Association of Paediatric Chartered Physiotherapists

New guideline from NICE recommends ensuring children and young people are fully informed about their health so that they are empowered to take an active role in their healthcare.

The CSP has been asked by the MS Society to disseminate the following survey to any networks and non-registered professionals

This is a DfE guide for all local authorities (LAs), health commissioning bodies and parents and young people in England, on the SEND Tribunal: single route of redress. This guidance can also be used to inform advice that Information, Advice and Support Services (IASS) and others provide to parents and young people.

Disabled children and young people up to 25 with severe complex needs: integrated service delivery and organisation across health, social care and education

A great opportunity to have your say….

APCP is pleased to announce the launch of its new Research Hub bringing together resources and information to support members involved,  or wanting to get more involved with, paediatric physiotherapy research.

‘The 2021 Rare Disease Framework, and the four national implementation plans that will come from it are welcomed. However, to know if we have truly succeeded, we should be judged on whether patients living with rare diseases notice an improvement in their experiences, treatment and care.’ (Baroness Nicola Blackwood, Public Projects – May 2021)

Cerebral Palsy Sport is the country’s leading national disability sports organisation, improving the health and emotional wellbeing of people with cerebral palsy through physical activity, and engaging the community in a number of programmes and interventions.

CSP members are asked to comment on the draft Equity, Diversity and Belonging Strategy.

The consultation will run until 31 July 2021