The Government absolutely recognises there are unacceptable delays in accessing assessments of need. My Department and the HSE are committed to addressing these delays. Under the Disability Act, an assessment of need is an assessment process carried out by the HSE where a person is of the opinion that he or she may have a disability for anyone born after 1 June 2002. It first establishes whether the person has a disability as defined within the Act and then identifies the health and education needs of the person with the disability and the service required to meet those needs.
As the Deputy said, last week the Government announced a series of reforms to the assessment of need process which will make the process more effective and efficient for children and families, and will move towards more assessments being delivered within the six-month statutory timeframe. These reforms include changes to Part 2 of the Disability Act, which provides for assessments of need. The general scheme of the disability (amendment) Bill 2025 was approved by the Government on 9 December and will be published on the Department’s website shortly. It is important to say these changes will not remove any rights for parents to apply for an assessment of need for their child, nor will they alter the statutory six-month timeline set out in the Disability Act.
Turning to access to treatment and therapies, I must emphasise that children do not require an assessment of need to access health services including primary care, children’s disability network teams, CDNTs, or mental health services. However, it is recognised that there can be delays for children and families in getting access to the treatments and therapies they need.
Children can be on a number of different waiting lists which can cause confusion for families. In 2026 the HSE will introduce a single point of access system, which will make it easier for families to be referred to the right service whether that is a CDNT, primary care, or a child and adolescent mental health team.
The recruitment of staff across the disability sector continues to be a key priority in ensuring children can access therapies in a timely manner. An intensive focus of my Department has been on increasing the staffing of CDNTs that deliver supports and services to children with complex needs. My Department has been in discussions with the Department of education on the need to phase out the requirement for an assessment of need to access special education class or school.