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A3150Assembly2019-2020 SessionSame asS3789

Family Rights for Disabilities Care

Official title

“Relates to the creation of a bill of rights for family and guardians of people with developmental disabilities that reside in residences certified or approved by the OPWDD”

Sponsor Thomas AbinantiAD-92Affects Health
Status
In Assembly Committee
Mental Health
Impact
4/10
Low
Passage
0%

Bill progress

Step 2 of 7

In committee · Mental Health

What's happening

This bill creates a "Family Bill of Rights and Privileges" for families and guardians of people with developmental disabilities in certified residences, outlining their rights to information, involvement, and advocacy.

Why it matters

  1. Empowers families and guardians with legal standing. By establishing a formal Bill of Rights, the legislation gives families and guardians a clear, enforceable set of rights, making it easier to advocate for their loved ones and navigate disputes with care providers.

  2. Enhances transparency and accountability. The bill mandates access to information on care, safety, and finances, as well as timely notifications of incidents, helping families stay informed and hold facilities accountable for the quality and safety of care.

  3. Expands involvement and oversight. Families and guardians gain the right to participate meaningfully in care planning, visit unannounced, be informed of staffing changes, and obtain facility safety and menu information, ensuring a higher level of day-to-day involvement in their loved one’s well-being.

  4. Increases public awareness and accessibility. By requiring providers to post the Bill of Rights prominently and the Office to distribute it in multiple languages and conduct public education, the bill seeks to ensure that all families, regardless of background or language, know their rights and how to exercise them.

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Who cares

  • Families and legal guardians of people with developmental disabilities

    The bill would establish rights to participate in care planning, visit unannounced, choose a care coordinator and access health, safety and financial information, subject to applicable confidentiality protections.

  • People with developmental disabilities receiving covered services

    The bill would allow individuals competent to do so to deny a specific representative a specific right, with the decision documented in writing and reasons provided to the representative.

  • OPWDD residential and non-residential service providers

    Covered providers would have to post the bill of rights at each facility and afford representatives its listed rights, including notice of staffing changes and access to safety plans.

  • Office for People With Developmental Disabilities

    OPWDD would have to publish and translate the bill of rights, establish a public education program, report implementation efforts in its statewide comprehensive plan and adopt implementing regulations.

Headline styles

Family Rights for Disabilities Care

Plain English, a few words. Used as the page title.

Sponsors

Primary sponsor
Thomas Abinanti

Assembly Member · Assembly District 92

No co-sponsors yet.

History

  1. Referred to mental health
  2. Referred to mental health

Companion bill

The same bill in the other chamber. A bill becomes law when one version passes both houses and the governor signs it, so either number can carry it.

S3789Senate

Family Rights for Disability Care

In Senate Committee · Mental Health And Developmental Disabilities · Sponsor David Carlucci

Impact 4 · Low0% to pass

Full text

3 pagesUnderlined is new[Struck] is removedOfficial text on nysenate.gov ↗

STATE OF NEW YORK

3150

2019-2020 Regular Sessions

IN ASSEMBLY

January 28, 2019

Introduced by M. of A. ABINANTI -- read once and referred to the Committee on Mental Health

AN ACT to amend the mental hygiene law, in relation to creating a bill of rights for family and guardians of people with developmental disabilities that reside in residences certified or approved by the office for people with developmental disabilities

The People of the State of New York, represented in Senate and Assembly, do enact as follows:

Section 1. The mental hygiene law is amended by adding a new section 13.04 to read as follows: § 13.04 Family bill of rights and privileges.

(a) The principles in the bill of rights and privileges set forth in this section are declared to be the public policy of the state.

(b) For purposes of this section:

(1) "qualified personal representative" means a spouse, parent, adult child, adult sibling, legal guardian or personal representative of an individual with developmental disabilities who is receiving services from a covered provider.

(2) "covered provider" means and includes any entity, providing residential services or non-residential services or programs to one or more persons with a developmental disability, that is licensed, operated or certified by the office.

(c) In addition to all other rights and privileges under law, a qualified personal representative shall have the following rights and privileges set forth below (the "Family Bill of Rights and Privileges") with respect to their individual family members with developmental disabilities.

"Family Bill of Rights and Privileges"

A qualified personal representative shall have the following generally-described rights and privileges concerning a family member with developmental disabilities receiving services; to:

EXPLANATION--Matter in italics (underscored) is new; matter in brackets

[ ] is old law to be omitted.

LBD02442-01-9

A. 3150 2

Be treated with consideration and respect.

Participate in and provide meaningful input into the development, review and revision of the individual's care plan, including placement or transfer within or between facilities.

Access information regarding the individual's health and safety, consistent with federal and state confidentiality protections.

Be notified within a reasonable time of any event that directly impacts the individual's health and safety, consistent with federal and state confidentiality protections.

Access information necessary for a qualified personal representative to make informed decisions, when appropriate, about the individual's care and care coordination.

Financial transparency, including access to budgetary information of the facility and individual expenses, consistent with federal and state confidentiality protections.

Visit unannounced.

Be informed of staffing changes.

Access a facility's fire and other safety plans and any information regarding a facility's passage or failure of any safety drills conducted by the facility and the office.

Access a facility's food menus.

Choose a care coordinator.

Consult and be represented by an independent advocate, mental hygiene legal services or an attorney; and if services are provided under Medicaid managed care, to have a Medicaid ombudsman.

Be informed in writing in plain language with up-to-date information about:

(i) the system of care and services for persons with developmental disabilities, including but not limited to managed care;

(ii) the laws, rules, and regulations applicable to the rights of family members and other personal representatives to participate in decisions about the individual's life and to access information, records, reports, care plans, etc.; and

(iii) the procedures to challenge any decision affecting the individual.

Nothing in this bill of rights and privileges shall limit any other right or privilege under law. If any residential facility or non-residential service provider fails to afford these rights and privileges, assistance may be sought from the facility or provider, or the office.

(d) A qualified personal representative may, in accordance with law and appropriate due process, not exercise a right or privilege described in this section if the subject individual receiving services, who is competent to do so, specifically affirms, in a reasonably contemporaneous manner, that such identified qualified personal representative shall not be afforded such specific right or privilege. Such determination by the subject individual shall be described and recorded in writing in the case file by appropriate staff of the facility or service provider and a statement of reasons for such denial shall be provided to the qualified personal representative.

(e) The statement of rights and privileges set forth in this section is intended to be a guide to the rights and privileges of qualified personal representatives of individuals with developmental disabilities receiving residential and non-residential services.

(f) Nothing in this section shall be read to limit any other rights or privileges that qualified personal representatives may have or limit any action or relief otherwise permitted by law. Nothing in this subdivi-

A. 3150 3

sion shall alter or affect any right of appeal, formal or otherwise, such personal representative may have concerning the denial of any such right.

(g) Each covered provider shall conspicuously post a copy of the bill of rights and privileges in a public place at each of the covered provider's facilities.

(h) The commissioner shall:

(1) Post a copy of the bill of rights and privileges on the office's website;

(2) Make copies of the bill of rights and privileges in English, and the top six languages other than English spoken in the state (according to the latest available data from the U.S. bureau of census) available to the public and every provider;

(3) Establish a public education program designed to disseminate information regarding implementation of this section;

(4) Include specific information detailing the efforts of the commissioner to effectuate this section in the statewide comprehensive plan required pursuant to section 5.07 of this chapter;

(5) Adopt all rules and regulations necessary to effectuate this section.

§ 2. This act shall take effect immediately.

Reflowed for reading: line numbers and page breaks removed. Cite the official text.

Summaries, headlines and scores are AI-generated from the official bill text. How we score bills. Source: NYS Open Legislation.