I am currently faced with an ethical dilemma that involves a child with CP who requires nasogastric tube feeding to feed safely (and is being worked up for a PEG). The family brought the child to the hospital to assist with persistent vomiting and poor feeding for 6 months. He is now severely malnourished. After 2 days of treatment they have decided that they want to take him off all treatment (feeding tubes and ARV treatment) in favour of using traditional medicine.
According to the children’s right: “A child with a disability or chronic illness has the right not to be subjected to medical, social, cultural or religious practices that are detrimental to his or her health, well-being or dignity”, would this decision not be detrimental to this child? When do we need to step in as healthcare professionals to follow this right vs respecting the autonomy of a patient’s family.