Synthetically altered blood @ 30,000 lumens, Darkfield. ---> LOOK <---
Blood cell images from the latest darkfield setup. Stunning detail !
https://open.substack.com/pub/managainstthemicrobes/p/synthetically-altered-blood-30000
KARL.C 2025.05.08 Thursday Substack
https://substack.com/@managainstthemicrobes
Darkfield Microscopy displays Carbon and polymer Nanotechnology in human blood post
Red blood cells showing polymeric altered membranes with clearly colourful synthetic material forming inside. Various RBC transformations can be seen in the image and these lend favor to them being altered and programmed differently also. Cell size and appearance is often completely out of biological norms these days and the effect worsens after just 30 mins viewing on the slide.
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Synthetically altered blood @ 30,000 lumens, Darkfield. ---> LOOK <---
Blood cell images from the latest darkfield setup. Stunning detail !
KARL.C
MAY 8
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It cant be long now, surely? The world still cant be pretending this was a vaccine roll out, but it is somehow despite all the clues and evidence.
Red blood cells showing polymeric altered membranes with clearly colourful synthetic material forming inside. Various RBC transformations can be seen in the image and these lend favor to them being altered and programmed differently also. Cell size and appearance is often completely out of biological norms these days and the effect worsens after just 30 mins viewing on the slide.
The video above shows our blood cells undergoing synthetic transformation at 12x speed. Notice the 2 RBC’s mid right, if you cant tell easily skip from the end to the beginning again and compare. I have been sharing all the hallmark signs of synthetic bio-engineering in full swing, and yet the world is still chasing spike proteins, vax gone wrong, etc. I even designed and modified adjustments to my Leica microscope several times so that I could produce imagery clear enough to debunk mainstream miss-information and agenda based retaliation. At least half of the world has no idea how far we are into the nanotechnology based biological computing science era. The microscope taking these images is a Leica DM2000 with 300w CRI97+ LED with huge cooling and lens refocusing system. The camera is a 1” industrial CMOS sensor by Sony and has also had a custom thermoelectric peltier added for darkfield noise reduction.
Apparently I was a bit shaky on the video below, but either way we can see unusual processes inside of what was RBC’s. The membrane is notably thick and unnatural (polymer-like), and there is a love heart shaped exotic membrane internally to the cell structure showing huge iridescence and mild birefringence. This is not lighting effects as 30,000 lumens passes through the membrane since these patterns are visually attributable to a solid tubular mass which is moving quite clearly. Also, if this were lighting effects from cell materials it would follow previous scientific understanding of how light passes through structures such as red blood cells in known literature, and this does not in any way whatsoever. Known lighting effects which might explain this phenomenon fall short where those expected lighting artifacts are traceable to the geometry of the cell. These visual findings are unique structures of partly solid and partly liquid or gel formation acting as separate entities where lighting effects and cell geometry are concerned. This is an easy observation to determine by visual analysis alone, not easy to debate.
Is there really references that tell us how birefringence and iridescence should behave in structures such as natural blood cells, Synthetic blood cells, liposomes, vesicles, exosomes, and other artificial cell types? Yes…there is.
This paper from the ‘Journal of Biomedical Optics’ shows measurement and characterization of optical phenomenon known to natural blood cells. In this case linearly polarized green light (λ ¼ 546 nm) is used to measure these optical features. However, nothing in this paper is even close to being able to plot, predict, or explain what is seen in my work results.
Much of the colourful effect seen in my images could only possibly be occurring more so at the curved edges of the blood cell and in curved areas near the concave dip. As this paper shows, intensely fluorescing and transforming shapes withing the cell are not part of optical effects. Instead, it was it is to be expected of complex vesicles with multiple membranes forming internally. Below is an extract from my private journal. Everyone’s blood can be seen forming this processes and much more clearly and cleanly after time on the slide has passed.
Focus into the geometry and optical specifics is still being profiled, but at this stage all massive arrows and current science knowledge direct us only to bio-engineering. The purpose of endless profiling like we can see in my other extract below is more to give us extra information regarding what type of synthetic process this is and how it all works, not to decide if the material is natural or synthetic since we can see that it is synthetic already for reasons above and more.
So, as we can see there are many different methods of characterizing optical and material data from samples, even just using software based scientific tools. morphology tools, FFT analysis, spacing, sizing, and exact geometries are all being catalogued for a larger perspective and explanation regarding the variances and behaviors of this synthetic material and processes. I do not advice using LLM/AI to output graphs and charts for reliable data. These clever platforms do not set optimal parameters in the image processing chain and this leads to it outputting vaguely useful data, but not accurate data. I used chatGPT’s ability to take an image, then perform certain algorithm based analysis and compared it to manual parameter entry or tweaked script/macro output in applications such as ImageJ and other scientific processing apps. The results were what I would say was close, but definitely not close enough for science.
An example of FFT analysis performed on human hair from my personal journal can be seen below. The LLM/AI does not provide clear and well organized frequency based visual analysis of structures in question. Manual calibration of parameter settings truly gives optimized processing like we see in my page below.
Typically different structure FFT analysis using LLM/AI provided output which was far less distinct, of lower resolution, and with many spacial errors. See the FFT graph below for an example, background artifacts were strong in the outer detail areas.
Without further deviation into technical methods being employed for optical analysis we can see how important this information is. It is a high resolution mapping of many optical properties that can indicate material properties and construction to some reasonable accuracy when correlated and compared to relevant databases for which i have been collecting from online. Everything is useful in presenting the full picture. What this all means will take more time in terms of interpreting the data, but some jobs have already been compared with interesting implications for material complexity and types.
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Above: recent collage of images taken from unvaccinated blood. At this stage trying to guess what exact unique structures are forming in terms of assembled material is still a fools erund. What we can confirm from this quality of imagery is that we are looking at constructs only known to the field of advanced nanotechnology. It isnt often in biological science you can say much about something you cannot see and yet still likely be right. But what is in the images is far too obvious to confuse with the appearance of natural biological structures. Previous science in biology does not align with what we see here, synthetic sciences do without any debate, this is a plausable conclusion. In this one collage alone we can tell several key factors which are synthetic mostly and only features. Membrane thckness of RBC’s, Inner layer vesicle membranes, varying membrane optical appearance, Polymeric type membrane attributes, Internal and observable morphological processes leading upto large complex structures of programmed nature, Presence of Hybrid lipid nanoparticles, extreme iridescence, and multi-domain inner vesicles showing seperate material properties. This isnt bevaiour of natural biology, its well known attributes applied to synthetic cell vesicles and altered cellular biology.
So, no ignorant nurse or doctor can really look at these while pretending they know it is normal, because it isnt and they most often have very limited experience in looking at blood themselves, or have never been allowed to use a dark field microscope since western medicine pretty much forbids it. They also have absolutely no experience or understanding in the field of nanotechnology/synthetic biological sciences. Thank god we have some awake and open minded doctors still thinking, it isnt many sadly, but its something. It seems we have too many of us which feel okay about fact checking things we havent even self investigated or have any background in. This doesnt help public awereness in a corrupt society and agenda based global takeover scenario either, we need to stand together! The end result of all this isnt meant to result in you being happy and having your freedoms. Its about AI, connected everything, dominance, population control, and future slavery for your loved ones and friends. I think many have started to realize that researchers, doctors, and some scientists wern’t making this stuff up the last 4 or 5 years. I only wonder what some people think is going to happen if they just do nothing? Many of us think we know, but we didnt guess it all, the answers were publicly provided in full. People just didnt listen and made excuses for why not to look, or why it must of all just been fake noise theyve been hearing.
Since weve made some headway on some of the projects been happening lately i shall leave you with a whole bunch of new images to feast the eye balls on. I dont want to say too much now since I have more to do, obviously. I am really pleased with the microscope upgrades and performance combined with software analysis techniques so far. It is best to only use high-resolution, quality work as accurate images processed into logical data and this setup certainly excels there so far. I am also excited to see where these libraries of data willg take things. Other analsysis is still running alongside also.
Back to cells from hell !
This cell is enlarged with objective aperture mostly closed, It enhances the ability to differentiate colour inside the cell and reveals properties of material which is different, ordered, and complex. What it loses is resolution and some light power, but it gives priceless insight in its own right. These internals are not known to normal human biology either. These have spread throughout the population mostly since the pandemic period. They may have been seen in older man-made and controversial diseases, but that is another story.
An RBC (Red blood cell) showing the complexity of material inside of our altered RBC’s. 40x oil, medium aperture. Nothing natural left of the blood cell. Image enlarged and taken on a 30,000 lumen dark field microscope, first of its power by 10x previous microscope capabilities.
Different altered cell sizes again, altered membranes, and almost what looks like blue structures possibly acting as linkers in this stage of the synthetic framework (a sort of joiner Lego brick).
Various sized altered RBC’s. After an RBC has gone through stages of transition it begins to start manufacturing material inside. The material has gained in complexity over the last year. Detailed images here show unnatural biomimmetic reformation.
More RBC,s revealing synthetic internal structures and altered membrane.
Here is the zoom out to get a wider grasp.
It is amazing, yet disturbing to see such a beautifal exhibition of all these sythetic details. At the same time as feeling priveledged and please the microscope is performing so well, im mortified. These variances and distinctly bold alteration effects are so easy to follow and capure now.
Various different RBC’s going through alteration. Some have always seemed like they are unique to others. Likely providing different functions.
We see the usual blue particles scattered and various complex lipid round bodies in the plasma. A good variation of the blood cell, sizes, alterations, and arrangements can be seen.
It would seem the blue cells are different to the clear, larger cells which have generally quite different material compostion inside. This is a sign of multiple processes and extreme product complexity in this view alone.
This image speaks of the above, but it is important to notice the diagonal chain of lipids which have floated up to the slide cover as fatty lipids tend to do.
In these post we do not focus too heavily on other structures but we can see some lipid trails exhibiting notable optical presentation which seems closer to that of anything but natural lipids when comparing other studies.
Here is another RBC enlarged and revealing more synthetic features.
Upstairs here we have another really detailed shot inside this RBC top left. Make no mistake, that isnt what proteins stripping or cell degredation looks like. Yet again, for many reasons including, size, difference, morphology, and layout this cannot be confused for natural biological material processes. These materials are polymerically chained often, have ordered or programmed assembly patterns, they are large materials after construction. ranging from low nm size all the way up to 2 um and more if assembling chains or other composite structures.
NOTHING TO SEE HERE………BACK AWAY FROM THE BLOOD VEHICLE!
Some of the altered RBC’s are far brighter than others with many taking on completely different sizes and final product appearances.
Another composition.
A REMINDER TO OTHER RESEARCHERS AND SCIENTISTS!
High-end optical equipment, powerful lighting, high-quality objectives with adjustable aperture, and industrial grade imagers are required to see this much detail and realism. I hope others explore the same, the right people really need to of course. I am reluctant to give away my personal system modifcation and designs freely. I am sick of everyone claiming things for themselves and not returning the favor in a productive, helpful, or meaningful way. Ill just sit on it for now, unless something comes up. I have little interest in personal gain since i don’t live a normal life with all this going on anyway. But, this is not a cheap line of work either and progress comes far quicker with resources as always.
At this earlier stage the centered RBC reveals a lipid like membrane structure to components forming on the inside.
Almost out of the vesicle form inside the above RBC and headed towards the material fabrication stages.
With the Objective aperture open more and showing less colour but more glare we can see the very bright membrane areas of the Hybrid lipid particles as they expand into complex vesicles that have even brighter halos.
above and below shows areas of dense and slowly forming artificial lipid structures, some reaching the large and massive lamellar vesicle sizes. Another detail many will never see with many microscopes, the colourful and differing material properties.
This is the same image as above, but with the aperture closed just over 2/3rds of the way. We get more colour and resolution, but lose light power. But it is essential to view some of the materials this way. Look at the lipids now, you see distinct colour and membrane differences. A broad range of complex materials can be seen in these shots.
Synthetic materials also forming outside of blood or other membrane areas such as vesicles. Part of this material can form in the plasma also.
Networked materials with crytsal phases appearing in some arease. (above).
A fantastic catch of both smaller hybrid lipids and altered RBC’s in different stages of working.
The colours seen in this cell are almost fluorescent, the outer membrane in mid transition stage as it loses any last natural RBC features and begins to transform into a thicker polymeric vesicle type cell. Wathcing the various transitions can be very intrigueing and there is no mistaking these repeat transitions processes.
The small round halos here with their thick yellow membranes really indicate the nasty nature of this material. We could only wish this is what an mRNA vaccine you didn’t even take looks like. But this is advanced materials at play. And no, it wasn’t china! it was all of them……see posts on swabs!
Another display of colourful lipid-polymer networks floated up toward sthe slide cover slip. Various transhuman RBC’s in the plasma just below the lipids and left/right.
Our video below catches smaller liposomes with blue particles moving internally on the left next to the RBC which has similar membrane apperance and highly reflective material instead. Other cell stages and types also present. Spherical bodies seen floating in the plasma of various sizes and types. Nanoparticles, lipid structures, and other debris.
Thank you everyone! Those who have supported have really helped get this cutting edge viewing ability to form. A small amount of contribution over the 2 years has taken me leaps and bounds while working with what little is afforadable to me. The Thermo nicolet FT-IR 6700 spectrometer still needs parts replaced or whole unit to be replaced since it isnt functioning yet still. It has a minor issue, but it takes a long time to troubleshoot complex technology without service documents that pharma industries stop you having for the very reason of controlling public research and knowledge. You would think they like to encourage science, but that isnt the case. They do the same with all types of high-end lab gear which could validate or detect chemical materials accurately, read small signals, and more, they hide technology and access to it behind contracts and pay walls. That isnt an accident, it is controlling knowledge. Those issues can be tackled with planning and special arrangements. but, it still costs even on used cost basis with parts scavanging.
If you appreciate my constant efforts and time, please help the cause and speed up research by contributing to equipment supplies and more. This cannot continue without the help other other living men and women !
Help out with KO-FI Thanks !
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