All Stories

  1. History of Psychology - Herman G. Canady
  2. Daily Loneliness Affects Quality of Life in Sickle Cell Disease
  3. Illness Intrusiveness in Adults with Sickle Cell Disease: The Role of Fatigue
  4. Marijuana use and health behaviors in a US clinic sample of patients with sickle cell disease
  5. Sickle Cell Disease, More Than Just Pain: The Mediating Role of Psychological Symptoms
  6. Metabolic syndrome among adults living with sickle cell disease
  7. Sociocultural contexts of health care use
  8. Multiple Levels of Suffering
  9. Interpersonal Contexts of Communication Between Sickle Cell Disease Patients and Providers
  10. Public Support for Sickle-Cell Disease Funding: Does Race Matter?
  11. The Association between Educational Attainment and Patterns of Emergency Department Utilization among Adults with Sickle Cell Disease
  12. Metabolic Syndrome Risk Among Adults Living with Sickle Cell Disease
  13. Perceived Discrimination in Health Care Is Associated With a Greater Burden of Pain in Sickle Cell Disease
  14. Perceived Discrimination, Patient Trust, and Adherence to Medical Recommendations Among Persons with Sickle Cell Disease
  15. An unequal burden: Poor patient–provider communication and sickle cell disease
  16. Sickle cell disease stigma
  17. Attitudes toward clinical trials among patients with sickle cell disease
  18. Perceived Discrimination In Health Care Is Associated With Daily Chronic Pain In Sickle Cell Disease
  19. Race and social attitudes about sickle cell disease
  20. Examining the characteristics and beliefs of hydroxyurea users and nonusers among adults with sickle cell disease
  21. Predictors of Employment Status among African Americans with Sickle Cell Disease
  22. Problematic Hospital Experiences among Adult Patients with Sickle Cell Disease
  23. Optimism and Perceived Stress in Sickle-Cell Disease: The Role of an Afrocultural Social Ethos
  24. Religious coping and hospital admissions among adults with sickle cell disease
  25. Hospital self-discharge among adults with sickle-cell disease (SCD): Associations with trust and interpersonal experiences with care
  26. The Association of Provider Communication with Trust among Adults with Sickle Cell Disease
  27. Sickle Cell Disease in a "Postracial" America
  28. Health care provider attitudes toward patients with acute vaso-occlusive crisis due to sickle cell disease: Development of a scale
  29. How feelings about being Black influence health care use for people with sickle cell disease
  30. Illness-specific and general perceptions of social relationships in adjustment to Rheumatoid Arthritis: The Role of Interpersonal Expectations
  31. Daily Mood and Stress Predict Pain, Health Care Use, and Work Activity in African American Adults With Sickle-Cell Disease.