SIP Launches ‘The Burden of Pain: A Societal Impact of Pain (SIP) Book of Evidence
The Societal Impact of Pain (SIP) Platform recently announced the launch of its newest resource entitled ‘The Burden of Pain: A Societal Impact of Pain (SIP) Book of Evidence’. Chronic Pain Ireland is delighted to support this initiative and our SIP Representative is CPI Chair Martina Phelan. The ‘Book of Evidence’ was created for individuals from a non-scientific background (e.g. policymakers and funding organisations) to help gain insights into what pain is, understand different definitions used (e.g. acute pain, neuropathic pain, nociceptive pain), and the debilitating effects pain has on patients and societies.
The document explains distinct types of pain conditions (e.g. headaches, low back pain), how common they are, and treatment approaches. Further, the document explains crucial concepts and challenges in pain field, including pain measurement and assessment, stigma, the importance of acknowledging the personal multidimensional nature of pain that requires an appreciation of the interplay between myriad biological/physical, psychological and sociocultural factors. You can read or download the Book of Evidence here.
Other Updates
SIP remains actively engaged in advancing pain management and treatment across Europe, advocating with the EU Commission, policymakers, and stakeholders on issues like Access to Treatment, the European Health Data Space, and mental health policies.
National Platforms (including Ireland of which Chronic Pain Ireland’s Chair is one of the two leaders) continue to receive support relating to advocacy, with relevant Members of the European Parliament engaged to shape effective policies. Recent publications include the report from SIP’s Stakeholder Forum, which set 2025 priorities, and the policy event ‘Pain Treatment, Management and Prevention – Is Europe Providing Adequate Access?’. Both highlight collaborative efforts among policymakers, specialists, and patient advocates across Europe.