Awesome work, Karl! Really great news that you finally have a spectrometer! Congratulations on getting that FTIR fully up and running — this is a huge step forward. From now on, your research will not only show fascinating structures, it will also be able to chemically identify them — which could reveal a lot of important information we still don’t have.
You dont want know what i think, it wont help anyone sleep at night. Just smile be tenaciscous, chin up keep calm and carry on. Progress and success relies on those things, fear always cripples a good plan !
And saying, The time is fulfilled, and the kingdom of God is at hand: repent ye, and believe the gospel.
🔸️Isaiah 55:7
Let the wicked forsake his way, and the unrighteous man his thoughts: and let him return unto the Lord, and he will have mercy upon him; and to our God, for he will abundantly pardon.
Ive come away from there right now. I keep to my sodium citrate all day, the nac, resveratrol, ip6, fulvic and humic, and several other things. Those are all doing great things, but not enough. Ive dropped thinking in that area until i know more about the composition specifically. I think i have scrapped the barrell for effective naturals with what is known at this point. There will ne no easy one thing, 2 thing or 3 thing cure for this i beleive. It seems to complex and well designed. Specific keys will be required to do more there. Its clever stuff, but methylene blue nicotine, master piece, ostrich antibodies, etc all are gatekeepers ideas to me. They show no relevant or logical affects from what i can see so far. Methylene blue is a risky idea if it doesnt nothing since it also weakens the DNA backbane facilitating genetic alteration of mammals if genetically altering material is present. I feel it is ni coincidence there are dodgy celebs and FB posts pushing unproven and quite frankly stupid ideas around basrd on no evidence. Its all old pathogen based medicinr ideas that have completely different meaning in the place of synthetics. Dont weaken your adNA backbane with methylene blue, it has the suggestive and studied properties to help your DNA be altered essentially. Nothing could be more risky than that if you think that a foreign agent needs to alter you in multiple ways. These are reasons why haste will slow you down and why the unkown needs to be known more before figuring whats what and why it could work. People are still pushing cures to remove a spike protein. What id a soike protein here ? Dr Arnold berkhardt foynd 231 proteins and heavy amounts of mettalics in clotss and tissue samples before sadly dying only a week after his public conference in germany. Anyone claming to have a cure based on the spike not showing or ehatever other false relabelled marker is likely not being honest. You cant claim to cure something you have not identified properly or taken someone elses word on in c9mb8nation with blood tests like that, not here. It has bren inyeresting watching all the false claims since most of the time it is obvious they cant know the thing they claim to know. Logic doesnt support most of these claims even closely.
Well, you dont actually require wireless signals to see behaviour like this. Things happen very quickly in wet phase self assembly systems when the conditions are right. A lot can happen very rapidly depending on how each individual chemical process occurs. On the other hand some structural assembly can take a long time visually before some of those frameworks finish.
One quick thought, Karl! Since some of these structures appear after plasma centrifugation, a very interesting approach could be to take FTIR spectra of normal plasma spread on the slide and also one of those structured networks. Then you could subtract one spectrum from the other.
If any extra spectral bands show up (beyond normal plasma proteins), that would be a very important finding. And it’s a straightforward comparison now that you have the FTIR running!
Agh, i see what you are saying now. There is no clean blood plasma to compare. I already have peer review documents detailing the correct structure of human blood. This is good because its the only other official type of record that is available for comparison. Using ftir the process will be a bit more technical. I can already see certain candidates to investigate from UV fluorescence work i did recently on blood and a few pharm products. Mostly whats there seems to be hiding close to natural blood peaks or masked by O2 and CO2 signitures, hence needing the gas. Most likely it will take chemical additions to shift and extend certain peak regions to indicate for instancea dye binding with groups or molecules in an unusual way. There are many tricks you can use if you have X amount of pre existing knowledge of what you are looking for. I already have my direction set. Struggling to afford the nitrogen purge kit at the moment. I ran out of money i saved for the spectrometer. Basically it is the same processes labs use with a range of synthetic products to characterize and evaluate emulsions and coacervates. So its a technique thats appropriate if you follow synthetic science over medical science approaches. You wont find suspiscious stealth materials without extended or alternative methods. There sre two things most have been doing wrong. 1: pretending they did spectrometry for gatekeeping purposes and 2: using the wrong techniques without understanding of complex synthetics in mind. Even an ftir spectrometer should be able to find almost trace sized components if the right techniques and methods are used. It wont likely find everything at all, but all you have to do is reliaably find anomalies which respond to other chemical or dye probing in a certain way enough to reveal x amount of components. That shiws that something foreign is there and yiu can prove it is self assembling by adding the correct cross linkkers, chelating them back out and more. Self asdembling systems have signiture responses that natural systems do not have.
Im finding this very interesting and something fun on days where i feel healthier lol. Its all a very heavy work load with so many unkowns.
Thanks a lot for the detailed reply, Karl! It’s really great to hear that you already have a clear strategy for the FTIR work and chemical probing techniques. I totally agree — standard methods alone won’t reveal stealth or hybrid materials. Your approach sounds absolutely on point.
Take care and keep us posted — your work is incredibly valuable!
What about compiling a record of RBC changes since start of live dark field microscopy in 90s, perhaps try to contact retired naturalpaths and like who may have treasure troves of old photos , videos.
Seems super major changes didn't start until 2019 but betcha each half decade will show relevant differences that could assist us in understanding more complex layers of nano now.
Do you know of any good old collections of microscopy online?
No these i can confirm as synthetic cells and not oommyctes. But years agi when i started out they were the go to. Since then working from synthetic studies and research it became evident that oomycytes and fungus can be mistaken for synthetic constructs. Who knew untill studting so much synthetic biology.
Awesome work, Karl! Really great news that you finally have a spectrometer! Congratulations on getting that FTIR fully up and running — this is a huge step forward. From now on, your research will not only show fascinating structures, it will also be able to chemically identify them — which could reveal a lot of important information we still don’t have.
We’re all looking forward to what comes next!
What does this mean for humanity?
You dont want know what i think, it wont help anyone sleep at night. Just smile be tenaciscous, chin up keep calm and carry on. Progress and success relies on those things, fear always cripples a good plan !
👇
🔸️Mark 1:15
And saying, The time is fulfilled, and the kingdom of God is at hand: repent ye, and believe the gospel.
🔸️Isaiah 55:7
Let the wicked forsake his way, and the unrighteous man his thoughts: and let him return unto the Lord, and he will have mercy upon him; and to our God, for he will abundantly pardon.
Hi Karl,
Haven't been here in a while. Great news on your new scope.
What's the latest as far as a treatment? Anything new?
Ive come away from there right now. I keep to my sodium citrate all day, the nac, resveratrol, ip6, fulvic and humic, and several other things. Those are all doing great things, but not enough. Ive dropped thinking in that area until i know more about the composition specifically. I think i have scrapped the barrell for effective naturals with what is known at this point. There will ne no easy one thing, 2 thing or 3 thing cure for this i beleive. It seems to complex and well designed. Specific keys will be required to do more there. Its clever stuff, but methylene blue nicotine, master piece, ostrich antibodies, etc all are gatekeepers ideas to me. They show no relevant or logical affects from what i can see so far. Methylene blue is a risky idea if it doesnt nothing since it also weakens the DNA backbane facilitating genetic alteration of mammals if genetically altering material is present. I feel it is ni coincidence there are dodgy celebs and FB posts pushing unproven and quite frankly stupid ideas around basrd on no evidence. Its all old pathogen based medicinr ideas that have completely different meaning in the place of synthetics. Dont weaken your adNA backbane with methylene blue, it has the suggestive and studied properties to help your DNA be altered essentially. Nothing could be more risky than that if you think that a foreign agent needs to alter you in multiple ways. These are reasons why haste will slow you down and why the unkown needs to be known more before figuring whats what and why it could work. People are still pushing cures to remove a spike protein. What id a soike protein here ? Dr Arnold berkhardt foynd 231 proteins and heavy amounts of mettalics in clotss and tissue samples before sadly dying only a week after his public conference in germany. Anyone claming to have a cure based on the spike not showing or ehatever other false relabelled marker is likely not being honest. You cant claim to cure something you have not identified properly or taken someone elses word on in c9mb8nation with blood tests like that, not here. It has bren inyeresting watching all the false claims since most of the time it is obvious they cant know the thing they claim to know. Logic doesnt support most of these claims even closely.
Hi Karl, hope you are well!
Have you read this from @Sam?
https://darkfield-enigma.com/events/theeraoftheborgsingularity/
It's got mw quite worried we are almost at the end here.
Much gratitude for all of your hard work... Please know, it is very much appreciated?!
Thank you simone, just know i appreciate all the good supportive folks like you also!
Amazeballs...Mind Blowing...Exceptional work. Thank you!:)
Thank you doria, warm wishes
Holy shit, this is wild looking.
Its a jungle in there egh
Sure is
WOW. OMG. FIRST VIDEO....
Mad on the big screen isnt it.
Absolutely. The First video. Blue movement clouding. Almost seems like 5G signaling movement influence….
Well, you dont actually require wireless signals to see behaviour like this. Things happen very quickly in wet phase self assembly systems when the conditions are right. A lot can happen very rapidly depending on how each individual chemical process occurs. On the other hand some structural assembly can take a long time visually before some of those frameworks finish.
Video 1.......
Is it just me or did I just see the wildest ever plasma fish tank
sporting the strangest looking
Fishlike creatures moving about ?
Absolutely stunning capture Karl
It almost had a very calming surreal
Feeling come from it as I watched these strangest activations occur.
You have taken exploring the unknowns to an epic degree of
Fantastic.
Thankyou so much for taking the time to share so much with us too.
KK
One quick thought, Karl! Since some of these structures appear after plasma centrifugation, a very interesting approach could be to take FTIR spectra of normal plasma spread on the slide and also one of those structured networks. Then you could subtract one spectrum from the other.
If any extra spectral bands show up (beyond normal plasma proteins), that would be a very important finding. And it’s a straightforward comparison now that you have the FTIR running!
Agh, i see what you are saying now. There is no clean blood plasma to compare. I already have peer review documents detailing the correct structure of human blood. This is good because its the only other official type of record that is available for comparison. Using ftir the process will be a bit more technical. I can already see certain candidates to investigate from UV fluorescence work i did recently on blood and a few pharm products. Mostly whats there seems to be hiding close to natural blood peaks or masked by O2 and CO2 signitures, hence needing the gas. Most likely it will take chemical additions to shift and extend certain peak regions to indicate for instancea dye binding with groups or molecules in an unusual way. There are many tricks you can use if you have X amount of pre existing knowledge of what you are looking for. I already have my direction set. Struggling to afford the nitrogen purge kit at the moment. I ran out of money i saved for the spectrometer. Basically it is the same processes labs use with a range of synthetic products to characterize and evaluate emulsions and coacervates. So its a technique thats appropriate if you follow synthetic science over medical science approaches. You wont find suspiscious stealth materials without extended or alternative methods. There sre two things most have been doing wrong. 1: pretending they did spectrometry for gatekeeping purposes and 2: using the wrong techniques without understanding of complex synthetics in mind. Even an ftir spectrometer should be able to find almost trace sized components if the right techniques and methods are used. It wont likely find everything at all, but all you have to do is reliaably find anomalies which respond to other chemical or dye probing in a certain way enough to reveal x amount of components. That shiws that something foreign is there and yiu can prove it is self assembling by adding the correct cross linkkers, chelating them back out and more. Self asdembling systems have signiture responses that natural systems do not have.
Im finding this very interesting and something fun on days where i feel healthier lol. Its all a very heavy work load with so many unkowns.
Kindest regards Christina
Thanks a lot for the detailed reply, Karl! It’s really great to hear that you already have a clear strategy for the FTIR work and chemical probing techniques. I totally agree — standard methods alone won’t reveal stealth or hybrid materials. Your approach sounds absolutely on point.
Take care and keep us posted — your work is incredibly valuable!
What about compiling a record of RBC changes since start of live dark field microscopy in 90s, perhaps try to contact retired naturalpaths and like who may have treasure troves of old photos , videos.
Seems super major changes didn't start until 2019 but betcha each half decade will show relevant differences that could assist us in understanding more complex layers of nano now.
Do you know of any good old collections of microscopy online?
Ho Lee Fuk - Som Ting Wong! Not being casually racist, 'seems wholly appropriate...
Yes, indeed. Thanks for sharing. Do you know that the bio-technocrats are openly redefining the human species? https://falkentheater.substack.com/p/humanity-in-the-crosshairs-the-great
No these i can confirm as synthetic cells and not oommyctes. But years agi when i started out they were the go to. Since then working from synthetic studies and research it became evident that oomycytes and fungus can be mistaken for synthetic constructs. Who knew untill studting so much synthetic biology.