People's health literacy needs change over time as their health changes and health services change.
Health literacy describes the skills and knowledge people need at any given time to:
- find their way around the parts of the health system they need to access
- understand their health conditions, including what makes them better or worse
- use their medicines safely
- give informed consent to medical procedures
- prevent illness so their health doesn’t get worse
- manage long-term health conditions well.
Historically, the language used to describe health literacy implied that low health literacy is an individual skill deficit, or community-wide deficit. People were described as having ‘low health literacy’. This person-deficit view of health literacy is unfair as it ignores the crucial role of the health system in creating or reducing complexity (eg, health literacy demands), and how delivering effective health care includes building the health literacy people and communities need.
For example, being diagnosed with a new health condition is the time when a person needs the opportunity to build new health knowledge and skills, and understand the relevant services they may now need, assisted by those with health expertise and experience. It's not fair to expect people to arrive for health care already knowing about all the possible health challenges they may encounter.