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Learning a new role with an illness |
Afraid of being categorized as “sick”; negative attitude toward the illness; comparing oneself to non-diseased individuals; sense of injustice (why me?) |
•As a human being |
• Being responsible for the illness and its treatment |
Learning from parents; feeling of self-efficacy |
• As a patient |
Participation in the decision; willingness to be viewed as an adult |
Learning a new lifestyle |
A need for information on general health matters; not identifying health care professionals as resources for health questions |
Learning a new health care service |
The change is not perceived in relation to oneself; the change is mostly perceived in relation to the parents; peace of mind regarding the change; the change is grasped after the fact; a modification in the relationship with the health care personnel; more biomedical consultations in the adults’ unit; administrative management is difficult to handle |
Maintaining a dual relationship with pediatric and adult care |
Trusting the pediatric doctor more for urgent or personal questions; needing time to trust new health care professionals; a sense of security provided by the dual relationship with pediatric and adult services |
Having experience sharing with peers |
Exchanging tips and tricks to live with the illness; sharing similar experiences; a common vocabulary |