Acid reflux riddle solved: what causes it?

Porphyromonas gingivalis.


This bacteria is easily killed quickly with food grade diatomaceous earth.

H pylori causes non-acidic reflux GERD.  But the addition of P. Gingivalis causes excess acid to be produced and erosion of the esophagus.


Hydroxyl Radical Electrochemical cell battery ("Vim Vitae Generator")

The hydroxyl radical battery is any device which utilizes a hydroxyl radical to create a potential energy or voltage.  The hydroxyl radical would likely need to be generated in real time as it is unstable.  The system can be aqueous or non aqueous but aqueous is preferred.

Any means to create this radical can be used but preferably we would use a biomimetic system that works how mammalian energy production works in order to create a sustainable system.  This is to use hydrogen peroxide and/or oxygen in combination with a catalyst to produce the hydroxyl radical.  Any catalyst or source of hydrogen peroxide or oxygen or air can be used or any other peroxide.  Preferably we would use a catalyst containing iron (II or III).  Iron (II) reacts with hydrogen peroxide forming Iron (III) and hydroxyl radical.  Iron (III) then reacts again with hydrogen peroxide forming Iron (II) again.  Another thing that can be done in this system is to supply something that can preferentially reduce Iron (III) to Iron (II) without consuming a hydrogen peroxide molecule.  Bicarbonate may be one such thing that can be used for this.  The iron atom can be free or bound to a structure.  In mammalian biology this structure is heme inside red blood cells.  Any structure to hold the iron atom is sufficient but not required.  For ease of use, power, and biodegradability EDDS can be used.  Acetic acid or citric acid or edta etc. can also be used.  Iron sulfides can also be used.  Anything can be used to sequester and/or improve the properties of the iron.  The structure can also fulfill any function including but not limited to aid in filtration or create a high surface area structure or keep the iron stationary or sequestered or stabilize oxidation states or facilitate oxidation or reduction.  The structure can be organic, inorganic, synthetic, or a combination.  It can be applied or deposited by any method to one or both sides of the membrane or create the membrane, etc.

In any kind of cell we need an oxidizing aspect and a reducing aspect.  The oxidizing aspect is hydroxyl radical fully or in part with other oxidizing agents.  The reducing aspect can be any reducing agent but preferably in an aqueous system; a reducing acid.  Most preferably formic acid or acetic acid or lactic acid or oxalic  acid or any combination etc.  Ideally formic acid will be used fully or in part at any concentration preferably at high concentration.  Hydrogen or hydrogen sulfide or -SH could also be used completely or in part.  Any means of generating any of these outside or inside the cell can be used.

Separating the oxidizing and reducing aspects of the cell can be anything that can achieve any sort of ion flow while keeping the solutions somewhat separated.  This separation need not be physical but can be based on the properties of the oxidizing and reducing aspects themselves like density, miscibility, solubility, etc.  There can be one or more than one separation.  Ideally a proton transfer membrane would be used allowing the H+ ions from the formic acid to flow through such as Nafion.


The formic acid hydroxyl radical flow battery: a biomimetic battery design (FAFB)

This is an open source patent and can be used by anyone to make a profit and/or change the world.

This electrochemical generator can be referred to as the radical generator, formic acid battery or any other term.

****Results: formic acid (95%) and hydrogen peroxide (35%) with paper separator 0.6 volts.  Acetic acid (99%) and hydrogen peroxide (35%) with paper separator 0.3 volts.  Sodium bicarbonate added to peroxide reduced voltage :(.  Hopefuly with a better membrane we will have better results.

Upon further study it looks like a iron 2 catalyst is needed to convert hydrogen peroxide to OH hydroxyl radical in a fenton type reaction which is enhanced by bicarbonate.

The formic acid flow battery uses formic acid (or any reducing acid, formic acid being the most preferable, acetic acid also good), hydrogen peroxide (or any peroxide, hydrogen peroxide being the most preferable), a catalyst (such as but not limited to any iron 2 or 3 containing molecule or compound or ion or atom), and optionally bicarbonate ions (or carbonate or carbonic acid or co2; bicarbonate being the most preferable- or any other additive that helps spare h2o2 in the regeneration of the catalyst).  It is believed that the hydrogen peroxide and catalyst form a hydroxyl radical.  Bicarbonate is thought to help improve the conversion efficiency or most probably to help the regeneration of iron 3 back into iron 2 but can be added for any other use as well.  Any other additives can be added as well to improve the cell in any way as long as the cell is producing hydroxyl radical.  The "bicarbonate" (or any previously mentioned alternative or combination) can be isolated or have alkali or alkaline counter ions or molecules like ammonia or combinations such as sodium or potassium or lithium or ammonia etc.  This isolation can be done inside or outside the battery or cell if desired.  One way (but not limited to) this can be done is with membranes and electrical potential

The solutions can be at any pressure including evaporated all the way (vapor phase, even plasma) to high pressure liquids, to solids.  Preferably probably at standard pressure for best practicality.  The solutions or cell or battery can be at any temperature, preferably probably around room temperature or body temperature 37 deg C for greatest practicality.  The liquids can be aqueous or non aqueous with any other additives desired for any purpose such as to improve power density, efficiency, practicality, membrane functionality, creation of the active molecules/compounds, etc.

The battery can either be recharged directly or the solutions replaced or a combination of these.  The battery can have single or multiple cells in series or parallel or combination; in any number or configuration; large or small.  The battery can be used for any use including but not limited to stationary or mobile power storage or generation, automotive applications, personal transportation, powering biologically interfacing devices, etc.

Ideally any separator of any material, shape, or surface area, including multiple layers with any spacing between; including most preferable a polymer membrane between the two solutions would keep the formate ion from crossing and only allow H+ to cross such as in a formic acid fuel cell.  A nafion type membrane would be a very preferable separator.  To make a biomimetic design there could be two membranes with an intermembrane space where bicarbonate/h2o2/h2co4/hco4 could cross from one side and H+ can cross from the other side; but this is not necessary.

Ideally the separator or polymer membrane would also only allow h2o2 and bicarbonate ion to cross from the other side; either separate or as an intermediate such as peroxycarbonate or peroxybicarbonate such as HCO4 or H2CO4; or not allow these ions to cross at all and only allow H+ to cross.

The "peroxycarbonate" (which will be used to imply any such item or combination as laid out above) would be the oxidizing agent on one side and "formic acid" as the reducing agent on the other side.

Each cell can have multiple membranes instead of just one if desired, for example but not limited to this; hydrogen peroxide linked to bicarbonate by a membrane and the bicarbonate linked to formic acid by a membrane.  Also multiple membranes can be use to separate counter ions like potassium from the bicarbonate ions or separate hydrogens from the formate ion.  Any number and in any format in 3 dimensional space can membranes or dividers be used.

The membrane can have any composition but most preferably it would only allow hydrogen ions and peroxy(bi)carbonate intermediates to cross or only hydrogen ions to cross.  Still very preferable would be if it allowed hydrogen ions, bicarbonate ions, and hydrogen peroxide to cross.  Less preferably but still reasonably it would allow anything to cross.  Things can cross directionally, bidirectionally, or omnidirectional; directional being most preferable.  Active transport of the ions or passive transport can be used.  Different solubility and/or density electrolytes could even be used so that no membrane or separator is needed.

Any current collectors or electrodes can be used but preferably noble type metals.  Copper and germanium can also be used as anode material and may make the battery into a hybrid of what is known as a "noble metal battery" which I have described in previous inventions.  Also any reducing gasses like hydrogen on the anode side and any oxidizing gasses like oxygen and nitrous oxide and co2 to the cathode side can be sparged or pressurized or otherwise added in as well making this a hybrid fuel cell.  Adding other molecules or materials to the anode or cathode side as catylysts for any purpose can also be done; including but not limited to photoreceptive compounds on the anode side to make this into a hybrid solar cell; or catalysts to convert oxygen or "air" into hydrogen peroxide, or creating bicarbonate with co2 and a alkali or alkaline metal and an electrical current or any other method.  These things laid out above can be done for any purpose such as recharging, adding additional power etc.  Also palladium or a palladium alloy of 0-100% palladium and any other metal or material may be an ideal material on the anode side since it is good at capturing hydrogen from "formic acid" (quotes used because any reducing acid or combination of reducing acids can be used).  For the cathode a most preferable material may be iridium or an iridium alloy 0-100%.  This is because iridium is the material most resistant to oxidation.  Other noble metals like rhenium, osmium, platinum, gold, ruthenium, etc. can be used as well as refractory metals like zirconium, niobium, tungsten, molybdenum, etc, can be used as well.  Any alloy as well.

The casing can be any material including but not limited to membranes, plastics, metals, etc.  It can be conducting or non-conducting but preferably non conducting.

The final active products h2o2/bicarbonate (or some type of peroxy(bi)carbonate) and H+ ion can be produced by any method and delivered by any method including but not limited to being produced in the battery itself via any method or produced externally and added into the battery automatically or manually.  The solutions can be dumped out of the battery if desired or recycled or recharged with or without dumping.  The solutions can be moved to other areas of the battery or outside the battery for any reason.  Any type of recharging or reforming the solutions can be done by natural (such as but not limited to enzymatically or biologically) or artificial means.


How to heal a sprain: MCL, ankle, knee etc.

First of all we have to attack the microbes that tend to be in the area.  If you are someone who wakes up too early they you are likely high in streptococcus and can benefit from adaptogens.  If you have trouble falling asleep you are likely high in proteus and can benefit from eucalyptus essential oil.

Now there are 3 more ingredients.  Ice obviously as a natural anti-inflamatory.

The last part is to take 2 tsp of potassium bicarbonate in water per day internally and apply a bragg's vinegar compress.  To best do this get a towel damp in vinegar and wrap on the effected area and wrap cellophane around that.  

The human body is a bicarbonate-acid battery and taking bicarbonate internally and applying vinegar externally charges up this healing battery.


Rechargeable CO2 Formic Acid flow battery; metabolic biological battery open source patent

*This flow battery is probaby most preferable to run as a hybrid fuel cell by sparging oxygen into the bicarbonate side and hydrogen into the formic acid side as this will help keep the voltage constant and also probably help with recharging.  At a minimum there would probably need to be an oxidizer constantly added whether that be air/co2/oxygen/nitrous/h2o2 in order to maintain a maximal voltage.*

This battery is very similar to the volcano battery but is a little more sophisticated and can be recharged not just the liquids refreshed to charge it.  Inthis case we are using either carbonic acid or alkali/alkaline bicarbonate and the other isde is formic acid.  The two sides are separated by a flow battery membrane.  The membrane ideally will only allow H+ ions (reducing equivalents) to cross from the formic acid (reducing) side into the co2 (oxidizing) side just like how biological organisms do it.

For example lets say the oxidizing side is carbonic acid or carbonate/bicarbonate ion and the reducing side is formic acid.  When the battery is depleted both sides would be carbonic acid (possibly because co2 is pressurized over the liquid).  A voltage can then be applied across the terminals and (with the help of a catalyst if desired) what happens is on the negative terminal formic acid is formed since co2 plus hydrogen ions plus electrons creates formic acid.  The hydrogen ions come from the water as co2 dissolved in water liberates hydrogen ions from the water.  On the other side you have carbonic acid/bicarbonate/carbonate ion (depending on how many protons you used up from making the formic acid and what pressure of co2 is above the liquid).

So in conclusion you have water or any suitable liquid.  You dissolve co2 in it (with or without sodium or potassium or whatever) under pressure and you have carbonic acid (or a bicarbonate in the case you used alkali/alkaline counter ion).  You now electrolyze the solution (still under co2 pressure if desired) to have formic acid form on one side and carbonic acid/bicarbonate on the other.  This is your Rechargable metabolic flow battery (RMFB) or rechargable biological flow battery (RBFB), formic flow battery (FFB), CO2 flow battery (CFB); whatever you wish to call it.

This technology can be used by itself or in combination with anode/cathode metals and/or in combination with sparged gasses.  Using all the above would make this a flow battery/regular battery/fuel cell hybrid/tribrid.

Volcano Battery: Baking soda and vinegar flow battery open source patent

*With standard vinegar and dilute potassium bicarbonate I get .16 volts per cell with vinegar bieng the + charge.  With hydrogen peroxide and vinegar I get 0.36 volts per cell with hydrogen peroxide bieng the + charge. With sodium hydroxide and vinegar I get 0.5 volts.  With sodium hydroxide and dilute hcl I get 0.36 volts.  Membrane is paper so that may effect things and artifically lower hcl figures since it dissolves paper. Dilute phosphoric acid and sodium hydroxide 0.48 volts.  In these acid/sodium hydroxide experiments adding hydrogen peroxide to either side lowered the voltage.  Still need to try formic acid and hydroiodic acid.  My steel probes are corroding so some of this voltage may be iron/iron oxide!  Needs more testing.  Yes it was contamination with good probes vinegar sodium hydroxide was .18 and phosphoric acid sodium hydroxide was ~0.*

This technology can be used by itself or in combination with anode/cathode metals and/or in combination with sparged gasses.  Using all the above would make this a flow battery/regular battery/fuel cell hybrid/tribrid.Well after a log time stumbling around trying to find a cheap easy and unique battery I made my way to flow batteres.  No electrodes to worry about which is very nice and no exotic gasses needed like the nitrous, oxygen, hydrogen (at very least air) to worry about.  In a flow battery all you have to worry about is pumping liquids which is easier that sparging with gasses.  So I realized instead of these exotic liquids they are trying to use in flow batteries like ionic lithium, why not just use some cheap and easy oxidizers and reducing agents?  Then I realized something I had known for a long time, our bodies are actually flow batteries!  Before I thought our bodies were flow batteries that used iron in heme as the oxidizing agent but now after trying out another "exotic material" called baking soda, I realized the iron is not needed.  How the body works and the premise of the volcano battery is the body works by oxidizing hydrogen ions (that were produced as an end-product of metabolism) with bicarbonate ion (which is produced in the red blood cell.  When these two neutralize eachother they release energy which is captured in the iron atom in heme I believe.  Since we will have metal current collectors in our volcano battery we won't need this iron to capture our released electrons; we will be able to use them directly.  It would be a good idea to charge up capacitors though probably.  

The body uses single hydrogen ions and single bicarbonate ions because it is a boss.  This means there is no counter ions like sodium and acetate to worry about gumming up the works.  But in our case we are not going to have hydrogen ion transporters like the body does so we need to compromise.  We can use a reducing acid like acetic acid (vinegar), formic acid (from ants), or oxalic acid (end product of metabolism).  For our oxidizer we can use baking soda or potassium bicarbonate or any type of peroxide like hydrogen peroxide.  Since the body uses bicarbonate (mabye in conjunction with some oxidizing metal ions) I think bicarbonate would be a great bet.  Also since vinegar is really cheap I think that would be a good bet too (but if you like farming ants you know what is even better than vinegar...;).

Also you can add a fuel cell to this setup by just sparging the bicarbonate side with oxygen/nitrous and the acid side with hydrogen.  Doing this will add about 0.7 volts per cell.

Now the hardest part of all this is the mechanical design as well as the membrane.  The membrane should be permeable enough to allow good ion flow between the bicarbonate and acid but not enough flow to allow super fast mixing.  Ultimatly both sides will ecome sodium acetate or sodium formate or whatever and the battery will pee that out and need to be refilled.  You can't charge this the traditional way.

This is 100% renewable and harmless.  You can make the bicarbonate solution by electrolyzing salt water and then pressurizing co2 into it.  You canmake vinegar  from fermenting sugar or ethanol or by reacting carbon monoxide with methanol.  Or you can distill ants to get the even better formic acid ;).

I'm not sure if the surface area of the metallic current collectors matter but may as well try a silver, nickel or copper mesh.  Possibly more noble metals will help improve voltage even more, it is worth a shot. If they do then you will want to select rhenium or iridium as those are #2 and #1 in my tests before.

This technology can be used by itself or in combination with anode/cathode metals and/or in combination with sparged gasses.  Using all the above would make this a flow battery/regular battery/fuel cell hybrid/tribrid.


How to make your own 75% Lugol's Iodine

Take a 1 liter beaker and add 456g Iodine crystals (I2).

Add 225g Potassium hydroxide (KOH)

Add 514mL distilled water.  Will get hot.  Mix with ceramic or glass untill fully dissolved.

Let white precipitate settle down and filter out (or pour out liquid and keep liquid).  This white precipitate is potassium iodate and isn't good to ingest.

Add 250g iodine crystals to the liquid.  Add more water as necessary and gently heat to get it to dissolve.

Vol to 1L.

This is 75% Lugol's iodine.


MOVI Fusion: Muon Oxygen Vacancy Implosion Fusion

Can be any type of fusion using any element compound in which vacancies can exist but preferably transition metal oxides performing "s-process" type fusion. (not exactly s-process but creating heavy elements, this would be a whole new type of fusion called MOVI fusion)  What this is is an oxide crystal lattice in which oxygen vacancies are present, for muons to fill those vacancies and cause a structural collapse to create heavier elements.  This can be used for any purpose.  Some preferable uses could be to create energy, create changes to isotopes leading to more or less radioactivity, but most preferably to create heavier elements de novo.  The most preferable would be to make noble metals such as gold and others.

This is a type of muon catalyzed fusion in which oxide compounds are used to collect the muons and an implosion of the structure (catalyzed by the muons filling the vacancies) occurs creating nuclear fusion.

"Cold fusion" or low energy nuclear reactions (LENR) are really just catalyzed fusion where the activation energy to cause fusion is reduced.  Therefore the MOVI process is also cold fusion.

This is a proposed process based on my theory of how gold is created in the earth.  

The MOVI process is an explanation which would provide a theoretical framework to explain how my theory for how gold is created in the earth could potentially happen.

This is also an open source process to create fusion which includes creating gold.

The minimum requirements for this invention are an oxide mineral, oxygen vacancies, and muons.  As stated before the muons fill the oxygen vacancies reducing the energy required for the atomic nuclei in the crystal structure to combine in a nuclear fusion reaction.

One example process would be to place hematite (Iron 2 oxide) between two charges that have a high potential difference.  These two charges could be crystals such as quartz, metals, or anything else that can carry the charge.  This can be any voltage but preferably a voltage on the order of millions of volts.  The other things needed are Iron 55 hematite and muons.  The muons and iron 55 may be created separately or produced in the process of the high voltage experiment.  On the positive charged side/electrode oxygen vacancies would form in the hematite.  These vacancies would migrate toward the negative charge/electrode since the vacancies are relatively positively charged.  When these vacancies move to the negative electrode they are partially or fully filled with muons.  These muons catalyze a structural implosion in the oxide mineral creating higher molecular weight atoms.  These muons are released and/or decay.  When they are released they can be reused creating a cascade of structural implosions and fusing of nuclei.  This could be termed "nuclear melting" or "atomic melting".  When they decay the release radiation which may or may not be used to create more muons and/or iron 55.

This is just an example process and will likely work with many different oxides.

In conclusion this is an open source process for creating catalyzed nuclear fusion.  This is the only process proposed for creating s-type fusion (but not limited to s-type fusion) that I am aware of.  The process at its minimum requires an oxide crystal lattice with vacancies and muons.  However these requirements are attained is of no consequence.  An example has been illustrated but is only one of many methods to accomplish muon oxygen vacancy implosion fusion.  Any process that uses one or more oxides and muons to accomplish fusion are covered by this open source patent.  Even more minimum requirement is any element or combination of elements, oxidizing conditions, and radiation.  These could be used to create an oxide and create muons and create oxygen vacancies.

Also things besides oxides can be used like hydrides, fluorides, chlorides, bromides, iodides, astantides, sulfides, selenides, tellurides, etc. and would be covered in this open source patent.

Any type of vacancy can be used, but preferably a vacancy of a negative atom like those just mentioned.  Perhaps positive muons could fill the vaciencies left by positive atoms.  So any vacancy and any type of muon can be used and are covered in this open source patent.

In essence just a muon needs to be used to catalyze the collapse of a lattice to create fusion of nuclei.  More external energy in the form of volts or electron volts may be required depending on the conditions.

In certain compounds like hydrides perhaps even just electrons could accomplish the goal and no muons are even needed which would also be covered by this open source patent.  But preferably muons would be used.


How to make a high voltage pulse transformer at home for cold fusion

Lets term this setup a "cold fusion transformer"

End from the beginning:

1. Neon sign transformer (or any high voltage high frequency AC)

2. CW transformer

3. Marx generator

4. Traditional multi layer transformer


We want an extremely high voltage and high current output.  For cold fusion we are not hot plasma mediated like a fusor is so we need to make up for that heat with more voltage (and maybe H+ ions but that is another topic.  See my cold fusion and making gold posts).

So how can we get both high voltage and high current?  Easy, we step up the voltage while also using capacitors to store up more current.

More specifically:
We want to have a high wattage high voltage starting point.  The best starting point I have seen is the neon sign  transformers that are 15kv and 60ma.  This gives around 900 watts which seems as good as you can get for an off the shelf 115v power supply.  So we start with that.  Amazing1 sells one google: 'amazing1 neon sign'

Now this is AC and we want to get it to DC.  To do this we use one step (or more) of a full wave CW transformer .  What this does is not only change the AC into DC but also multiply the voltage depending on how many stages you use.  For practical reasons I only suggest you use one stage, and get a 30kv output.  This will make sourcing 30kv resistors and capacitors possible for the next stage, the marx generator.  Now we have a continuous current at 30kv.  However we halved the amperage to 30 ma.  Not only do we want to boost the amperage, but we want to boost the voltage much higher.  How can we do both?  A marx generator.  This device takes the 30kv to charge capacitors in parallel and discharge them in series.  This will multiply your 30kv by however many stages you have and improve the amperage because you stored up a long times worth of power and it discharges fast in pulses once every few seconds.  I suggest maybe 1-10 stages (the fewer stages the faster it should spark but the lower voltage you will have).  This will bring us up to 300kv.  Now you may ask why not just use more stages of the CW transformer instead of using a marx generator?  Well because we need pulsed DC.  In order to elevate our voltage even more we need pulsed DC.  Only pulsed DC will work to input into a transformer.  And since we want to go for insane voltages, we need to use a transformer.  Now we just make an ultra high voltage transformer.  You make it ultra high voltage by making there be big gaps between the transformer layers of the secondary so sparks can't jump the gap.  Also make sure the primary is also separated from the secondary with a big gap or insulator.

If we use a 1:10 winding (induction) ratio between the primary and the secondary we will multiply our voltage another 10 fold... bringing us up to 3 million volts or 3 mv megavolts.  Also we should have decent amperage because of our marx generator.  So we have 3 million volts of pulsed DC power.  Just what we need for cold fusion.  Cold fusion will not work with AC (like a tesla coil or magnifying transmitter) as far as I am aware because the frequency is too high to support neutron production / generation.

Also for the end transformer, you should have a soft iron core or mild steel.  As big diameter as possible.  Wind the primary (input coil) on the iron rod.  Then put insulating material then put iron foil (0.5mm-0.1mm, reduce thickness as you move away from the center of the rod) then more insulator then wrap your next layer of copper wire.  The primary and secondary are not connected but the multiple layers of secondary coil are all connected.

PS: Decided to go with a 12" long 4" diameter 1018 steel rod (onlinemetals.com) for my transformer core.  Primary will be wound first with 8 awg magnet wire.  Then 30 mil nomex sheet (insulator) then 20 mil pure iron sheet then 30 mil nomex then secondary 18 awg (not connected to primary).  Then nomex/iron/nomex (the iron sheets can get thinner as you go outwards if desired) then 23 awg wire wound up connected to the 18 awg one.  This is the tertiary.  Nomex/iron/nomex then 27 awg wire wound up connected to the 23.  This is the quaternary.  Nomex/iron/nomex then 30 awg wire wound up connected to the 27.  This is the pentary.  The guages were carefully selected based on what the input voltage is compared to the input voltage of the last coil.  So if the voltage was 3 times higher at the output of the 27 awg for example then I selectedthe next wire to have a power current rating of 3x less amps as the last one had.  I started with 18 awg arbitrarily though and worked down from there.  To  calculate voltage I used turns of the primary (92) and turns of the coil of interest.  If say the coil of interest had 184 windings to make it the whole 12 inches then the voltage doubled from the original 60kv.  If there was a secondary coil before that one I added the voltage from there plus 120v.  Then I did the new voltage divided by the previous voltage to find out how much that coil changed the voltage.  That multiplication constant then was used to divide the power amperage carrying ability of the old wire to find the awg of the new wire that carried that amount times less.  That is how I determined what wire awg to use for each coil.  The resources I used were:




So my current build is 15kv .06 amp power supply.  Feed that into 1 stage of CV multiplier to get 30 kv.  Feed that into 1 stage of Marx generator to get 60kv.  Feed that into my transformer to get 1.745 MV. My transformer will also preferably be submerged in liquid nitrogen to reduce resistance losses.  Why not right?  

Also the reason I used iron sheets was to basically effectively enlarge the iron core helping bring more magnetic flux to the outside wire coils.  Also wrap the finished thing in iron too then some nomex.  Allow it to breathe so it can soak in the liquid nitrogen which will also work as a dielectric better than mineral oil.

So the three innovative things I brought to the transformer was 1. liquid nitrogen to improve conductivity 2. stepping down the wire size in relation to the reduction of amps as the voltage multiplies 3. iron sheets between transformer coil layers. 

And of course this entire circuit, the high voltage ac through a cv multiplier then through a marx generator, then into a transformer.

PSS:  If you want you can substitute out the initial ac neon sign transformer and the CW multiplier for a high voltage DC power supply.  But I coupdn't find nearly as good (high watts) of a hv dc power supply compared to the neon sign ac transformer.

PSSS:  Actually planning on using a full wave CW multiplier so that would be 15kv x3 from the CW = 45kv x2 for the marx is 90kv x 29.1 for the transformer = 2,619,000 volts.

PS4: Always point the B field of every winding (if they are on top of eachother) up towards the north star and make sure every winding is wrapped counter clockwise (negative side up?)

PS5:  The best magnet would be a magnetized iron sphere within another iron sphere that are connected to eachother through the poles (mabye the earth is this?).  If you want to make a toroid out of the transformer by attaching iron sheet to the top and botton; attach it to the corner s at 45 degree angles.  Even just making the top and bottom of a bar "flared out" would also help.  Ideally one would want to input a frequency of DC pulses into the transformer that matches the ringing frequency of the transformer itself.  Basically the magnetic field produced on the core by the primary will induce current in the secondary which itself will induce a magnetic field (in the same direction as the primary if it is wound right; use the "right hand rule") which will induce a current in the tertiary which, by virtue of the magnetic field it creates induce another current in the secondary again... and so on and so on. Sp basically you are looking to create the highest anplitude standing waves of power; basically just look for the best ratio of power out of the pentiary vs power in to the primary.  So vary the frequency of input pulses from the marx generator (by varying the capacitance and/or number of stages, but voltage of each capacitor should be the same) to get the best ratio of output power from the pentiary vs input power into the primary.


Cold Fusion using acidic electrolysis of regular light water

I have been attempting to make gold when I stumbled upon an interesting find,  acidic hydrolysis produced much more heat than alkaline hydrolysis and also seems to produce neutron radiation.

I used two iron electrodes (but could be any conductive material) submerged in distilled water and 30 volt power supply running at about 10 amps by putting in a slight amount of sulfuric acid into the distilled water.   Just enough acid to get 10 amps at 30 volts.  

What I noticed was incredible heat produced and peripheral neuropathy like I was bombarded with neutron radiation. Even a foot of sand wasn't enough to stop the effects, adding water to that sand did however reduce the effects.  This leads me to believe we are dealing with neutron radiation.

The mechanism for this may be that the H+ ions in acidic solution were undergoing electron capture or 'positron emission' and being converted into neutrons.

To harness this power lithium or boron compounds and water can be used to absorb the neutrons and convert the energy into heat.

Alternating current can also seemingly produce large amounts of heat in water and may also produce cold fusion effects.

Electric Cold Fusion of atomic nuclei mechanism: How gold is made in the earth

In my past posts I have talked about creating gold with a strong electric charge.  Now I am going to propose a theory on exactly how electric charge can induce fusion.

In this hematite lattice we can see each oxygen is bound to 3 irons.  Now the theory here of electric fusion is that since we know a strong electric charge can create oxygen vacancies in a crystal structure, these vacancies coupled with the neutralization of the iron atoms from the same electric charge, allow the three iron atoms to collide/implode along with 2 oxygens fusing them together creating plutonium 200.  This plutonium 200 decays with 15 electron captures/positron emissions and 3 neutron emissions.  (Now I don't believe in positron emission, I believe it is just a high energy electron capture producing a gamma ray instead of an x-ray, but regardless it doesn't effect this theory.) 
What may happen is when 5 neutrons are created rapidly that one is lost as a neutron emission.  Or that neutron loss leads to gamma ray emission (positron emission).  Something to this effect would be needed to explain why both positron emission/electron capture and neutron emission are both happening to convert plutonium 200 to gold 197 and not mercury 200.

Now the iron/hematite is just an example of exactly how this works, but electric fusion in general just requires:

1. a crystal structure 
2. Negative atom vacancies being  produced by an electric charge (ie: oxygen, chlorine, fluorine)
3. An electric charge that neutralizes positive atoms that are a part of the crystal structure that are in proximity to the vacancies (probably the same electric charge from #2 but not necessaarily)

The predictions of this theory are:
1. We will see x-rays (from electron capture) and/or gamma rays (from 'positron emission') emitted which signify electric fusion is happening.
2. We will see neutron emission. (unless the exact amount of atomic mass units are produced ie: iron 55 is being made/used to produce plutonium 197.)
3. We should see elements being transmuted.

**Update** high mercury contents found in gold!
This means that the Iron 55 method is probably right, so we need neutron radiation to convert Iron 56 and 54 to 55 in orderto make gold.

So all that is needed is an oxide of the form of hematite and a strong electric charge to transmute elements.  The charge just needs to be protected so that it doesn't induce a chemical bond between ions instead of electric fusion within the crystal lattice.  So negative ions should be blocked from interacting with the target oxide.  

This can also work with other elements besides iron; Manganese in this form may be able to create platinum for example.


Making gold from iron electrolysis appears to have worked, update later today

So I have been working on making gold and this is how I did it.

two 3/8" steel bars put in distilled water in a glass (not touching each other). Put in a tsp or so of sulfuric acid.  Hook up the bars to a 30 volt power supply around 2 amps or so.

Electrolyze for a long time but changing the polarity of the electrodes often (switching which electrodes is positive and which one is negative).  Run it for as long as you can.

All of that muck is your gold "concentrate".  Now wash it (by adding water, letting it settle, and pouring off the excess water) and then dissolve it using hydrochloric acid and peroxide and heat.

Once it is all dissolved and the liquid is clear, let it cool then add SMB (sodium metabisulfite), you may need quite a bit but if you add too much it will turn all opaque and foggy, you don't want that.  You just want enough until it stops fizzing when you add it, maybe a little bit more.

Now wait a day and you should see a dusting of tan to blackish powder on the bottom of the glass.  This should be gold.  Carefully pour off the liquid.  Add more distilled water (only use distilled water in this whole process) let it settle another day, then pour off the liquid again.  Do this once more.  Now when you pour off the liquid, heat up the remaining powder and water to evaporate all water.  

This is what is left: (looks like gold but who knows)

Now put this remaining powder in a crucible and melt it into gold. (may need to add borax, doesn't seem to want to easily melt into gold)

I am at the final step now, once I melt it and verify it is gold I will let you know.  

ps: since I don't really have enough to reliably melt into gold I am aquiring a stannous (tin) chloride test solution to test this for gold rather than trying to melt it.


Clean legal nuclear power reactor using bismuth lead thallium

Here is the invention of a clean safe and legal nuclear reactor.

We use our neutron production from our previous method of generating neutrons from hydrogen sulfide/selenide/telluride and quartz/hydroxide/iron oxide system.

To the iron oxide we add beryllium oxide (or another high temperature neutron moderator).  This slows neutrons down so that we can capture them later.  Now we take a large atom like bismuth (largest easy to acquire element) to capture our slowed (thermal-like) neutrons.  The reason we want big elements is they decay quickly and release radiation that we will absorb to produce heat.

To add the neutron capturing atom we include that in the quartz crystal described in the how to make gold post. Quartz crystal can act as a neutron filter to only allow slow neutrons to enter.  Now the slow neutrons interact with the bismuth atoms in the glass and create unstable bismuth isotopes.  These emit radiation which is captured by a neutron absorber, preferably borax or boric acid infused water.  This setup is preferably placed underground for safety or is shielded with heavy elements to protect against gamma rays from escaping.

Also we can tune the temperature of the reactor so that neutron capture is effected.  Anywhere from near absolute zero to high temperatures can be used to vary the reactor properties like neutron capture/reemission rates and how many neutrons can be captured before decay. Having todo with the resonance of the atomic nucleus with the neutron it is trying to capture.  R and S process and what isotopes are formed can also be effected.  If the temperature is low and the neutron speed is low and constant then likely we will expect greater frequency of neutron capture since the resonance peak is higher and narrower.  This can allow for more R process capture happening.

Notes on clean independent high power generation

How to make power

so we need neutron creation, moderation, filters, acceptors, reflectors, and absorbers.

creation and moderation coupled.  Iron oxide (creation) and beryllium oxide (moderation).

filter and acceptor coupled; quartz is the filter and bismuth is the acceptor.  Bismuth oxide added to glass then made into quartz.

Neutron stuff

neutron filter bismuth quartz


neutron reflector beryllium graphite

neutron absorber boric acid

neutron moderator (thermal neutron)

moderator vs reflector (lighter moderates heavy reflects)

the slower the neutrons the more lighter elements reflect.


Appendicitis is caused by bacteroides infection

This bacteria was isolated from the majority of removed appendixes that tested positive for bacteria.  It is especially present in more severe cases. This is a gram negative bacteria so that means appendicitis can be prevented or treated with food grade diatomaceous earth.


Where cold fusion really shines: Thorium production

So as we have seen, cold fusion doesn't produce excess energy.  Creating neutrons from electrons takes a lot of potential energy, and really the best we can hope for is to get our electrons back.  If we could break even in energy usage we would be very very happy (and could make gold from iron for free).  

Well then how does this help us on our quest for better energy for all?  Well since we can make heavier elements we can make elements that are typical nuclear fuel.  

So lets take thorium for example.  Thorium is produced probably from Rubidium.  Thorium is 4 spaces to the right of rubidium and 3 spaces down just like gold is to iron.  I believe this is the standard difference that usually can produce a new element.

Things that support this notion is that rubidium is found in high concentrations of seawater and thorium is insoluble in water.  Thorium is found in high concentrations on the sea floor.  So it could easily be that rubidium is converted into thorium on the surface of the ocean by light and probably the reducing action of phytoplankton and it falls to the bottom of the ocean.  

In order to figure out exactly how to replicate this we should study the electron transport chain of phytoplankton and figure out the intercellular reducing compounds that the creature makes.  Also we should see where exactly rubidium would fall into that metabolic chain knowing that rubidium would be analogous to potassium so it would be found inside cells.  So we want to find reducing compounds found inside  phytoplankton cells.  When we know this we can use those compounds to convert rubidium to thorium without the cells --or we could farm phytoplankton and feed them extra (below 50% of potassium) rubidium and collect the sediment on the bottom of the tank.--

Anyway after we have thorium the next step is to make it into material that can provide us cheap power.  I believe up to 12% uranium 233 is allowed to be in thorium legally.  This should be plenty for us for small scale power.  We convert the thorium to uranium 233 by including thorium in the process we did earlier where iron was converted into gold.  Mixed in the iron oxide we should have some thorium.  As the iron oxide "nuclear melts" some of the thorium also is given some extra neutrons as the iron oxide nuclear melts from the electrons provided by the quartz crystal.  This should make some of our thorium take up extra neutrons and to create a slightly enriched version of thorium.  We need to stay below the 12% mark to stay legal which is beyond the limit we will achieve anyway.  Then we can use that to make energy from.


Recipe to make gold

gold recipie

3 stage.  First stage is the hydrogen sulfide generating mix.  Careful as hydrogen sulfide gas is deadly.  Make sure you really know what you are doing! 2nd stage is dry ice.  Third stage is iron-quartz.  For the theory of how this works see my previous post(s).

To make the first stage get sulfur and tellurium and make molten and mix.  I will start out trying 75% sulfur 25% tellurium.  Mix in graphite.  I will start with 50% graphite 50% sulfur/tellurium mix. Let cool so you have a solid.  Now grind this into a powder.  That is stage 1.

Stage 3 is alkali quartz hematite.  Get iron (III) oxide (rust/hematite) powder and mix with silicon dioxide and sodium hydroxide.  I will start with 65% sio2, 25% iron(3)oxide, and 10% sodium hydroxide.  Melt this then immediately crystalize at 750-900c.  Let cool and if it looks crystalline then smash to a coarse powder.  That is stage 2.

Now take a test tube that can withstand high temperatures and place the sulfur-graphite powder at the bottom.  Next layer on some clean (not dusty) sand.  Next layer some dry ice.  Maybe now layer cotton.  And now layer your iron-quartz.  Above this you will want to put a cotton layer, then a sodium hydroxide layer to capture excess hydrogen sulfide.  Careful, this won't catch all the hydrogen sulfide and it can be deadly so watch out!

Now once the reaction has run use tweezers to remove the cotton and sodium hydroxide.  Now carefully remove your now hopefully gold rich iron-quartz layer.  Assay your iron-quartz to see if you made gold.  The iron oxide should have partially turned to gold.


 Tellurium is probably better than sulfur but I feel sulfur will catalyze the tellurium sulfide generation.  

try this test tube:


The Co2 may interfere with the bisulfide production on the alkali quartz hematite and produce carbonates.  But we probably need the low temperature to make the gas superconducting and to create gold.


NatureHacker's Cold Fusion Theory

This is not your grandaddy's "free energy" cold fusion.  This is real and no extra energy is gained, the only thing to be gained is creating higher elements and if you do it perfectly it would cost you very little energy (and very cheap raw materials).  So right now the most valuable thing cold fusion can do is create gold, mabye create some even higher elements too.

Cold fusion and nuclear chemistry hinges on one spectacular process;  creating neutrons.  One proton plus one electron combined equals a neutron. This is a well established fact proven by NASA but it is not well known yet by the public.  Neutrons can be created.  The cool thing about neutrons is they are no longer repelled by the nucleus like a proton would be.  They are more free to move.  So the cold fusion theory is that you convert protons into neutrons, add the neutron to an atom's nucleus, the nucleus now expells an electron (beta decay) and the neutron is now a proton and you have a new element.  Sound complicated to do?  Need a CERN particle accelerator?  Nah it's easier than you think.

Electrons are easy to come by.  Electricity.  The problem is that it is difficult to make the electrons leave their defined clouds and to join up with a proton in the nucleus.  There is an elegant way to do this though; superconductivity.  If you can create a superconducting cloud then when you provide extra electrons they can make their way to the nucleus to join with protons much easier.  Think of this superconducting "cloud" as a solvent to dissolve an atom's typical electron cloud configuration and allow electrons to join the nucleus.

Also you can't add electrons to the proton's of a metal.  We know that metals allow electrons to flow through them too easily without interacting with the atoms.  So we need oxides for this (since pretty much every solid and pure element is metal-like).

So lets take hematite (iron oxide) for example.

Our superconductor will be cold depressurized hydrogen sulfide (the best superconductor known; but hydrogen telluride and selenide will be found to be even better superconductors, and probably hydrogen bisulfide too).

Anyway not coincidentally hydrogen sulfide is an excellent reducing agent.  It isn't a coincidence that excellent reducing agents (lots of free electrons) make very good superconductors.  So we get hydrogen sulfide into its superconducting state and put some hematite in there.  Now what we need is to get some free electrons that are at a high energy state.  Enter quartz.  Quartz (silicon dioxide) has a negative surface charge... ie: free electrons.  Also it can very likely capture excess electrons from hydrogen sulfide and store them on it's surface as well.  Since quartz is not conductive these electrons will stay on the surface of the crystal/rock.  Now since our superconducting gas/fluid is hydrogen sulfide which has extra electrons of it's own, we may not need the quartz but it will still be helpful.  We have a downhill reaction catalyzed by a superconductor; electrons move from the quartz into the hematite nucleus via the superconducting fluid/cloud.

Now these electrons get so up close and personal with the protons of the iron oxide via the superconducting pathway that they can combine with the protons and form neutrons.  Turning an atoms protons into neutrons makes the atom "melt" (I'll term it "nuclear melting") into other atoms combining with them.  Since neutrons aren't repelled by the other atoms protons, two nuclei (atoms) can combine into 1.  And when this happens you have a heavier element.  In the case of hematite; it seems that the most favorable element to be formed is gold.

The neutrons now release their electrons as beta decay in order to stabilize once they are in their new home (another atoms nucleus).  These extra electrons can be salvaged if you want, but they aren't going to give you more energy than you had before.

Viola...you just made gold.

And that's cold fusion.


What we likely give Homo Capensis as a society

1.  Our blood plasma.
2.  Glucose from the production of high fructose corn syrup.
3.  Lauric acid.
4.  Plutonium that they use in their anti-gravity craft in order to counter "gravity" (which is really just induced electrical charge).

probably much more.

Gold making attempt 2 recipie

Since I know that light is just the vapor form of electrons, this should work well to cause cold fusion and produce gold.  What I will do is use a large fresnel lens and dig a hole in the ground.  Set the fresnel up to focus at the bottom of the hole.  Put a mixture of the below in the hole and leave!: (the hole will help block radiation produced and leaving will help you not be exposed to sulfide gas and radiation in the process.  Wait at least a couple hours.)

silicon dioxide
sodium hydroxide.

(not sure on exact proportions, experiment)

Sulfur selenium tellurium when combined with heat and a hydrogen source like graphite will produce the respective hydrogen -ides (like sulfide telluride etc). These are our potent electron sources (along with the sunlight).  Now these -ides combined with sodium hydroxide will create bi-ides like bisulfide.  This is an even more potent reducing (electron giving) compound.  Hematite is what transmutes into gold, and silicon dioxide seems to be some sort of catalyst.  Maybe electrons are stolen from it, not sure.


How to make cold fusion theory

We thought about this all wrong.  You don't need to bombard an atom with protons and neutrons to make it grow.  All you have to do is provide it with extra electrons.  When you really give an atom more electrons what happens is it melts. The atom will pull another atom's nucleus into it to share the electrons.  Think of an electron cloud as a fence and the protons and neutrons in the nucleus as cows.  If you enlarge the pasture (make the fence bigger by adding more electrons) then the other nearby pastures will combine into 1 and all your cows will be together.  This is how cold fusion works.  You don't shoot cows at the fence (nuclear bombardment) if you are smart.  You simply open and enlarge the fences to encompass your neighbors cows.  This is what cold fusion is.  The melting of nearby atoms into one.

Now this sounds hunky-dory and peaceful.  And it is for the most part but these atoms could create unstable versions when they combine and could possibly release radiation in order to stabilize.  So be careful and make sure the contraption is underground so gamma rays or alpha/beta particles don't do damage to you.  We are doing nuclear chemistry after all.

You can't use metals for this.  Metals are way too conductive and instead of electrons sticking to them it will flow right through and nothing will happen.  We need oxides.

Now I don't claim to have it all figured out, this is just the beginning of the research.  But in order to make gold we need quartz (silicon dioxide) and hematite (fe2o3).  I believe its the hematite that transforms into gold but for some reason quartz seems to be needed. 

Anyway what we need is a STRONG source of electrons.  Or maybe just a superconducting pathway between the silicon dioxide and hematite.  Nature uses H2S and H2Te.  At the temperatures and pressures underground these gasses can be superconducting when they are rapidly cooled and depressurized.  This happens in an earthquake.  As the superconducting h2s (or better yet h2te) rush by the quartz and hematite maybe  electrons are siphoned from the quartz and given to the hematite, or maybe the quartz isn't needed and the superconducting sulfide gas just melts the hematite on its own into gold.  In any case the hematite gains extra electrons and the atoms of hematite melt together into gold.  Like I said there are probably neutrons/protons/gamma rays lost so be very careful if trying experimentation.

The element to the left of iron on the periodic table (manganese) may react in the same way as iron but instead of producing gold, may produce the element to the left of gold, platinum.  And maybe  the elements to the left (and/or right) of those too do the same thing and so on.

Microwaves and light and electricity are also sources of electrons so may also work but it would be much more difficult to achieve than with superconducting sulfide gas.

One method to make sulfide gas superconducting at room temperature may be to turn it into a plasma in something like a halogen light bulb.  Have a hematite electrode(s) and conduct electricity through the sulfide gas and maybe gold will form.  Or do it the old fashioned way and pressurize/heat sulfide gas and rapidly depressurize and chill it through hematite/quartz mix and see if gold forms.  Be very careful not only could the gold produced let off gamma rays but also hydrogen sulfide gas is deadly!  So don't do this without really knowing what you are doing!


How to (mabye) make gold

I do not recommend trying this without adequate protection from gamma radiation.  Creating gold may create gamma rays.

Coarsely crush quartz and mix in hematite powder.  Run superconducting hydrogen sulfide or hydrogen tellurium through the mix.  Collect the gold produced.  Getting the h2s or h2te to be superconducting is the tricky part, you would need high temperature high pressure tanks of it and run it through a (dry ice) chilled expansion valve into a tube containing the quartz-hematite mix.

the below was from old thoughts and didn't work
The mix would be iron powder and food grade diatomaceous earth melted at very high temperatures like the 5,000f with an HHO torch or oxyacetylene.  Potassium hydroxide may also help catalyze the reaction.  This is based on the notion that burning silicon can create iron and as iron is created it could catalyze gold creation.

I have been studying gold veins in quartz and it seems that superconducting hydrogen sulfide with quartz in the presence of catalysts (iron containing minerals and possibly others) can create gold.

"At pressures above 90 GPa (Gigapascal), hydrogen sulfide becomes a metallic conductor of electricity. When cooled below a critical temperature this high-pressure phase exhibitssuperconductivity. The critical temperature increases with pressure, ranging from 23 K at 100 GPa to 150 K at 200 GPa.[11] If hydrogen sulfide is pressurized at higher temperatures, then cooled, the critical temperature reaches 203 K (−70 °C), the highest accepted superconducting critical temperature as of 2015. By substituting a small part of sulfur with phosphorus and using even higher pressures, it has been predicted that it may be possible to raise the critical temperature to above 0 °C (273 K) and achieve room-temperature superconductivity"

hydrogen telluride is probably a superconducter at higer temperatures and is why telluride bearing gold viens can go deeper into the earth.  This would be great for gold production.


Bookmark my Guide to Gut Microes!

This is what my next book will primarily reference:


Please bookmark it and check it regularly!  I update 
it constantly and there is a treasure trove of information on
how to keep your gut and body healthy!


Hacking drug withdrawl

As a curious youth in college I experimented heavily with Salvia divinorum use.  I wanted to experience the hallucinogenic states to gain insights about the truth behind reality.  Basically to understand more about life.

Well it was a drug and drugs have consequences.  For receptor agonists like salvia (very potent kappa opioid agonist), they cause a down regulation in receptors.  When you overwhelm the body with a agonist (activator) the body responds by reducing the amount of receptors so excessive activation can't happen.  It basically adapts to the new normal.

Bow problem is when you stop taking the drug you are now below the new normal and experience the effects of bieng low on it.  So if you take morphine all the time and stop taking it, your body will think it is now low in morphine and you will wothdrawl.

Well I stopped taking salvia about 13 years ago but I still haven't recovered.  I believe my sleep disordered breathing is caused by low kappa opioid receptors.  I have two reasons to think this; first some erowid trip reports of heavy users mention that they have severe sleep disordered breathing.  Also kappa receptors block the sleep disordered breathing that opiates cause.  So if salvia over time down regulates kappa receptors, then there is nothing to stop opiate induced sleep disordered breathing (sleep apnea, etc).  Obviously I don't take opiates but the body produces opiates naturally.

So what do I do?  Well you have to fight fire with fire in this case.  If the cause of your problems was a drug, it will take a drug to fix them.

Kappa receptor antagonists.  Since I caused a down regulation of receptors with the agonist salvia, I have to cause an up regulation with an antagonist.  This antagonist is a plant called selaginella tamariscina.  This plant contains the perfect antagonist; amentoflavone.  This kappa antagonist is very selective to only antagonize kappa receptors.  This will mean that by taking it I will increase the amount of kappa opioid receptors without effecting the other receptors like mu and delta.  This should cure my problem and may help many people fighting central or obstructive sleep apnea (or especially a mix of the two).


Cold Stone Ice cream hacked real recipe

So I reverse engineered cold stone's actual base ice cream (sweet cream) recipie.  They use this recipie for the base of all their ice cream then add vanilla or other flavoring and more sugar depending on the flavor.  I did this using their ingredient list and the nutrition facts.  With just those two things and enough mathmatical calculations, you can reverse engineer any recipie.

Makes roughly 1kg (2.2 lb)

390g heavy whipping cream
390g skim milk
41g whole milk
3.75g whey powder (pure)
61g corn syrup
132g white sugar


200g half an half 1cup
15g corn syrup 2 tsp
33g sugar 2.5 tbsp

turns out half and half is not actually half milk and half cream so we need to do...

so simplified recipie:

1 cup heavy whipping cream

1 cup skim milk (or water even if sensitive to milk)

5 tbsp sugar

4 tsp corn syrup

Use your favorite method to turn this recipe into ice cream.  Cold Stone uses capigiani 502g batch freezer.  The quicker the ice cream machine freezes the ice cream the better.


Treating central cerebral edema naturally

Strep seems to be a bacteria associated with this so adaptogens for that.

Looks like I took a little too much rennet (10 drops or so over a couple days) and felt a little pressure in my head.  Aspartic proteases are good at extracting collagen and it may have stripped some collagen from my blood brain barrier causing a fluid pressure imbalance.  It turns out that the CSF is deficient in potassium and bicarbonate and protein  and glucose compared to the blood.  This means if you take potassium bicarbonate and protein and glucose/starch it will osmotically pull fluid from the csf into the blood.  I took about a half tsp of potassium bicarbonate and slightly elevated my head at night and feel better now.



TEEF Powder up and running again!

Turns out an HHO torch will work to make tetra calcium phosphate! (the key ingredient to teeth remineralization).  Picked up the micro flame polisher H180A from ebay for a couple hundred bucks and couldn't be happier!  Never have to buy gas tanks or refill gas since it just uses water to make hydrogen and oxygen!  I can run two torches at once with it, one for each hand!  Just mix 12g CaOH with 50g TCP thoroughly  and put in a flame proof container and start torching it!  Only melts a little powder at a time and you will need to wear 2 pairs of polarized sunglasses so you can see what you are doing.

Hair-loss male female pattern baldness is caused by a pepsin (aspartic protease) deficiency

Pepsin deficiency:
H pylori
heart disease (Coronary artery disease)
high cholesterol
gluten sensitivity

Hair loss is caused by the buildup of collagen in the hair follicle.  This is caused by type XVII collagen being destroyed which leads to triggering the body to synthesize more collagen and subsequent buildup.  Kind of like in the game tetris, if you can't eliminate the bottom rows then it builds up and you have a crash.

So how do we eliminate the collagen properly?  Aspartic proteases.  Aspartic proteases like pepsin are used in biology research to extract collagen without destroying it.  These enzymes are needed to maintain a health scalp (and also healthy brain against Alzheimer's and healthy blood vessels against plaque buildup from an aspartic protease cathepsin d). In order to achieve this we could supplement aspartic (cheese making) enzymes from plants like cardoon and thistle flowers, animal rennet, or pepsin itself.  Don't go overboard though because enzymes are powerful medicine and may make cancer grow more rapidly.

H pylori is either the cause or result of pepsin deficiency and pepsin deficiency also causes gluten sensitivity.

rennet chymosin



buy veal rennet

cardoon stamens cynarase 

cardoon rennet

mutagen studies


cathepsin d alzheimers breast cancer but also metastasis.

cathepsin b cystine protease

pepsin extracts collagen

collagen follicles

collagen breakdown products cause collagen synthesis and buildup.