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!
Neil
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.”