With Lupus affecting more than 1.5 million Americans, predominantly women of childbearing age, there are many complex psychosocial challenges for the health care provider, the patient and the family. This book provides a comprehensive overview of the psychosocial impact of Lupus as a range of health care providers in the field explain the medical, sociocultural and psychological frameworks particularly critical for a better understanding of this perplexing autoimmune disease.
With original qualitative and quantitative research and rich case studies and examples from both care providers and patients, this book provides essential information about diagnosis, treatment, mental health issues, and cultural competency issues relevant to all that live with Lupus or provide care to those living with it.
This book was originally published as a special issue of Social Work in Health Care.
Betal enkelt med kort, Klarna, Apple Pay eller Google Pay. Ikke fornøyd? Du har alltid 14 dagers angrerett. Les mer i våre vilkår. Har du spørsmål, send oss en e-post på hello@memmo.org.
Memmo gjør det enklere å studere – uansett hvor du er i verden. Hos oss samler du pensumbøker og smarte studieverktøy på ett og samme sted: sammendrag, quizer, podkaster og flashcards. Og så Ted, din studiekompis som svarer på alt du lurer på. Over 50 000 studenter studerer allerede her – bygget for at du skal lære raskere og stresse mindre.