Children With Autism Face a Year Long Wait for Education Support
By Janaki Mahadevan | Children & Young People Now
Almost half of all children with autism wait for More than a year for Appropriate Educational support, a report by the National Autistic Society (NAS) HAS found.
The Findings Accompany the launch of the charity’s Great Expectations campaign, Aimed at Influencing Government Reform on Special Educational Needs (SEN) to Ensure the expectations of Both children and parents are met.
More than 1.000 parents of children with autism Were Surveyed by the society, with 48 per one hundred Saying THEY Waited More than a year to get the right support for Their 27 per child and one hundred WAS Saying the wait More than Two Years.
Eighteen per one hundred parents of Said THEY HAD taken legal action to get support for Appropriate and Their Children HAD gone to court year average of 3.5 times each.
Only 52 per one hundred of parents Said Their child WAS Making Good Educational Progress and seven out of 10 Did not Think It Had Been easy to get the education support Their child needed, while a further Top 47 per one hundred Said Their Child’s Needs Were not Picked Up in Timely a way.
Mark Lever, NAS chief executive, said: “It Is Completely Unacceptable That So Many parents are still fighting a daily battle for Their Fundamental right to get education year for Their child. The government Rightly Recognise That Action Is Needed, and THEY That Need to Reform That system has continued to Many Children with autism let down.
“Our report sets out the Practical, Often simple steps That Can the government take to create a system That Works for everyone. Let’s get it right. “
NAS Is Now That recommending Local Authorities work with schools and Other Services Such as to Ensure Health Have access to all schools and specialist support for chairs of governing bodies to Be Given Specific Training in SEN. According To the charity, health visitors and school staff must aussi Have Specific training in autism to Ensure THEY Can Identify early signs of the condition.
Referring to the new Health and Wellbeing boards, the report Said There Should Be more representation from schools. CYP Now Reported Earlier this month That initial research HAD Shown schools look Unlikely to Be Among the hand is on the boards.
NAS aussi wants Local Authorities to Increase transparency by publishing Their Strategic Plan for Children with SEN. The charity Said government must work with councils Also, parents and the Voluntary Sector to explore how Local Authorities Can Become parent champions.