Get the free National Intellectual Disability Database Committee annual

National Intellectual Disability Database Committee annual report 2006 Item type Report Authors Health Research Board (HRB) Rights Health Research Board Downloaded 8Jan2016 11:55:53 Link to item http://hdl.handle.net/10147/45439

How to fill out national intellectual disability database

1. To fill out the national intellectual disability database, you will need to gather relevant information about the individuals with intellectual disabilities.
2. Start by collecting basic demographic details such as their name, date of birth, gender, and contact information. This information is crucial for identification and communication purposes.
3. Document the individual's diagnosis and any specific conditions they may have. This helps in categorizing and understanding their unique needs and challenges.
4. Include information about their educational history, including where they attended school and any specialized programs or services they have received.
5. Record details about their medical history, including any relevant diagnoses, medications, and past surgeries or treatments. This information helps healthcare professionals understand the individual's overall health and any specific medical considerations.
6. Include information about their family or caregivers, such as their names and contact information. This allows for effective communication and involvement of key stakeholders in the individual's care.
7. Provide details about any additional support or services the individual receives, such as therapy, vocational training, or social programs. This helps in assessing the effectiveness and impact of these interventions.
8. It is essential to ensure the database is kept updated with any changes in the individual's circumstances, such as new diagnoses, changes in medication, or modifications to their support plans.

Who needs the national intellectual disability database?

1. Researchers and policymakers: The national intellectual disability database serves as a valuable resource for researchers and policymakers in understanding the prevalence, characteristics, and needs of individuals with intellectual disabilities. It helps in identifying trends, informing policy decisions, and promoting evidence-based practices.
2. Healthcare professionals: Medical professionals can benefit from the national intellectual disability database by accessing relevant information about a patient's diagnosis, medical history, and support needs. This assists in providing personalized and coordinated care, avoiding duplication of services, and identifying any potential health risks or complications.
3. Service providers and educators: By accessing the national intellectual disability database, service providers and educators can gain a comprehensive understanding of an individual's support needs and tailor their interventions accordingly. This promotes effective service delivery, improves outcomes, and ensures individuals receive appropriate assistance and accommodations.
4. Families and caregivers: The national intellectual disability database can be a valuable tool for families and caregivers, providing them with access to resources, support networks, and information about available services. It helps in navigating the complex system of care, connecting with relevant professionals, and advocating for the best interests of the individual with intellectual disabilities.
5. Individuals with intellectual disabilities: The database can empower individuals with intellectual disabilities by ensuring they have a voice, facilitating their access to appropriate services and supports, and promoting inclusion and self-advocacy. It gives them the opportunity to participate in research studies, contribute to policy discussions, and access various resources for their overall well-being.

In summary, filling out the national intellectual disability database requires gathering information about the individual's demographics, diagnosis, medical and educational history, and support services received. The database serves various stakeholders, including researchers, healthcare professionals, service providers, families, caregivers, and individuals with intellectual disabilities, by providing valuable insights, coordinating care, and promoting inclusive practices.

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What is national intellectual disability database?

The national intellectual disability database is a system that collects and stores information about individuals with intellectual disabilities.

Who is required to file national intellectual disability database?

Healthcare providers, social workers, and other professionals working with individuals with intellectual disabilities are required to file the national intellectual disability database.

How to fill out national intellectual disability database?

The national intellectual disability database can be filled out online through a secure portal provided by the government. Users will need to input information such as demographic details, medical history, and support needs of individuals with intellectual disabilities.

What is the purpose of national intellectual disability database?

The purpose of the national intellectual disability database is to improve coordination of care, monitor outcomes, and generate data for research on intellectual disabilities.

What information must be reported on national intellectual disability database?

Information such as personal details, medical history, support needs, and services received by individuals with intellectual disabilities must be reported on the national intellectual disability database.