NATIONWIDE DOOR TO DOOR “FORCED” OBAMACARE HOME INSPECTIONS START OCTOBER 1ST 2013
According to an Obamacare provision millions of Americans will be targeted. The Health and Human Services’ website states that your family will be targeted if you fall under the “high-risk” categories below: Families where mom is not yet 21. Families where someone is a tobacco user. Families where children have low student achievement, developmental delays, or disabilities. Families with individuals who are serving or formerly served in the armed forces, including such families that have members of the armed forces who have had multiple deployments outside the United States. There is no reference to Medicaid being the determinant for a family to be “eligible.” In 2011, the HHS announced $224 million will be given to support evidence-based home visiting programs to “help parents and children.” Individuals from the state will implement these leveraging strategies to “enhance program sustainability.”
IS THE GOVT PLAN TO SIMULTANEOUSLY CAUSE THE DOLLAR CRASH DURING A WORLDWIDE ELECTRICAL GRID BLACKOUT,FOLLOWED BY “FORCING” THE MARK OF THE BEAST UPON THE ENTIRE NATION? (RFID CHIP)
WHY DO YOU THINK THE UNITED STATES DEPT. OF AGRICULTURE IS NOW PREPARING FOR PLANET X?
BY THE WAY, PRINCE WILLIAM HAS TAKEN OVER OBAMACARE.
THESE 2 LINKS PROVE IT, READ IT AND WEEP. OBAMA DOES NOT CONTROL THE AFFORDABLE CARE ACT ANYMORE.PRINCE WILLIAM HAS A COMPANY NAMED SERCO THAT NOW CONTROLS OBAMACARE HERE IS EVEN MORE PROOF
MUSLIMS DON’T HAVE TO TAKE OBAMACARE
CONGRESS GETS A WAIVER SO THEY DON’T HAVE TO TAKE OBAMACARE
(USA Hitman) Below is a pretty big list of past events and current ones which are pretty much listed in order, and these events point to something big happening in FEMA Region Three which has DC, DE, MD, PA, VA, WV.
Many different things are happening but they seem to be geared towards a monthly disaster that will collapse society and leave a shortage of food and possibly water. Read them below and remember this speculation on current purchases and political movement:
Forced Home Inspections Will Implemented sometime in 2013.
FEMA purchase orders for over $14.2 million for MREs and heater meals to be delivered to Region III by October 1st.
FEMA purchase orders for 22 million pouches of emergency water to be delivered to region III by October 1st.
FEMA purchase orders for $13.6 million for MREs and heater meals to be delivered to Austin by October 1st.
Nine-week training course for UN Peacekeepers in CONUS to learn Urban Warfare, English, and US weapons systems beginning 4th week of July for 386,000 troops to be completed by October 1st. $11 million in antibiotics to be delivered to FEMA region III by October 1st ordered by CDC.
World Health Organization held second emergency meeting in its history to discuss MERS Coronavirus. Determined a vaccine MUST be in place by October 1st.
2800 MRAPs must be delivered to DHS by October 1st. No leave will be allowed for US military from September 28th thru November 5th. NORCOMM yearly training for civil unrest suspended until September 27th. To be performed in northeast coastal areas. Date for release of QE3 report moved to October 16th.
All DHS agents MUST qualify with sidearm, shotgun and AR 15 by September 28th. No mention of yearly less lethal qualification. Sporadic testing of GPS and Communications satellites is coordinated for the first time with a testing date of September 29th.
All National Guard units will complete riot control and disaster assistance training during this years annual two week training. All units MUST have their training complete by September 30th.
Daily testing of the Emergency Broadcast System to begin on September 25th and run thru October 2nd.
Eastern-based Coast Guard units to perform massive group training, usually performed in the Gulf, in the Virginia and Delaware areas. This is a 10-day training mission to begin September 26th.
Wake Up Sheeple!
The following section of the ObamaCare Bill (H.R. 3590) is the root of the ObamaCare microchip rumor.
H.R. 3590 amends Section 519 of the Food, Drug and Cosmetic Act (21 U.S.C .360i). Here is the applicable language from H.R. 3590 (page 1,014):
(g)(1)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
(i) a class III device; or
(ii) a class II device that is implantable, life-supporting, or life-sustaining.
(2) In developing the registry, the Secretary shall, in consultation with the Commissioner of Food and Drugs, the Administrator of the Centers for Medicare & Medicaid Services, the head of the Office of the National Coordinator for Health Information Technology, and the Secretary of Veterans Affairs, determine the best methods for—
(A) including in the registry, in a manner consistent with subsection (f), appropriate information to identify each device described in paragraph (1) by type, model, and serial number or other unique identifier;
(B) validating methods for analyzing patient safety and outcomes data from multiple sources and for linking such data with the information included in the registry as described in subparagraph (A), including, to the extent feasible, use of—
(i) data provided to the Secretary under other provisions of this chapter; and
(ii) information from public and private sources identified under paragraph (3);
(C) integrating the activities described in this subsection with—
(i) activities under paragraph (3) of section 505(k) (relating to active postmarket risk identification);
(ii) activities under paragraph (4) of section 505(k) (relating to advanced analysis of drug safety data); and
(iii) other postmarket device surveillance activities of the Secretary authorized by this chapter; and…
3(B) In this paragraph, the term ‘data’ refers to information respecting a device described in paragraph (1), including claims data, patient survey data, standardized analytic files that allow for the pooling and analysis of data from disparate data environments, electronic health records, and any other data deemed appropriate by the Secretary.
Note: The FDA has established standards for an implantable radiofrequency transponder systems (RFID chips) that are Class II compliant (http://www.fda.gov/Radiation-EmittingProducts/RadiationSafety/ElectromagneticCompatibilityEMC/ucm116647.htm). However, these RFID chips will have patient identification and health information. While the bill does not require mandatory RFID microchip implantation, it does establish an initial framework where the scope could be expanded with future legislation and regulation.
To learn more about the uses of RFID chips in the healthcare field please read the linked section of this wiki article on RFID and healthcare.