German ME/CFS Society Offers Free Information, Aims to Improve Understanding
The German Society for ME/CFS (DG.ME/CFS) has been actively providing free information on Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) to patients, relatives, doctors, and health professionals. The society aims to raise awareness and improve understanding of the condition.
DG.ME/CFS offers a wide range of information, including general topics like 'What is ME/CFS?', 'Pathophysiology', 'Post-Exertional Malaise', and 'Brain Fog'. They also provide specific guidance on 'Pacing', videos, FAQs, and translated scientific articles for patients and relatives. For medical professionals, the society offers an accredited on-demand training course through the Doctor's Portal.
In the last year, DG.ME/CFS has published eight information leaflets in collaboration with the Charité Fatigue Centre and the Chronic Fatigue Centre for Young People. These leaflets cover a variety of topics, from ME/CFS overviews to specific aspects like diagnosis, treatment, and care. The society also provides targeted information for the press and politically active individuals, aiming to enlighten the public and influence policy.
DG.ME/CFS continues to expand its information offerings, with a focus on improving the situation of ME/CFS sufferers. Their comprehensive resources, including printed leaflets and online materials, cater to patients, relatives, doctors, and the wider public. By providing accurate and accessible information, the society seeks to foster understanding and support for those affected by ME/CFS.
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