Education, Health and Care Plans

Debate between Tanmanjeet Singh Dhesi and Marie Goldman

Wednesday 22nd January 2025 Westminster Hall

[Marie Goldman]

Of course, and my hon. Friend raises an important point. We must tackle that inequality. The Government will say, “We put £1 billion of extra funding into special educational needs.” That is great—it is much better than no extra money for special educational needs—but it will not touch the sides. Local authorities are saying that they have a deficit in the high needs block of £3 billion, and some estimates say that that will go up to £8 billion in the near future. We are looking at a massive funding shortfall.

[Mr Tanmanjeet Singh Dhesi (Slough) (Lab)]

I congratulate the hon. Lady on securing today’s important debate. In Slough, attainment outcomes for children with special educational needs and disabilities were below the national average, and that is precisely why we need more funding and resources for Slough children. As a parent, I can only imagine the anguish of parents who have to navigate the complex and time-consuming process of gaining an EHCP, particularly given that only half of EHCPs are issued within the statutory 20-week limit and 98% of appeals are successful. Does the hon. Lady agree that, to improve EHCPs, we need first to regain the trust and confidence of parents?

[Marie Goldman]

Absolutely. Parents’ trust in the system is important, so we need to show that we are listening to them. We also need to show that we are giving them the information they need to alleviate their stress. Someone who has a child with special educational needs knows that their child needs extra support. This is already a stressful time in their life; they then have to sit and wait for an EHCP to land in their inbox, perhaps in week 19 —it is supposed to be 20 weeks, so of course it should land in week 19—but then it does not turn up, and keeps on not turning up. That is incredibly stressful, and it takes away parents’ trust in the system. We should be more transparent about that.

We talk about an EHCP being issued within 20 weeks, but across England 37.4% of decisions took six months or longer—that is just ridiculous—and 5.7% took a year or longer. That is completely unacceptable, and it leaves parents in a very difficult place. We need to be more honest with parents and to make that information much more available to them. My new clause 3 to the Children’s Wellbeing and Schools Bill would help to make the system much more transparent for parents by making local authorities publish how well they are performing against those statutory deadlines. That would be much better for parents.

What is the impact on children? We must remember that we are not talking about random numbers or about figures on a spreadsheet somewhere; these are real children who have real lives, real parents and real families. They have aspirations in life, and we need to support them. What does all this mean for them? One SEND professional wrote to me about one child’s case:

“This child, who is autistic, non-verbal, and has sensory processing challenges, applied for an Education, Health, and Care Plan (EHCP) in October 2023. It is now January 2025, and they are still waiting for their EHCP to be issued. In the meantime, they are placed in a mainstream school with no tailored support. The result has been incredibly stressful for the child, their family, and the staff working with them. The school has now reached a point where they cannot cope, and the child is being home-schooled, isolated from peers and without access to the specialized education they need and deserve.”

One SEND co-ordinator, who is also a teacher, wrote to me:

“It is very frustrating with the length of time it is taking for EHCPs to be finalised. Although they are back-dating the funding (which is great), by the time the EHCP actually is agreed, it is often too late for parents to request school placements ready for a transition at the start of the school year, which is often what we need it for.”

There is a preference for mainstream, and I hear the Government say that we should educate as many children as possible in mainstream. I do not fundamentally disagree, but mainstream is not suitable for all children, and certainly not when mainstream schools do not have the resources they need to provide education and support.

Mainstream sounds good in principle. However, Contact—a charity for families with disabled children—wrote to me, saying, “Local Authorities like Essex”—again, that is where I am—

“are reducing the provision in section F for a child with an EHCP as they believe that a lot of the provision in section F comes under ordinarily available provision, which they say the school can provide as standard. All the special educational provision that a child with an EHCP needs is legally required to be stated in section F of an EHCP. It is through section F that there is a legal duty for Local Authorities to make this provision. Parents have been told by schools that there is no funding for SEN provision or ordinarily available support. How can children be reliant on SEN support when there is no funding for it?”

Schools are really struggling to deal with the situation. The idea of mainstream and of “ordinarily available” provision is great, but not if schools are not provided with the funding they need. I know that the Government can say, “Well, we have increased the funding for schools,” and they have also increased teacher pay, which is great— teachers absolutely should be paid more—but they have also told schools that teacher pay needs to be funded out of their budgets, which makes the situation very difficult.