From: treon3verdery@gmail.com   
      
   If the first laser foil has refractive index or negative refractive index that   
   focuses the percussing laser onto the next laser foil. Making the second laser   
   foil to have the opposite of a transparency grating causes immediate higher   
   amplitude laser    
   percussing from higher laser concentration and percussing. At a crystalline   
   metal laser foil the crystal face the laser reaches (i have heard of 111   
   crystal face) could effect laser percussion effects on the foil, making many   
   more particles, like pions->   
   muons occur as an output. Another possibility is to simply make the entire   
   first laser foil, or an optical element,  a holographic grating that   
   multiplies a single 1-11 watt laser into thousands or millions of spatially   
   separate dot-beams. A million dot    
   beams could produce a million times more pions->muons, useful in muon   
   technologies like muontricity, if the frequency of femtosecond pulse laser   
   foil percussing can be raised to a million laser percusses per second or   
   higher than the amount of muons    
   produced from pions becomes a trillion times larger from the combination of   
   dot beams and 1MHz frequency of the femtosecond laser pulses. Replacement of   
   electrons with muons at chemistry, and noting muon atoms are 200 times smaller   
   than electrons there    
   is lots of all new muon atom chemistry, including catalysts. Multiply   
   retroreflected muon beams travelling through ch4 gas could cause 1 or more of   
   the atoms at CH4 to be a 200 times smaller atom, which very extremely   
   destabilizes the CH4, causing the    
   ch4 molecules to be willing to combine with each other to make more valuable   
   longer hydrocarbons.    
      
   Lasered PMMA enterosorbents, swell in gi tact and have tremendous dendritic   
   channel sorface area optimally higher than activated carbon. Enterosorbents   
   are published as making mice live 40% longer, PMMA or other polymer that   
   swells to 2K its original    
   volume could make a .5 gram pill occupy the volume of 2 Kg of activated carbon   
   when it puffs up. PMMA is optically transparent so 3D channelizing the new   
   enterosorbent with lasers is likely to work well, it could be cheap to   
   holographically, with a    
   single laser exposure laser dendrify and channelize 100 gram PMMA ingots that   
   are then ground to optimally sized powder for putting in capsules. Enteric   
   capsules might be used to keep the enterosorbent from absorbing stomach   
   contents. The new    
   enterosorbent is then tested on marmosets and human (Homo sapiens and branch   
   species) age batched volunteers. Its possible that the very highest dose   
   potency enterosorbents would have the very largest amount of dendritic and   
   connector surface area,    
   suggesting subwavelength of light laser zapping from metamaterials could raise   
   the fineness of feature size an order of magnitude, making a 40 mg   
   entersorbent pill sequester 2 pounds of lower gi tract digesta. The 40 mg pill   
   could be an enteric coated    
   fizzy pill to optimize distribution.    
      
   CAD based Holograms of beamsplitter elements at a dot plurality of a billion   
   beamsplitter elements produce a large plurality of quantum entangled photon   
   pairs for technologies like arrays of delayed choice quantum eraser, MWI test,   
   and Y shaped fiber    
   optic communication over networks. Computers 1 and 2 can be at branches of the   
   Y and share state 10,000 times faster than the speed of light just from their   
   particular photon at the paired photons, femtosecond lasers could be used for   
   trillion cycles per    
   second laser pulse data narrowness. Half lead and half lag photon pairs could   
   be used for computer 1 and computer 2 so either one could lead or receive the   
   bit change. Also i think it is possible to use nested sequential beamsplitters   
   to address 64 bits    
   simultaneously, assisting the computers in their communication.   
      
      
   mRNAs of different sexually excited states in rodents are published, they   
   could try getting both fMRI light up area during human (Homo sapiens and   
   branch species) female orgasm and mRNA profiles and their associated proteins   
   and receptors of marmoset    
   female orgasms and create a drug suite that gives humans, male or female, the   
   experience of female multiple orgasms. Sexually experienced orgasmic women   
   could critique and grow the multiple female orgasm suite of drugs so that at   
   99.9% of them the sexual    
   excitement and orgasm quality is better from the protein or small molecule or   
   peptide drug suite alone, and the drug suite with one or more partners having   
   sex is even better than the drug suite alone.   
      
   Topical fast penetrating NMN, NR, NAD, and atp could all be tested to see if   
   they, or neural/nerve stimulants like acetylcholine drugs or glutamate drugs   
   increase the pleasurable sense of touch, after harmless or beneficial topical   
   drugs that increase    
   the pleasurable sense of touch are found they could be made into ingredients   
   for a bodywash, sexual pleasure entire body surface oil or massage oil, or at   
   high dose potency drugs (fluorination, ethynylization, cell membrane passing   
   moieties or peptides)    
   a single drug michael reaction to keratin (like transparent henna) diffuses   
   the enhanced pleasure drug at all body surface through the skin for 3-6   
   months. It is a whole body surface technology but there could be additional   
   concentrations at the nipples,    
   breasts, other erogenous zones, and genitals. Whether you are simply having a   
   hug, getting a massage, or making out with kissing, or having sex pleasurable   
   activity at nerves would go up.   
      
      
   [continued in next message]   
      
   --- SoupGate-Win32 v1.05   
    * Origin: you cannot sedate... all the things you hate (1:229/2)