Our Reports

A rapid literature review carried out by Patient Experience Library in May 2024 and commissioned by the Neurological Alliance as part of preparations for the 2024 iteration of the My Neuro Survey. The review was undertaken during a four week period in May 2024 and supports the Neurological Alliance in deepening our understanding of how […]

This epilepsy resource navigator tool is designed for commissioners, providers and professionals working with the epilepsy population in England. The tool identifies and directs you to the best available resources to commission, design and improve services for people with epilepsy, their families and carers. The information and resources in the tool can help local systems […]

The Neurological Alliance has developed a number of proposals for RightCare pathways. You can read more about RightCare pathways

What needs to change for people with rare neurological conditions.

Restarting services for people with neurological conditions after the COVID-19 pandemic and planning for the longer term.

Is there a gender gap in experiences of, and access to, neurological services in England?