Per extends his curiosity of what the commotion has been about regarding folks consistently displaying foreign materials in blood since the 2020 period.
That was a very well concise overview of humanity finding itself already having been unknowingly seeded from long ago with the mechanics and mechanisms marching forwards
relentlessly in a fusion of synthetic replacement - intent
on total theft of what you were.
The most gripping moment in all of which,...the unnerving eerily
Paused moment as we saw
Cells melted away to something else not remotely "us"......
Karl's 6 last minures of the interview are most significant for me. No matter if and what remedies exist or could be discovered, it might already be too late for the Humankind to defeat this evil.
If you study nanotechnology courses online, they actually talk about how to prevent nanocarriers and other nanostructures from connecting. This is something nanotechnology developers generally try to avoid, but they don't have all of the bugs worked out yet. The bubbles (spheres/nanocarriers) connecting bit is an issue nanotechnology developers talk about a lot, because when they connect accidently, the surface area gets reduced, which is considered undesirable for certain functions. The debunkers could learn an awful lot by just looking into official information that's already out there, but they usually don't.
This great commentary. When you say there is a nano carrier prevention source, do you have a link. I think I already have been working on the most viable options so far, but 8 might be wrong. Nice work! There is peer reviews showing all this too, but more often showing a perspective where a product is hindered in a process or to characterise it's behaviour with chemical addition. For vesicles surfactant and enzymes are often the go to. They often use red o, Sudan black, fast green, dapi and other dyes to highlight the vesicle and components.
Did you try scihub with the DOI? did you know electrolyte levels alter the spacing of some particles in solution. I think I've found a few new a hills heals for part of the framework layers. Hopefully I can find a few more as a targeted multi-key strike. I'm feeling a lot smarter and brighter since my last find. Can't say what that is yet until I find a safe consumable alternative.
I will certainly try to find a link. I've come across this information two or three times in educational videos on nanotechnology. The professors/speakers were essentially telling students how to design spherical nanocarriers so that they wouldn't stick together, as this happens if you don't take precautions when you're designing them. (I'm pretty sure the instructions weren't meant to be a protocol. Instead, they were meant to enable nanotechnology to work better.) But, ff you can somehow figure out how to help everyone with the nanotech designers' own information, that would be wonderful! I'll start looking for a link.
The issue of whether microspheres or nanocarriers connect with each other is not trivial. The connectors allow for a magnetic and optical phenomenon to occur between microspheres. Is it a communication and/or activation system? Depending on whether there is more or less light, it can be better appreciated. It was Zandré Botha who highlighted this while looking at a Janssen. Karl C. I want to send you a document that I have prepared about this.
Feel free Ruth. But I have to admit that I stopped listening to those outlets long ago with all the other weird stuff that came from there. Had everyone puzzled. The lipids connectivity is part of the templating system. It's how it assemblies internally and the branches to the next structural or connective stage. So yes, it is a necessary process. I didn't think anyone but myself had characterised the lipid system yet in any detail as I hv e been doing. Dr botha isn't sure what the bubbles are from what I can tell. Hybrid-LNP's, lipid vesicles, nano structure formations, bi-layer vesicles, I to tissue scaffoding. End result - - - > technical biomimetic tissue scaffolding. As far as I am aware the understanding here so far goes beyond Dr botha's identification at this stage. But if there is anything useful such as genuine spec analysis or other information that would be helpful. Mail to humankarl@protonmail.com. Thank you Ruth!
Okay, so I started looking for things on how to prevent nanocarrier aggregation and it brought up information on how to prevent the aggregation of liposomes (fair enough) and nanoparticles. The funny part is, two of the sources with reasonably good information, appear to be company websites. Anyway, this should help you figure out if there's a way of using any of this information to test anything. I've been looking at sound frequencies, because sound waves can affect nanotechnology. I've attached a response I got to one of my google queries below the links. The question I asked was: How do you prevent Nanocarrier aggregation? It gave me liposome info. and nanoparticle info., depending on when and how I asked.
polyethylene glycol (PEG) or other polymers, adjust the Zeta potential by adding charge-inducing components to increase repulsion, use cryoprotectants like sugars to protect against freezing damage, control lipid composition, maintain proper pH, avoid harsh storage conditions like freeze-thaw cycles, and use antioxidants if unsaturated lipids are present.
Surface Modification Strategies
• PEGylation:
Incorporate PEG-modified phospholipids onto the liposome surface to create a steric barrier, which prevents liposomes from interacting and aggregating.
• Other Polymers:
Apply other hydrophilic polymers, such as chitosan or pectin, to the liposome surface using methods like layer-by-layer electrostatic deposition to provide a protective coating.
Zeta Potential Control
• Increase Zeta Potential: A high positive or negative Zeta potential (typically > ±30 mV) provides a strong electrostatic repulsion force between liposomes, keeping them dispersed and preventing aggregation. You can achieve this by incorporating lipids with charged head groups.
Cryoprotectants for Storage
• Add Cryoprotectants: When freezing liposomes, especially for long-term storage, add cryoprotectants such as sucrose, trehalose, glycerol, or dimethyl sulfoxide. These protect the liposomes from damage caused by ice crystal formation.
Environmental and Compositional Controls
• Control pH:
Liposome stability can be sensitive to pH. Ensure your preparation's pH is in the optimal range for your specific lipids to minimize aggregation.
• Use Antioxidants:
If your liposomes contain unsaturated lipids, add antioxidants like tocopherols to prevent oxidative damage and lipid degradation that can lead to aggregation.
• Minimize Exposure to Freezing/Thawing:
Repeated freeze-thaw cycles are known to promote aggregation. Store liposomes under conditions that avoid these cycles.
• Control Lipid Concentration:
The total lipid concentration can affect aggregation. Keep concentrations at an appropriate level for your formulation to prevent clumping.
Advanced Techniques
• Spray Freeze Drying:
This advanced processing technique can be used to create stable, dry liposomal products with improved stability and desired particle properties.
• Microfluidics:
This technology offers precise control over fluid flow, enabling the production of uniform liposomes and minimizing aggregation during manufacturing.
• Poly(ethylene glycol)-modified phospholipids prevent aggregation during covalent conjugation of proteins to liposomes
The reason I made the comment originally, was in response to one of Per's questions. I remember him asking about two bubbles joined together, and something about how we knew they weren't regular bubbles. I hope this helps. Daisy
Good thinking. I will say the desire to bond between vesicles looks very well directed. I believe there is charge manipulation external to vesicles as well. Often they form very close or in networks. I would say spreading techniques are a minor combatent tool due to the fact you can't keep your fluids in that state. Ultra sound can have negative effects on your own molecules too. Ultra sound can be rather aggressive if not well understood and targeted exclusively towards the right functions. I love all the technical stuff because I can rig up electronic designs and calibrate them fairly well. But with electronic and audible methods there is risk depending on the situation. Do see what comes up. I love what you are doing. If only everyone was in it like this daisy. Hopefully your research will angle something out. If the odds a nd concept seem unflawed or not dangerous then I'm all for attempting tests assuming I can get the right parts and gear. Thanks daisy
Thank you, Karl, for consistently sharing your research and findings so clearly and generously!
In this article, I was especially struck by one of the images, because I have identical observations in my cat’s blood (this time without EDTA): filaments accompanied by hydrogel-like material, with the same morphology you show in your photo (by the way, also observed by Dr. Nixon in cat blood as well)!
Seeing this coincidence confirms to me that what I have been documenting are not just isolated artifacts in cat blood, but part of a recurring pattern appearing in other contexts as well. Precisely, I am preparing a short article with images for Substack where these observations can also be seen. Unfortunately, I can barely understand the video of your interview, but I truly appreciate the effort you make to share it.
First of all, I would like to thank you for your utmost effort.
I have 3 dental surgery in 2019, and a year later, I got sick high fever, coughing badly, and very weak. Although my fever gone, I still unable to walk properly let alone jogging (i was regularly jog). Much later on, I heavily suspect the anestetic has same ingredieents of the covid jab. I could not verify it, as dont have access to darkfield microscope. I tried many things, eventually tried MMS (or Chlorine dioxide) as describe in wonderful book "Healing autism" by Kerri riverra (free pdf book). After approx 5-6 months, there are black things that goes to certain part of my skin (in the stomach, back, on the feet), which is very painful so I tried to take it out by cupping (suck blood with incission on the skin). After this painful episode lasting 2-3 weeeks, my legs become somewhat normal again, at least I could walk and jog a little. Mabee Cl02 not the best, but I dont have much choicee. Laterr on I tried Sodium Citrate, but now I use minimum ammount of MMS (plus citric juice from citric fruit) and sodium bicarb with honey. I now maybe still a way to go to full recover, but the progress although slow is worthwhile.
Again thanks for your dilligent effort to uncover mistery jab.
I found CD chlorine dioxide or MMS to have surprising low affect on sames. Isopropyl and h202 have slightly different actions and they certainly do disrupt albeit it temporarily. The sodium citrate seemed to score far higher given the extra amount of junk that came out in urine when we went over this a few years back. The symptoms for some. Can be rather visual and even more disturbing. I had those too in the begin. I looked like a radiation victim crossed with outbreak. It scared the life out of me as does everyone. I hope you find a key. Serrapetase, and various other agents in the above may be very useful. I personally take the max dose for all supplements like nac, qeurcetin, resversatrol. Less feels far less effective symptom wise. My tinnitus goes up and down.
Thanks for valuable insight. I will get sodium citrate. As for h2o2 i used it for nebulizer. (Specially for lung). 0.5percent with saline solution (.9 percent sea salt in water). Do you recomend to drink as well? Someone said “couple of 6 percent drops in glass of water”… i could not found any ref to this.
Honestly, I told an older lady years ago about the h202 nebulizing for copd sent her info since I knew her. She was on a gas tank, She tried everything. I said to her that science papers and clinics have had great success with it. I left her with h202 Saline solution for her neb. It helped, then after she said to me that drinking the safe amount was far more effective. It was her first hopefully sign of success where her illness had taken her. I was pleasantly surprised to hear she had excellent results. Surprising how many clinics popped up and specialise in this now for copd.
There is actually many other cross actions for some of those supplements. But it's very hard to bamboozled folks with all the literature. But I have seen papers where many of these agents have been tested on synthetic materials in lab settings for one reason or another. They are the safest sensible choices with proven actions. That's good for me, I don't do pharma, and I don't do things with negative implications like DNA weakening and alteration pathways.
Amazing photos...do you have any thoughts on near infrared light and its interaction with the self-assembling particles? For instance, infrared sauna can be a detoxifier, but recently a subscriber of mine said you had alluded to NIR potentially exacerbating harm from these particles.
We heard bad stuff from folks goint to infrared treatment places and then going to their naturpaths. The naturpaths couldn't beleive how many of them were really getting ill from it. I heard this several times and considered it unlikely these guys were all Wrong. But in all truth noone at this point can say infrared is specifically good or bad where the stuff in the blood is concerned. Infrared can impact synthetic frameworks differently depending on their designs. Some can absorb he energy and use it or be triggered by it, and some can be destroy by it in certain exposure settings. It may make some folk feel better but not actually anything to do with affe ting the synthetic material. I hope. This is the correct way to put it.
Thank you Karl for clarifying. I would also think that since many of the infrared saunas emit a ton of EMF, that this would also weaken the immune system (Udinstev 1978). However there are saunas out there, like the one I use from Sauna Space, that has a faraday cage and bulbs are shielded.
This is an interesting perspective, thank you. I spent 3 months reading IR sauna specifications before buying one for a daughter recovering froma bone tumor. She would experience high pain when in the presence of a EMF feild so she was our canary in the gold mine for several years...taught us so much. (She is ok today.) Sunstream was one model I found where the wifi speakers could be disabled completely and the heaters had low EMF, food grade glue and no toxic wood treatment.
Hi Carol, thanks for sharing that. There is also the issue of dirty electricity that can come through the outlet, regardless of Sauna...but that's wonderful news that your daughter is doing much better! Do you still use the sauna?
We do. I have family members with bone and muscle injuries and they use it instead of pain medication. But there are questions about infrared and EMF exposure feeding some artificial processes in the body, so I think each persons situation is different. We listen carefully to the body - it signals when a treatment is not beneficial. There's so much we don't know and sometimes instinct is more valuable than knowledge. Doing the best we can in a weird world!
I certainly here you on that Carol - doing the best we can here as well. Intuition and listening to one's body is just like a muscle - use it or lose it! Have you looked into/ heard of Stetzerizer dirty electrical filters?
Good to put a face to your posts. This is the first time I have heard your health story and how you started studying the blood. Thanks for sharing your journey and for continuing to produce fascinating evidence and solutions.
Yes, thank you. I purposely don't like to talk about why I got in to this. It was extremely traumatic. I've been offered to talk on shows about it but I felt that I didn't want to stigmaitize my efforts with with what happened in case some folks didn't beleive it. I like to keep focused on what's important. 😁
That was a very well concise overview of humanity finding itself already having been unknowingly seeded from long ago with the mechanics and mechanisms marching forwards
relentlessly in a fusion of synthetic replacement - intent
on total theft of what you were.
The most gripping moment in all of which,...the unnerving eerily
Paused moment as we saw
Cells melted away to something else not remotely "us"......
This really got to me, I'm shaken
KK
Karl's 6 last minures of the interview are most significant for me. No matter if and what remedies exist or could be discovered, it might already be too late for the Humankind to defeat this evil.
Nice work Karl! Thank you for sharing the conversation.
If you study nanotechnology courses online, they actually talk about how to prevent nanocarriers and other nanostructures from connecting. This is something nanotechnology developers generally try to avoid, but they don't have all of the bugs worked out yet. The bubbles (spheres/nanocarriers) connecting bit is an issue nanotechnology developers talk about a lot, because when they connect accidently, the surface area gets reduced, which is considered undesirable for certain functions. The debunkers could learn an awful lot by just looking into official information that's already out there, but they usually don't.
This great commentary. When you say there is a nano carrier prevention source, do you have a link. I think I already have been working on the most viable options so far, but 8 might be wrong. Nice work! There is peer reviews showing all this too, but more often showing a perspective where a product is hindered in a process or to characterise it's behaviour with chemical addition. For vesicles surfactant and enzymes are often the go to. They often use red o, Sudan black, fast green, dapi and other dyes to highlight the vesicle and components.
Here's something else that looks interesting. The abstract mentions ways of redispersing nanoparticles that have aggregated. I think we all pretty much want to dissolve, destroy, vaporize, or otherwise make them disappear. Redispersing sounds promising! The trouble is, like so many articles, you need an institutional link to access the whole thing. I was hoping David Nixon might have one. Here's the link: https://www.sciencedirect.com/science/article/abs/pii/S0001868619304816#:~:text=This%20review%20article%20is%20focused,relevant%20to%20controlling%20NP%20aggregation
Did you try scihub with the DOI? did you know electrolyte levels alter the spacing of some particles in solution. I think I've found a few new a hills heals for part of the framework layers. Hopefully I can find a few more as a targeted multi-key strike. I'm feeling a lot smarter and brighter since my last find. Can't say what that is yet until I find a safe consumable alternative.
Thanks for that tip. I didn't know about SciHub. Go Karl!
I will certainly try to find a link. I've come across this information two or three times in educational videos on nanotechnology. The professors/speakers were essentially telling students how to design spherical nanocarriers so that they wouldn't stick together, as this happens if you don't take precautions when you're designing them. (I'm pretty sure the instructions weren't meant to be a protocol. Instead, they were meant to enable nanotechnology to work better.) But, ff you can somehow figure out how to help everyone with the nanotech designers' own information, that would be wonderful! I'll start looking for a link.
The issue of whether microspheres or nanocarriers connect with each other is not trivial. The connectors allow for a magnetic and optical phenomenon to occur between microspheres. Is it a communication and/or activation system? Depending on whether there is more or less light, it can be better appreciated. It was Zandré Botha who highlighted this while looking at a Janssen. Karl C. I want to send you a document that I have prepared about this.
Feel free Ruth. But I have to admit that I stopped listening to those outlets long ago with all the other weird stuff that came from there. Had everyone puzzled. The lipids connectivity is part of the templating system. It's how it assemblies internally and the branches to the next structural or connective stage. So yes, it is a necessary process. I didn't think anyone but myself had characterised the lipid system yet in any detail as I hv e been doing. Dr botha isn't sure what the bubbles are from what I can tell. Hybrid-LNP's, lipid vesicles, nano structure formations, bi-layer vesicles, I to tissue scaffoding. End result - - - > technical biomimetic tissue scaffolding. As far as I am aware the understanding here so far goes beyond Dr botha's identification at this stage. But if there is anything useful such as genuine spec analysis or other information that would be helpful. Mail to humankarl@protonmail.com. Thank you Ruth!
Okay, so I started looking for things on how to prevent nanocarrier aggregation and it brought up information on how to prevent the aggregation of liposomes (fair enough) and nanoparticles. The funny part is, two of the sources with reasonably good information, appear to be company websites. Anyway, this should help you figure out if there's a way of using any of this information to test anything. I've been looking at sound frequencies, because sound waves can affect nanotechnology. I've attached a response I got to one of my google queries below the links. The question I asked was: How do you prevent Nanocarrier aggregation? It gave me liposome info. and nanoparticle info., depending on when and how I asked.
https://www.mdpi.com/2305-7084/9/3/56#:~:text=To%20address%20stability%20concerns%2C%20liposomal,Filtration%20and%20Aseptic%20Processing%20Equipment:
https://pubs.acs.org/doi/10.1021/bc00032a006
https://www.satnanomaterial.com/blog/how-to-effectively-control-the-agglomeration-of-nanoparticle-powders_b205#:~:text=Nanoparticles%20can%20be%20surface%20modified,be%20treated%20with%20citric%20acid.
https://www.getnanomaterials.com/kb/how-to-properly-disperse-nanoparticles-or-microparticles-and-avoid-agglomeration-issues/#:~:text=How%20It%20Works:%20Stabilizers%20are,and%20mechanical%20properties%20in%20composites.
https://pubs.rsc.org/en/content/articlelanding/2018/nr/c7nr09011k
One AI Overview response:
polyethylene glycol (PEG) or other polymers, adjust the Zeta potential by adding charge-inducing components to increase repulsion, use cryoprotectants like sugars to protect against freezing damage, control lipid composition, maintain proper pH, avoid harsh storage conditions like freeze-thaw cycles, and use antioxidants if unsaturated lipids are present.
Surface Modification Strategies
• PEGylation:
Incorporate PEG-modified phospholipids onto the liposome surface to create a steric barrier, which prevents liposomes from interacting and aggregating.
• Other Polymers:
Apply other hydrophilic polymers, such as chitosan or pectin, to the liposome surface using methods like layer-by-layer electrostatic deposition to provide a protective coating.
Zeta Potential Control
• Increase Zeta Potential: A high positive or negative Zeta potential (typically > ±30 mV) provides a strong electrostatic repulsion force between liposomes, keeping them dispersed and preventing aggregation. You can achieve this by incorporating lipids with charged head groups.
Cryoprotectants for Storage
• Add Cryoprotectants: When freezing liposomes, especially for long-term storage, add cryoprotectants such as sucrose, trehalose, glycerol, or dimethyl sulfoxide. These protect the liposomes from damage caused by ice crystal formation.
Environmental and Compositional Controls
• Control pH:
Liposome stability can be sensitive to pH. Ensure your preparation's pH is in the optimal range for your specific lipids to minimize aggregation.
• Use Antioxidants:
If your liposomes contain unsaturated lipids, add antioxidants like tocopherols to prevent oxidative damage and lipid degradation that can lead to aggregation.
• Minimize Exposure to Freezing/Thawing:
Repeated freeze-thaw cycles are known to promote aggregation. Store liposomes under conditions that avoid these cycles.
• Control Lipid Concentration:
The total lipid concentration can affect aggregation. Keep concentrations at an appropriate level for your formulation to prevent clumping.
Advanced Techniques
• Spray Freeze Drying:
This advanced processing technique can be used to create stable, dry liposomal products with improved stability and desired particle properties.
• Microfluidics:
This technology offers precise control over fluid flow, enabling the production of uniform liposomes and minimizing aggregation during manufacturing.
• Poly(ethylene glycol)-modified phospholipids prevent aggregation during covalent conjugation of proteins to liposomes
The reason I made the comment originally, was in response to one of Per's questions. I remember him asking about two bubbles joined together, and something about how we knew they weren't regular bubbles. I hope this helps. Daisy
Good thinking. I will say the desire to bond between vesicles looks very well directed. I believe there is charge manipulation external to vesicles as well. Often they form very close or in networks. I would say spreading techniques are a minor combatent tool due to the fact you can't keep your fluids in that state. Ultra sound can have negative effects on your own molecules too. Ultra sound can be rather aggressive if not well understood and targeted exclusively towards the right functions. I love all the technical stuff because I can rig up electronic designs and calibrate them fairly well. But with electronic and audible methods there is risk depending on the situation. Do see what comes up. I love what you are doing. If only everyone was in it like this daisy. Hopefully your research will angle something out. If the odds a nd concept seem unflawed or not dangerous then I'm all for attempting tests assuming I can get the right parts and gear. Thanks daisy
Thanks Karl. And, thanks for the encouragement! We need it in this challenging field!
Thank you, Karl, for consistently sharing your research and findings so clearly and generously!
In this article, I was especially struck by one of the images, because I have identical observations in my cat’s blood (this time without EDTA): filaments accompanied by hydrogel-like material, with the same morphology you show in your photo (by the way, also observed by Dr. Nixon in cat blood as well)!
Seeing this coincidence confirms to me that what I have been documenting are not just isolated artifacts in cat blood, but part of a recurring pattern appearing in other contexts as well. Precisely, I am preparing a short article with images for Substack where these observations can also be seen. Unfortunately, I can barely understand the video of your interview, but I truly appreciate the effort you make to share it.
Yes, seth showed us wild trout blood and other animals 2 years ago too since he lives out back and hunt in the USA. Crazy what we all saw.
That’s really striking, Karl. It perfectly shows how this goes beyond humans
First of all, I would like to thank you for your utmost effort.
I have 3 dental surgery in 2019, and a year later, I got sick high fever, coughing badly, and very weak. Although my fever gone, I still unable to walk properly let alone jogging (i was regularly jog). Much later on, I heavily suspect the anestetic has same ingredieents of the covid jab. I could not verify it, as dont have access to darkfield microscope. I tried many things, eventually tried MMS (or Chlorine dioxide) as describe in wonderful book "Healing autism" by Kerri riverra (free pdf book). After approx 5-6 months, there are black things that goes to certain part of my skin (in the stomach, back, on the feet), which is very painful so I tried to take it out by cupping (suck blood with incission on the skin). After this painful episode lasting 2-3 weeeks, my legs become somewhat normal again, at least I could walk and jog a little. Mabee Cl02 not the best, but I dont have much choicee. Laterr on I tried Sodium Citrate, but now I use minimum ammount of MMS (plus citric juice from citric fruit) and sodium bicarb with honey. I now maybe still a way to go to full recover, but the progress although slow is worthwhile.
Again thanks for your dilligent effort to uncover mistery jab.
I found CD chlorine dioxide or MMS to have surprising low affect on sames. Isopropyl and h202 have slightly different actions and they certainly do disrupt albeit it temporarily. The sodium citrate seemed to score far higher given the extra amount of junk that came out in urine when we went over this a few years back. The symptoms for some. Can be rather visual and even more disturbing. I had those too in the begin. I looked like a radiation victim crossed with outbreak. It scared the life out of me as does everyone. I hope you find a key. Serrapetase, and various other agents in the above may be very useful. I personally take the max dose for all supplements like nac, qeurcetin, resversatrol. Less feels far less effective symptom wise. My tinnitus goes up and down.
Thanks for valuable insight. I will get sodium citrate. As for h2o2 i used it for nebulizer. (Specially for lung). 0.5percent with saline solution (.9 percent sea salt in water). Do you recomend to drink as well? Someone said “couple of 6 percent drops in glass of water”… i could not found any ref to this.
Honestly, I told an older lady years ago about the h202 nebulizing for copd sent her info since I knew her. She was on a gas tank, She tried everything. I said to her that science papers and clinics have had great success with it. I left her with h202 Saline solution for her neb. It helped, then after she said to me that drinking the safe amount was far more effective. It was her first hopefully sign of success where her illness had taken her. I was pleasantly surprised to hear she had excellent results. Surprising how many clinics popped up and specialise in this now for copd.
Oh wow,,, thanks for the info
Yes. Outstanding work Karl.
I’m impressed with your intelligence and perseverance!
Great video Karl. I am so proud of you... and all your wonderful research and work.
Karl kept it smooth talking , that way stay away from trouble,
Coffee sent
Haha, no way to soften the blow of what comes next. Thanks keyes!
Great stack list! I wasn't aware of all of those things!
There is actually many other cross actions for some of those supplements. But it's very hard to bamboozled folks with all the literature. But I have seen papers where many of these agents have been tested on synthetic materials in lab settings for one reason or another. They are the safest sensible choices with proven actions. That's good for me, I don't do pharma, and I don't do things with negative implications like DNA weakening and alteration pathways.
OUTSTANDING Presentation Karl!
Would love your help in this if you have the capacity:
https://substack.com/@michaelginsburg/note/c-148737643
Excellent, Brother.
Thank you very much.
Amazing photos...do you have any thoughts on near infrared light and its interaction with the self-assembling particles? For instance, infrared sauna can be a detoxifier, but recently a subscriber of mine said you had alluded to NIR potentially exacerbating harm from these particles.
We heard bad stuff from folks goint to infrared treatment places and then going to their naturpaths. The naturpaths couldn't beleive how many of them were really getting ill from it. I heard this several times and considered it unlikely these guys were all Wrong. But in all truth noone at this point can say infrared is specifically good or bad where the stuff in the blood is concerned. Infrared can impact synthetic frameworks differently depending on their designs. Some can absorb he energy and use it or be triggered by it, and some can be destroy by it in certain exposure settings. It may make some folk feel better but not actually anything to do with affe ting the synthetic material. I hope. This is the correct way to put it.
Thank you Karl for clarifying. I would also think that since many of the infrared saunas emit a ton of EMF, that this would also weaken the immune system (Udinstev 1978). However there are saunas out there, like the one I use from Sauna Space, that has a faraday cage and bulbs are shielded.
This is interesting, it really depends on whether it is IR or the EM responsible for any Interactions. I wouldn't make any guess yet eeek
This is an interesting perspective, thank you. I spent 3 months reading IR sauna specifications before buying one for a daughter recovering froma bone tumor. She would experience high pain when in the presence of a EMF feild so she was our canary in the gold mine for several years...taught us so much. (She is ok today.) Sunstream was one model I found where the wifi speakers could be disabled completely and the heaters had low EMF, food grade glue and no toxic wood treatment.
Hi Carol, thanks for sharing that. There is also the issue of dirty electricity that can come through the outlet, regardless of Sauna...but that's wonderful news that your daughter is doing much better! Do you still use the sauna?
We do. I have family members with bone and muscle injuries and they use it instead of pain medication. But there are questions about infrared and EMF exposure feeding some artificial processes in the body, so I think each persons situation is different. We listen carefully to the body - it signals when a treatment is not beneficial. There's so much we don't know and sometimes instinct is more valuable than knowledge. Doing the best we can in a weird world!
I certainly here you on that Carol - doing the best we can here as well. Intuition and listening to one's body is just like a muscle - use it or lose it! Have you looked into/ heard of Stetzerizer dirty electrical filters?
Good to put a face to your posts. This is the first time I have heard your health story and how you started studying the blood. Thanks for sharing your journey and for continuing to produce fascinating evidence and solutions.
Yes, thank you. I purposely don't like to talk about why I got in to this. It was extremely traumatic. I've been offered to talk on shows about it but I felt that I didn't want to stigmaitize my efforts with with what happened in case some folks didn't beleive it. I like to keep focused on what's important. 😁
Thank you for your research!!!