Nazarene Space

Tonight the Senate votes to give the Government the power of Life and Death

I am getting old and I am sick. I am a prime prospect for the eugenics program -- Obamacare. No longer are U.S. Progressives happy with murdering people in the womb, now they are trying to expand their power of life and death to beyond the womb. That means they want the power to kill you -- leagally, of course.

These are the decendants of the same people who formed the American Eugenics Society in the early 20th century, today going under the name of Planned Parenthood. But you can be sure other euthansia organizations will pop up as soon as Congress gets a death, or rather, a healthcare bill passed.

These are the dark days that the Biblical prophets warned us of, I just didn't think it would happen to America in this way. I was pretty sure that we would be hit by a few Russian SS-18s (NATO code named: SATAN), a 10 warhead nuclear ICBM. But the Democratic Party has become a Marxist fifth column in our nation, and can we escape the Godly curses that He leveled on other nations who took this Godless road? I think not. So before we are hit by SS-18s brace for a societial and economic breakdown, and a government that wants to murder you for the bottom line.

This is the "Hope and Change" America got with the Obama Administration, now this nation is at the tender mercies of radical Marxist progressives led by Barack Hussein Obama. So are you ready to fight for your rights as a citizen of the Kingdom of Heaven here on earth? You might as well get ready to die for your Savior, because one way or another this government wants you dead.

Our nation was founded as an outpost of the Kingdom of Heaven with Jesus ruling supreme. Now the elite want to rebel against this nation's KING. Don't choose the rule of man over the rule of God. God tells us over and over again to be compassionate to the weaker members of our society -- to help them, not kill them.

If this healthcare bill passes make up your minds to go out and vote for anyone who isn't a Democrat in 2010, from the school board to the Congress. Remember -- like the Nazi Party of the 1930s -- the Democratic Party wants to kill you for the bottom line. That's not "The American Way!"

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Views: 28

Comment by S Scott C on November 21, 2009 at 8:53pm
Yeah, we must be careful to prapare for ourselves besides the governments orders in these last days! And to remember that our Father in Heaven is abiding over even the most powerful of heads in our paths. And that His son will be coming soon in His redeemption and love, Oamain.
Comment by Mikha El on November 21, 2009 at 9:44pm
Nobama bowing excessively to the emperor above is sure sign of his incompetence.


This is a bit discomforting also...


----- Forwarded Message ----
From: ROBB BERRY

Sent: Sat, November 21, 2009 12:34:34 PM
Subject: OUR WORLD CHANGES AFTER TONITE . . . . . .

I SENT THIS OUT A COUPLE OF DAYS AGO AND WAS TOLD THIS COULDN'T BE TRUE . . . . WRONG IT IS TRUE. BELOW IS THE ACTUAL COPY OF THAT ACTUAL PART OF THE BILL THAT CONTAINS IT. LET US PRAY THAT THOSE WHO SAID IT WOULDN'T HAPPEN OPEN THEIR EYES. BIRTH PAINS OR TRIB . . . EITHER ONE IT IS HERE


Micro-Chipping Of US
Citizens To Be Mandatory?

By Jack Williams
11-20-9



Already, It Looks As if Micro-chipping of US Citizens Will Soon Be Mandatory.



US federal legislation seems to be written by illiterates, or by foreigners, none of whom seem to understand English very well, which the Controllers prefer as that gives them more latitude with interruption and enforcement: Obama's health care bill is a case in point.



Congressman John Conyers (D-Michigan), Chairman of the House Judiciary Committee, even questioned the sense of reading Obama's 1,990 page health care bill by saying, "I love these members, they get up and say, 'Read the bill.' What good is reading the bill if it's a thousand pages and you don't have two days and two lawyers to find out what it means after you read the bill."



Sorry to have to expose you to a portion of that very poorly written, 1990 page health care bill (Subtitle C-11 Sec. 2521 National Medical Device Registry), but maybe you can tell me what it means.



"... 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 that has been used in or on a patient; and (B) is a Class III device; or (ii) A Class II device that is Implantable..."



Well, enough of that, a person can take only so much nonsense at one sitting. But, ask yourself a simple question: Are we to be multi-chipped, complete with updates, like a computer program, with our yearly rounds of multi-inoculations?



J. Speer-Williams

THE FOLLOWING COPIED DIRECTLY FROM THE US CONGRESS OFFICE BILL. I SUBMIT THAT WE ARE CLOSER THAN WE CARE TO BELIEVE.






Subtitle C—National Medical

10 Device Registry

11 SEC. 2521. NATIONAL MEDICAL DEVICE REGISTRY.

12 (a) REGISTRY.—

13 (1) IN GENERAL.—Section 519 of the Federal

14 Food, Drug, and Cosmetic Act (21 U.S.C. 360i) is

15 amended—

16 (A) by redesignating subsection (g) as sub17

section (h); and

18 (B) by inserting after subsection (f) the

19 following:

20 ‘‘National Medical Device Registry

21 ‘‘(g)(1) The Secretary shall establish a national med22

ical device registry (in this subsection referred to as the

23 ‘registry’) to facilitate analysis of postmarket safety and

24 outcomes data on each device that—

25 ‘‘(A) is or has been used in or on a patient; and

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1002

1 ‘‘(B) is—

2 ‘‘(i) a class III device; or

3 ‘‘(ii) a class II device that is implantable,

4 life-supporting, or life-sustaining.

5 ‘‘(2) In developing the registry, the Secretary shall,

6 in consultation with the Commissioner of Food and Drugs,

7 the Administrator of the Centers for Medicare & Medicaid

8 Services, the head of the Office of the National Coordi9

nator for Health Information Technology, and the Sec10

retary of Veterans Affairs, determine the best methods

11 for—

12 ‘‘(A) including in the registry, in a manner con13

sistent with subsection (f), appropriate information

14 to identify each device described in paragraph (1) by

15 type, model, and serial number or other unique iden16

tifier;

17 ‘‘(B) validating methods for analyzing patient

18 safety and outcomes data from multiple sources and

19 for linking such data with the information included

20 in the registry as described in subparagraph (A), in21

cluding, to the extent feasible, use of—

22 ‘‘(i) data provided to the Secretary under

23 other provisions of this chapter; and

24 ‘‘(ii) information from public and private

25 sources identified under paragraph (3);

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1003

1 ‘‘(C) integrating the activities described in this

2 subsection with—

3 ‘‘(i) activities under paragraph (3) of sec4

tion 505(k) (relating to active postmarket risk

5 identification);

6 ‘‘(ii) activities under paragraph (4) of sec7

tion 505(k) (relating to advanced analysis of

8 drug safety data); and

9 ‘‘(iii) other postmarket device surveillance

10 activities of the Secretary authorized by this

11 chapter; and

12 ‘‘(D) providing public access to the data and

13 analysis collected or developed through the registry

14 in a manner and form that protects patient privacy

15 and proprietary information and is comprehensive,

16 useful, and not misleading to patients, physicians,

17 and scientists.

18 ‘‘(3)(A) To facilitate analyses of postmarket safety

19 and patient outcomes for devices described in paragraph

20 (1), the Secretary shall, in collaboration with public, aca21

demic, and private entities, develop methods to—

22 ‘‘(i) obtain access to disparate sources of

23 patient safety and outcomes data, including—

24 ‘‘(I) Federal health-related electronic

25 data (such as data from the Medicare pro-

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1004

1 gram under title XVIII of the Social Secu2

rity Act or from the health systems of the

3 Department of Veterans Affairs);

4 ‘‘(II) private sector health-related

5 electronic data (such as pharmaceutical

6 purchase data and health insurance claims

7 data); and

8 ‘‘(III) other data as the Secretary

9 deems necessary to permit postmarket as10

sessment of device safety and effectiveness;

11 and

12 ‘‘(ii) link data obtained under clause (i)

13 with information in the registry.

14 ‘‘(B) In this paragraph, the term ‘data’ refers to in15

formation respecting a device described in paragraph (1),

16 including claims data, patient survey data, standardized

17 analytic files that allow for the pooling and analysis of

18 data from disparate data environments, electronic health

19 records, and any other data deemed appropriate by the

20 Secretary.

21 ‘‘(4) Not later than 36 months after the date of the

22 enactment of this subsection, the Secretary shall promul23

gate regulations for establishment and operation of the

24 registry under paragraph (1). Such regulations—

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1005

1 ‘‘(A)(i) in the case of devices that are described

2 in paragraph (1) and sold on or after the date of the

3 enactment of this subsection, shall require manufac4

turers of such devices to submit information to the

5 registry, including, for each such device, the type,

6 model, and serial number or, if required under sub7

section (f), other unique device identifier; and

8 ‘‘(ii) in the case of devices that are described in

9 paragraph (1) and sold before such date, may re10

quire manufacturers of such devices to submit such

11 information to the registry, if deemed necessary by

12 the Secretary to protect the public health;

13 ‘‘(B) shall establish procedures—

14 ‘‘(i) to permit linkage of information sub15

mitted pursuant to subparagraph (A) with pa16

tient safety and outcomes data obtained under

17 paragraph (3); and

18 ‘‘(ii) to permit analyses of linked data;

19 ‘‘(C) may require device manufacturers to sub20

mit such other information as is necessary to facili21

tate postmarket assessments of device safety and ef22

fectiveness and notification of device risks;

23 ‘‘(D) shall establish requirements for regular

24 and timely reports to the Secretary, which shall be

25 included in the registry, concerning adverse event

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1006

1 trends, adverse event patterns, incidence and preva2

lence of adverse events, and other information the

3 Secretary determines appropriate, which may include

4 data on comparative safety and outcomes trends;

5 and

6 ‘‘(E) shall establish procedures to permit public

7 access to the information in the registry in a manner

8 and form that protects patient privacy and propri9

etary information and is comprehensive, useful, and

10 not misleading to patients, physicians, and sci11

entists.

12 ‘‘(5) To carry out this subsection, there are author13

ized to be appropriated such sums as may be necessary

14 for fiscal years 2010 and 2011.’’.

15 (2) EFFECTIVE DATE.—The Secretary of

16 Health and Human Services shall establish and

17 begin implementation of the registry under section

18 519(g) of the Federal Food, Drug, and Cosmetic

19 Act, as added by paragraph (1), by not later than

20 the date that is 36 months after the date of the en21

actment of this Act, without regard to whether or

22 not final regulations to establish and operate the

23 registry have been promulgated by such date.

24 (3) CONFORMING AMENDMENT.—Section

25 303(f)(1)(B)(ii) of the Federal Food, Drug, and

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1007

1 Cosmetic Act (21 U.S.C. 333(f)(1)(B)(ii)) is amend2

ed by striking ‘‘519(g)’’ and inserting ‘‘519(h)’’.

3 (b) ELECTRONIC EXCHANGE AND USE IN CERTIFIED

4 ELECTRONIC HEALTH RECORDS OF UNIQUE DEVICE

5 IDENTIFIERS.—

6 (1) RECOMMENDATIONS.—The HIT Policy

7 Committee established under section 3002 of the

8 Public Health Service Act (42 U.S.C. 300jj–12)

9 shall recommend to the head of the Office of the Na10

tional Coordinator for Health Information Tech11

nology standards, implementation specifications, and

12 certification criteria for the electronic exchange and

13 use in certified electronic health records of a unique

14 device identifier for each device described in section

15 519(g)(1) of the Federal Food, Drug, and Cosmetic

16 Act, as added by subsection (a).

17 (2) STANDARDS, IMPLEMENTATION CRITERIA,

18 AND CERTIFICATION CRITERIA.—The Secretary of

19 the Health Human Services, acting through the

20 head of the Office of the National Coordinator for

21 Health Information Technology, shall adopt stand22

ards, implementation specifications, and certification

23 criteria for the electronic exchange and use in cer24

tified electronic health records of a unique device

25 identifier for each device described in paragraph (1),

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1008

1 if such an identifier is required by section 519(f) of

2 the Federal Food, Drug, and Cosmetic Act (21
3 U.S.C. 360i(f)) for the device.
Comment by Mikha El on November 22, 2009 at 9:34pm
Reading this paragraph caught my eye...

"... 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 that has been used in or on a patient; and (B) is a Class III device; or (ii) A Class II device that is Implantable..."

This appears to be the law as written....

‘‘(g)(1) The Secretary shall establish a national med22

ical device registry (in this subsection referred to as the

23 ‘registry’) to facilitate analysis of postmarket safety and

24 outcomes data on each device that—

25 ‘‘(A) is or has been used in or on a patient;


I have not taken the time to substantiate this information. Given the current mindset of the dimwits in control, I wouldn't put it past them. Especially after seeing the amendments as written will go forward for debate and a final vote to come soon. The Dems may not hold together though. One or 2 are against the "public option". aspect.

(If this were to become law, I will claim it would violate my "religious beliefs" due to the prick required,)

PRAY and PRAY some more!

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