DG.ME/CFS Offers Comprehensive Free ME/CFS Info
The Deutsche Gesellschaft für ME/CFS (DG.ME/CFS) has been actively providing comprehensive, free information about Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) to patients, relatives, doctors, and healthcare professionals. Their website offers a wealth of resources, including information leaflets, videos, and FAQs, covering various aspects of the condition.
The society's website provides an overview of current information, featuring general articles, resources for patients and relatives, and printable information leaflets. Topics range from symptoms and diagnosis to therapy, pacing, PEM, orthostatic intolerance, fatigue, brain fog, and long COVID. A FAQ section addresses common queries about diagnosis, therapy, children, law, social issues, and the DG.ME/CFS itself.
In the last twelve months, DG.ME/CFS has published eight information leaflets in cooperation with other institutions. These cover topics such as ME/CFS overview, pacing, school, employers, diagnosis and treatment, hospital care, physiotherapy, and supporting psychotherapy. The society plans to continue expanding its information offering in the future.
DG.ME/CFS also provides targeted information for the press and politically active individuals, aiming to enlighten the public and medical professionals about ME/CFS. Additionally, the doctor's portal offers information, diagnosis and therapy recommendations, and an accredited on-demand training course on ME/CFS and Long COVID. The website features videos illustrating PEM and pacing, developed with Long COVID Germany and supported by Charité and TUM.
DG.ME/CFS continues to be a vital resource for anyone seeking reliable, up-to-date information about ME/CFS. With a wide range of topics covered and a commitment to expanding its offerings, the society ensures that patients, relatives, doctors, and healthcare professionals have access to the information they need.
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