Service Users’ families’ surveys
At The Richardson Partnership for Care we have an open-door policy so the family members and friends of the service users in our care can visit at any time. As this is not practical for everyone we also include supported home visits in individuals’ care plans. As well as contributing to the service users’ well-being and family relationships, it also helps to encourage feedback from family members about the care that their loved one is receiving. In addition, we send out an annual questionnaire so that we can formalise the feedback process and identify any changes that are needed. Our service users have acquired brain injuries, learning disabilities and/or complex needs, so everyone’s requirements are different, but this process helps us to see the overall picture, identify trends and flag up any issues.
The questionnaires can be anonymous and they are optional, so we may only receive a relatively small number of responses. However, we are very grateful to the family members who complete them. Once again, we have received some very positive feedback and some lovely comments, but we are never complacent. We regularly step back and review our services and are always looking to improve.
The same questionnaire is sent to the families of service users who have learning disabilities and those who have an acquired brain injury. We ask all families whether they strongly agree, agree, don’t know or disagree with the following statements: