Don't take the MARK people! ObamaCare Mandates RFID Chips to be Implanted in all Americans by March 23rd 2013?

Well post it you Dick!!

obama is the world leader he is the head of the united nations 1st president to reside as president of the USA and the UN at the same time.. It is the mark of the beast. 1 it will forced upon us which it has and continue to (rev 13:9-12), 2nd it will also link your financial info on it. this is not in writting now but its a no brainer to know that they will link it.. dont fear if you trust in GOD

You've got it all figured out, don't you? THIS is the Mark of the Beast, without a doubt. It couldn't be something to come later. It's THIS, right now. You know this because on some other website, someone once wrote that the "Mark of the Beast" would be an RFID tag. You believed that person, and now you know that this is it. It all just makes perfect sense doesn't it? It couldn't possibly be any more complicated.

People and their egos.

You have to pass it before you can find out what's in it.- nancy pelosi

This

LOOK UP HEALTHARE NULLIFICATION ACT

what about the frequencies emitted from these chips? these will cause serious problems with people's minds.

even if one doesn't believe in the mark, this chip mandate is a VERY bad idea.

Jesus Christ OP you are fucking stupid and so is anyone buying your bullshit.

OP, just wanted to let you know, that you're dumb. Really, really dumb. If you read that that bill and think it said anything about mandatory implants of RFID chips, then your reading comprehension is at about a Grade 3 level. Maybe lower.

But I strongly suspect that you may not be dumb, and that like most people on this site, you're just a flat out liar.

[link to www.youtube.com]

You're right, of course. And all should watch the video.

Another liar...

It says that very thing.

You're also a liar.

It says that very thing.

I haven't read it, but you obviously have, so you would know exactly where it says it. So why not copy and paste what it says?

You keep saying that to everybody so why don't you post it??

If they try chipping me, they will not do it without a fight to the death with me.

I'm NOT going to live in a tyrannical state.

This law doesn't take effect until 2014. So this is BS.

this is not the mark of the beast; but the RFID isn't even in the bill that was passed.

I wouldn't want to either. In fact, I think most people that can think for themselves wouldn't want to live in a tyrannical state.

Speaking of thinking for myself, I find it strange that nobody can post actual evidence from the wording in the bill that supports mandatory RFID implants for everybody.

Here's the bills as they are written,the same bills this dick wad claims to contain the rfid law.

Here's HR4872 and HR3590

[link to housedocs.house.gov]

[link to www.gpo.gov]

Just Copy and paste the RFID clause so we can see it..

wow! great clip! I've always been huge fan of twilight zone, but somehow missed that one. thanks!

So...we're all still waiting for the proof that the bill mandates RFID implants.

OP? OPs minions? Anyone? Bueller? Bueller?

OP. You lying sack of crap. Chip my ass. You know, I wasn't gonna vote for Obama again, but when I read lies like this, from people like you...I actually think I will.

Now, We have see it all. sick world sick people.

Page 1014 of hr4872, then read down about 5 pages to have it in context.

Well??...Is anybody going to copy and paste the RFID clause??

first link

20 Subtitle C—National Medical
21 Device Registry
22 SEC. 2521. NATIONAL MEDICAL DEVICE REGISTRY.
23 (a) REGISTRY.—
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•HR 4872 RH
1 (1) IN GENERAL.—Section 519 of the Federal
2 Food, Drug, and Cosmetic Act (21 U.S.C. 360i) is
3 amended—
4 (A) by redesignating subsection (g) as sub5
section (h); and
6 (B) by inserting after subsection (f) the
7 following:
8 ‘‘National Medical Device Registry
9 ‘‘(g)(1) The Secretary shall establish a national med10
ical device registry (in this subsection referred to as the
11 ‘registry’) to facilitate analysis of postmarket safety and
12 outcomes data on each device that—
13 ‘‘(A) is or has been used in or on a patient; and
14 ‘‘(B) is—
15 ‘‘(i) a class III device; or
16 ‘‘(ii) a class II device that is implantable,
17 life-supporting, or life-sustaining.
18 ‘‘(2) In developing the registry, the Secretary shall,
19 in consultation with the Commissioner of Food and Drugs,
20 the Administrator of the Centers for Medicare & Medicaid
21 Services, the head of the Office of the National Coordi22
nator for Health Information Technology, and the Sec23
retary of Veterans Affairs, determine the best methods
24 for—
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•HR 4872 RH
1 ‘‘(A) including in the registry, in a manner con2
sistent with subsection (f), appropriate information
3 to identify each device described in paragraph (1) by
4 type, model, and serial number or other unique iden5
tifier;
6 ‘‘(B) validating methods for analyzing patient
7 safety and outcomes data from multiple sources and
8 for linking such data with the information included
9 in the registry as described in subparagraph (A), in10
cluding, to the extent feasible, use of—
11 ‘‘(i) data provided to the Secretary under
12 other provisions of this chapter; and
13 ‘‘(ii) information from public and private
14 sources identified under paragraph (3);
15 ‘‘(C) integrating the activities described in this
16 subsection with—
17 ‘‘(i) activities under paragraph (3) of sec18
tion 505(k) (relating to active postmarket risk
19 identification);
20 ‘‘(ii) activities under paragraph (4) of sec21
tion 505(k) (relating to advanced analysis of
22 drug safety data); and
23 ‘‘(iii) other postmarket device surveillance
24 activities of the Secretary authorized by this
25 chapter; and
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•HR 4872 RH
1 ‘‘(D) providing public access to the data and
2 analysis collected or developed through the registry
3 in a manner and form that protects patient privacy
4 and proprietary information and is comprehensive,
5 useful, and not misleading to patients, physicians,
6 and scientists.
7 ‘‘(3)(A) To facilitate analyses of postmarket safety
8 and patient outcomes for devices described in paragraph
9 (1), the Secretary shall, in collaboration with public, aca10
demic, and private entities, develop methods to—
11 ‘‘(i) obtain access to disparate sources of
12 patient safety and outcomes data, including—
13 ‘‘(I) Federal health-related electronic
14 data (such as data from the Medicare pro15
gram under title XVIII of the Social Secu16
rity Act or from the health systems of the
17 Department of Veterans Affairs);
18 ‘‘(II) private sector health-related
19 electronic data (such as pharmaceutical
20 purchase data and health insurance claims
21 data); and
22 ‘‘(III) other data as the Secretary
23 deems necessary to permit postmarket as24
sessment of device safety and effectiveness;
25 and
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•HR 4872 RH
1 ‘‘(ii) link data obtained under clause (i)
2 with information in the registry.
3 ‘‘(B) In this paragraph, the term ‘data’ refers to in4
formation respecting a device described in paragraph (1),
5 including claims data, patient survey data, standardized
6 analytic files that allow for the pooling and analysis of
7 data from disparate data environments, electronic health
8 records, and any other data deemed appropriate by the
9 Secretary.
10 ‘‘(4) Not later than 36 months after the date of the
11 enactment of this subsection, the Secretary shall promul12
gate regulations for establishment and operation of the
13 registry under paragraph (1). Such regulations—
14 ‘‘(A)(i) in the case of devices that are described
15 in paragraph (1) and sold on or after the date of the
16 enactment of this subsection, shall require manufac17
turers of such devices to submit information to the
18 registry, including, for each such device, the type,
19 model, and serial number or, if required under sub20
section (f), other unique device identifier; and
21 ‘‘(ii) in the case of devices that are described in
22 paragraph (1) and sold before such date, may re23
quire manufacturers of such devices to submit such
24 information to the registry, if deemed necessary by
25 the Secretary to protect the public health;
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•HR 4872 RH
1 ‘‘(B) shall establish procedures—
2 ‘‘(i) to permit linkage of information sub3
mitted pursuant to subparagraph (A) with pa4
tient safety and outcomes data obtained under
5 paragraph (3); and
6 ‘‘(ii) to permit analyses of linked data;
7 ‘‘(C) may require device manufacturers to sub8
mit such other information as is necessary to facili9
tate postmarket assessments of device safety and ef10
fectiveness and notification of device risks;
11 ‘‘(D) shall establish requirements for regular
12 and timely reports to the Secretary, which shall be
13 included in the registry, concerning adverse event
14 trends, adverse event patterns, incidence and preva15
lence of adverse events, and other information the
16 Secretary determines appropriate, which may include
17 data on comparative safety and outcomes trends;
18 and
19 ‘‘(E) shall establish procedures to permit public
20 access to the information in the registry in a manner
21 and form that protects patient privacy and propri22
etary information and is comprehensive, useful, and
23 not misleading to patients, physicians, and sci24
entists.
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•HR 4872 RH
1 ‘‘(5) To carry out this subsection, there are author2
ized to be appropriated such sums as may be necessary
3 for fiscal years 2010 and 2011.’’.
4 (2) EFFECTIVE DATE.—The Secretary of
5 Health and Human Services shall establish and
6 begin implementation of the registry under section
7 519(g) of the Federal Food, Drug, and Cosmetic
8 Act, as added by paragraph (1), by not later than
9 the date that is 36 months after the date of the en10
actment of this Act, without regard to whether or
11 not final regulations to establish and operate the
12 registry have been promulgated by such date.
13 (3) CONFORMING AMENDMENT.—Section
14 303(f)(1)(B)(ii) of the Federal Food, Drug, and
15 Cosmetic Act (21 U.S.C. 333(f)(1)(B)(ii)) is amend16
ed by striking ‘‘519(g)’’ and inserting ‘‘519(h)’’.
17 (b) ELECTRONIC EXCHANGE AND USE IN CERTIFIED
18 ELECTRONIC HEALTH RECORDS OF UNIQUE DEVICE
19 IDENTIFIERS.—
20 (1) RECOMMENDATIONS.—The HIT Policy
21 Committee established under section 3002 of the
22 Public Health Service Act (42 U.S.C. 300jj–12)
23 shall recommend to the head of the Office of the Na24
tional Coordinator for Health Information Tech25
nology standards, implementation specifications, and
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•HR 4872 RH
1 certification criteria for the electronic exchange and
2 use in certified electronic health records of a unique
3 device identifier for each device described in section
4 519(g)(1) of the Federal Food, Drug, and Cosmetic
5 Act, as added by subsection (a).
6 (2) STANDARDS, IMPLEMENTATION CRITERIA,
7 AND CERTIFICATION CRITERIA.—The Secretary of
8 the Health Human Services, acting through the
9 head of the Office of the National Coordinator for
10 Health Information Technology, shall adopt stand11
ards, implementation specifications, and certification
12 criteria for the electronic exchange and use in cer13
tified electronic health records of a unique device
14 identifier for each device described in paragraph (1),
15 if such an identifier is required by section 519(f) of
16 the Federal Food, Drug, and Cosmetic Act (21
17 U.S.C. 360i(f)) for the device.

Nah, you'll do what you've been doing all along. You'll take it lying down, then to back to watching reality shows.