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Home/Bills/AR 85California · 2025–2026 Regular Session
Assembly MeasureChaptered/Signed

AR 85: Relative to Angelman Syndrome Awareness Day.

California · Assembly · 2025–2026 Regular Session · last verified May 14, 2026

What AR 85 does, verified May 14, 2026

<p>The bill aims to raise awareness about Angelman Syndrome, a rare genetic disorder that affects approximately 1 in 15,000 births. It designates a specific day each year to promote education and support for individuals with Angelman Syndrome and their families. The bill encourages schools, healthcare providers, and community organizations to observe this day by providing educational materials and resources. By increasing awareness, the bill hopes to improve the lives of those affected by the disorder and promote a better understanding of its effects.</p>

Bill journey
✓IntroducedComplete
✓In CommitteeComplete
✓First Chamber FloorComplete
✓Second ChamberComplete
✓GovernorComplete
6ChapteredCurrent
Last action: Read. Adopted. (Ayes 69. Noes 0. Page 4035.). (2026-02-19)Alert me
Author and sponsors
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Coauthors
Cecilia Aguiar-CurryPatrick AhrensJuan AlanisJoaquin ArambulaRebecca Bauer-KahanSteve BennettMarc BermanBlanca RubioTasha BoernerMia BontaLisa CalderonJessica Caloza
Recent actions5 total · showing 5
Feb. 19, 2026Read. Adopted. (Ayes 69. Noes 0. Page 4035.).
Feb. 19, 2026Coauthors revised.
Feb. 17, 2026From committee: Be adopted. To Consent Calendar. (Ayes 6. Noes 0.) (February 17).
Feb. 17, 2026Referred to Com. on RLS.
Feb. 12, 2026Introduced.
Latest bill textIntroduced version, February 12, 2026 · 335 words


CALIFORNIA LEGISLATURE— 2025–2026 REGULAR SESSION

House Resolution
No. 85


Introduced by Assembly Member Nguyen

February 12, 2026


Relative to Angelman Syndrome Awareness Day.


LEGISLATIVE COUNSEL'S DIGEST


HR 85, as introduced, Nguyen.

WHEREAS, Angelman syndrome is a rare neurogenetic disorder that occurs in 1 in 15,000 live births and affects approximately 500,000 individuals worldwide; and
WHEREAS, Angelman syndrome is caused by a loss of function of the UBE3A gene in chromosome 15 derived from the mother, and a gene that is needed to develop and control speech and movement; and
WHEREAS, Individuals with Angelman syndrome begin experiencing developmental delays starting from 6 and 12 months of age, inclusive, and these developmental delays are often the first signs of Angelman syndrome; and
WHEREAS, In addition to delayed development, Angelman syndrome causes problems with speech and balance, mental disability, and sometimes seizures; and
WHEREAS, Angelman syndrome shares symptoms and characteristics with other disorders, including autism, cerebral palsy, and Prader-Willi syndrome; and
WHEREAS, Individuals with Angelman syndrome have an overall happy and excitable demeanor, and they smile and laugh often; and
WHEREAS, Angelman syndrome is rare. Most individuals with Angelman syndrome do not have a family history of the syndrome, and researchers often do not know what causes the genetic changes that result in the disease; and
WHEREAS, Angelman syndrome can lead to several complications, including trouble feeding, hyperactivity, sleep troubles, scoliosis, and obesity; and
WHEREAS, The treatment of Angelman syndrome focuses on managing medical, sleep, and developmental issues; and
WHEREAS, There is currently no cure for Angelman syndrome, but organizations such as the Angelman Syndrome Foundation note that with further research, there may be a cure in the future; and
WHEREAS, Organizations worldwide recognize February 15 as International Angelman Day to raise awareness about Angelman syndrome; now, therefore, be it
Resolved by the Assembly of the State of California, That the Assembly hereby recognizes February 15, 2026, as Angelman Syndrome Awareness Day; and be it further
Resolved, That the Chief Clerk of the Assembly transmit copies of this resolution to the author for appropriate distribution.
Text of AR 85 as introduced, from the official record. Connect Plus keeps every version and highlights what changed.Compare versions
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