Category: ME/CFS
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Een persoonlijke reflectie over long COVID, ongeloof en medische geschiedenis. Van kanker tot burn-out en hiv: telkens liep de wetenschap achter op wat patiënten al voelden. Over ziek zijn, geloofd willen worden en waarom begrip soms het belangrijkste medicijn is.
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Living with long COVID has taught me how lonely disbelief can feel. Looking at the history of cancer and burnout, I realized we’ve seen this pattern before. Science catches up, but people need understanding now.
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This is a follow-up to my earlier blog about using LDN for Long COVID / ME-CFS. This time, I write about something less visible: the loneliness that grows when you’re surrounded by people but slowly losing access to yourself. A personal reflection on illness, connection, and being unseen.


