Act now! Sign and Share the Parliamentary Petition to PROTECT SEND RIGHTS!

** Read the updates to this post**

If you’re a SEND parent or a teacher, certain headlines last week likely made your blood run cold – headlines like “250,000 SEND pupils could lose their legal guarantees of extra support”. Behind those headlines were comments from Dame Christine Lenehan, former head of the Council for Disabled Children and now strategic government advisor on SEND. We discussed her comments here (in less click-baity terms) last week.

Dame Christine confirmed consideration was being given to statutory plans no longer being available to children in mainstream schools. She is quotes as stating (inaccurately) that EHCPs were only ever meant for children who needed support from health and social care as well as education. 

No time to read all the article now? Click for the petition link

Buy SNJ Ad
SNJ FLOW CHARTS
SEND LAW & OPEN RESEARCH

Shock and Flaw…

The government has been insistent that “inclusive mainstream” is the way forward for the SEND system, so Lenehan’s comments came as a shock even to us. The thought of shoehorning almost all disabled children into mainstream schools, without any promise of the provision they need, is chilling.

The only way to achieve this would be a change to the current law. Once that particular Pandora’s Box is opened, all bets are off—and this is the main reason we have steadfastly opposed any reform of the Children and Families Act.

Despite Dame Christine saying we shouldn’t be worried, parents and teachers will be terrified by these suggestions. If needs outstrip resources now, imagine what that will be like with even more children who should be in specialist provision but can’t get an EHCP, crammed into mainstream with inadequate staffing. We can foresee increased exclusions, an even bigger increase in applications for statutory assessments, and far more children than now out of school without any kind of provision. Is this what the government wants? Dame Christine has written about her comments in The Independent, but when she says “I have every reassurance that for the hundreds of thousands of children with EHCPs, there will continue to be high-quality support,” is neither reassuring or explanatory.

This is NOT the way to solve the SEND crisis

If the government wants to build a fantastic system where EHCPs are rarely ever needed, bring it on. In an ideal world, our schools would be sufficiently resourced and trained to offer immediate and effective support to every child who needs it, and we’d watch as the need for EHCPs gradually fell. This would be a long, careful program of change with both High Needs debt written off and a massive increase in school funding, ringfenced for SEND. Given that all of this is predicated on the need to save money, that seems beyond unlikely. 

Back in December, we wrote about the Institute for Fiscal Studies report into SEND spending. They asked “What would need to change for parents to trust the system to meet their children’s needs without statutory obligations?”. It seems the government have taken that question to heart, but hasn’t bothered to seek an answer they don’t want to hear. Unless we see dramatic change, where needs are being met effectively at a non-statutory level, there is nothing that will reassure us that needs will be met unless the law requires it. If they’re not going to ask, we need to tell them this – right now.

Promoted

The thin end of the wedge?

While we need to remember that these are NOT YET published proposals, forewarned is forearmed. And this Government has form in targeting the elderly and disabled adults and children, instead of the wealthy to bear the brunt of the financial “black hole”.

Let’s not forget, anyone’s child, grandchild or close relative can be born disabled or become disabled, so if your family is not affected now, you could be in the near future.

How can anyone stand by as the government visits the pain of the previous government’s failures on those least able to bear it? This is the thin end of the wedge—if disabled children’s inconvenient rights are stripped away, whose rights will be next?

Send a message to parliamentarians—SIGN the petition.

Without a strong response to these proposals, the back room discussions about the future of our children’s rights will continue unimpeded. We need to be loud, and it needs to be now – before decisions are made. Signing a petition may not seem much—but it sends a message abotu what people want and don’t want

Over the last few months, I’ve worked to get a parliamentary petition in place, which asks the government to commit to maintaining disabled children’s existing legal rights to assessment and support in education. There has been a fantastic response, with the petition receiving over 8,000 signatures on Sunday alone. This is a testament to the number of families and professionals who would be affected by a change in law. 

We’ve passed the 10,000 signature target, which will ensure a response from the government, but these are often minimal. We’ve passed 20,000 after sharing the petition on our socials yesterday—but we need 100,000 signatures to ensure this petition is debated in the House of Commons, and your support will help us to achieve that. 

Please sign the petition and share this information with your families, friends, schools and SEND groups. There will be more to come, and I know we are all exhausted from the fight. Let’s focus on the actions we can take now and make our voices heard. You can hear me talking more about this here

IPSEA has today created a template for you to write to your MP about this too. You can find and download it here

We are all parent carer volunteers at SNJ, but we still have costs to cover. If you can DONATE—even a small amount—you will help us continue. If not, you can still help by sharing this article—share links below ⤵️ ⤵️—follow us on social media, and/or offer to volunteer.


Disabled Children’s Rights are Under Attack.
We’re fighting, but we can’t do it alone: we need your help more than ever.
We’re volunteer-run, but costs are rising. To help us keep going, please consider a one-off or, if it’s possible, a regular donation.
Read more about being a regular donor here.
We use Zeffy to fundraise, which doesn’t charge us a fee, so 100% of your donation reaches us.


SNJ FLOW CHARTS
Books SNJ recommends

Also read:

Don’t miss a thing!

Don’t miss any posts from SNJ – simply add your email address below. You must click the link in the confirmation email you’ll receive to activate your free subscription.

You can also keep up with us by following our

Want more? Be an SNJ regular donor!

SNJ is a non-profit and everyone who writes here does so voluntarily. We need your support to help us with costs by donating once or as a regular patron. Find out more here

Rachel Filmer
Follow

Discover more from Special Needs Jungle

Subscribe to get the latest posts sent to your email.

We LOVE to hear what you think... please take a minute to add your views here, so your comment is seen by all!

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Discover more from Special Needs Jungle

Subscribe now to keep reading and get access to the full archive.

Continue reading