The

Grid.

CONFERENCE OF CREATIVES

Medical Graffiti

Medical graffiti page one.

but it really is meant to be condition based, for many pages condition named, and each page is like a web-board where facts you consider true, or theories you have can be posted like graffiti, to help with that condition.

even patients can state what diet helped say. And docs can graffiti things they have discovered. The grid is the basic grid of where you can form ideas, with nothing calculated but the medical graffiti placed on an xy page. A very basic system, of making a page of graffiti'ed things.

Later organisation may occur.

A page called parametric medical, where there is an info-parametry system and other fields auto update vs others, through all medical; conditions with the body as in its natural state being the normal info parametry zero'ing. And you can output programming field tests of new theories vs data observed. say get it down first to

observations on one side, and theory linking on the other side.

But really its meant to be biochemical cycle linked, and test test theories vs biochem cycles, and then vs physical test procedure outputs, or observations.

Is also meant to find common biochemical cycles across the board of conditions, and link them. Can be PLL type system also (phase locked loops, as in electronics) in the programming to find ever nearer biochemical truth for the test theories.

but this whole site and the state of medicine, we need the scientific bias check (from other theories) check system made parametric so each time you gain bias check data, and can also help with the condition anyway, of side notes, of things you never knew about it before, and a sci bias check system even if some ideas fail, would always bring people nearer to the answer, (but I would like like it parametric on top, so you never waste time or money, cause becomes linkable).

Its what I want this to become, a non fail bias check system, that is parametric and always gets nearer to that condition, or links to others too, and doesn't produce no useful result ever. So time and money never wasted.

And also the "really real link" tm haha kidding, of actually can be used in altered metabolism disease states, from patients statements, and how to actually use it real world. and this may be running parametrically opposed, while you are doing the biochem one of them using diet, so they might be faster than biochem. but yeh.

eventually might end up with some medical condition periodic table, or fields to be filled,

but this is much harder than the making of the chemical periodic table. and it has to work real world, and cures real world, from the "really real link"

Cancer/HIV:

Heres one from me:

no marmite, no milk,

poss bgh,

and vit mimics, and vit mimics like dna base mimics, as carcinogenic, and also maybe calcium amping, and too much b12 cobalt, and zn disregulated due to low copper, and hep changes the dump rates of any elements, may be good for hiv too if is actually HIV is a archaefungus, and needs copper and ascorbic acid as well, you know the copper antifungals are the thing you may need.

and maybe helps with ebola too, some copper.

And with cancer.

so my cancer diet:t:

you can remove marmite, and beer yeast if combines with carcinogens in tarred bodies.

you can not have calcium pills. Not have dairy for Bovine growth hormone. taken zinc from protein source only, but not from bacon or ham as it contains nitrites, which can produce floating cyanide possibly with gut methane pressure, and can kill you if you have been eating gluten, or have intestinal/bowel cancer.

Maybe some copper to stabilise zinc, but you need only trace amounts. If you drink you may aslo be losing elements. Cancer is prob a system that leaches bone to find copper. It will go anywhere it can to get some, and is often made of rogue immune cells, or allowed by rogue immune cells. But the vitamin mimics are also involved, as well as BGH, making cancer more than a quick energy storage medium as well as element seeker.

They def need to element test people more often, and people with HIV could have lowered copper.

The DNA BIOS of Na,K, Mg,Ca, and the dopers maybe be disturbed in hiv, allowing retroviral entrance. I believe it is a fungus because retrovirus cell wall lyse and release is like sporing, and it just screws everything up.

HPV thought of in cancer recently is prob a fungi virus too, cause although it is called a virus, it infects the DNA BIOS and creates fungal effects, like happens on plants.

ebola is another tropical fungus really rather than a virus. Maybe we just call fungi fungi from the effects seen, so even though we know its a virus, WE are its medium so it is egotistical to call it just a virus, and not a fungus.

could people need nickel too. copper and nickel in traces to make zinc function well in HIV and cancer. Maybe viruses mimic element holography and looks like certain element poisonings or deficiencies. as to idea on right.

nickel would be bad in less than trace, as would copper, but hows the bone storage of copper and nickel in cancer and hiv. and the dump rates through urine and foecal.

ie. does this nickel-zinc-copper triangle prism of control need to be there to help cancer and maybe HIV too. you need to make a program for bone elements, and if they are being accessed by bone eat enzyme (the osteoporosis one) and the dump rates, and test flaws from bone eat, of high calcium, and the urine and foecal elements test in a parametric spreadsheet system, with html output say, for ease of use. or a form field box for nurses once you have it working.

Virtual element conditions in the body

remember that thing on New Scientist, where you can make virtual atoms as holograms,

well say you had no copper say, and was factors happenning bn nickel and zinc, well maybe virtual copper atoms can occur, and there is a flaw in that it can create stable holes, but something in this could allow the energy barrier of trace cadmium or stuff like that to replace it, or else ther can be holographic cadmium or palladium conditions causes by say low copper, and hey then you get HIV, except for that virus that was doing it. or virtual element atom conditions in the body could help retroviridae work, it gives them this process mechanism which is very powerful, and which current science cannot understand.

It can alter tests too. water is the bodies transistor, and thats a great medium for holographic virtual element effects, all those water prisms (slash inverse prisms)

god knows how some of these viruses really work, holography wise, and virtual element wise.

Gearing machines:

On the backbone of the dna, there are phosphates. To these phosphates, the dna main bios elements combine of mg, ca, K, Na.

The twist of teh helical dna happens naturally from entropy flow in water.

But can the dna helix be a worm gear?

A dna helix that worm gears the water structures that form with the transition metals. Ie. I am talking about water wheels made of triangle water molecules, bound in transition metal chelates. And there may actually be worm geared wheels off the dna helix, for the water transistor, and this may be the function of the further tranition metal doping part of the water transistor bios, some sorty of CMOS or something, using water wheels.

The bios may bind to the dna backbone, and runs electronically directly these water wheels, or else it also be mechanical, ie. non chemical debond-bond off the dna backbone, as in teh bios chemicals bound to the backbone are not chemically debonded, but actually physically (at least by electrostatic forces, if not touch, turn water chelate wheels)

OR bioth systems may run for turnover of the BIOS at once.

It may be true that these water wheels created DNA in the first place.

but I guess they could be 3d spheres as well for cnc water movements in 4 axis movements, or 5 axis.

They could interchange water as set blocks of a chelator and some amount of h2O's, all sorts. so its like dna too, but an evolutionary waterwheel system.

I bet you this is prob how dna first got formed, from these cnc chelate waterwheels and spheres.

All it has to do is move amino acids into position by acid end and cooh end, and probably can cnc move sugars too. But it would be able to position them with intense accuracy, and would love making helices off water spheres.

Tjhey are math opposites.

So thats probably the evolution of life for you right there. then combine that with normal lipospheres auto arrranging.

hOW'S THAT FOR SELF ORGANISING MOLECULES THOUGH AYE? CNC BOTS EMPLACING AND COMBINING DNA BASES. WHOOPS I SAID AMINOS BEFORE. SHIT MAYBE BOTH BUT WHAT CAME FIRST THE ENZYME OR THE EGG? THE ENZYME OR THE DNA BASES WITH SUGAR AND PHOSPHATE ON THEM (PLUS THE FOUR MAGIC SALTS, (IN A MASS AND PERIODICITY FOUR SQUARE MAGIC SQUARE)

LIKE I RECKON THAT HAS LITERALLY GOT TO BE TRUE. DEF THE CNC MOVEMENTS AND POSITIONING OF EITHER AMINO PROTEIN MAKING FIRST, OR DNA MAKING TOO.

YOU JUST GO LOOK UP SOME YOU TUBE VIDEOS ON 5 AXIS CNC MACHINES, SEE THEM ROTATE OBN TEH AXES ETC. i RECKON COULD MAKE EVOLUTIONARY PROGRAM FOR IT. IN SOFTWARE, BY SPHERE AND HELIX AND AMINO ACIDS MADE ON THE OTHER SIDE OF THE SPHERES SAY, OR SEVERAL SPHERES ON, BY GEARING, (HEY AND THE GEARS OF MANY COULD HAVE BEEN PRE-ORGANELLE), TO FORM PROTEINS WHILE FORMING FORMING DNA AT THE SAME TIME. tHEN SOMETIMES AFTER THAT GOOD PROTEINS WOULD DESTROY THE DNA OR ALTER IT IN WAYS, AND MAYBE ALTER OTHER PROTEINS OR WATER WHEEL FUNCTION IN AREA ELECTROMAGNETIC STATS TOO.

OUT OF IT.

ANYWAY. THE WHOLE BODY PROBABLY DOES ACTUALLY WORK BY ELECTRONICS COMPUTING PLUS GEARING COMBINED. SAME WITH PROTEIN FOLDING, ITS MECHANICAL AND ELECTRICAL.

AND THE BIOS WOULD BE ELECTRICAL AND MECHANICAL TOO.

THE WHOLE OF BIOCHEM WILL BE JUST THESE TWO AND THATS IT.

BUT ELECTRICAL MIGHT MEAN BONDING, AND MECHANICAL MEANS EM FORCE REPULSION OR ATTRACTION TO CAUSE A PHYSICAL MOVEMENT OF THE ELEMENTS/ MOLECULES INVOLVED. HIGHER PHYSICAL MOVEMENTS ARE MAYBE STILL REALLY THAT BUT IS THAT BIOPHYSICS FOR STRUCTURE MOVEMENTS.

If not the organelles the chelate waterwheels could have acted as a core former for such cell cycles as the citric acid cycle and then dropped away later. or at least i assume they have dropped away, and there not still some chelate waterwheel or element sitting in the middle of a tca wheel/effective wheel over fluidity of a an area, but with the wheel ratio of that metal chelate amount vs the tca.

GEAR PATCHES:

SO OK ON THE RIGHT IS THAT GEAR THING. BUT WHAT IF CANCER AND HIV ETC CAN BE SORTED OUT BY THE PERIODIC TABLE.

YOU NEED TO THINK ABOUT WHY CANCER HAS WOBBLED OFF CORRECT BIOS FUNCTION.

AND ALSO WHY HIV CAN SPIRAL IN

THINK ABOUT ANIONS FOR THE TRANSITION METALS MAYBE

LIKE BIOCHEMISTRY ONES.

SO YOU CAN MAKE A SHAPE GEAR PATCH. OF SAY CANCER VS NORMAL CELL, AND SEE IF IT WORKS.

PO4

Cl-

H+

HERES A GEAR PATCH FOR CANCER FOR THE TRANSITION METAL WHEELS HAVE FAILED DUE TO LOW COPPER, AND CANCER IS RUNNING THIS TRI ANION PRISM INCORRECT.

IT CAN AFFECT:

ATP

DNA BACKBONE

PROTON PUMPS

CHLORIDISATION OF CANCER FUNGI, FROM STOMACH ACID PLUS BASICITY BINDING IS TIED

prob crap

hERES MORE PATCHES:

SOME 4 FACTOR THING, WITH ONLY RECTANGULAR CONSTRAINTS

a SQUARE EFFECT FOR DEF ITS DIRECTLY REVERSED TO THE BIOS, FOR CANCER FIND ALL four FACTORS,

BUT THE BIOS IS MAGIC DIAMOND OR SOMETHING REALLLY. OR A PAIR OF RECTANGLES OR SOMETHING, FOR MASS AND PERIODICITY.

The waterwheels theory:

wouldn't mind calling the above the waterwheels theory.I used to theorise that dna formed inside zeolite tubes but no, its probably this cnc waterwheels system

I suppose another name could be "waterwheel pick and place QNC robotic self organisation theory"

QNC for Quantum Numerically Controlled, or BNC for bond Numerically Controlled.

or FNC for Field Numeric Control, of em fields off those molecules. or Force Numeric Control, Van-Derwaal plus molecular bonding forces involved.

Legal: The data on this page is not to be trusted as correct until confirmed, and this page doesn't do confirms. If something sounds great, it may still end up being rubbish. so beware this page, but also beware the status quo. There can be deadly theories not changed for years nor challenge checked, or have never been really checked for truth well to proper standards and socially accepted in the status also. But don't be silly and not use your head on anything here. This IS the wild west.

ACORBIC, RIBOSE FOR DNA AND ATP.

ACORBATE PROB CLEANS DNA BASES OF THE KEKULES TO MAKE SURE NON CARCINO FROM OX ATTACK.

TRUST ME :

GOTTA BE A CLEANER, OH SHIT BUT THINK ABOUT IT, WHAT ARE GENETIC CONDITIONS? DO DNA BASES GET DUMPED, OR CHUCKED OUT UNTIL YOUR METAB IS RIGHT. SHIT YOU GET STUFF LIKE PHENYLKETONURIA AND STUFF MAYBE. JUST TEMPORARY DUMPING.

AND, WILL BE DUMPING PHEN UNTIL HAS REROUTED THE WATER WHEELS

FOR REFIX THE DNA.

SHIT ITS CONTINUOUS. IT CONTINUES TO THIS DAY, THE WATER WHEELS HAVE BEEN RETAINED AS BACK CMOS TO REROUTE DNA AND AMINOS TOO.

BUT THEY DO IT CAREFULLY THOUGH, CAUSE USUALLY THE PROGRAMS ARE RIGHT. SO THIS EVO GOES ON TO THIS DAY, OR THE WATERWHEEL SAVE CHANGE, BY YOU PROB LOWER PHEN IN PHENYLKETONURIA, AND IT CAN LATER THE DNA AND WATER WHEEL CNC'S BACKWARDS AND REUOUTE THEM OFF THE TRIANGLE BY REMOVE AMINO OF PHEN, THEN IT WILL REOUTE THE CRAP DNA, OF ALL OTHER AMINOS USED, AND THIS TRI SYSTEM IS FAIR TO ALL HUMANITY, BUT YOU DO HAVE TO DEAL WITH IT AT TIMES. BUT NOTHING PERMANENT WITH THIS TRIANGLE PROCESSOR.

In the days before archimedes, everyone was a fool, so nowadays I am a new archimedes then, besides the math, for the dna and protein problems never used to be very intelligent at all of using two systems without waterwheel base.

HIV in cows grows general antibodies fast

This is the big symposia going on at the moment, about cows being used to griow HIV antibodies, and it makes the general affector ones faster.

Well one bias is that the cows don't have hepatitis, and are fed well with plenty of copper, zinc, nickel and the other d blocks of manganese, chromium, vanadium, scandium and iron of course, and cobalt is there with no b12 mimics from marmite.

Well it WILL help them make antibodies fast and well, and the no vit mimics will be there too. Monkeys handle HIV better due to this too I guess.

We make our own viruses? Viruses appear from nowhere? Like spontaneous creation

I remember coming up with this theory that the immune cells could use immunoglobulins to manufacture viruses, and it would be great for altering body conditions, like with T-phage dna alteration say, but it may do it due to low copper to change the waterwheels to dna to protein system, and patch it for low d block conditions. ANd HIV could be the bodys own virus. used for dna alteration. Having your own virus making stuff ready in the immune cells repertoire could be evolutionarily more advantageous.

BUT

if this is true and d block giving can help HIV, then it is just unwriting the viral use procedure of the immune cells backwards system, as we don't need it. In this context, what are general antibodies.(which is not the actual name of them, more like general affector antibodies or something). But what are they again, just some float around whole encompassing does stop HIV ones, without detail, which actually works better for hiv since is aretro, and specific ones are bad, so that's what they are.

but in this context, what are they?

Not the synthesiser antibodies.

Are these cows getting human genes in them here?

as a side note.

generally in health, with d blocks, the dna etc. and all immune cells work well, but in d block deficiencies, it would make sense there was a dna alter phage, and HIV might be one. It works close to the human cell, and is a hard drug target.

but its attacking immune cells? Imagine how much change would be required in the metabolism if some serious d block elements weren't there. An internal virus t phage'y thing but a retroviridae maybe could make sense, for rewriting the genome temporarily until the d block element is back.

Poss cancer and HIV related in ways also. needs to be parametric info table-ing checks I think.

but I am sure that all conditions run waterwheel-DNA-protein system to self correct at any of the three places. I think this is a rule written as to how life formed first and must be annotated as a scientific self correcting cycle, and made connectable to old medical theory systems, which are pretty poor. Thew system may need to be made deeply parametric.

hiv in cows

A note about antibiotic resistance

I thought an interesting thing to think about would be that if herbology herbs in some cases did not cure a bacterial infection say, that still they are or could be important as "mutation re-aligners".

I know that some do actually have antibiotic and antiviral properties of course.

In this theory however, the herbal substances,can realign bacteria, and the oddity mutations that have occurred off use of singular non tri/fibbo antibiotics(:will explain later), that have turned the bacteria in variious strange and dangerous directions.

The theory of tri/fibbo antibiotics, is that herbs are these, or some, and these contain a chemical array in a triangulation of bacteria, or viruses, and use slight differences of compounds, but these are all there, perhaps in a fibbonacci sequence, and if were coloured would be the chromatographic rainbow of them. But this array mechanism of slightly aleter antibiotics can kill bacteria or viruses in a better way.

I also have this other idea that the immune cell is a snobby gourmet eater, and likes to engulf any new bacterium strain most of all, and but however may also be a preservationist of rare bacteria, by allowing the bacteria that are rare into its immune cell ram or genome, (to create an "ignore effect") (hey or perhaps it just hasn't found tri-strain immunity and formed tri-antibodies yet.

Also another idea for tri antibodies is that the y-antibody, can actuyally post process, and be released with the third back end of the y in some cases becoming a coagulator of viruses or bacteria, to enmesh them liek a spider, so then even HIV or ebola could be fixed, if it were only sitting still. This coagulation mechanism may also be a mechanism, of the triple headed y antibody.

Anyway, the alignment of bacterial mutations back to the natural plant animal relationship is very important, and this may be needed in todays age of failing antibiotics.

Also for cancer, the "ignore effect" above may be occurring, from a vitamin mimic process.but sometimes things like viruses, say HPV, or bacteria can make possible carcinogens or vitamin mimics also, but some viruses work into the dna, which i suppose hpv does.

Makes you wonder if viruses or bacteria alter our vitamins or some regular molecules to use for mating calls, or pheromones.

But AFM wise, I wonder if you could study mating calls of viruses and bacteria, for at least bacteria have a pillus. and listen to them by sound conversion of the AFM tip as bacterai go past the tip, But it would be great to know something liek the ebola mating call and the phereomones it uses, which are probably converted from our molecules.And if you can screw with them which may not be possible perhaps, you might be able to slow them or confuse them, or pheromone attract them towards the bladder or something.

Another random idea about HIV:

mm, so if with the d blocks for low amounts of them and the immune system can make its own dna changer stuff for changing metabolism so as to deal with low elements.:

Well do you think there could be low phosphate in hiv too.

This may also happen just from the idea that hiv is from outside, and is not an immune system created one, (or even allowed one, from snob-eater immune cell theory):

but it could be bad too. If under the conditions youi need nmore phosphate in HIV infection, then you give phosphate, it might crank up rna production maybe. or it may help. don't know.

you could try some copper phosphate or other d block phosphate too, if the phosphate way is the best way to kill an hiv virus, (for the deeep-reach idea, of salts deep reach, as antifungals for archaeofungi.

But you wouldm't think the immune system would create viruses for rerouting dna, by just low phosphate right. Prob not until the bones were near gone.(appearing to be osteoporosis)

HIV AS ARCHAEFUNGUS AGAIN: MORE ON:

Well, the micreme stuff is supposed to be the best stuff for fungal infections. I wonder if the chemical can be ingested in HIV. Miconazole nitrate or something.

I wish I has done drug design and synthesis at Uni but had to leave due to brain cancer.

God- dammit. So I don't really know.

You know that famous HIV guy that combined three drugs together, as a cocktail.

That worked well apparently.

I wonder if you could make an antiviral/antifungal mixed molecule that kills HIV. Or if just miconazole nitrate would work. But at least it would work in petri dishes, surely, which you would try first of course. Apparently sometimes they don't work the same in vivo and in vitro due to metabolic alterations that occur, or if the drug reaches where it needs to go.

That triple dose thing must have triangulated it well. Maybe one was an antiviral and one was an antifungal and one something else. Who knows though, but that would eb a good thing to try.

But mutations are really worrying, is the problem. I wish you could have a mutation studier, which would use antivirs vs antifungals, and the molecules are used in 2 paired, or two of one and one of the other etc. until you can triangulate the best HIV drug. But I don't think you can do this in people, I guess.

Maybe its better to try it in silico first, to give you some clues.

But it might fit in with that array theory I came up with ages ago of the way natural herbs have a range of variations on a single molecule to create a triangulation (this also is true for mutating viruses and bacteria well to reflash them back to plant animal relationship way, from dodgy new mutations, off the silly way we use now, and could cure majorly mutated bacteria or viruses , by retraining them.)(in theory at least).

It might be true that combined antifungal and antivirus one although may be neat, if was in one molecule, still could suck cause of non triangulation, by floating in water of two different ones are better. I dunno.

But you can do in silico math and sims on it.

THEN you can make some generic sim amth triangulation theory software tool

THEN you can fix ebola

and EVERYTHING ELSE!!!

using that same software tool.

but they already have those viral things of inserted rna that work already.

But good to think about other methods too. Unless you are a purist analist.

Its a fairly purist analist new basket in itself to put eggs in to.

Rheumatic fever:

I reckon its maybe some bacterial infections and virus colds and shit, but also its like roack bites which have eaten white tails when have low food, and hence they bite you for some food. But always its evolutionary for insects to by pphysical oragns to isolate bac or even white tail or any poisons in their bite, so maybe cockroaches can poison concentrate too, All it does is run poisons to a body position for the insects. It jsust concentrates it and gets rid of it, but when you get bitten if was a hungry roach that had to go rogue and eat white tails, or daddy long legs'es, umm then it can bite you and teh rheumatic fever is like a bite, and its just bullshit its not part of it is a bite.

Fucking like fuck its just that, of bacteria normal.THATS BULLSHIT!

IT SERIOUSLY LOOKS LIKE A SNAKE BITE OR SOMETHING.

WHAT THE FUCK IS THIS BULLSHIT

Ebola:

I wonder if prebioticaly, if ebolas rna could be compared to higher worms. like roundworm, hookworm, threadworm whatever. even earth worms.

Ebola has the surface area to act like a worm instead of a virus that they call it.

They call it the ebola virus maybe they should call it the ebola worm.

And with this computer circuit thing I have going on, for the body is one, you could compare it to a computer worm too. which are reall assholes, and so is ebola.

Cancer again.

I remember having an idea that cancer was a bioplastic. I had various ideas on it. A bioplastification process, yet still its alive supposedly. Probably it could be considered, if plasticising to be about as alive as a virus.

What about butanoic acid as a plasticising thing. From the two incidents after drinking chico-de-oro coffee with orange juice x a litre or more, led to polyp in veins, which can cause heart attacks and strokes, thought was caffeine ascobate formed under stomach HCl, could be old coffee, and a bit butanoic acidy. dunnno about that one really, the coffe was not that acidic, but r-cooh does restrict veins.

but yeh it formed a ball that i could not crush with my fingers as it went through my leg veins. I reckon it formed a rubbery sphere. one that was equal or greater to the rubberiness of the vein cause could not crush it. A very strange thing to happen twice.

causes dangerous sleep apnoeia also.

not good.

bioplastic wise, maybe butanoic acid, or just methanic acid. but maybe H2S can do it too.

Anyway cancer may be a bioplastic, but a metabolic one that can grow.

may not fit with mrs gren.

Maybe should add an IQ thing to mrs gren at least. cancer seems too uncontrolled/non regulating to be alive.

Or could have a second type of mrs gren thing, with deals with self regulation/intelligence.

MRS GRENI maybe.or MRS GRENIRS.

What might be a cool thing is trying to use gases perhaps to make cancer bioplastics. and if its not gases then some other way. Its easy to synthesise in vivo cancers from kekule structrues which are carcinogenic, but out of a body, it is hard isn't it. well is it.

It may not be.

But perhaps the first carcinogen thing is not the plasticising factor, th repeat thing. dunno how wasteed the time may be on this unclear/incorrect poss thing.

I also had this idea on with the computing theory of the body stuff, water transistors etc. that the body works as a crystal system off kekule carbon cyclic crystals. And it actually does. The vitamins are an example and theres haeme, theres plenty. But yeh when carcinogens come in they disrupt this kekule crystallisation in the body.

Like with minerall crystal formation say, (you could have bio crystal geology as such, but named something non geo maybe) but with the body there is an added factor of time and the IRS on MRS GRENIRS. If that could be made into math theory of even compare the two, then . ie. the bio geology, and the IRS addition made math too, you could get some great stuff.

HIV vit mimic post processing

If cancer pause diet is remove bgh and vit mimics, like caramelisedf yeast extract, perhaps hiv can add side groups to vitamins and create a similar immune and cell screwup, that vit mimics do. very interesting.

focus on just rna into cells may be prior/in conjunction. maybe if you could bind viral free radicals created it would make also a change for many viruses being combatted.

Maybe with diabetes

maybe with diabetes, youi would need maltobacillus, or some sort thing off wheat grain, that coexists. even some gluten eating bacteria,

but yeh can lactobacillis already break any double sugras, like maltose from beer and bread or what, and cause we cook bread a lot all those bacteria die I think.

Another idea for diabetes:

some emulsification enzyme:

emulsifiers do help, but that was from fizzy lollies, which have sugar in them, so not a great test, or from ice cream which has lactose sugar, and sucrose.

You'd have to try isolated food emulsifiers in the correct delicate amounts, but these also can release cigarette toxins and poisons, and yeh,

if you don't know the marmite and bgh remove pause cure you can be killed possibly.Plus you need to know how to detox. if was an emulsification enzyme though, dunno how specifically metab related it would be, so emulsifier drugs, dunno.

HIV as archaefungus: VY dangerous!!

I probably shouldn't have this public.

But will put it on here for intelligent people.

Well,

I think that the colour substances from archaebacteria may have controlled teh archaefungi from infecting them, the sort of colour molecules you get in those famous rock pools coloured.

but umm, if we did use the archaebac colours, couldn't HIV mutate over them to forma full blown new virus worse!!!!.

Right from a really basic things that used to happen deep down in the annals of the formation of life times.

The mutations may be very bad.

ANd also just isolating those colurs is not really using the bacteria themselves for their in vivo factors, and this controlled the archefungi.

It would be worrying. What do those archaebac colour molecules look like.

I know that colours in fruit skins can be antibiotic. They have to be to protect the plant. They may be antiviral and anti fungal as well, which is the colour kekule electron zapping of the viruses I guess. Pretty much could burnm them maybe even. But it def disrupts them. The old lock and key thing too from my biochem papers dunno.

So yeh these archebac colours. waht the fuck are they, are they metal based?

Anyway in silico for ages.

Pi units:

base pi units:

I am sure if you had a mathematic system of base pi, for the complicated schroedinger stuff, that you could just use integers instead of using pi each time for calculating stuff, and then for specific thing calculated, pi gets calculated then. But if you knew what you were looking for.

Also I reckon there should be a pi computer that they make and you can even arrange the circuitboards in overlapping circles. You could probably make a quantum computer that way with regular compnents. maybe.

But pi computers at least whatever they are would be really good. you could even have a special programming language converter for holographic or pi circuitboards. If the circuit boards were circularly holographic, sort of radio light speed back effecting transistors and shit, they would calculate pretty fasr through the many circoles overlapping on the circuit board. you could make new transistors that have a radio metal dish plate on them and it can transmit as a holo quadristor within that circuitboard circle, and then hence effect a change in another circle connected to that holo quadristor.

Cancer caused by vitamin and stimulants combined:

heres another idea:

I wonder if there can be crossovers between cell cycles and these crossovers can help cause cancer. perhaps half of the molecule is a vitamin, and the other half is a stimulant perhaps.

Nicotine is a stimulant and vitamin mimic in one.

a dangerous thing liek caffeine ascorbate that binds in the stomach from OJ and caffeine is perhaps a cancer causer also. but causes stroke polyps at least poss if have scurvy first only, and is desperately trying to uptake vit c. Some sort of at least stroke causing collagen balls can form, or else it is cancer also.

So interesting.

Either a stimulant salt of a vitamin,

or the simulant and vitamin being in one molecule.

Theres one idea.

It is interesting also, like the vitamin mimic idea. However these could come under vitamin mimics perhaps.

But an interesting idea of

simulant- vitamin confusion causing cancer.

They do have oncogenes apparently however that stop cell growth control.

vitamin-protein translation linked incorrectly in cancer?

In use of methamphetamines, I think at least most times, they have amine groups on them right, and sometime methyl groups hence methamphetamine I think, anyway, when used, I had this idea that it makes people lose protein by binding into peptide groups. SO they become very skinny.

Well with vitamin stimulant salts, and the cancer idea.

Perhaps the vitamin stimulant can screw up protein translation and this mechanism becomes coupled with vitamin using pathways. Which the theory is that that is not meant to ever be coupled metabolically.

And this creates cancer???

are oncogenes real, can genes be made from feedback from altered translation, if cancer sticks around after these vit stimulant salts are gone.

Cancer and metabolic solder cross joints:

Along with the electronics analogy of metabolism, in biochemistry, you can call them circuits. so, supposedly, cross solder joints, from bad soldering can make the rest of the metabolism die, cause voltage alterations and current leaks through the solder joints over, and pretty much can make the rest of the chip or in this case the human life metabolism dead.

BUT: to be clear: In molecular

terms, a molecule that is a salt or of a specila cross structure for some special thing molecule, can cross over metab cycle 1 and metab cycle 2. and make a dnagerous solder joint. so this would be the cancer mechanism, just "cross cell cycle solder joint molecular solder breaches of di cycle molecular molecules" to make cancer, and leave the rest of the life circuit in death. to die like a dying circuit itself. A voltage crossover, wahtever, stop a cap working dunno, but althought those people and their metabolism may seem alive, its dying in fact. simply from these solder cross joints.

ie. cross metab cycle doublex molecules. VERY INTELLIGENT!

yeh essentially it can make the rest of the metab really dead also in definition anyway. think about it. And this is how cancer kills them. You can't even get up again from it. Your metab is fucked, from ONE solder cross joint.

cross metab cycle solder joint theory, or "CMCSJ theory" can be used audited for viruses.

addd on for CMCSJ theory is that for vit mimics from burnt cause cancer, maybe is basic oxygenation and deox pathways from these mimics, cross soldered, cancer wise, could be some oxidating run factor for anti ox-no antiox process but gone nuts with that at least of cross soldered.

post processing immuno globulin tri release viral/bacterial

coagulators

or "tri-globulins coagulator theory"

Interesting idea that the y immunoglobulins can become tri coagulator immunoglobulins for released as just coagulators, for static time attack by immune cells, and could hiv screw with the tri release, or but does that take three strains before immune cells will allow post process coagulator tri globulin release, or could hiv screw with that.

shit post processing ig tri release can explain high ig rates in cancer well a system of release anyway, but that actual cells though. instead of coagulator killers. mm stikll rthinking on that. how come it has a crank mechanism, of too many cells, maybe its some cancer crank of something, but not tri immunoglobulin, but cancers making it fruit instad of tri globulining.

there has to be this time hold thing with coagulators for immune system though ate. gotta be a time stop holder thing aye coagulator system aye,. Shit that holds these things still while the immune system checks their time diffferential parameteres. but hiv and prbably cancer has stuff up the time check holders.

You sit your ass still motherfucker.

and ebola even too has even wormed the "sit still coagulator" process, as new sci term.

sit still thing like getting a haircut from the barbers when young.

but the sit still thing might be the parameter difference for hiv, and ebola worming. like thats all theyd do is control the sit still immune release globulin tris by some wier shit for both, hiv just a triple feect maybe in time and ebola a quad in time , something like that, and can prob if its immunoglobulin tri fior post process, like they use it even to help them, or even nick the globulin or yeh time out the post priocess or know hoow to use it for themselves, but i have never heard of time stop tri post y globulin post processing ever spoken, it must drop off like a flower bud then gets third addition globulin. but if noone knows and it does happen, they couyld be fucking withj it either way even with normal drugs. maybe is a post process enzyme undiscovered even

for tri coagulator globulins and all it has to do is fuck with that.

maybe vit mimic post process though also.

You sit your ass still motherfucker.

and ebola even too has even wormed the "sit still coagulator" process, as new sci term.

sit still thing like getting a haircut from the barbers when young.

for tri coagulator globulins and all it has to do is fuck with that.

maybe vit mimic post process though also.

You sit your ass still motherfucker.

and ebola even too has even wormed the "sit still coagulator" process, as new sci term.

sit still thing like getting a haircut from the barbers when young.

for tri coagulator globulins and all it has to do is fuck with that.

maybe vit mimic post process though also.

That might be ebola and HIV, as well as the vit mimic post processor thing, or even double post processor stuff from hiv's reductant shit viral capsid reductors or vit adders or something, but also like goes along with immune globulin tri post priocessing coaggulator stoppers. Maybe double so have never even seen it test wise.

hold still in time dim pathogen theory or "HSTDP" theory

As well as post process time tri globulin coagulators, for still holding of pathogens by coagulation for correct immune attack, there is also another for this.

this is that antioxidants, of the colour substances are higher above vitamins, and that vitamins are abused by bacteria, as they are part of their metabolic internals often also. it is analogous to say sulphur above carbon on the periodic table, and can "still-kill" pathogens.

And on third theory, just if you fail to have the already elements required above lower elementts in basic elemental periodicity, there will be strange pathways occurring as well and that these are also non combatitive against pathogens, and also that hep post dump rates are higher. and that sugar metab is required to move on for post hep with that basic sugar move form of diabetes.

so there are four, and must whole society include post hep by patch.

So thats the three traingle first fibbo sequence and with fourth start on the start of new fibbo layer.

of these four things for the HSTDP theory which will create a very intellgent method of understanding pathogenicity, and how to avoid its effects.

If from DOD NZ, check above too in other texts above well the whole page for IQ'ing the full HSTDP theory as recents emails related.

old haircut barbers from my youth were on to something all along. Didn't like that much at the time though. But the immune system can do this too. It must remove massive infinities.

yeh the thing of how they just cranked in heaps of plastic coffins for the climate change and the viral changes and shit. maybe some of the plastic coffins will degrade to plastic dust if have this HSTDP theory also, plus other data digital stuff. That WOULD be good.

NEGATIVITY READINESS COULD SLAM CREATE POSITIVITY FIXES. well realism, made unreal some way.

Blood filters

Ages ago I came up an idea of using blood filtering. Talked about it. Not sure if was from some idea from new scientist back in the days though so credit where is due.

Anyway. If its a good idea I will put it here.

For HIV or any virus, you could have blood filters consisting of antibodies bound to a nanolayer. Ones that will hold that specific virus you are filtering for in place on the grid, and so as to lower the blood count.

The pooir points about it is that there may be other things that bind? Unknown. Blood has a lot in it.

Another poor point is that if ebola or HIV or whatever virus trying to heal has put itself into cels already. you would only be filtering the external cell viruses, which might be only half of them.

Possibly you can also find cell binders that bind only infected cells also, poss through a second filter. You might even be able to centrifuge the blood then reintroduce it. But assumedly it wouldn't work, with masses and weights.

Another idea if it doesn't, is to in the body tissue use sonographic ultrasound to kill say liver cells containing the virus, but sound zapping them, but is this really going to help also. You might want the viruses only sound zapped in the filter, or not in the filter by an mri converted.

However it may help in increasing viral time spans for infection kills, which might be handy.You could semi pause it only I suppose. Like 1/3 pause it perhaps with 2/3 of kill rate time gone.

Might be good in an outbreak of something very bad, not that ebola or hiv isn't.

Another idea is refeed the completely sonically wasted and virus released cells of blood into the stomach, with blood regiven from outside. But you would run out of blood quick. I used to have this other idea with HIV or any virus that the HCL coagulated proteins if eaten would provide immune cell lamella proprius intelligence to double blind HCl coagulated proteins vs ones in the blood for creating a food type allergy.Whether its true or not is a different story. Perhaps you can even eat cancer and find the HCL coagulated to dna bios of mag, cal, k, Na free blood double food allergy. or the food allergy makes it able to allergy aids or cancer.

Could create very general food allergy antibodies, which might work. Perhaps there is just not enough cannibalism nowadays haha joke.

But yeh wierd I am sure HCl is like a skin layer bios protection coagulator differential. However look at food poisoning.That seems to be able to bypass it at least temporarily.But is bacteria of course, but yeh.

If you have a blooded up gut, no good either I guess.

It's great when you don't know something however scientifically.

I am sure HCl could be BIOS related.

prob can cure aids with chlorinated dna bios base phosphates or something. Like with AZT. but no. you can't go that far, prob better than AZT though aye. Silly talk though. Phosphato chlorides may be something for dna base Bios salts on dna backbone plus globally over ATP metab etc. but yeh not exactly curing it here, just some data. I know at least is a new idea that the HCl acidity could be involved in HIV bios salt regulation. But I don't really know that either. I just think it may be good as a data check thing for the dna bios, plus general e metab of atp, gtp whatever.

and can they be chlorinated, else acidified from h+ and cl release even for chloride ion kills of retros. Really pie in sky. just more data, but very good basic sci research if done with stomach coagulated by hcl also. like how a proton pump on tail rotor of bacteria could be removing h+ from the system.

But just nah except for stomach coagulants by hcl to blood immunities to acidity of dna bases, and poss chlorine bind. we all know chlorine is a good antibiotic also. Pretty good general research project.

The ultrasound holography is def from new scientist, and can kill cancer cells too.They should make an MRI of that.

Withe the blood filtering, I wonder what lab processes could be done to blood, before reintroduced. There are biochem techniques, but I guess the cells must be alive again after reintroduction for non blood around in mass outbreaks. I wonder how could you could get the lab processes, then the cells reorganise if lysed maybe, for a good filter.

And one day it might get micro-ed to a bench box unit in one fundable and repeatable.

It's an interesting idea, but requires that you try to reform the cells after lysing say, by self molecular organisation processes, once the virus is gone. Possibly possible to have it lab revert also for a filter. A dual lyse then un-lyse system maybe. Has never been that sort of dual thinking of recreate with lab systems before.

All the lab gear is there already, so this might be good to have this dual lyse system. Very well established industry systems basically so may as well use what you have got already. That couid be fast for a mechanical filtration system of viruses, even ebola if got early.And no blood new needed by the military. which can be a constraint often I think.

Or you can do mndatory blood drives, but always yeh just new needle systems of course. Nothing allowed unpackaged. Just a machine makes those packaged needles and are cranked well above requirement by a third. So can reorder in triangular time.

And if for africa had to, they don't have to, and the third on the side of machine packaged needles still remains long term good stock. I suppose after bleach on it or something for enironmental plastic bind of say ebola to packets.. or they might just chuck it. If machine made would be real quick and cheap. Prob just burn it after an outbreak.

But you have to have triangular stock systems, for outbreaks always. And don't let the poorness nurse in africa say being like that for re-use, off poor thought. Good IT connect and traingular restock.

mil should prototype mini cell towers portable like just with extension poles prototyped.

They prob have sat uplinks but for small rural african towns say, they need ex mil looks after you of socialist sat uplink systems too, of these mini towers also, just the rural shit.

prob virus app too, with symptom checklist across whole of africa, generically obn cell phones as orderered when they pay for them.

If its those bats for ebola, what about gamma food baiting to study semi dino semi mammal virus chaos, of bat moves by hubble turned around. saurely has gamma detect on it. just use radiological chems used for cancer, (if cannot mutate ebola: prob wont)

i don't know though. It will be semi biased off the bait though. They seek natural food is better. bloody semi dino cold bloodeds aye, cranks in dino cold blooded virus, from dino days, which is ebola. no wonder it bloods you up. Its a time virus off Infrared detect, or something bn mammal and dino cold blooded. can snakes get ebolsa prob not, lizards nuh prob not. unless it goes backwards too towards cold blooded also.

but its prob the lizard myoglobin vs haeme nmammalian virus.

some wierd infiltrator bn, wher can use old myoglobin pathways or works bn myoglobulin and haemoglobulin, as a worming mechanism. could be fruit bat shit added also of fructose mutate too, of bat near genome friendly too.

imagine a fructose virus, with myoglobin:haemoglobin hole too. shit, and bloods you up quick. I think vit c as pentagonal acid can heal dna 5 prime sugar mutations a bit.

but the dna is all 5 base sugars. its hard.

poss sometimes the vampire bats try and root the fruit bats too on the side when horny, and ebola then happens.

looks like a bat to my ass. quite rare but then their immune bounce makes obola output, well yeh maybe. but what a crazy outbreak start point.

You wouldn'[t even know when it would start,

but maybe 5 prime sugar use by ebola worm, and as well as cold blooded/warm blooded, but add fructose and can styop vit c, and can do 5 prime through dna bases. Its good as theory. I bet those bats do fuck each other when just horny though aye. Fancy pants fruit bat chick. I bet my cock still works up there. Those fancy pants fruit eating snobby bitches need some good cock.

something liek this, but somehow ebola happens off it as a cold dino/mammal/vit c or 5 prime virus worm happens

Be nice to us mice! Use your brain instead of death create requirement, at fix rate.

Info periodics:

(as not related to vit periodicity but to the site, and human health fibbo periodicity) or anti entropy human periodicity, all life is antientropy.

All the ideas on this site are in a messy structure. Perhaps one day they can be used in a form field mind map system, and post that to a periodic table of ideas. I guess with human evolutiion it is on a much different stage to atoms and elements, and you would not really have a mass weight periodic table of course on this stage of evolution, it seems to be social IQ evolution. perhaps the best we can get is linkers with form fields, but this may just because we are not atoms. but it could get the cleanest possible, and the form fileds act on the mind map below in a linked spreadsheet, then check through that for any dtat code clearing, retaining holes in IQ, much like when the periodic table first formed. But they can be beta tested for checking theories really well. And others ideas too.

Sometime you might get a human fibbo table. which is like the periodic table of humans and their struggle to overcome health issues. And it could be real clean. But still open with holes available before its completed perfectly.

and can change the whole main file fibbo organisation system if needed too, and test those on main file layer.

The immunoglobulin buds are budding off aye's, but can become tris post processed, and yeh this metabolism is not understood. This can help with ebola and HIV. and maybe a post process enzyme. and even these thing screw with that. but trinarisation is important for the immune cells but nothing is yet known, but it can bud off likie a y flower too, from release, and then become a tri coagulator. and prob this is what HIV's about, or worming by ebola. We don't know this metrab of post process antiglobulins. top make tri coagulator globulins for sit still factors, and yeh I guess there could be wo enzymes, one in random chaos and the other one does the y's, as growth bud. and prob hiv and ebola are stopping proper triangulation. by this in millelu post post processing stuff. Shit so its not all about rna input. and maybe nearly nil at all if they are pre-preparing for cell input this way, of this viral process. So a good new side focus.

and very important as theory of budding and post process y's

I think they had to bud,, cause it would need some place to be built upon, then post processed after release enzyme lets its go, then it gets the third post processing, but I suppose this might take an intelligent antibody binder too, to make sure the right ones are post processed., and the right tri put on it.

Perhaps it is this we don't understand yet for HIV abusing that system, or ebola too.

cancer and fumigatens fungus?

(cancer acts as a fungus thing) looks like one, acts like one.

not a fibbo cell based life lifes whole cell bioplastic then dude.

despite the vit mimics and shit, maybe cancer and aspergillus fumigatens.

Interestingly cigs prob kill fumigatens in lungs but not arse. All delicate clues. sorry about the fancy language there.

Auditing requirement is req.

I think are antifungals naturally in cig smoke yet much else. Well theres every molecule in it. I love clarification. It brings one step closer always. I don't endorse cigarettes for health. might be useful militarily poss, cause are currently avail anywhere. Also does mutations! but yeh. check below anyway.

A few emails cancer soc nz MOD NZ and to UNAIDS

hi d jones.

If HIV and ebola are fungi, well archae ones perhaps, then perhaps it may be interesting to trial in hiv or ebola if going to die, which do very quickly, aspergillus orzyae, as a competitive plant fungus probiotic to compete directly with these animal archaefungi. It could be that they are directly genetically symmetrical. which would be great, or side on slightly, but yeh you could try it.

ebola sounds too hardout for it to work for that, but it could be some wierd lamella proprius regulating fungus factor for plant to animal fungi which may be the issue.

No promises, but try it out.

I have done many ideas, but try this one. Eats starches probably for: this cancer email check this out;

<head> / Hi djones again

Hmm

perhaps rheumatic fever is actually caused by aspergillus fumigens, and I have that.

I figure the orzyae strain must be competitive. It is available for brewing by credit card. I have to repin my card but yeh, will tomorrow.

Perhaps rheumatic fever is from this, instead of insect bites etc.or the tetanus idea.

check this out I sent to cancer nz.

Hi D Jones

What do you think about the orzei strain of aspergillus being a good idea to take as a tablet for helping in cancer in that it would compete with any fumigatus, and also that it may have the ability to produce its own resveratrol and may in fact be a probiotic required to kill cancer. And also may be required in diabetes for breaking down starches.

This is an interesting idea.

Would you like to research it please.

It might be the cure but am definitely not sure yet as have not tried it but it does make some sense.

Yours Sincerely

Daniel Jones

year1 of biochem papers, and chem etc. But yeh whoever.

So yeh maybe. I will buy some though and try it out. I have recently started taking probiotics of lactobacillis, but I notice some starches etc. are still in stool, which I previously thought may have been from just bowel polypsual cancers. which it is but I wonder if that is due to no orzyae strain.

Oh well thought you'd like to know.

Yours Sincerely

Daniel Jones

(the fumigatens strain must be the strain that infects milk/cheese I guess) I sent this to MOD but yeh has the cancer society one inside it

/<head>.

Daniel Jones

yes just check it out. just stuck the head start and end for clarity of when it starts and ends. don't know programming.

Theory Life in the fast lane with medical graffitti definitely, but I always email my ideas instantly too. So you might be looking at old data, IF it got funded.

no longer whole cell bioplastic process then. The bioplastic theory does have some merit, and reretain if above fail.

Life in the fast lane

Vits low in cancer, low uptake from bowel polyps. Also stomach cancer. (mine at mo, is the sub interest of the title)

I wonder if carcinogens are sometimes used as vit precursors hence leading to strange small molecule bi-products which enter cell cycles and create strange metabolic cycles, and hence growth odd to create cancer.

Would be interesting to compare this with b vitamin mimic theory of:

A: pre reacted externals like burnt b’s in caramelised yeast extract

And

B: in vivo reactions with b vitamins or other vitamins with either these small molecules and carcinogens directly, or the small molecule biproducts from above attacking b vits or other vits creating vit mimics again. Some sort of oddity cycle that becomes growth incursive.

Also cofactors and stuff could be involved. A lot of things are metab influencers that are not vits but cofactors still.

It will be interesting to find the proper metabolic cancer cycles. You need a bioreactor doing it, and do it piece by piece finding small molecules and discovering the vit mimics involved.

Remember any bias of the antioxidant like chemicals being broken down to vitamins also. I think they are higher periodicities of vitamins. Plant post cursors of vits maybe, and act in the body to be used downgraded to create vits in times of need, as carcinogen cyclics might be also if no vits around. Or in a mix with low vits, from bowel polyp uptake poor, both may be used as post cursors of vits, which then are obviously pre cursors, as is the terms meaning in definition.

Wow I must be up to about 200 cycles of pausing and unpausing over ten years using bgh and b vit mimic removal. I really want a cure though.

But it is sure statistically relevant for

pausing cure is true.

I wish there was a bioprocessor bot that could be made to create cancer CAD piece by piece with the cell biproducts found and teh cell cycles put into cleanly true files one at a time. Leading finally to pure

CANCER CAD. You might be able to do it with cells but it would be better to use mice, but I don't think you have to kill the mice, just use more delicacy so can cure them after and minute doses, or possibly could use some human organ kept alive or something.

or just cells would probably be very fast. I guess the prob with cancer is that the immune cells get the same metab probs, so maybe using cancer cells with immune cells present doesn't matter too much, or just compare immune cancer cells and normal cells, then both together in the reactor.

Then maybe one day patch that in to mri testing scans by a program input for checking against real people and organisms.

No mice allowed! Not to kill them by ridiculous mass doses of carcinogen rubbish like in the past, just uncure then cure by known removal. I am sure we can all handle small amounts, but post hep don't know.

Check dna against it too. But yeh maybe no mice. BE NICE TO MICE.

There should be a mini mouse MRI also, the size of a pencil case.

Sometimes I wonder if the dna if it changes is just a floating change which is a sensible dna change as related to when carcinogens have become the precursors/ plant higher periodicity post-cursors for current vitamin creation needs, and may be reversible and only temp ram dna, needs based. prob cancer is storage of needed metabolic things under error issues of no fruit post-cursors, and that reintro of fruit post cursors and removal of the carcinogens might change the dna back, but possibly they need to go into protein eat to burn the cancer also poss.Go into ketosis.

can also test with mice, the hep on/ off and if they cannibalise, but maybe three strains of hep and get them together after the cancer and make trinary (tri strain immunity) post hep to fix them too, could eat some killed baby ones or just have sex with each other for tri immunity. but definite tri strains of the three mice in three different colonies then reintroduce them into one. see if can cure it, and try anti viral herbs in a second tri colony one.

prob need field mice instead of shitty immune deficient albino mice too, and maybe try putting in black currant etc. for the post-vits stuff too. But work it well in a diagram. They might eat blackberries maybe naturally. maybe those and various other things they might eat besides grain, which is so generic, as are use of albino mice.

I wonder how many expt.s are poor from just using albino mice. Its good for human redheads with white skin though, but yeh. Not greatly double blinded yet I don't think.

Its definitely dumb stuff. Field mice with natural fibbo ratios and leave the natural viruses in them maybe too could help with other areass for a continuous experiment. But be nice to the mice, ie. non kill, then release back to fields. The viruses should be alright, they will just eat some more blackberries or something or weeds and herbs. which stop mutate because are tri antivirals, or antibiotics, in natural triangulate array form. Prob A-OK.

humans always fuck things up. even if they retain starins for rebreed, the strains are triangularly isolated, by plant array to non mutate too highly. This is why rats survived the black plague no worries at all. (which you may have previously thought was from breed to death rate lifecycle time of darwinian stuff). They are less snobby too for breeding and kissing too, and sense of smell can smell virus type symptoms of different organic molecules with scent are given off based on different metab cycle changes from viruses. Nose touch micro post nose immune tissue microtouches too from nose touching for testing immunity stage.

side note: perhaps mice eat natural orzyae? hoe long have field mice been bullshitting about cancer and getting us to use lab mice albinos, when really other field mice ate natural orzyae strains. this is assuming the ge straibn they made to make resveratrol was already a naturally occuring thiing they tried to amp to make caplets. Like was laready an orzyae biproduct the resveratrol. we'd be needing raw infected grain like mice might get.

GODDAM INFO HOLES!

Something like this much later on maybe.but first spreadsheet to mind map form field fill.

Multiple sclerosis

Yeh I have this theory that if you were not infected by some listeria or soil bac, or even if that there is protein helix periodicity, almost there with the fish oils but not like caveman doc, or to be man, eat like bear, including fish scale, which has keratin, and I think prob keratin powder, as a periodic hel;ix higher periodicity over myelin, it can help you, and also the theory that the helix nature of keratin is antiviral as a helix, due to the fact a lot of viruses might use antientropy, but are pi float around ones, so maybe keratin powder supplementation can help. They prob give anti virs, but scews you up, and is not functional against the fact you don't have keratin spinner in there. The other two anti entropy helices are viral rna and human dna. Very interesting data for MS. Better a maybe than nil. It is of hypothesis nature good. So just eat keratin powder, lose marmite, lose bgh, lose gluten, massage methane away from heart. And maybe survive.

lose nitrite meat too for microcyanide rxn with gut pressure methane. Thats it. check for listeria. maybe need soil probiotics. check for tetany.check for bad soil bac too, non related to probiotics. also dis-iq from docs non iq about keratin as anti vir for gave anti virs, which may have screwed up the natural way. immuhne cell may be keratin dependant. strange antiviral autoimmunity code occurrences could occur from docs, but mainly no marmite

Speakers

CANCER TRIANGLE:

FOR FIND HEART OF CANCERS FUNCTION AS A MOLECULE OR TYPE OF MOLECULAR GROUP: A TRI MOLECULE.

TO FIND THE HEART OF CANCER FUNCTION AS A Ca-Vit-Ox TRI

MOLECULE.

Is from metabolic cycle solder jump joint theory, but this one might jump around and double or triple bond, and be more rotary.

a good way for tests to fail here too, if can choose double or triple bond,

if ends up as true, they will be saying oh no, it's been a fidget spinner thats been doing it for so long.

SOME PROOF:

calcitosis: calcium and cancer, may need calcium to grow, removal of calcium may stop growth. calcium mediated endocytosis is some thing i can't remember.

yeast extract, a caramelised (smoked/burnt) form of b vits, hence ox group, grows cancer well

bgh grows cancer well too, this also has calcium in it

cancer can hook up veins for itself, so may be able to fiddle with respiration signalling

ANOTHER UNRELATED CANCER IDEA:(CAUSE AM ON COMPUTER NOW) BURNT MALT OR BURNT SUGAR MAY DO THINGS. I KNOW CAN CREATE CARCINOGENS AT LEAST.

The

Grid.

CONFERENCE OF CREATIVES

Medical Graffiti

HIV in cows grows general antibodies fast

Cancer and metabolic solder cross joints:

BUT: to be clear: In molecular

ie. cross metab cycle doublex molecules. VERY INTELLIGENT!

yeh essentially it can make the rest of the metab really dead also in definition anyway. think about it. And this is how cancer kills them. You can't even get up again from it. Your metab is fucked, from ONE solder cross joint.

cross metab cycle solder joint theory, or "CMCSJ theory" can be used audited for viruses.

​

​

addd on for CMCSJ theory is that for vit mimics from burnt cause cancer, maybe is basic oxygenation and deox pathways from these mimics, cross soldered, cancer wise, could be some oxidating run factor for anti ox-no antiox process but gone nuts with that at least of cross soldered.

post processing immuno globulin tri release viral/bacterial

coagulators

or "tri-globulins coagulator theory"

hold still in time dim pathogen theory or "HSTDP" theory

Blood filters

Be nice to us mice! Use your brain instead of death create requirement, at fix rate.

Info periodics:

(as not related to vit periodicity but to the site, and human health fibbo periodicity) or anti entropy human periodicity, all life is antientropy.

cancer and fumigatens fungus?

(cancer acts as a fungus thing) looks like one, acts like one.

not a fibbo cell based life lifes whole cell bioplastic then dude.

​

CANCER TRIANGLE:

FOR FIND HEART OF CANCERS FUNCTION AS A MOLECULE OR TYPE OF MOLECULAR GROUP: A TRI MOLECULE.

TO FIND THE HEART OF CANCER FUNCTION AS A Ca-Vit-Ox TRI

MOLECULE.

a good way for tests to fail here too, if can choose double or triple bond,

if ends up as true, they will be saying oh no, it's been a fidget spinner thats been doing it for so long.

BONE: Ca, Mg etc.

Phosphate

BONE STORE RELEASE

CYCLE, OR CALCIUM /

PHOS CYCLES IN MILLILEU

Vitamin, eg.

B12, or b vits, or maybe

other vits and even

cofactors considerable

VIT CYCLE

Oxygen factor:

CO, O2, CO2,

RESPIRATION CYCLE