminology, I sincerely appreciate the work you do and the analyses you put together. How do you spoke with the best person I know today and they thought most likely these issues would be explained by the spike proteins homology with factor XII, so what we are going to do over the next week and see if the correct region of factor XII is mimicked on the spike proteins, what occurs in the simulated docking experiments and how this region of the spike protein compares to the original SARS virus which did not cause clotting under any circumstances.
Also, Wi-Fi and other forms of microwave radiation does interfere with zeta potential.
"PEGylation of reduced graphene oxide induces toxicity in cells of the blood-brain barrier: an in vitro and in vivo study" actually puts a little table with your potentials, here a cut and paste for you:
Table 2. Physicochemical characteristics of non-PEGylated and PEGylated rGO.
"A comparison of zeta potential revealed that the charge associated with the non-
PEG rGO had a greater negative zeta potential (тИТ25 ┬▒ 0.18 mV) than the PEGylated rGO (-4.2 ┬▒ 3.8 mV). This suggests the existence of positive amino-ended branches, resulting in a lesser negative electrostatic charge for PEGylated rGO than rGO (Vila et al. 2012). The PEGylation of rGO leads to a decrease in PDI values (0.56 ┬▒ 0.03 to 0.39 ┬▒ 0.04), resulting in the diminished polydispersity of particles, probably due to a lower susceptibility to aggregate formation.
A significant increase in size, from 342 ┬▒ 23.5 nm up to 910 ┬▒ 32.7 nm, was
found after PEGylation. Although this increase offers evidence for the PEGylation of
nanoparticles, confirmation of the attachment of PEG to rGO is essential."
The PEG2000 in the shots is rather large, but still 3x smaller than the size used in this paper, thus these rGO+PEG clusters would be smaller in comparison to these sizes mentioned here.
Thanks. I may be a retired chemist (not physical or electro, but organic, I've worked for one of the more notorious pharmaceutical firms in an earlier incarnation), but didn't know what zeta potential be. This? https://en.wikipedia.org/wiki/Zeta_potential
Zeta potential is a critically important concept for a living systems because when it is not maintained all the fluid in the body can clot or coagulate together, and proteins will commonly miss fold precipitate out of solution. My present belief is that the primary reason why vaccinations are so harmful is that they are highly effective at interfering with the state of tension on the body (and to a lesser extent causing the lymphocytes to block the capillary circulation), and for some reason, the spike protein on SARS-CoV-2 was modified from the original SARS spike protein to have a very high density of positive charges so that it was an ideal agent for destroying data potential in the body. Amongst other things I think this is why the vaccines cause very odd clots that do not respond to anitcoagulants.
I have looked at hundreds of medical models, and my present perspective is that is it a potential is one of the things that most directly correlates with health and vitality.
If you want to understand this concept, look up how they flocculate sewage with aluminum for municipal water treatment.
I will be honest, I had never come across this concept before you left that comment. I do not think that a zeta potential collapse or agglomeration of a suspended colloids is the same as a coacervates forming, but I may be wrong however the end result you are describing, sludge in the circulation is white occurs within the blood.
Phenomenal article, and I'd love to hear more about your plan for zero-medical system interaction in older age, that's super interesting!
Basically you have to:
-Maintain the Zeta Potential of the Body
-Periodically do chelation therapy (which to some extend maintains the Zeta Potential)
-Make sure you've properly healed any old injuries.
-Do something that regularly moves the fluids in your body (large trampollene is best, daily walking also works)
-Be on top of catching issues that emerge in your body before they progress to something more serious (ie. a hip going out of allignment).
-Do regular Tai Chi or something equivalnt.
-Periodically water fast.
-Avoid processed foods.
A lot of the people I know who have done this successfully (ie I know a highly active 88 year old who everyone thinks is in their 50s) also believe regular sunlight exposure is important but I am not sure how important that one is.
Do you know how does the Zeta Potential change after the covid gene modifying injections???
One of the very first things I noticed with Covid was that it had all the clinical signs of destroying zeta potential within the body, which is something you almost never see (and many other clinicians have observed the same things I have although very few of them are aware of this and a potential concept and hands do not have an explanation for what they are observing). Since that time, I have also noticed the vaccines will often do the same thing. Some of the signs are very hard to pick up on (and may make me sound a little weird once you go into fluids besides the blood), but one of the key ones is that the blood starts to clump together and becomes significantly more viscous. For example, all of you have seen the microscope slides of vaccinated blood being clamped together, and I have started hearing stories of vaccinated patients where is not possible to do blood draws on them even through their external jugular vein (because the black keeps clotting), which is something most of us had never run into. Who is one of these people, it took about six weeks of them being on proteolytic enzymes before it was actually possible to do a large vein blood draw, which is extremely concerning put it mildly.
That is unheard of! Are you talking about living patients actually??? Do the unjabed patients with Covid have identical symptoms of that severe clamping or it is 'just' the jabbed? Thank you very much for sharing all this... Actually I wrote many posts with the genetic analysis of the Spike code, which has pieces of everything, including every single clotting factor out there, as if the Spike sequence was made for hemophiliacs, to keep their blood running properly...
Oh that's crazy, I had no idea that spike protein had clotting factors in it. Could you like me to that post? That is really interesting.
Regarding your question, I have seen patients with Covid who had a very thick blood, and blood that was very dark and look different (which I know from having done a lot of blood draws correlates with low zeta potential), and I have friends who have had Covid whose body filled with major clots (to the point they needed blood transfusions once the clots were removed).... but the blood clotting being described here has only occurred in alive and vaccinated patients.
In 2021 I've send the entire list of the Spike and human proteins homologies to FDA. Parts of that letter to them I posted at:
https://mejbcart.substack.com/p/why-cdcfda-ignore-the-spike-protein
Here the list of part of the factors for you. Descriptions are in my post:
- human coagulation factor VII (75% sc, 45% id)
- human coagulation factor VIII (94% sc, 32% id)
- human coagulation factorIX (97% sc, 31% id)
- human coagulation factorX (85% sc, 35% id)**
- human coagulation factorXI (89% sc, 22% id)
- human coagulation factorXII (82% sc, 35% id)
That is really interesting. As you probably know, one of the major issues with Covid blood clots and vaccine damage is that they don't really respond to anticoagulants. Each of the anticoagulants on the market (the main ones are heparin and Xarelto and Plavix) don't really workтАж Plavix is the only one that seems to stop the blood clots. This will probably make more sense if you look at it yourself, but it's very likely one of the things that's happening is that the spike protein is messing with the coagulation cascade in a way that are not designed to address. I do not have a good enough background in hematology to say anything definitive on this, but I suspect that there's some extent, the spike protein coagulation factors are able to activate sequential parts of the coagulation cascade. Would you be open to taking a deep dive on this and seeing if the structure of any of the coagulation factor like domains could cause a subsequent part of the coagulation cascade to activate? This might require some In Silico modeling or docking analysis. If that's beyond your ability to do, I might know someone who could figure this out. Overall, I do not think this is that complicated and disco potentially be a really big deal for what all the clinicians are working with in the field.
Factor IX Induced Hypercoagulable State ...
do you know that FActor IX is also called Christmas Factor? Named after the first AIDS patient who needed lot of blood transfusions and subsequently died? Guess when the biggest HIV specialist has his birthday: 24 Dec, on Christmas. I'm talking Dr. Fauci.
I also wonder if one of the reasons why you periodically see clotting disorders and severe hemorrhages after exposure to the spike protein is because they are having antibodies to the clotting factor form within the body (I am the most familiar with this occurring in hemophiliacs from foreign factor VIII).
if you know the part sequence of those anti-bodies just check it with the known Spike sequence. Once you chop it down, you end up with all these pieces! There is a good paper about the epitopes within the spike, every single segment of it is an epitope, wrote abut it in the last few posts all the time...
if you are performing the 'official medicine' then yes, normal drugs won't help, you need new drugs, more drugs.. Was just listening to Dr. Klinghard on acu2020 hearing:
https://odysee.com/@Corona-Ausschuss:3/s110de:0
He is using 3ple combo, of which heparin is just one component, which won't work on its own. He adds hydroxychloroquine and zinc, with antibiotic. I think they will translate his 1 hour interview so you can listen to it yourself and get the formula.
I used to do macromolecular modeling years back, but no more for the last quite few years, do not have the software for that. Just do the open source support in the bioinformatics area, but can check out if online support is available. Also I must say, people need HELP NOW, FAST. The NATURAL remedies for anticoaglation are out there, just have the guts to use it, against your board of .... Last but not least, the ANTI-venom remedy is equally worth to try out. Even I, as NON-MD, know what to use to help myslef...
https://www.jabfm.org/content/18/2/147
https://pubs.asahq.org/anesthesiology/article/62/4/515/28531/Factor-IX-Induced-Hypercoagulable-State
How can spike protein be confirmed? Clotting can be caused by the omnipresent graphenes alone; no need for "spike proteins" (applying Occam's Razor).
I would argue that the clotting found in Covid infections and vaccine injuries been caused by the spike protein rather than graphene oxide is actually Occam's razor here, and I am relatively sure at least 95% of people would agree with that assessment.
Thank you for your reply.
My problem with the spike protein narrative is that, as far as I understand, the hydrogel-embedded mRNA starts up a chain reaction that cannot be controlled.
The number of people echoing the same thing doesn't make it true...
Hydrogels are supposedly degraded by EDTA, the strongest metal chelator out there. To destroy the toxic synthetic genetic material should be known too, at least by those criminals who produce it.... Even the synthetics needs to be 'protected' by the lipids and nanos, thus something should be able to get rid of it, enzymes which can cut it down. Well, once you have the wrong building blocks I don't know how the body gets rid of that 1-methy-pseudouridine....
Hydrogels tend to be deadly, too, but not as bad as the mRNA stuff, which is, according to Dr. Andreas Noack, it a red herring:
https://rayhorvaththesource.substack.com/p/mrna
one could find that out, maybe even done already.. Get the commercial Spike powder and rGO. Concentrate both to appropriate level in physiological solutions and mix up with blood under microscope while filming what is happening. The difference between what is happening while having the jabs is, that the Spike or its parts (S1 or S2 ) is actually embedded in the cell membranes which bind ACE2, which is in all blood vessels and on surface of many organs.... The pathological findings from Prof. BRurkhardt showed that the SPike is also freely floating in cells, thus that suggested experiment would give the proper answer at least in part. Reduced Grahene Oxide (rGP) is a FLAT, electrically and thermally conductive surface capable to cut proteins/DNA via the edges, get into brain directly^1, etc. but it would be hard to imagine it is capable of stacking the entire red blood cells regularly or clumping them entirely, like what is known to be done by wi-fi radiation, interacting with iron dipole moments of the hemoglobin molecules. While cutting comepletely randomly in blood rGO would create a mass of byproducts seen as a big clump, but not as a regular organized entity.
I'm looking for papers on the graphene influenced blood stacking, so far nothing out there. Thus the suggested experiment could be useful.
1. PEGylation of reduced graphene oxide induces toxicity in cells of the blood-brain barrier: an in vitro and in vivo study. 06 Oct 2016 Molecular Pharmaceutics.
I just want to note that even though we have a little bit of a disagreement over the vaccine terminology, I sincerely appreciate the work you do and the analyses you put together. How do you spoke with the best person I know today and they thought most likely these issues would be explained by the spike proteins homology with factor XII, so what we are going to do over the next week and see if the correct region of factor XII is mimicked on the spike proteins, what occurs in the simulated docking experiments and how this region of the spike protein compares to the original SARS virus which did not cause clotting under any circumstances.
Also, Wi-Fi and other forms of microwave radiation does interfere with zeta potential.
Thank you. That paper I just mentioned:
"PEGylation of reduced graphene oxide induces toxicity in cells of the blood-brain barrier: an in vitro and in vivo study" actually puts a little table with your potentials, here a cut and paste for you:
Table 2. Physicochemical characteristics of non-PEGylated and PEGylated rGO.
Samples Size (nm) Zeta potential (mV) PDI
Non-PEGylated rGO 342 ┬▒ 23.5 тИТ25 ┬▒ 0.18 0.56 ┬▒ 0.03
PEGylated rGO 910 ┬▒ 32.7 -4.2 ┬▒ 3.8 0.39 ┬▒ 0.04
and a quote, in case you can't get this paper:
"A comparison of zeta potential revealed that the charge associated with the non-
PEG rGO had a greater negative zeta potential (тИТ25 ┬▒ 0.18 mV) than the PEGylated rGO (-4.2 ┬▒ 3.8 mV). This suggests the existence of positive amino-ended branches, resulting in a lesser negative electrostatic charge for PEGylated rGO than rGO (Vila et al. 2012). The PEGylation of rGO leads to a decrease in PDI values (0.56 ┬▒ 0.03 to 0.39 ┬▒ 0.04), resulting in the diminished polydispersity of particles, probably due to a lower susceptibility to aggregate formation.
A significant increase in size, from 342 ┬▒ 23.5 nm up to 910 ┬▒ 32.7 nm, was
found after PEGylation. Although this increase offers evidence for the PEGylation of
nanoparticles, confirmation of the attachment of PEG to rGO is essential."
The PEG2000 in the shots is rather large, but still 3x smaller than the size used in this paper, thus these rGO+PEG clusters would be smaller in comparison to these sizes mentioned here.
Thanks. I may be a retired chemist (not physical or electro, but organic, I've worked for one of the more notorious pharmaceutical firms in an earlier incarnation), but didn't know what zeta potential be. This? https://en.wikipedia.org/wiki/Zeta_potential
Zeta potential is a critically important concept for a living systems because when it is not maintained all the fluid in the body can clot or coagulate together, and proteins will commonly miss fold precipitate out of solution. My present belief is that the primary reason why vaccinations are so harmful is that they are highly effective at interfering with the state of tension on the body (and to a lesser extent causing the lymphocytes to block the capillary circulation), and for some reason, the spike protein on SARS-CoV-2 was modified from the original SARS spike protein to have a very high density of positive charges so that it was an ideal agent for destroying data potential in the body. Amongst other things I think this is why the vaccines cause very odd clots that do not respond to anitcoagulants.
I have looked at hundreds of medical models, and my present perspective is that is it a potential is one of the things that most directly correlates with health and vitality.
If you want to understand this concept, look up how they flocculate sewage with aluminum for municipal water treatment.
The jabs, esp. this highly charged sequence, form coacervates? (Essentially sludge in the circulation.)
I will be honest, I had never come across this concept before you left that comment. I do not think that a zeta potential collapse or agglomeration of a suspended colloids is the same as a coacervates forming, but I may be wrong however the end result you are describing, sludge in the circulation is white occurs within the blood.
Awesome! I'm doing some of those and need to research and incorporate some of the others
Aging is largely a process of all the fluid circulations in your body shutting down.