Arbeit von #MillionsMissing Deutschland
Wir sind eine politisch engagierte Initiative, die sich der Aufklärung über ME/CFS widmet. Unser Ziel ist es, Personen aus Politik, Medizin, Institutionen und Journalismus zu informieren. Darüber hinaus bieten wir Informationen für Betroffene von ME/CFS sowie deren (pflegende und betreuende) Angehörige an, die zum Herunterladen und Ausdrucken zur Verfügung stehen.
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PEM ist messbar „Veränderungen der Skelettmuskulatur bei Post-COVID-Syndrom & ME/CFS“ | Dr. Rob Wüst
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