The Specific Needs Register was set up in 2000. It is used to provide parents with relevant information as well as to help improve services in Pembrokeshire.
What is the purpose of the Register?
The register is used to improve current services to disabled children/young people in Pembrokeshire. It is also used to provide quarterly and annual statistical information which helps to improve the planning process for all agencies and to identify changing trends and needs so that services can be put in place to meet them.
How will it benefit me?
As a parent of a disabled child/young person on the register, you will receive a newsletter twice a year containing useful and interesting information. You will also be invited to attend relevant training courses throughout the year run by both ourselves and other voluntary organisations throughout Pembrokeshire. We also hold an annual fun day for registered children/young people.
How do I register my child/young person?
Registering your child/young person is simple. Just complete a form, you can download this form below. They are also available via us at the Hawthorn Project, from your Health Visitor, or from your School Nurse, make sure all the relevant details are complete and that you have signed the form, and then return it to us. We will do the rest.
To download the following documents, please click on the links below
The Data Protection Act
Click to Download:
Data Protection Act Documentation
Guidance Notes for Registration
Click to Download:
Guidance Notes Documentation
Specific Needs Register Registration Form
Click to Download:
Specific Needs Registration Form