Comment to 60-Day FRN

Burroughs, Kennya L. (CDC/00/0ADS)
Jean Public
Monday, June 29, 2015 2:51 PM

From:

Sent:
To:

OMS-Comments (CDC); [email protected];

Subject:

[email protected]
Fw:PUBUC COMMENT ON FEDERAL REGISTER cdc pushing mammography which has
been shown to be useless and can in fct bring on cancer

Follow Up Flag:

Follow up

Flag Status:

Flagged

THESE TESTS BRING ON X RAY EXPOSURE WHICH CAN BUILD UP OVER YEARS OF
TESTING SO THAT YOU BRING ON BREAST CANCER OVER THE PERIOD OF YEARS FROM
THE TESTS THEMSELVES. THIS KIND OF ADVOCACY IS SECRET, SNEAKY AND THE WOMEN
DONT GET THE FULL INFROMATION WHEN THEY ARE URGED TO HAVE THESE TESTS. THIS
AGENCY IS NOT HONEST WITH THE PUBLIC. IT TENDS TO PROMOTE AND PUSH BENEFITS
AND HIDES THE CONTRAINDICATIONS OIF VARIOUS DRUGS AND TESTS. THAT IS
DISHONEST TO THE AMERICAN PUBLIC.

LET ME POINT OUT THAT THE AMERICAN PUBLIC HAS BEEN SKEWERED BY THE GOVT
HEALTH CARE PROFITEERS OVER THE YEARS. TESTS DONE FOR THEIR OWN BENEFIT NOT
FOR THE AMERICAN PUBLIC BENEFIT. the below catalogue of attacks against american citizens
by these health care agencies is hereby made part of my comment on this issue. this comment is for
the public record. please receipt. jean publi jeanpublic1 @gmail.com

A History Of US Secret Human Experimentation

A History Of US Secret Human Experimentation
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Subject: cdc pushing mammography which has been shown to be useless and can in fct bring on cancer

[Federal Register Volume 80, Number 122
[Notices]

[Pages

(Thursday,

June 25,

2015)]

36539~36540]

From the Federal Register Online via the Government Publishing Office [·.-:;·.".·:.

[FR Doc No: 2015-15550]
1

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. ;

===============~======~'-"=.0."-'~-'-'~========="--"-'-'===="'-'-'--'-"--==~====='-=-'-'-'-~~'-''-"'-"'-''-'

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-15-057l] ;

[Docket No. CDC-2015-0015]

Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services {HHS).
ACTION: Notice with cowment period.

SUMMARY: The Centers for Disease Control and Prevention {CDC), as part
of its continuing efforts to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies to take this opportunity to comment on proposed and/or
continuing information collections, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on the collection of
Minimum Data Elements (MOE) for the National Breast and Cervical Cancer
Early Detection Program {NBCCEDP). CDC collects information about the
cancer screening services provided through the NBCCEDP to support
program management.
DATES: \'Jritten comments must be received on or before August 24, 2015.
ADDRESSES: You may submit comments, identified by Docket No. CDC-20150015 by any of the following methods:
Federal eRulemaking Portal: i--:.· ';- cj" : .
-~1'··. Follow the instructions
for submitting comments.
Mail: Leroy A. Richardson, Information Collection Review Office,
Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS074, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. All relevant comments received will be posted
without change to ~<~<~- ~ ,t_l,- r.: . _l· ,\', including any personal information
provided. For access to the docket to read background documents or
comments received, go to ~>-·~r.:-·__:___2 -_) or by U.S. mail to the
address listed above.

FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact the Information Collection Review Office,
Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS074, Atlanta, Georgia 30329; phone: 404-639-7570; Email: JL.l :j·
SUPPLEMENTARY INFORMATION:
Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 35013520), Federal agencies must obtain approval from the Office of
Management and Budget {OMB) for each collection of information they
2

conduct or sponsor. In addition, the PRA also requires Federal agencies
to provide a 60-day notice in the Federal Register concerning each
proposed collection of information, including each ne~o-J proposed
collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
Comments are invited on: (a) ~Vhether the proposed collection of
information is necessary for the proper performance of the functions of
the agency, including whether the information shall have practical
utility; (b) the accuracy of the agency's estimate of the burden of the
proposed collection of information; (c) ways to enhance the quality,
utility, and clarity of the information to be collected; (d) ways to
minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques or other
forms of information technology; and (e) estimates of capital or startup costs and costs of operation, maintenance, and purchase of services
to provide information. Burden means the total time, effort, or
financial resources expended by persons to generate, maintain, retain,
disclose or provide information to or for a Federal agency. This
includes the time needed to review instructions; to develop, acquire,
install and utilize technology and systems for the purpose of
collecting, validating and verifying information, processing and
maintaining information, and disclosing and providing information; to
train personnel and to be able to respond to a collection of
information, to search data sources, to complete and review the
collection of information; and to transmit or otherwise disclose the
information.
Proposed Project
Minimum Data Elements (MOE) for the National Breast and Cervical
Cancer Early Detection Program (NBCCEDP) (OMB No. 0920-0571, exp. 10/
31/2015)--Extension--National Center for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
t-:lany cancer-related deaths in women could be avoided by increased
utilization of appropriate screening and early detection tests for
breast and cervical cancer. Ma~~ography is extremely valuable as an
early detection tool because it can detect breast cancer well before
the woman can feel the lump, when the cancer is still in an early and
more treatable stage. Similarly, a substantial proportion of cervical
cancer-related deaths could be prevented through the detection and
treatment of precancerous lesions. The Papanicolaou (Pap) test is the
primary method of detecting both precancerous cervical lesions as ~~ell
as invasive cervical cancer. !1ammography and Pap tests are underused by
women who have no source or no regular source of health care and women
without health insurance.
Despite the availability and increased use of effective screening
and early detection tests for breast and cervical cancers, the American
Cancer Society (ACS) estimates that 231,840 new cases of invasive
breast cancer will be diagnosed among women in 2015, and 40,290 women
will die of this disease. The ACS also estimates that 12,900 new cases
of invasive cervical cancer will be diagnosed in 2015, and 4,100 women
will die of this disease.
The CDC's National Breast and Cervical Cancer Early Detection
Program (NBCCEDP) provides screening services to underserved women
through cooperative agreements with 50 States, the District of
3

Columbia, 5 U.S. Territories, and 11 American Indian/Alaska Native
tribal programs. The program was established in response to the Breast
and Cervical Cancer tvlortality Prevention Act of 1990. Screening
services include clinical breast examinations, manunograms and Pap
tests, as well as timely and adequate diagnostic testing for abnormal
results,
[[Page 36540]]
and referrals to treatment for cancers detected. NBCCEDP at<~ardees
collect patient-level screening and tracking data to manage the program
and clinical services. A de-identified subset of data on patient
demographics, screening tests and outcomes are reported by each awardee
to CDC twice per year,
CDC plans to request OMB approval to collect MOE information for an
additional three years. There are no changes to the currently approved
minimum data elements, electronic data collection procedures, or the
estimated burden. Because NBCCEDP awardees already collect and
aggregate data at the state, territory and tribal level, the additional
burden of submitting data to CDC will be modest. CDC will use the
information to monitor and evaluate NBCCEDP awardees; improve the
availability and quality of screening and diagnostic services for
underserved women; develop outreach strategies for women who are never
or rarely screened for breast and cervical cancer; report program
results to stakeholders including Congress and other legislative
authorities; and inform program planning and management.
There are no costs to respondents other than their time.
Estimated Annualized Burden Hours

Average

Number of
burden
Type of respondents
response
Total burden
hrs. l

Number of

responses per

respondents

respondent

Minimum Data

67

536

Elements.

Total . . . . . . . . . . . . . . . .
536

Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2015-15550 Filed 6-24-15; 8:45 am]
BILLING CODE 4163-18-P

4

per

(in

(in hrs.)

NBCCEDP Grantees .....
4

Form name

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