§ 1074d. Certain primary and preventive health care services

Pub. L. 118–159, div. A, title VII, § 709, Dec. 23, 2024, 138 Stat. 1945, provided that:

“(a)“(a)

Demonstration Program.—

Not later than one year after the date of the enactment of this Act [Dec. 23, 2024], the Secretary of Defense shall carry out a demonstration program to reimburse covered members for expenses incurred in the retrieval, testing, cryopreservation, shipping, and storage of gametes of such covered members in a private storage facility determined appropriate by the Secretary.

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“(b)“(b)

Elements.—

“(1)“(1)

Amount of reimbursement.—

A covered member participating in the demonstration program shall receive not more than the following amounts per year:

“(A)“(A)

$500 in the case of a member who preserves sperm.

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“(B)“(B)

$10,000 in the case of a member who preserves eggs.

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“(2)“(2)

Information.—

“(A)“(A)

Providers.—

The Secretary shall provide to a covered member participating in the demonstration program information regarding providers of services described in subsection (a) located near the covered member.

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“(B)“(B)

Promotion.—

The Secretary shall promote the demonstration program to covered members in the course of annual health examinations and pre-deployment screenings.

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“(3)“(3)

Use of military medical treatment facilities.—

The Secretary shall encourage the use of military medical treatment facilities that offer services described in subsection (a) to provide services under the demonstration program.

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“(c)“(c)

Duration.—

The Secretary shall—

“(1)“(1)

publish in the Federal Register the date on which the Secretary will commence carrying out the demonstration program; and

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“(2)“(2)

carry out the demonstration program for a three-year period beginning on such date.

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“(d)“(d)

No Liability or Contractual Obligation.—

The United States shall not be—

“(1)“(1)

considered a party to any agreement between a covered member who participates in the demonstration program and a private gamete storage facility; or

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“(2)“(2)

responsible for the management of gametes cryopreserved or stored for which a covered member receives reimbursement under such demonstration program.

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“(e)“(e)

Advanced Medical Directive.—

A covered member who participates in the demonstration program shall complete an advanced medical directive that specifies how gametes preserved under the demonstration program shall be handled upon the death of such covered member.

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“(f)“(f)

Reports; Briefings.—

“(1)“(1)

Initial report.—

Not later than one year after the date of the enactment of this Act [Dec. 23, 2024], the Secretary shall submit to the Committees on Armed Services of the House of Representatives and the Senate a report containing a plan to implement the demonstration program.

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“(2)“(2)

Report.—

Not later than one year after the Secretary commences carrying out the demonstration program, the Secretary shall submit to the Committees on Armed Services of the Senate and the House of Representatives a report on the demonstration program. Such report shall include the following:

“(A)“(A)

Usage by covered members.

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“(B)“(B)

Demographics of participating covered members.

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“(C)“(C)

Costs of services to participating covered members.

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“(D)“(D)

The feasibility of expanding the demonstration program.

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“(E)“(E)

The feasibility of making the demonstration program permanent.

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“(F)“(F)

Other information determined appropriate by the Secretary.

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“(3)“(3)

Briefings.—

Not later than one year after the date of the enactment of this Act, and annually thereafter for the duration of the demonstration program, the Secretary shall provide to the congressional defense committees [Committees on Armed Services and Appropriations of the Senate and the House of Representatives] a briefing on—

“(A)“(A)

the design, use, and costs of the demonstration project; and

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“(B)“(B)

any other observations of the Secretary with respect to the demonstration project, such as the effects of the demonstration project on recruitment and retention.

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“(g)“(g)

Definitions.—

In this section:

“(1)“(1)

The term ‘covered member’ means a member of a covered Armed Force serving on active duty—

“(A)“(A)

who has received orders (including deployment orders) for duty for which the member may receive hazardous duty pay under section 351 of title 37, United States Code;

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“(B)“(B)

whom [sic] the Secretary determines is likely to receive such orders in the next 120 days;

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“(C)“(C)

who will, under orders, be geographically separated from a spouse, domestic partner, or dating partner for a period of not less than 180 days, including sea duty; or

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“(D)“(D)

whose application to participate in the demonstration program is approved by the Secretary.

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“(2)“(2)

The term ‘covered Armed Force’ means the Army, Navy, Marine Corps, Air Force, or Space Force.

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“(3)“(3)

The term ‘deployment’ has the meaning given such term in section 991(b) of title 10, United States Code.”

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Pub. L. 115–91, div. A, title VII, § 708, Dec. 12, 2017, 131 Stat. 1436, provided that:

“(a)“(a)

In General.—

The Secretary of Defense shall implement processes and procedures to ensure that a covered beneficiary under the TRICARE program whose pregnancy is complicated with (or suspected of complication with) a fetal condition may elect to receive expedited evaluation, nondirective counseling, and medical treatment from a perinatal or pediatric specialist capable of providing surgical management and intervention in utero.

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“(b)“(b)

Definitions.—

In this section, the terms ‘covered beneficiary’ and ‘TRICARE program’ have the meanings given those terms in section 1072 of title 10, United States Code.”

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Pub. L. 114–92, div. A, title VII, § 718, Nov. 25, 2015, 129 Stat. 868, provided that:

“(a)“(a)

Clinical Practice Guidelines.—

“(1)“(1)

Establishment.—

Not later than one year after the date of the enactment of this Act [Nov. 25, 2015], the Secretary of Defense shall establish clinical practice guidelines for health care providers employed by the Department of Defense on standards of care with respect to methods of contraception and counseling on methods of contraception for members of the Armed Forces.

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“(2)“(2)

Updates.—

The Secretary shall from time to time update the clinical practice guidelines established under paragraph (1) to incorporate into such guidelines new or updated standards of care with respect to methods of contraception and counseling on methods of contraception.

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“(b)“(b)

Dissemination.—

“(1)“(1)

Initial dissemination.—

As soon as practicable, but commencing not later than one year after the date of the enactment of this Act, the Secretary shall provide for rapid dissemination of the clinical practice guidelines to health care providers described in subsection (a)(1).

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“(2)“(2)

Dissemination of updates.—

As soon as practicable after each update to the clinical practice guidelines made by the Secretary pursuant to paragraph (2) of subsection (a), the Secretary shall provide for the rapid dissemination of such updated clinical practice guidelines to health care providers described in paragraph (1) of such subsection.

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“(3)“(3)

Protocols.—

The Secretary shall disseminate the clinical practice guidelines under paragraph (1) and any updates to such guidelines under paragraph (2) in accordance with administrative protocols developed by the Secretary for such purpose.

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“(c)“(c)

Access to Contraception Counseling.—

As soon as practicable after the date of the enactment of this Act, the Secretary shall ensure that women members of the Armed Forces have access to comprehensive counseling on the full range of methods of contraception provided by health care providers described in subsection (a)(1) during health care visits, including visits as follows:

“(1)“(1)

During predeployment health care visits, including counseling that provides specific information women need regarding the interaction between anticipated deployment conditions and various methods of contraception.

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“(2)“(2)

During health care visits during deployment.

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“(3)“(3)

During annual physical examinations.”

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Pub. L. 103–337, div. A, title II, § 241, Oct. 5, 1994, 108 Stat. 2701, provided for the continuance of the Defense Women’s Health Research Program established pursuant to the authority in section 251 of the National Defense Authorization Act for Fiscal Year 1994 (Public Law 103–160; 107 Stat. 1606, formerly set out below) and appropriated funds to the program for fiscal year 1995.

Pub. L. 103–160, div. A, title II, § 251, Nov. 30, 1993, 107 Stat. 1606, authorized the Secretary of Defense to establish a Defense Women’s Health Research Center to serve as the coordinating agent for multidisciplinary and multi-institutional research within the Department of Defense on women’s health issues related to service in the Armed Forces and required the Secretary to report to Congress on the decision to establish the Center no later than May 1, 1994.

Pub. L. 103–160, div. A, title VII, § 735, Nov. 30, 1993, 107 Stat. 1698, directed the Secretary of Defense to prepare a report evaluating the provision of primary and preventive health care services through military medical treatment facilities and the Civilian Health and Medical Program of the Uniformed Services to female members of the uniformed services and female covered beneficiaries eligible for health care under this chapter, and directed the Secretary, as part of such report, to conduct a study to determine the health care needs of female members and female covered beneficiaries, and to submit such report to Congress not later than Oct. 1, 1994, and a revised report not later than Oct. 1, 1999.