-------------------------------------------------------------------------------- From: Sent: Monday, October 30, 2017 7:07 PM To: Subject: FW: The Levamisole experiment, Looking to gain knowledge in the suboptimum dose configuration, and the use of body oils, body sulfur thinner, and other moderation techniques to prevent chain reaction killing of threadworm infections -------------------------------------------------------------------------------- From: Sent: Monday, October 30, 2017 6:42 PM To: Subject: Threadworm elimination time = 1 year Clearing Co Infections, Clearing Strongyloides Using aforementioned methods and techniques, The treatment time will be greater than 6 months for threadworm elimination, and possibly 6 months to eliminate the gigantic flat worm species from the body. This places a benchmark time to eliminate threadworms at one year -------------------------------------------------------------------------------- From: Sent: Monday, October 30, 2017 5:16 PM To: Cc: Subject: FW: The Levamisole experiment, Looking to gain knowledge in the suboptimum dose configuration, and the use of body oils, body sulfur thinner, and other moderation techniques to prevent chain reaction killing of threadworm infections And use less GuaiAid? -------------------------------------------------------------------------------- From: Sent: Monday, October 30, 2017 5:13 PM To: Subject: The Levamisole experiment, Looking to gain knowledge in the suboptimum dose configuration, and the use of body oils, body sulfur thinner, and other moderation techniques to prevent chain reaction killing of threadworm infections Worms are able to force cells into G1 replication as method to protect kill of aggressive fast and oversaturated Strongyloides tissue. If raster is to be maintained in fluid tissue structure, lower Levamisole salt must be used, As the infection quells, increase of LEV % increases, as dying parasites release their Levamisole, essentially causing a chain reaction that causes the body to flow melt tissue. Higher IVM dosing using skin tissue fat to moderate the dose, can be done with lower level oral dosing to create a Invermectin reacted solution Optimum kill rate would ensure low white worm, red worm, and flatworm infections exist at the time of the Strongyloides purge. Once started, the reaction point is unstable and unregulated. Rapid body kill causes raster distortion and the body essentially melts. Key structures can be lost, including urine structures, flow structures, and other critical area tissues. The replication of melt, in a Levamisole moderated kill is unstable. The most stable participant is either IVM, or Praziquantel. Moving to a IVM dominant med causes little improvement in the final kill of Strongyloides in the body. The correct or best guess improvement in the threadworm killing process, is to use body skin dosing to increase the killing power of IVM by almost an order of dose magnitude. The time precision of 4 doses per day is assumed to be required. Pulse time of Praziquantel, lower Levamisole levels, with less parasite Levamisole storage in body tissues, lowers the possibility of instability Drink more Pepsi, phosphate chemistry would have added to instability possibly, but also could have stabilize the rate of kill and the ability of the parasite worm to liquefy structures by introducing a genetic card of forcing the tissue into replication as a defense mechanism. 6 months was used, 3 months red worm kill, then 3 month max level kill rate without stroke, to remove deep bone and tissue infections, but as the infection became unstable with to many works dying and offering up Levamisole lag in removal due to damage to kidneys, and liver, with an underestimated burden of large flat worm gigantic structures led to a poor retention of raster in the genetic replication, leading to a substandard cure, with higher than acceptable tissue structure retention.