Not sure if anyone else has posted this... it's a big win for Norway. http://esme-eu.com/news/cfs-me-know...and-care-services-in-norway-article493-7.html CFS/ME Knowledge summary, evaluation and recommendation for Ministry of Health and Care Services Many patients need services in an interaction between the primary- and specialist care. This interaction does unfortunately not function well enough today. The Directorate of Health has answered the mission from the Ministry of Health and Care Services with the following main conclusions and recommendations. The full answer can be read in the box to the right. (Translation of the full answer will be posted later.) Link to the reports from the Center of Knowledge will follow later. Main conclusions: It does not exist today a evidence based knowledge fundament to publish national guidelines or a general guide. With the background from the present reports, The Directorate of Health sees that it will still take time to build good, robust patient care for this group of patients. The knowledge review does not support an earlier recommendation made to use the NICE-criteria. The knowledge revies does not on a general level give support for recommending graded exercise therapy and/or cognitive therapy to everybody with CFS/ME. Recommendations: The knowledge review of Kenny De Meirleirs research makes that the Directorate of Health, on the basis of todays knowledge, can not recommend that the public health sector finances this kind of treatment. It is recommended that one identifies ongoing studies and makes a summary about existing studies regarding causality and diagnostics. New research projects and recommendations about interventions must be seen in regard to the severity of the disease; mild moderate severe or very severe, and in what phase of the disease the patient is; unstable phase of stabilisation phase of rehabilitation/(reconstruction). An increase in funding for research on causality and treatment is recommended. Collection and dissemination of experience-based knowledge will be facilitated amongst other things through regional conferences of experience. The creation of a national treatment-/competence-service for CFS/ME for a limited time is considerated. The biobank at Oslo University Hospital Aker will be closely related to the national service. It is recommended that ambulant/outpatient-teams is being created for children, youth and adults in all health regions. It is recommended that an effort is started to develop good models for how kids as relatives/next of kin should be given follow-up. It is recommended regional polyclinic for CFS/ME. It is recommended rehabilitation services built on the experiences and competence from amongst others Slvskottberget. It is recommended regional Learning- and coping-courses for patients and next of kin. It is recommended to extend the national Information Telephone Service for CFS/ME.