Special Educations Needs: Getting Started with Statements – the parent to parent guide to getting your child the help they need
Reviewed by NAS Surrey Branch member Emma Searle, mother of a 4 year old recently diagnosed with ASD
"This is a brilliant little book. We are just starting on the statementing process and it’s a bit depressing to find that it’s such a battle, but it is refreshing to get an honest and real account of what happens. I really liked the detail on the process – for example, I hadn’t realised that you don’t have to stick to the form to give your evidence, but can write your own account. It was really useful to have all the detail and being able to read extracts from other people’s statements is invaluable.It shows you how to use the SEN Code of Practice – I haven’t seen any other examples of this. Because it’s written by parents for parents, it can give you information you don’t get on official we sites. I found it quick and easy to read and easy to dip into when you’re waiting at school for example."
A huge thank you to Emma for taking the time to write the review and I hope very much the book has helped you so far. If anyone else has found the book useful and would like to leave a review, I would be delighted if you would post it on the Amazon book page
Founder, CEO, Editor at Special Needs Jungle
Founder of Special Needs Jungle. Parent of two young adults with autism. New grandma. Tania is a member the Ofsted SEND Inspections Stakeholders Advisory Group, and sits on the Advisory Board of the Royal Holloway, University of London Centre of Gene and Cell Therapy. She is also on the Editorial Board of Springer Nature Gene Therapy journal
She is also an experienced broadcast and print journalist & author. Tania also runs a PR, web & social media consultancy, SocialOro Media. She is a rare disease & chronic pain patient advocate with Ehlers Danlos syndrome.
She is also an experienced broadcast and print journalist & author. Tania also runs a PR, web & social media consultancy, SocialOro Media. She is a rare disease & chronic pain patient advocate with Ehlers Danlos syndrome.
Latest posts by Tania Tirraoro (see all)
- Poor advice for Post-16: Why Katie & Harvey Price’s long hunt for a suitable college is far from unique - March 2, 2021
- Free back-to-school legal WEBINAR! What to do if your child’s SEND education rights are denied when schools fully-reopen - February 25, 2021
- SNJ’s 10-point “Grab & Go” version of the DfE’s Back-to-School Guidance for SEND learners - February 23, 2021
