As policy officer in the external affairs team at the Alzheimer's Society, I would like to hear from you about your experiences of user involvement in local NHS or social care services. This could be acting as a representative from the local Alzheimer’s Society, as an individual, or supporting individuals with dementia or carers to get involved. Do you think user views were properly considered and influenced service development? Do you have suspicions about ‘tokenism’? What about the practicalities of ‘user involvement’ – were meetings arranged to support user involvement? If you have any views about this, please get in touch. I am collecting views to inform a short report I am preparing on the topic. Thank you.