AuSends Consultancy

AuSends Consultancy Independant, Neurodivergent, SEND & Disability Advisor, Speaker, & Trainer for families, professionals and organisations. Identify-Understand-Connect.

Individual support to help understand triggers and needs, no diagnosis needed.

29/03/2026

The National Education Union says schools need more funding to be able to make all classrooms inclusive.

28/03/2026

Many children with selective mutism are misunderstood. Their silence isn’t a choice, it’s the result of intense anxiety in certain situations.

With understanding, patience, and the right support, children with selective mutism can build confidence and find their voice. 💛

Latest Devon SEND news! This one has frustrated me!!  A new “neurodiversity advice line”!! Where’s the inclusion? Given ...
27/03/2026

Latest Devon SEND news!

This one has frustrated me!!

A new “neurodiversity advice line”!!

Where’s the inclusion?
Given many neurodivergent adults struggle to use phones for various reasons, a phone number is not accessible!

What about those in the D/deaf community who can’t hear/process audio calls. How do we use this?

Lack of inclusion in and the increasing amount of “helplines”, is really infuriating.

They are not “helplines” if there not accessible!!

Parent Carer Forum Devon
National Autistic Society
I.P.S.E.A
Jade Farrington - Counsellor and Therapist
Tigger Pritchard: Neuroaffirming Advocate, Consultant and Trainer
Deaf - not stupid.

Disability Together

Livewell and CFHD are working together to provide a free, confidential advice line for children, young people and their families on the Neurodiversity Pathways in Plymouth and Devon. Advice can include: Contact us Phone: 01752 435404 the Neurodiversity Pathway advice line is open, Monday to Friday,....

27/03/2026

📣 Help Us Work Together to Improve SEND Services for Families in Devon

We bring parent carers and services together to create positive change — and your views help guide that shared work 💛

Our survey:
✅ Takes around 10 minutes
✅ Is anonymous
✅ Helps shape positive change

👉 Take the survey
https://forms.cloud.microsoft/e/zcjT0GCVbW

25/03/2026
This is by far the most common misconception I come across. People assuming that every D/deaf person communicates by sig...
23/03/2026

This is by far the most common misconception I come across.
People assuming that every D/deaf person communicates by signing. We don’t.

I lipread alongside the heating I do have in my right ear and wear hearing aids.
I can use SSE- sign supported English when needed. SSE uses BSL but follows English grammar rules.

With BSL the topic goes first. You’d ask “name what?” as opposed to “what is your name?”

If somebody feels able to tell you they’re deaf, hard of hearing or have another hearing issue. Please ask how they communicate.
Sign, lipread, speaking, writing boards/note books, and AAC are all different methods.

High five to those who already knew this!🖐️⁠

Believe it or not many people don't know these facts, and we're sharing this so that you can take part in raising Deaf Awareness and celebrating British Sign Language (BSL)⁠.⁠
⁠⁠
⁠Happy Sign Language Week 2025!⁠




⁠Alt text: ⁠An educational graphic titled "Did You Know...?" listing key facts about sign language: it does not represent spoken language, is not universal, not all Deaf people use hearing aids or sign language, Deaf people can do everyday activities like reading and driving, and that a lack of hearing does not indicate a lack of intelligence. The design includes a blue and purple gradient background with www.deafumbrella.com at the bottom.⁠

⁠ SignLanguage

21/03/2026

On SNJ TODAY: Statutory Guidance for Supporting Pupils with Medical Conditions at school is being updated. SNJ's Tania looks at the consultation document to see what's new, what's missing and what you need to know to respond, including a handy table laying out the changes. Link in the first comment

20/03/2026

For anyone on PIP or a with a young person on PIP.
The consultation for feedback on the Timms report on changes to PIP has opened.
Any feedback has to be received by 28/5/26.

What an amazing tool.
17/03/2026

What an amazing tool.

14/03/2026

ARFID and Medication.

People with ARFID, avoidant, restrictive food intake disorder often find it difficult to take medication for several reasons.
Physical, sensory, and psychological.

Many ARFID sufferers have heightened sensitivity to taste, texture, smell, or even the feeling of things in their mouth or throat.

Medications often don't taste very pleasant. They may taste bitter, have a chalky texture or have unpleasant smells. All of these can trigger strong aversive reactions, such as gagging, vomiting and anxiety.

Sometimes even flavored or liquid medicines may be rejected as it can be overwhelming and smell/taste unfamiliar.

For many people, ARFID involves fear-based avoidance. For example, they may have a fear of choking, vomiting, or other negative responses to eating.

Swallowing tablets or capsules can feel risky or unsafe. Some people (R included) say they feel as though their throat closes as soon as they try to swallow it. This can cause heightened anxiety and create a physical inability to swallow.

Many people with ARFID have a very narrow range of "safe" or "tolerated" foods and drinks that they trust, so introducing anything new, even Calpol can disrupt the feeling of safety.
For this reason some people avoid ANY change in taste or texture in their mouth such as toothpaste, it isn'tjust food they struggle with.

Pills or capsules may be too big or hard to swallow
Liquid medicines may have a nasty taste or have a grainy texture.

Chewable medication and gummies may have a powdery or squishy texture that can't be tolerated. And the flavor of them may also be an issue.

The distress may not be about the actual medication itself. Though that is a problem for many.
We all know that ARFID is often linked to anxiety for many people and a need for predictability and control over their oral intake can be very important to them, so taking a new medication, just like trying a new food, can be too unpredictable. They may worry about what it will taste like or if it may make them feel sick, will it get stuck in their throat, etc.. This can increase avoidance.

Taking medication can be challenging for anyone, nut moreso fornpeople with ARFID because it can activate the same sensory and fear based challenges that make eating difficult.

What others, including health care professionals see as them being difficult, is actually a genuine, overwhelming feeling of distress.

It's really important to try not to hide medication in their "safe" foods/drinks.
I know this can be tempting when we are desperate and it can work for some people. However it can lead to them losing the food or drink.
If they are old enough to understand, it is always better to be honest about how important it is that they take the medication and try together to find a way to help them take it.

For example, R has medications she takes daily. She absolutely cannot swallow them. For many years she has had them crushed to a fine powder and buried in a spoonful of yogurt.
Yogurt was once an occasional safe food but she sees it as medicine now, so can literally only take it with the medication in.
We discussed different things to try and settled on Yogurt. It works for her, but I know that may not work for everyone.
Paracetamol suppositories can be really helpful for younger children.
Many children need to be admitted to hospital to have essential medication administered via IV, some have an NG tube fitted when they need consistent medication.
So the inability to take medication orally can be a really serious complication of ARFID.
A complication that many people.are not aware of or take seriously. 💜

13/03/2026

What a historic moment for BSL in Wales! 💙

The BSL (Wales) Bill reaches its final stage — a huge step for Deaf community across Wales. Recognition of British Sign Language means greater visibility, inclusion, and respect.

Today we celebrate this achievement and the amazing community that made it possible! 🎉

12/03/2026

I always try to give praise where it’s due. Our EHCP caseworker has been great, communicating well with me and chasing other professionals alongside me.

However, we are now having to trigger our 3rd EHCP appeal in 3 years due to no provision for a handful of identified needs which require social care input specifically PFA transition.

It’s an absolute waste of public expenditure forcing Familes to appeal simply because certain professionals are unable to meet their statutory obligations and responsibilities.

Tonight I have formally requested mediation and issued another pre-action protocol letter.

It is unacceptable!
It is incomprehensible and sheer incompetence that they hope a family will go away if they simply ignore them.

On the positive. My son has a specialist post-16 place set for 2 years.

Address

Exeter

Opening Hours

Tuesday 10am - 2pm
Wednesday 10am - 2pm
Thursday 10am - 2pm
Friday 10am - 2pm
Saturday 10am - 1pm

Alerts

Be the first to know and let us send you an email when AuSends Consultancy posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to AuSends Consultancy:

Share

Share on Facebook Share on Twitter Share on LinkedIn
Share on Pinterest Share on Reddit Share via Email
Share on WhatsApp Share on Instagram Share on Telegram