Patient advocates respond to ‘Utilizing Patient Advocates…’ by Feeney et al

by Sara Riggare, Benjamin Stecher, Jon Stamford
Published 2020-08-01

“You have to know why you're doing this”: a mixed methods study of the benefits and burdens of self-tracking in Parkinson's disease

by Sara Riggare, Therese Scott Duncan, Helena Hvitfeldt, Maria Hägglund
Published 2019-08-01

Six countries, six individuals: resourceful patients navigating medical records in Australia, Canada, Chile, Japan, Sweden and the USA

by Sara Riggare, Selina Brudnicki, Maho Isono, Cecilia Rodriquez, Louise K Schaper, Jan Walker, Tom Delbanco
Published 2020-09-01