Neil Lipken (27 July 2012)
"Every American To Be Microchipped In 2013 Per Obamacare"

Revelation 13:16 & 17 King James Bible

"And he (the false prophet, one of the satanic trinity-----antichrist, false prophet, and satan) causeth all, both small and great, rich and poor, free and bond, to receive a mark IN their right hand, or IN their foreheads:  and that no man might buy or sell, save he that had the mark........"

Did you catch that?  "IN" the right hand or "IN" the forehead!  Now just how could John, who was given the book of Revelation from God on the Greek Island of Patmos late in the first century, just exactly how could he have known such a thing?!  Only very recently have implantable microchips come into use, at just precisely the right time now that we are late into these End Times (Israel is now over 64 years old).  And you know what?  Most people will just put their heads in the sand and refuse to consider these things!  And they will find themselves here AFTER the Rapture, facing the worst 7 year time period in all of human history!  


Every American To Be Microchipped In 2013 Per Obamacare
Wednesday, July 25, 2012
A major news story broke on AOL and countless other mainstream news media outlets, this past week, that the Obama Health Care Bill will require all U.S. citizens and babies to receive a microchip or Medchip by March 23, 2013. Whether or not the microchip requirement in the bill is implemented by 2013, remains to be seen.
In 2010, my book “Are You Ready for the Microchip?” was released, and I asked the question, “Is the microchip implant hidden in the Healthcare Bill? Are newborn children starting in 2013 going to receive a microchip shortly after birth?” Then in the book, I wrote, “ In the massive US HEALTHCARE BILL, which your elected representatives voted for without reading, there is a section titled: Subtitle C-11 Sec. 2521 – National Medical Device Registry which states:Continued below.
“The Secretary shall establish a national medical device registry (in this subsection referred to as the ‘registry’) to facilitate analysis of postmarket safety and outcomes data on each device that—‘‘(A) is or has been used in or on a patient; and ‘‘(B) is a class III device; or ‘‘(ii) a class II device that is implantable.”