Learning Disabilities and Autism Support
One to one and group support for children with learning disabilities and autistic children, built around communication, sensory needs and routine.
The environment causes most of the difficulty, so we start there
Support for autistic children and children with learning disabilities goes wrong most often when it is built around making the child fit a setting. Our starting point is the reverse. A great deal of what gets called challenging behaviour is a child in an environment that is too loud, too bright, too unpredictable or too fast, without a way of saying so that anybody is listening to.
So the first work is understanding the child. How they communicate, whether that is speech, signing, symbols, a device or behaviour. What their sensory profile is, what overwhelms them and what settles them. What their routine is and which parts of it are load bearing. What they actually enjoy, which is asked far less often than it should be.
From that we write a support plan covering communication, sensory needs, daily routine and activity choices, and then we work to it consistently. Consistency matters enormously here. A plan followed by one worker and ignored by the next is worse than no plan, because the child learns that the rules depend on who turned up.
Support can be one to one or in a group, at home, in the community or at our day service. Where a child needs a higher ratio we staff two to one rather than stretching one worker and calling it support.
All Providence staff working with children and young people are trained in line with the Oliver McGowan Code of Practice on Learning Disability and Autism, which became statutory for CQC registered providers in September 2025.
We are a care and support provider, not a diagnostic or therapy service. Assessment, diagnosis and speech, occupational and behavioural therapy come from health services, and we work to their plans rather than writing our own version.
This is likely right if
- A child has a learning disability, is autistic, or both
- Communication needs are not being met consistently across settings
- Sensory needs are driving distress that is being read as behaviour
- A family needs support at home, in the community or during holidays
- A higher staffing ratio is needed for a child to take part safely
Something else may fit better if
- What is needed is assessment or diagnosis, which comes through health services
- Speech, occupational or behavioural therapy is what is being sought
- Support is needed in school, which is arranged through the school and local authority
How we work with a child
Slowly at first, and then very consistently. Both halves matter.
Learning how they communicate
Speech, signing, symbols, a device, or behaviour. Whatever it is, we learn it and use it rather than expecting the child to meet us halfway.
Sensory profile
What overwhelms and what regulates. Noise, light, texture, crowds, smell. This goes in the plan properly rather than as a note at the bottom.
Protecting routine
Knowing which parts of a routine are load bearing, and giving proper warning before anything changes. Most avoidable distress comes from unannounced change.
Consistency between staff
The same approach from every worker. A plan that only some people follow teaches a child that the rules are arbitrary.
Real choices
Choosing the activity, the order, the ending. Children with high support needs are given very few genuine choices and it matters more than almost anything.
Working with everybody else
School, therapists, the social worker and the family. A child supported four different ways in four settings does not do well.
What is included, and what is not
Set out plainly so there is nothing to discover later. Anything not listed here can still be discussed, and often arranged.
Included as standard
- A bespoke support plan covering communication, sensory needs, routine and activities
- Staff trained in line with the Oliver McGowan Code of Practice
- One to one support, and two to one where the assessment calls for it
- Access to our day service in Dagenham, including a sensory room
- Support at home, in the community or at the day service
- Joint working with school, therapy services and the social worker
- Enhanced DBS checked staff, trained before working alone
Arranged separately
- Diagnosis and clinical assessment
- Speech and language, occupational or behavioural therapy
- Education, which is the school responsibility
From first call to first visit
Referrals come from local authorities, health teams and schools, and directly from parents.
Referral or enquiry
From a social worker, a health professional, a school, or a parent ringing us directly.
Getting to know the child
Time spent with the child and the people who know them best, before any plan is written. Rushing this produces a plan that does not survive week two.
The support plan
Communication, sensory needs, routine and activities, agreed with the family and shared with everybody who works with the child.
Gradual start and review
Introductions rather than a new adult appearing. Then review, because the first plan is never quite right.
How this is paid for
Usually funded by the local authority through the children with disabilities team, or through an Education Health and Care Plan where the support is part of that plan. Short breaks funding is a common route for group and holiday activity.
Direct Payments are widely used and let families choose the provider and shape the support themselves. Ask about them by name if nobody has raised it with you.
Read the full guide to fundingWhat families ask us about this
What is the Oliver McGowan Code of Practice?
A statutory code requiring CQC registered providers to ensure staff are trained in learning disability and autism at a level appropriate to their role. It became statutory in September 2025. All Providence staff working with children and young people are trained in line with it.
Do you provide two to one support?
Yes, where the assessment says it is needed. Stretching one worker across a situation that genuinely needs two is unsafe for the child and for the staff member.
Do you have a sensory room?
Yes, at our day service. For a lot of children a sensory space is not an extra, it is what makes the rest of the day possible.
Can you support a child who is non speaking?
Yes. Communication is the first thing we work out, whatever form it takes. A child who does not use speech is not a child without communication.
Do you provide therapy?
No. Speech and language, occupational and behavioural therapy come from health services. We work to their plans consistently rather than inventing our own approach alongside them.
Will the same staff work with my child?
The same small team, protected as far as the rota allows. Consistency is central to this work and we treat it as part of the support rather than a scheduling preference.
Services that often go together
Day Activities for Children and Young People
A structured programme of activities outside school hours and through the holidays, with transport and meals included.
Read morePersonal Care for Children
Care in the child own home, built around their routine and around the family that is already doing most of it.
Read moreSEMH and Behavioural Support
Support for young people whose behaviour is telling everybody something that nobody has worked out yet.
Read moreTell us about your child, not their diagnosis
What they like, what they cannot bear, how they tell you things. That is where good support actually starts.
Emergency placements are answered 24 hours a day, seven days a week.