Special Educational Needs Debate

Full Debate: Read Full Debate
Department: Department for Education
Wednesday 21st April 2021

(3 years ago)

Westminster Hall
Read Full debate Read Hansard Text Read Debate Ministerial Extracts

Westminster Hall is an alternative Chamber for MPs to hold debates, named after the adjoining Westminster Hall.

Each debate is chaired by an MP from the Panel of Chairs, rather than the Speaker or Deputy Speaker. A Government Minister will give the final speech, and no votes may be called on the debate topic.

This information is provided by Parallel Parliament and does not comprise part of the offical record

Tulip Siddiq Portrait Tulip Siddiq (Hampstead and Kilburn) (Lab) [V]
- Hansard - -

It is a pleasure to serve under your chairmanship, Sir Edward. I start by thanking my hon. Friend the Member for Slough (Mr Dhesi) for initiating this important debate. He was completely right to say that children with SEND have been forgotten, left behind and overlooked, and that their parents have had to fight at every single stage of the process to get their needs met. It is shocking that some children in Slough have had to wait up to two years for a diagnosis. My hon. Friend the Member for Norwich South (Clive Lewis) made similar points about his area and about how the system has completely failed parents, with appalling social services infrastructure and, in effect, a two-tier system for those who can afford it.

I want to take the opportunity offered by this debate to pay tribute to the fantastic staff at Swiss Cottage School and Manor School in Brent. Both are specialist schools in my constituency and have done phenomenal work in supporting children with SEND. The shadow Secretary of State for Education, my hon. Friend the Member for Stretford and Urmston (Kate Green), and I had the privilege of speaking to the headteachers of those schools and other special schools across the country in a virtual roundtable earlier this year. Many of the headteachers pointed out to me that much of the digital support that schools have been given, such as laptops, is not even appropriately tailored for the needs of children with SEND.

My hon. Friend the Member for Liverpool, West Derby (Ian Byrne) also explained how he had heard many concerns about resources when he met headteachers in his region. My hon. Friend the Member for Bedford (Mohammad Yasin) made powerful arguments about the devastating impact of coronavirus on the funding situation for special schools. My hon. Friend the Member for Reading East (Matt Rodda) also made a powerful speech about the impact of the pandemic on these services. I hope that the Minister, who has always had an open door with me, will respond positively to his request for a meeting.

As a mother of two young children, I know just how tough this pandemic and school closures have been on young people and their parents, but I simply cannot imagine how much harder it has been for those who have had their specialist support withdrawn. At the height of the third lockdown, just 16% of children with EHCPs were getting all the support set out in their plan, according to research by the Disabled Children’s Partnership. Some 21% of parents said that their children were not getting any support set out in their EHCP. Remember that this is support to which the children are legally entitled, and which all too often represents a compromise that is below the level of support they actually need.

That is just children who have already secured EHCPs. Getting an appropriate EHCP in good time has unfortunately become a postcode lottery, after a decade of cuts to local government that have been felt unevenly across the country, not to mention the impact of the relaxations on timescales misguidedly introduced last April for assessing EHCPs. My hon. Friend the Member for Jarrow (Kate Osborne) spoke movingly about the huge problem in getting EHCPs, drawing on her own experience of looking after a child with SEND. I appreciate her taking the time to contribute to this important debate.

As horrifying as some of the statistics are, the results are scarier. Half of the children with SEND have seen their conditions worsen this past year. I will focus specifically on the impact of loss of access to such therapies as speech and language therapy, occupational therapy, and physiotherapy, which a shocking 70% have been unable to do in recent months. Dan told us about his daughter Elisa, who has cerebral palsy. Elisa relies on regular physiotherapy from her education, health and care plan to manage her condition. Sadly, she missed out on that support for a year during the pandemic and her condition has worsened. My constituent Elisa has dystonia, a very uncomfortable condition where muscles contract uncontrollably. She can no longer use her wheelchair due to the worsening dystonia.

Then there is Suziie, my constituent who cares for her nephew, aged 11, who has a complex series of physical and neurological disabilities. During the pandemic, her nephew has been isolated from other children and has lost access to vital series and therapies that he needs to manage his condition. Awfully, he is now regressing and has lost vital abilities in communication and other essential life skills. He needs sensory rooms and hydrotherapy in his covid-19 recovery plan, and Suziie needs additional respite care.

Those heartbreaking cases tell a story about what has happened during the pandemic: a loss of support and declining health and social outcomes for children with SEND. As has been mentioned in the debate, the Women and Equalities Committee concludes that the Government’s catch-up package will not be enough to tackle the disproportionate impacts on children with SEND. It is all very well issuing guidance saying that they will be a priority, but unless that is followed up with targeted funding there is no guarantee that they will get the support that they desperately need.

I have previously criticised Ministers for treating children as an afterthought in the pandemic, but I believe that those with SEND have been completely left behind. That is certainly how parents feel when I speak to them. However, not all politicians have forgotten about these children. My hon. Friend the Member for Luton North (Sarah Owen) highlighted the important work that Councillor Javed Hussain and other Luton councillors are doing on local autism hubs and park upgrades, bringing benefits for those who use wheelchairs. We should be learning from them.

Although lessons must be learned from the failures that my colleagues have outlined, I want to look to the future. We need proper support for EHCP provision to be restored in full. We need a plan from Ministers to clear the backlog of assessments and health appointments. There must be a proper co-ordinated catch-up plan that goes beyond the Government’s narrow ideas about educational catch-up. We have to have targeted support for children with SEND to make up for months of lost development in communication, social skills and wellbeing.

Rather than downgrading the legal duties to children with SEND, as the Government did at the start of the pandemic, the SEND review should be an opportunity to upgrade the resources that local authorities have to deliver support, and to listen directly to families about how services can be reshaped so that they operate in the best interests of our young people.