AuSends Consultancy

AuSends Consultancy Independant, Neurodivergent, Neuro-affirming SEND & Disability Advisor, Speaker, & Trainer for families, professionals and organisations.

Identify-Understand-Connect. Individual support to help understand triggers and needs, no diagnosis needed.

25/02/2026

Devon.

For those that aren’t aware.
A local SEND Specialist school burnt down over the weekend.

The resources, equipment and impact will knock on for the foreseeable future.

A request from a teacher at the Promise School, Okehampton.

https://www.facebook.com/share/p/1cPaDPa1mp/?mibextid=wwXIfr

25/02/2026

Department for Education. What a joke!! You run an event about SEND reforms white paper and it’s not inclusive!!

Can’t join with a teams account, and no option for captions. Completely discriminatory for D/deaf and those who need captions. And people say so far back, can’t even lipread!!

How do you expect inclusion in schools when you’re not even inclusive for parents and professionals with additional needs!

No inclusion at all!

Absolute joke!!!

RNID - For Deaf & Hard of Hearing People
Deaf - not stupid.
DeafNation
Neuroverse Community
National Deaf Children's Society

24/02/2026

Mum Billie, , has shared her young son Jess’s anaphylaxis experience. She wants to raise vital awareness that anaphylaxis symptoms may not present themselves as they have in the past or as you might expect.

“ANAPHYLAXIS does not always happen the way you think it will. For Jess, it wasn’t instant, loud or dramatic like in movies. It’s the silence, for me, that my mind keeps playing back to.” – Billie

⚠️ Jess has an allergy to dairy and is at risk of anaphylaxis. When he accidentally ingested milk, his lips became sore and his hand itchy. I called an ambulance as soon as I realised, and I’m so glad I did. He was in hospital when the anaphylactic reaction started.

⚠️ In hospital, Jess didn’t immediately go into anaphylaxis. It didn’t appear until an hour after ingesting the milk, while we were sitting in the A&E waiting room.

⚠️ There was no screaming or crying. Jess looked at me and told me he felt sick. Within 20 seconds, his ears were burning. He had hives on his tummy and his eyes began to get gunky.

⚠️ Instinct told me anaphylaxis was beginning. I ran, carrying him to the nearest nurse, and she grabbed an EpiPen. I could see he was unable to swallow his own saliva and he struggled to speak.

Vigilance saves lives. Stories like Billie’s are so important. In this instance, it could help raise awareness that anaphylaxis symptoms don’t always appear immediately; they can escalate at great speed, highlighting the importance of acting quickly.

Thank you, Billie, for sharing 💜

*Natasha’s Foundation does not provide medical advice. All medical information is sourced from reputable medical sites, experts and publishers. Always seek the advice of your physician or other qualified healthcare provider.

I agree that this proposed model will increase trauma, and likely leave more choosing to Home educate meaning more paren...
24/02/2026

I agree that this proposed model will increase trauma, and likely leave more choosing to Home educate meaning more parent carers will be forced to leave jobs.

How is that supporting families, the economy or the children.

Cerebra has issued an initial response to the Government’s proposed SEND reforms, focusing on the rights of disabled children, the desire to push disabled children to mainstream schools and the reduction of powers of the SEND Tribunal. We are very concerned about the likely increase in Systems Generated Trauma:

For many reasons, families of children with disabilities know what it is like to live with uncertainty. After six and a half years, one of those uncertainties has been removed, as the Government’s review into education for children with special educational needs has concluded with the publication today of the Schools White Paper.

This represents a fundamental rethink into how children with special educational needs will be educated. The Government intends to replace the Children and Families Act 2014, which, along with regulations and a code of practice, sets out the current rights and entitlements to special education provision with a new law.

There is nothing wrong with the current statutory framework, it is good law. We believe that the primary reason that the Government wants wholesale change is to contain costs, which have been increasing significantly over the last few years and are forecast to increase further. It intends to do this by increasing capacity in mainstream schools by creating inclusion bases and reducing access to more expensive special schools.

We agree with the principle that, where appropriate, children should have their special educational needs met in their local mainstream school and be educated alongside their non-disabled peers, but for some children this is not appropriate and places at special schools should not be restricted for children who need them.

We entirely oppose the removal of any rights for children with special educational needs.

We are extremely concerned that this will be accompanied by the reduction or removal of disabled children’s rights by making access to Education Health and Care Plans (EHCPs) much harder, leaving schools to decide what provision a child needs.

An EHCP sets out a child’s special educational needs and the special educational provision to meet every one of those needs. It is the legal mechanism by which families can enforce their child’s right to an education in what is a very broken system.

If the proposed system works as the Government intends, the demand for EHCPs would naturally reduce as needs will be met out of ordinarily available provision in mainstream schools.

There would be no need to remove rights. But the Government needs to demonstrate this works. It should not remove rights at all, and it definitely should not legislate to remove rights based on an untried and untested model.

We entirely oppose the reduction in powers of the SEND Tribunal, which is a key mechanism available to parents to hold local authorities to account. These include removing the power of the SEND Tribunal to direct a local authority to provide a place at a specific school, which could be potentially disastrous for a child.

The job of the SEND Tribunal is to step into the local authority’s shoes and remake the decision that is being appealed. Local authorities lose 99 percent of all appeals because they consistently make unlawful decisions. There is no reason to think this will change in the proposed new system.

Removing rights and accountability mechanisms will not solve the problem. The Government are proposing to improve complaints and mediation processes. We help many families with social care complaints and know this system works poorly.

We are not convinced that making families go through a complaints system, before being able to make a more limited appeal to the SEND Tribunal, will be fair, timely or effective.

We welcome the increased funding that is attached to the proposals and the intention to increase access to specialist support in mainstream schools. There Government has come forward with some solid proposals. Whether these will be sufficient to meet needs remains to be seen.

Our report, Systems Generated Trauma, published in November 2025, found that a large percentage of families are traumatised as a result of fighting for the right educational provision for their children.

We are deeply concerned that the proposed changes set out in the White Paper will have the unintended consequence of traumatising even more families because we believe that the changes are fundamentally about saving money, rather than meeting children’s special educational needs.

Read the full statement here: https://buff.ly/HZVzEVB

23/02/2026
Government white paper has been released. I will share two links below one is a full paper and one is the School week su...
23/02/2026

Government white paper has been released. I will share two links below one is a full paper and one is the School week summarised version.

I’m interested to hear from any professional professionals and their thoughts I would give them more detailed response later when I’ve read it again and processed it.

Most importantly to remember is that these reforms are not due to start until 2030 so all (current) laws remaining placed and nothing changes.

Schools week:
https://schoolsweek.co.uk/schools-white-paper-the-key-send-reform-policies/

Full copy:
https://www.gov.uk/government/publications/every-child-achieving-and-thriving

Reforms to the schools and SEND systems in England to ensure that every child can achieve and thrive.

21/02/2026
19/02/2026

When a child is melting down, our instincts can take over — and not always the helpful ones.
We might lecture, rush to fix, or tell them to calm down… but these actually block co-regulation rather than build it.

Let’s talk about what not to do — and what to try instead — so we can truly help a child borrow our calm instead of our chaos.

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It’s setting up to fail. Schools have too much already without being expected to wrote independent support plans (which ...
19/02/2026

It’s setting up to fail. Schools have too much already without being expected to wrote independent support plans (which “may” have legal parts!).
How are they proposing consistency? That’s half the issue at the moment, schools don’t have enough funding, support or staff to ensure all needs are met.

Children with special educational needs and disabilities (SEND) will have their right to support reviewed as they move into secondary school, leaked government plans suggest.

Read more: https://bbc.in/3MxevNc

Very true. Whatever else maybe leaked the law has not changed and will not change until due process etc.
19/02/2026

Very true.

Whatever else maybe leaked the law has not changed and will not change until due process etc.

Just a gentle reminder to our families and those we work with 💛

We know that recent press leaks about potential SEND reforms in the forthcoming Government White Paper may feel worrying or unsettling. It’s completely understandable to have questions or concerns when you see headlines like these.

For now, though, nothing has changed. The law remains exactly the same today as it was yesterday, and it will be the same tomorrow. Any future changes would need to go through formal consultation and parliamentary processes before they could come into effect.

When the consultation opens, we will make sure families have clear information and the support needed to understand the proposals and share their views. You won’t be navigating this alone — we’re here to support you every step of the way.

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