Meet Ivy
Ivy is 11 and attends Pace School full-time. She has quadriplegic cerebral palsy and uses specialist switch access and a track system to get around in her motorised chair.
Policies and feedback
Your feedback and suggestions can help improve Pace services.
Our statutory information and policies
All of our statutory information and polices can be accessed here, as well as details for how you can give feedback to us.
Statutory policies and other information:
- Accessibility Policy
- Attendance Policy
- Behaviour Management Policy
- Biometric Policy
- Child Protection Policy
- Data Protection Policy
- English as an Additional Language Policy
- Equality and Cohesion Policy
- Early Years SEND Policy
- Special Educational Needs and Disability Policy
- School Visits Policy
- School Closure due to Bad Weather (Guidance for Parents)
- SMSC Policy
- PHSE Policy
- Curriculum Statement
- Anti-Bullying Policy
- First Aid Policy
- Admissions Policy
- Remote Learning Policy
- Cold Weather Guidelines
- Staff Code of Conduct Policy
- Assessment and Impact Policy
- Teaching and Learning Policy
- Health and Hygiene Policy
- Health and Safety Policy
Feedback, concerns and complaints
Parents can also make a complaint directly to Ofsted at:
Ofsted, Piccadilly Gate, Store Street, Manchester M1 2WS
Tel: 0300 123 1231
Formal complaints 2022-2023
The number of formal complaints registered
during the academic year 2023-2024 was 2
Real life Stories
Meet Annie
Annie has a diagnosis of dystonic cerebral palsy, with associated involuntary movements which can be distressing and uncomfortable for her at times. Annie is a verbal communicator, although her tone and state of alertness can significantly impact her voice volume and how well she is heard and understood by others.
Meet Sonny
Sonny has cerebral palsy. The damage to his brain results from being born 10 weeks prematurely. As his mother Lou says, “I had heard of cerebral palsy, but I didn’t really know what it was or what it meant for my baby. The worst thing was, nobody did. We just had to wait and see what this disorder meant for my little boy. It was a matter of time.”
Connect with other families
Ask questions, join in the conversation and support other families in our community forum.