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[Congressional Bills 118th Congress]
[From the U.S. Government Publishing Office]
[H.R. 6412 Introduced in House (IH)]
<DOC>
118th CONGRESS
1st Session
H. R. 6412
To amend title XXVII of the Public Health Service Act to provide
certain informational resources related to Down syndrome.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
November 14, 2023
Mr. Molinaro (for himself, Ms. Budzinski, and Mr. Lawler) introduced
the following bill; which was referred to the Committee on Energy and
Commerce
_______________________________________________________________________
A BILL
To amend title XXVII of the Public Health Service Act to provide
certain informational resources related to Down syndrome.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``Down Syndrome Diagnosis Act''.
SEC. 2. PROVIDING INFORMATIONAL RESOURCES RELATED TO DOWN SYNDROME.
(a) In General.--Subpart II of part A of title XXVII of the Public
Health Service Act (42 U.S.C. 300gg-11 et seq.) is amended by adding at
the end the following new section:
``SEC. 2730. INFORMATIONAL RESOURCES RELATED TO DOWN SYNDROME.
``(a) In General.--In the case of an individual enrolled under a
group health plan or group or individual health insurance coverage who
is diagnosed with Down syndrome while so enrolled (or who is pregnant
and is given a diagnosis of Down syndrome with respect to the fetus
while so enrolled), not later than 60 days after such plan or coverage
is made aware (through claims data or otherwise) of the relevant
diagnosis, such plan or coverage shall provide the informational
resources described in subsection (b) to--
``(1) the individual; or
``(2) if the individual is under the age of 18, a parent or
legal guardian of the individual.
``(b) Informational Resources Described.--For purposes of
subsection (a), the informational resources described in this
subsection are the following:
``(1) Written information about Down syndrome, including
information on the range of physical, developmental,
educational, and psychosocial outcomes for individuals living
with Down syndrome, that--
``(A) is up-to-date, evidence-based, and culturally
and linguistically appropriate for the individual; and
``(B) was developed by--
``(i) medical experts or representatives of
national medical or genetics organizations; and
``(ii) disability experts or
representatives of patient advocacy groups.
``(2) Contact information for 1 or more organizations that
specialize in Down syndrome support, such as the National Down
Syndrome Congress, the National Down Syndrome Society, or the
Global Down Syndrome Foundation.''.
(b) Effective Date.--The amendment made by subsection (a) shall
apply with respect to plan years beginning on or after January 1, 2024.
<all>
Introduced in House
Introduced in House
Referred to the House Committee on Energy and Commerce.
Referred to the Subcommittee on Health.
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