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SENDIASS Support for PDAers

Available to purchase individually, or access this content as part of our monthly or annual subscription plans.

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£10.00

Overview

SENDIASS Support for PDAers (Two-Part Podcast)

This two-part audio resource is included in our monthly and annual subscriptions, or can be purchased individually. It offers clear, practical guidance and insight into engaging with SENDIASS to support the needs of a PDAer at home and at school.

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Learn how to make the most of SENDIASS (Special Educational Needs and Disabilities Information Advice and Support Service) when supporting a PDAer in educational settings. This two-part series blends essential information, lived experience and practical tips to help you advocate effectively and navigate the systems around education, support and rights.

In Part 1, we focus on using SENDIASS at home and school: what the service offers, how it can support you in understanding processes, building confidence in meetings, and clarifying your child’s needs from a place of strength.

Part 2 explores what support SENDIASS can provide in more detail, including working with schools, understanding statutory rights and assessments, preparing for reviews, and practical ways to collaborate with professionals to make education more accessible for a PDAer.

Created by the PDA Society with contributions from people with lived experience and professionals in the field.

Disclaimer

The views and opinions expressed by guest speakers in this podcast/audio guide are their own and do not necessarily reflect those of the PDA Society. While we aim to provide balanced and inclusive discussions, individual experiences and perspectives may vary. The PDA Society is committed to using language and terminology that reflects the preferences of PDAers and autistic people, but sometimes our guests may use language and terminology which differs. Appearance on our podcast is not an endorsement of an individual, and not all of our guests will align with our position on the issues discussed.

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This content was developed by the PDA Society together with PDAers, family members, and professionals, drawing on a wide range of lived and professional experiences.

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