---
title: SR 567. State Prader-Willi Syndrome Awareness Day; express support for the designation
collection: bills
id: 2025-2026/sr567
cite_as: SR 567, 2025-2026 Regular Session (Ga.)
canonical_url: https://georgiacommons.org/bills/2025-2026/sr567
md_url: https://georgiacommons.org/bills/2025-2026/sr567.md
text_url: https://georgiacommons.org/bills/2025-2026/sr567/text
source_url: https://www.legis.ga.gov/legislation/72189
date: 2026-02-26
status: passed
corpus_version: bills-2026-09-13
license: Public record of the Georgia General Assembly, via LegiScan; see about.md
publisher: Georgia Commons, an independent project of Georgia Civic Data. Not the State of Georgia. Not legal advice.
up: https://georgiacommons.org/bills/2025-2026.md
previous: https://georgiacommons.org/bills/2025-2026/sr566.md
next: https://georgiacommons.org/bills/2025-2026/sr568.md
index: https://georgiacommons.org/bills/index.md
omitted: votes and history
omitted_chars: 463
omitted_url: https://georgiacommons.org/bills/2025-2026/sr567.md?full=1
bill_number: SR 567
session: 2025-2026 Regular Session
session_slug: 2025-2026
chamber: Senate
bill_type: resolution
status_date: 2026-02-26
last_action: Senate Passed/Adopted By Substitute
sponsors:
  - Kay Kirkpatrick
  - Chuck Hufstetler
  - Ben Watson
  - Max Burns
  - Bo Hatchett
  - Carden Summers
  - Jason Anavitarte
  - John Albers
  - Shawn Still
  - Randy Robertson
  - Greg Dolezal
  - Larry Walker
  - Blake Tillery
  - Clint Dixon
  - Bill Cowsert
text_version: Enrolled
has_text: true
legiscan_url: https://legiscan.com/GA/bill/SR567/2025
upstream_id: 2073965
summaries_model: claude-sonnet-5
topic_tags:
  - Prader-Willi syndrome
  - disability awareness
  - genetic disorders
  - Georgia Senate resolutions
  - public health
---

# SR 567. State Prader-Willi Syndrome Awareness Day; express support for the designation

## Text

Senate Resolution 567
By: Senators Kirkpatrick of the 32nd, Hufstetler of the 52nd, Watson of the 1st, Burns of the
23rd, Hatchett of the 50th and others
ADOPTED SENATE
A RESOLUTION
Expressing support for the designation of a Prader-Willi Syndrome Awareness Day at the
Capitol to raise awareness of and promote research on the disorder; and for other purposes.
WHEREAS, occurring in approximately 1 out of every 15,000 births, Prader-Willi syndrome
is a complex genetic disorder that causes an extreme and insatiable appetite, which often
results in morbid obesity; and
WHEREAS, morbid obesity is the major cause of death for individuals with Prader-Willi
syndrome; and
WHEREAS, Prader-Willi syndrome is the most commonly known genetic cause of
life-threatening obesity, affecting males and females with equal frequency across all races
and ethnicities; and
WHEREAS, Prader-Willi syndrome further causes cognitive and learning disabilities as well
as behavioral difficulties, including obsessive compulsive disorder and difficulty controlling
emotions, and studies have shown that individuals with the syndrome have a high morbidity
and mortality rate; and
WHEREAS, the hunger, metabolic, and behavioral characteristics of Prader-Willi syndrome
force affected individuals to require constant and lifelong supervision in a controlled
environment; and
WHEREAS, although there is no known cure for Prader-Willi syndrome, early diagnosis
allows families to access treatment, intervention services, and support from health
professionals, advocacy organizations, and other families who are dealing with the
syndrome; and
WHEREAS, recently discovered treatments, including the use of human growth hormone,
are improving the quality of life for individuals with the syndrome and offer new hope to
families, but many difficult symptoms associated with Prader-Willi syndrome remain
untreated.
NOW, THEREFORE, BE IT RESOLVED BY THE Senate that the members of this body
express their support for the designation of a Prader-Willi Syndrome Awareness Day at the
Capitol in recognition of the efforts of the many advocates and organizations that encourage
awareness, promote research, and provide education, support, and hope to those impacted by
Prader-Willi syndrome.
BE IT FURTHER RESOLVED that the Secretary of the Senate is authorized and directed
to make appropriate copies of this resolution available for distribution to the public and the
press.

## Summaries written by Georgia Commons

The following was written by claude-sonnet-5 from the text above and is not part of the resolution. Quote the text, not the summary.

A Georgia Senate resolution expresses support for designating a Prader-Willi Syndrome Awareness Day at the Capitol to raise awareness of the genetic disorder and encourage research.

### Plain-language summary

This resolution does not create new law. Instead, the Georgia Senate uses it to state its support for setting aside a day at the Capitol to recognize Prader-Willi syndrome, a genetic disorder that causes extreme hunger, obesity, cognitive and behavioral difficulties, and a need for lifelong supervision.
The resolution recites background on the disorder, including its rarity, its health effects, and the lack of a cure, then formally resolves that Senate members support the awareness day designation. It also directs the Secretary of the Senate to make copies available to the public and the press. It does not fund programs, create legal requirements, or change any Georgia statute.

### What it does

- States the Senate's support for designating a Prader-Willi Syndrome Awareness Day at the Georgia Capitol.
- Recognizes advocates and organizations that promote research, education, and support for people affected by Prader-Willi syndrome.
- Directs the Secretary of the Senate to distribute copies of the resolution to the public and the press.
- Creates no funding, legal requirement, or change to Georgia statute; it is a statement of the Senate's position.

### Who it affects

The resolution mainly speaks to people living with Prader-Willi syndrome and their families, along with advocacy organizations and health professionals who support them. It does not impose any obligations on state agencies, businesses, or the general public.

### Why it matters

While the resolution carries no legal force, it signals official recognition from the Georgia Senate of Prader-Willi syndrome and the challenges it causes, which can raise public awareness and support the visibility of advocacy and research efforts tied to the disorder.

### Key provisions

- The whereas clauses describe Prader-Willi syndrome's prevalence (about 1 in 15,000 births), its link to morbid obesity, and its cognitive and behavioral effects.
- The resolved clause states the Senate's support for designating a Prader-Willi Syndrome Awareness Day at the Capitol.
- A further resolved clause directs the Secretary of the Senate to make copies available for distribution to the public and press.

## Status

- Status: Passed (2026-02-26)
- Last action: Senate Passed/Adopted By Substitute (2026-02-26)
- Sponsors: Kay Kirkpatrick, Chuck Hufstetler, Ben Watson, Max Burns, Bo Hatchett, Carden Summers, Jason Anavitarte, John Albers, Shawn Still, Randy Robertson, Greg Dolezal, Larry Walker, Blake Tillery, Clint Dixon, Bill Cowsert
- Official page: https://www.legis.ga.gov/legislation/72189

> The history, votes, and amendments (463 characters) are at https://georgiacommons.org/bills/2025-2026/sr567.md?full=1
