One of the newest ( last 3 months or so) things I have noted is what I have been calling aromatics in the blood. Its when there is a haze formed, under certain areas of the cover slip, of "bubbles" that makes it hard to see what's underneath. What you can see underneath does not look normal nor healthy. A gas would make 100% sense of this.
yes - but this would mean that more of it appears as the infestation increases and the process is accelerated. The question that arises from this - what can be used to bind it so that it does not continue to multiply?
Wonderful SAM!!! I think you just solved (discovered?) one of the most important medical issues of the past 50 years. I have been racking my brain for the triggering factor in the debilitating health issue that has tormented me for 40+ years, and effects just about everybody now. In 2024, it seems to hammer particularly hard most everyone I know over 45 years old, and many younger healthier people too. I'd like to say more later, but I need to blast this information out to a couple of hundred people. No worries, I'll suggest to them that they subscribe to your substack too <g>!
Yours and the good doctor in the video's mention about the concept of "archae" sparked a memory of where I last saw discussion of the concept. I happen to have an entire document devoted to my findings on the uber creepy optogenetics and how it is used to remotely "manage the herd" using light of various origins. Could it seem to square with the whole concept of the non-linear optics conversation?
Here's an excerpt from my Optogenetics document:
"Bacteriorhodopsin
Bacteriorhodopsin (BR) is one of the simplest and best studied optoelectrical transducers from the microbial (class I) opsins, found in archae, eubacteria, fungi, and algae. It is a protein with seven transmembrane domains that acts like a light-gated active ion pump—it captures photon energy via its covalently bound chromophore, retinal—and moves protons against their electrochemical gradient from the cytoplasm to the extracellular space. Since their discovery, the microbial opsins have been viewed as potential components for bioelectronics and a new generation of optical memory because of their ultra-fine spatiotemporal control by light (i.e., their ability to address single molecules by focused light at very fast rates). The latter is of equal interest in control of eukaryotic cells. Structurally and functionally, BR provides good insight for optogenetics as it shares high homology with all (class I) opsins currently in use.
The New Generation of Single-Unit Optical Actuators
Current-day optogenetics began with the characterization and cloning of ChR1 and the higher-conductance light-sensitive ion channel ChR2 from green algae by Nagel, Hegemann, Bamberg, and colleagues in 2002 and 2003. This was followed in 2005 by the first robust demonstrations of the use of ChR2 to stimulate mammalian cells. Upon heterologous expression, these microbial ion channels provide excitatory (cation-mediated) current with relatively fast kinetics and can effectively trigger electrical impulses (action potentials) in excitable cells upon light stimulation at relevant physiological rates.
This demonstrated usefulness in neuroscience revived interest in other types of microbial opsins, discovered earlier and extensively studied within the microbial photobiology field. These include the chloride pump halorhodopsin (HR)10 and the BR-like proton pump archaerhodopsin (AR). Both have proved capable of providing outward/hyperpolarizing current in mammalian cells."
Hi Sam,
One of the newest ( last 3 months or so) things I have noted is what I have been calling aromatics in the blood. Its when there is a haze formed, under certain areas of the cover slip, of "bubbles" that makes it hard to see what's underneath. What you can see underneath does not look normal nor healthy. A gas would make 100% sense of this.
Best Regards,
Matt.
Hello Matt!
yes - but this would mean that more of it appears as the infestation increases and the process is accelerated. The question that arises from this - what can be used to bind it so that it does not continue to multiply?
Replication via the gas level is something new...
Best regards
SAM
Wonderful SAM!!! I think you just solved (discovered?) one of the most important medical issues of the past 50 years. I have been racking my brain for the triggering factor in the debilitating health issue that has tormented me for 40+ years, and effects just about everybody now. In 2024, it seems to hammer particularly hard most everyone I know over 45 years old, and many younger healthier people too. I'd like to say more later, but I need to blast this information out to a couple of hundred people. No worries, I'll suggest to them that they subscribe to your substack too <g>!
Then please take a look at the article https://open.substack.com/pub/sam368/p/pegasus-and-medusa-nanotechnology?r=2xsfdn&utm_medium=ios
Silvia and company,
Yours and the good doctor in the video's mention about the concept of "archae" sparked a memory of where I last saw discussion of the concept. I happen to have an entire document devoted to my findings on the uber creepy optogenetics and how it is used to remotely "manage the herd" using light of various origins. Could it seem to square with the whole concept of the non-linear optics conversation?
Here's an excerpt from my Optogenetics document:
"Bacteriorhodopsin
Bacteriorhodopsin (BR) is one of the simplest and best studied optoelectrical transducers from the microbial (class I) opsins, found in archae, eubacteria, fungi, and algae. It is a protein with seven transmembrane domains that acts like a light-gated active ion pump—it captures photon energy via its covalently bound chromophore, retinal—and moves protons against their electrochemical gradient from the cytoplasm to the extracellular space. Since their discovery, the microbial opsins have been viewed as potential components for bioelectronics and a new generation of optical memory because of their ultra-fine spatiotemporal control by light (i.e., their ability to address single molecules by focused light at very fast rates). The latter is of equal interest in control of eukaryotic cells. Structurally and functionally, BR provides good insight for optogenetics as it shares high homology with all (class I) opsins currently in use.
The New Generation of Single-Unit Optical Actuators
Current-day optogenetics began with the characterization and cloning of ChR1 and the higher-conductance light-sensitive ion channel ChR2 from green algae by Nagel, Hegemann, Bamberg, and colleagues in 2002 and 2003. This was followed in 2005 by the first robust demonstrations of the use of ChR2 to stimulate mammalian cells. Upon heterologous expression, these microbial ion channels provide excitatory (cation-mediated) current with relatively fast kinetics and can effectively trigger electrical impulses (action potentials) in excitable cells upon light stimulation at relevant physiological rates.
This demonstrated usefulness in neuroscience revived interest in other types of microbial opsins, discovered earlier and extensively studied within the microbial photobiology field. These include the chloride pump halorhodopsin (HR)10 and the BR-like proton pump archaerhodopsin (AR). Both have proved capable of providing outward/hyperpolarizing current in mammalian cells."