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Bill > SJR81
NJ SJR81
NJ SJR81Designates October 23 of each year as "Aromatic L-amino Acid Decarboxylase Deficiency Awareness Day."
summary
Introduced
02/12/2024
02/12/2024
In Committee
02/12/2024
02/12/2024
Crossed Over
Passed
Dead
01/12/2026
01/12/2026
Introduced Session
2024-2025 Regular Session
Bill Summary
This resolution establishes October 23 of each year as "Aromatic L-Amino Acid Decarboxylase Deficiency Day" in New Jersey. The State of New Jersey supports protecting the health of vulnerable populations and young children, as well as educating the public and medical communities about rare diseases. A rare disease is generally considered to be a disease that affects fewer than 200,000 people in the United States at any given time. Aromatic L-Amino Acid Decarboxylase ("AADC") Deficiency is a life-limiting, severely debilitating genetic neurologic rare disease that significantly impacts a patient's development, motor skills, growth, cognition, and language skills. While some patients who are born with AADC Deficiency may be asymptomatic at birth, AADC patients typically experience symptoms within the first year of life such as developmental delay and involuntary eye movements. Caregivers of patients with AADC Deficiency are often responsible for the overall care of the patient due to the debilitating nature of this disease and patients may need life-long care. The State of New Jersey can raise awareness of AADC Deficiency in the public and medical communities within this State in order to support individuals with AADC Deficiency and their caregivers by designating this awareness day.
AI Summary
This joint resolution designates October 23 of each year as "Aromatic L-amino Acid Decarboxylase (AADC) Deficiency Awareness Day" in New Jersey, aiming to raise public understanding about this rare genetic neurological disorder that affects approximately 1 in 100,000 people. The resolution highlights that AADC Deficiency is a severe condition where patients lack the enzyme needed to create dopamine, which can prevent them from achieving basic motor skills, communication abilities, and life milestones. While some patients might be asymptomatic at birth, symptoms typically emerge within the first year of life, including developmental delays and involuntary eye movements. The resolution calls on the Governor to issue an annual proclamation and encourages public officials, private organizations, and citizens to participate in awareness activities that support individuals with AADC Deficiency and their caregivers, who often provide lifelong care due to the disease's debilitating nature. By establishing this awareness day, New Jersey seeks to educate the public and medical communities about this rare condition and support vulnerable populations affected by the disorder.
Committee Categories
Health and Social Services
Sponsors (1)
Last Action
Introduced in the Senate, Referred to Senate Health, Human Services and Senior Citizens Committee (on 02/12/2024)
Official Document
bill text
bill summary
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bill summary
| Document Type | Source Location |
|---|---|
| State Bill Page | https://www.njleg.state.nj.us/bill-search/2024/SJR81 |
| BillText | https://pub.njleg.gov/Bills/2024/SJR/81_I1.HTM |
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