Bill of Rights for People Living with Epilepsy

  Novartis Pharma US

The Bills of Rights for People Living With Epilepsy

3. People living with epilepsy have the right and responsibility to be active members of their healthcare team.
Many people living with epilepsy work with a healthcare team to treat their condition. They should feel comfortable asking for the qualifications of the people taking care of them.

The healthcare team may include (but is not limited to) primary care doctors, neurologists, epileptologists, nurses, physicians' assistants, speech and language pathologists, physical and occupational therapists, social workers, pharmacists and emergency personnel.

People living with epilepsy are encouraged to share their treatment and quality of life goals with their healthcare team and ask for these to be considered and incorporated into their healthcare plan. They are also encouraged to ask for accurate information about their condition on an ongoing basis.

People living with epilepsy have the right to seek a second opinion from another doctor and to ask for a copy of their medical records to provide to the new doctor. However, insurance policies vary, so a visit to a new doctor may not be covered for certain individuals.

People living with epilepsy can ask their healthcare providers and insurance company about the financial costs of medical tests and treatments.




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