Imagine a world in which cancer treatments are based on the evidence available from medical research, from research in other fields of science, from the best practices developed in clinics and health centres (Moerman, Gerson, Qi Gong), and from the stories and narratives of individual cancer patients, and last but not least, from individuals involved directly with the cancer patient.

To me it seemed, and still seems, logical to tap into all these sources of information in my role as an active participant, rather than accepting the role of a passive cancer patient and leaving the decision making to others.

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