Skip to main content

Self-Advocacy in Health Data

Meaning

Self-Advocacy in Health Data describes the patient’s active, informed exercise of their rights to access, understand, correct, and direct the use of their own clinical and physiological data, including their comprehensive hormonal profile. Self-advocacy empowers the individual to partner effectively with their healthcare team, ensuring that their personal narrative and data preferences are fully integrated into their personalized treatment plan. This active participation is a cornerstone of truly patient-centered and personalized endocrine care.