I welcome many aspects of the special educational needs and disabilities White Paper, especially those on early intervention and increased funding. We know that most local authority SEND staff care deeply, and we are grateful for them for that, but local authority SEND provision is chronically underfunded and too often this has led to corner cutting, a culture of dishonesty and brutalisation. I fear that the Government have seriously underestimated the scale of harm. One mum wrote on my Facebook page:
“My daughter is self-harming and suicidal. EHCP behind by weeks. Discharged by CAMHS as educational setting is the main reason for mental health struggles and has to change before any work can be done. We are just left watching our children suffer. How is breaking the law by all these services allowed and not prosecuted?”
To this point, Mathew Purchase KC has said that the schools White Paper has
“a lot of good intentions, but which, on the face of it, are going to reduce the ability for children and families to enforce what they are legally entitled to.”
Last week I published, with The Times, 20 cases of avoidable SEND child suicide caused by failures by local authorities. All 20 of those children would have had their education, health and care plan rights removed under the Government’s plan, so would potentially have been even more vulnerable. Three of their mums have asked me to speak about their children.
Patricia Alban is here today. Her son Sammy was autistic. His local authority removed his EHCP. Despite 13 referrals by the police to the council, it refused to provide him with any of the support he needed. After a history of suicide attempts, Sammy died, aged 13, after falling from a harbour wall. His inquest concluded that he died from
“inadequate support from the local authority and mental health services.”
My constituent, Jen Bridges-Chalkley, started college in October 2021. She was 17 and had been diagnosed with autism and attention deficit hyperactivity disorder. Her local authority failed to update the college, through her EHCP, about her risk of suicide. One month later, she was dead. Her 81-page inquest report detailed continuous and prolonged failures by her local authority to provide the support she needed.
Eivie White was 13 when she killed herself, after years of denials and failures by her local authority to provide the support she needed for her autism. Her older sister found her body. She had to continue sleeping in the same bedroom in which Eivie had hanged herself because the local authority would not provide new housing. Six months later, Eivie’s best friend killed herself, aged 13.
Those are just three of over 200 testimonies I have received about avoidable SEND child suicide—it is an epidemic. It is our country’s duty to protect our most vulnerable citizens. How can the Government even consider cutting children’s rights?