Wolf-Hirschhorn/4p- Syndrome Awareness Day

2026 Regular Session Introduced by Michelle Salzman

The bill designates an annual Florida Wolf-Hirschhorn (4p-) Syndrome Awareness Day to raise public awareness and education without creating new laws or funding.

Adopted by Publication

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Summary of HR 8037 (Florida, 2026) – Wolf-Hirschhorn/4p- Syndrome Awareness Day

Purpose and intent

The bill designates a new commemorative observance: Wolf-Hirschhorn Syndrome Awareness Day (also referred to as 4p- Syndrome Awareness Day) in the state of Florida.

The aim is to raise awareness about Wolf-Hirschhorn syndrome, a genetic condition caused by deletion on the short arm of chromosome 4, and to promote understanding, support, and resources for affected individuals and families.

Key provisions and changes

Establishment of observance: Creates an annual awareness day focused on Wolf-Hirschhorn syndrome (4p-), its symptoms, diagnostic considerations, and the needs of individuals living with the condition.

Focus areas for the day: Likely includes education for the public and healthcare professionals, dissemination of information about diagnosis, treatment options, research, and support services, though the exact activities are not specified in the summary.

Commemoration scope: The bill authorizes recognition at the state level by appropriate agencies or through ceremonial/recognition channels, without imposing new regulatory or funding burdens on local governments or private entities.

Sponsorship: Co-sponsor listed as Michelle Salzman, indicating bipartisan or cross-party support within the chamber.

Who/what is affected

Primary impact: Individuals and families affected by Wolf-Hirschhorn syndrome (4p-), and the broader public who would benefit from increased awareness and education.

State agencies and institutions: May participate in observance events or provide information, but the bill does not appear to create new mandates or appropriations.

Medical and advocacy communities: Could leverage the designation to promote awareness campaigns, partnerships, and resources.

Procedural and timeline notes

Status: Filed February 11, 2026.

Legislative action: On February 17, 2026, the bill was read a second time and adopted by publication, and placed on the Ceremonial Resolutions Calendar for publication only. This indicates the measure is non-substantive in nature, focusing on ceremonial recognition rather than new law or funding.

Next steps: If advanced, it would proceed through the ceremonial calendar and, depending on chamber rules, may be adopted by publication and ultimately become an officially recognized observance in Florida’s ceremonial records.

Practical impact

Recognition without funding: The bill creates awareness and ceremonial acknowledgment without imposing new regulatory requirements or state spending.

Public education potential: Could catalyze information dissemination and partner organizations to raise public understanding of Wolf-Hirschhorn syndrome.

Advocacy alignment: Provides a formal platform for families, patient groups, and healthcare providers to advocate for research, services, and supportive resources.

If you’d like, I can compare this proposed observance to similar awareness days in Florida or summarize related educational resources commonly associated with Wolf-Hirschhorn syndrome.