Swedish healthcare advocates call for improved chronic pain and ME treatment

In Sweden, political and patient advocacy groups are calling for improved standards and accessibility in healthcare for patients suffering from chronic pain and ME (Myalgic Encephalomyelitis).

Christofer Bergenblock of the Center Party emphasized the need for permanent, regional specialist clinics for ME to ensure equitable care regardless of whether a patient lives in a city or a rural area. The party proposes a one-billion SEK investment to train healthcare personnel and suggests expanding the 1177 portal to allow patients to compare providers and waiting times. They also advocate for strengthening home healthcare and ensuring patients have a dedicated contact nurse to coordinate complex care.

Simultaneously, the Rheumatism Association (Reumatikerföreningen) has highlighted significant regional disparities in pain management. While a person-centered care pathway for long-term pain was published in November 2022, implementation remains inconsistent across the country. Advocates argue that regions must share successful examples of pain treatment to spread knowledge more effectively. Concerns were also raised regarding a Vårdanalys report indicating that primary care has not received sufficient financial or personnel resources to support the transition to 'Nära vård' (Close Care).