This petition has been running for about 4 months now so I'm just popping in to remind everyone why this new system is important and necessary.

Anecdotally, it has been known for years that non-pharmaceutical 'treatments' harm some patients with all sorts of illnesses. Patients complain to their Dr, NHS Trust, CCG, PALS, and Healthwatch. Complaints are dealt with internally and are not recorded centrally or counted.

This means there is no quantitative data available when the time to make policy or research decisions comes around.

This new system will lead to data collection so that informed policy and research decisions can be made. This will lead to much better, and more appropriate, care for patients with a range of conditions, including Myalgic Encephalomyelitis (M.E).

Thank you for your support.