D. D. Leo and K. Spathonis, “Do Psychosocial and Pharmacological Interventions Reduce Suicide in Schizophrenia and Schizophrenia Spectrum Disorders?” Archives of Suicide Research, Vol. 7, No. 4, 2003, pp. 353-374. http://dx.doi.org/10.1080/713848945
 M. Ostman and K. Andersson, “Family Burden, Participation in Care and Mental Health—An 11-Year Comparison of the Situation of Relatives to Compulsorily and Voluntarily Admitted Patients,” The International Journal of Social Psychiatry, Vol. 46, No. 3, 2000, pp. 191-200. http://dx.doi.org/10.1177/002076400004600305
 A. Caqueo-Urízar, J. Gutiérrez-Maldonado and C. Miranda-Castillo, “Quality of Life in Caregivers of Patients with Schizophrenia: A Literature Review,” Health and Quality of Life Outcomes, Vol. 7, 2009, p. 84.
 L. Boyer, A. Caqueo-Urízar, R. Richieri, C. Lancon, J. Gutiérrez-Maldonado and P. Auquier, “Quality of Life among Caregivers of Patients with Schizophrenia: A Cross-Cultural Comparison of Chilean and French Families,” BMC Family Practice, Vol. 13, No. 1, 2012, p. 42.
 J. C. Coyne, R. C. Kessler, M. Tal, J. Turnbull, C. B. Wortman and J. F. Greden, “Living with a Depressed Person,” Journal of Consulting and Clinical Psychology, Vol. 55, No. 3, 1987, pp. 347-352.
 F. Pharoah, J. Mari, J. Rathbone and W. Wong, “Family Intervention for Schizophrenia,” Cochrane Database of Systematic Reviews, Vol. 12, 2010.
 L. Dixon, W. R. McFarlane, H. Lefley, A. Lucksted, M. Cohen and I. Falloon, et al., “Evidence-Based Practices for Services to Families of People with Psychiatric Disabilities,” Psychiatric Services, Vol. 52, No. 7, 2001, pp. 903-910. http://dx.doi.org/10.1176/appi.ps.52.7.903
 G. Thornicroft and E. Susser, “Evidence-Based Psycho-Therapeutic Interventions in the Community Care of Schizophrenia,” The British Journal of Psychiatry, Vol. 178, No. 1, 2001, pp. 2-4.
 J. Reid, C. Lloyd and L. De Groot, “The Psychoeducation Needs of Parents Who Have an Adult Son or Daughter with a Mental Illness,” Advances in Mental Health, Vol. 4, No. 2, 2005, pp. 65-77.
 A. Rotondi, C. Anderson, G. Haas, S. Eack, M. Spring, R. Ganguli, et al., “Web-Based Psychoeducational Intervention for Persons with Schizophrenia and Their Supporters: One-Year Outcomes,” Psychiatric Services, Vol. 61, No. 11, 2010, pp. 1099-1105.
 S. M. Glynn, E. T. Randolph, T. Garrick and A. Lui, “A Proof of Concept Trial of an Online Psychoeducational Program for Relatives of both Veterans and Civilians Living with Schizophrenia,” Psychiatric Rehabilitation Journal, Vol. 33, No. 4, 2010, pp. 278-287.
 S. R. Cotten and S. S. Gupta, “Characteristics of Online and Offline Health Information Seekers and Factors That Discriminate between Them,” Social Science & Medicine, Vol. 59, No. 9, 2004, pp. 1795-1806.
 J. Powell and A. Clarke, “Information in Mental Health: Qualitative Study of Mental Health Service Users,” Health Expectations, Vol. 9, No. 4, 2006, pp. 359-365.
 L. J. Barney, K. M. Griffiths and M. A. Banfield, “Explicit and Implicit Information Needs of People with Depression: A Qualitative Investigation of Problems Reported on an Online Depression Support Forum, “ BMC Psychiatry, Vol. 11, No. 1, 2011, p. 88.
 J. Preece, “Empathic Communities: Balancing Emotional and Factual Communication,” Interacting with Computers, Vol. 12, No. 1, 1999, pp. 63-77.
 K. P. Davison, J. W. Pennebaker and S. S. Dickerson, “Who Talks? The Social Psychology of Illness Support Groups,” American Psychologist, Vol. 55, No. 2, 2000, pp. 205-217.
 A. N. Joinson, “Understanding the Psychology of Internet Behaviour. Virtual Worlds, Real Lives,” Palgrave MacMillan, Houndmills, Basingstoke, Hampshire, New York, 2003.
 R. Fuhrer, S. A. Stansfeld, J. Chemali and M. J. Shipley, “Gender, Social Relations and Mental Health: Prospective Findings from an Occupational Cohort (Whitehall II study),” Social Science and Medicine, Vol. 48, No. 1, 1999, pp. 77-87.
 K. Y. Chuang and C. C. Yang, “Interaction Patterns of Nurturant Support Exchanged in Online Health Social Networking,” Journal of Medical Internet Research, Vol. 14, No. 3, 2012, p. e54.
 C. E. Cutrona and J. A. Suhr, “Controllability of Stressful Events and Satisfaction with Spouse Support Behaviors,” Communication Research, Vol. 19, No. 2, 1992, pp. 154-174. http://dx.doi.org/10.1177/009365092019002002
 I. Skarsater, “The Importance of Social Support for Men and Women, Suffering from Major Depression. A Comparative and Explorative Study,” Sahlgrenska Academy, Division of Health and Caring Sciences, Institute of Nursing, Gothenburg University, Gothenburg, 2002.
 T. Takizawa, T. Kondo, S. Sakihara, M. Ariizumi, N. Watanabe and H. Oyama, “Stress Buffering Effects of Social Support on Depressive Symptoms in Middle Age: Reciprocity and Community Mental Health,” Psychiatry and Clinical Neurosciences, Vol. 60, No. 6, 2006, pp. 652-661.
 G. J. Meissen, D. F. Gleason and M. G. Embree, “An Assessment of the Needs of Mutual-Help Groups,” American Journal of Community Psychology, Vol. 19, No. 3, 1991, pp. 427-442.
 S. Stjernsward and M. Ostman, “Illuminating User Experience of a Website for the Relatives of Persons with Depression,” International Journal of Social Psychiatry, Vol. 57, No. 4, 2011, p. 375.
 U. Josefsson, “Coping with Illness Online: The Case of Patients’ Online Communities,” The Information Society, Vol. 21, No. 2, 2005, pp. 143-153.
 C. Feste and R. M. Anderson, “Empowerment: From Philosophy to Practice,” Patient Education and Counseling, Vol. 26, No. 1-3, 1995, pp. 139-144.
 J. Rappaport, “Terms of Empowerment/Exemplars of Prevention: Toward a Theory for Community Psychology,” American Journal of Community Psychology, Vol. 15, No. 2, 1987, pp. 121-148.
 B. R. Shaw, R. Hawkins, F. McTavish, S. Pingree and D. H. Gustafson, “Effects of Insightful Disclosure within Computer Mediated Support Groups on Women with Breast Cancer,” Health Communication, Vol. 19, No. 2, 2006, pp. 133-142.
 J. Smyth, “Written Emotional Expression: Effect Sizes, Outcome Types, and Moderating Variables,” Journal of Consulting & Clinical Psychology, Vol. 66, No. 1, 1998, pp. 174-184.
 J. W. Pennebaker and J. D. Seagal, “Forming a Story: The Health Benefits of Narrative,” Journal of Clinical Psychology, Vol. 55, No. 10, 1999, pp. 1243-1254.
 S. Stjernsward, M. Ostman and J. Lowgren, “Online Self—Help Tools for the Relatives of Persons with Depression—A Feasibility Study,” Scandinavian Journal of Caring Sciences, Vol. 26, No. 1, 2012, pp. 70-80.
 W. B. F. Brouwer, N. J. A. V. Exel, B. V. Gorp and W. K. Redekop, “The CarerQol Instrument: A New Instrument to Measure Care-Related Quality of Life of Informal Caregivers for Use in Economic Evaluations,” Quality of Life Research, Vol. 15, No. 6, 2006, pp. 1005-1021.
 The INDIGO Study Group, “Discrimination and Stigma Scale DISC 12?,” 2008.
 E. Brohan, D. Rose, S. Clement, E. Corker, T. Van Bortel, N. Sartorius, et al., “Discrimination and Stigma Scale (DISC), Version 12. Manual Version 3,” HSPRD Institute of Psychiatry, King’s College London, 2012.
 A. Piatidis, “Anvandbarhetsstampel pa Konsument-Produkter. Ett satt att Underlatta Kundernas kop och Paverka Foretagets Arbetssatt,” TRITA-NA-E02001, CID-187, 2002.
 J. Brooke, “SUS—A Quick and Dirty Usability Scale,” In P. W. Jordan, B. Thomas, B. A. Weerdmeester, A. L. McClelland, Eds., Usability Evaluation in Industry, Taylor and Francis, London, 1996.
 A. Bangor, P. Kortum and J. Miller, “An Empirical Evaluation of the System Usability Scale,” International Journal of Human-Computer Interaction, Vol. 24, No. 6, 2008, pp. 574-594.
 U. H. Graneheim and B. Lundman, “Qualitative Content Analysis in Nursing Research: Concepts, Procedures and Measures to Achieve Trustworthiness,” Nurse Education Today, Vol. 24, No. 2, 2004, pp. 105-112.
 L. Flyckt, A. Lothman, L. Jorgensen, A. Rylander and T. Koernig, “Burden of Informal Care Giving to Patients with Psychoses: A Descriptive and Methodological Study,” International Journal of Social Psychiatry, Vol. 59, No. 2, 2013, pp. 137-146.
 T. Connolly and B. K. Thorn, “Discretionary Databases: Theory, Data, and Implications,” Organizations and Communication Technology, 1990, pp. 219-233.
 B. Nonnecke and J. Preece, “Why lurkers lurk,” Americas Conference on Information Systems, 2001.
 H. L. Provencher, K. T. Mueser, “Positive and Negative Symptom Behaviors and Caregiver Burden in the Rela- tives of Persons with Schizophrenia,” Schizophrenia Research, Vol. 26, No. 1, 1997, pp. 71-80.
 J. Addington, E. Coldham, B. Jones, T. Ko and D. Addington, “The First Episode of Psychosis: The Experience of Relatives,” Acta Psychiatrica Scandinavica, Vol. 108, No. 4, 2003, pp. 285-289.
 S. Barker, T. Lavender and N. Morant, “Client and Family Narratives on Schizophrenia,” Journal of Mental Health, Vol. 10, No. 2, 2001, pp. 199-212.
 L. E. Rose, “Families of Psychiatric Patients: A Critical Review and Future Research Directions,” Archives of Psychiatric Nursing, Vol. 10, No. 2, 1996, pp. 67-76.
 C. K. Coursaris and M. Liu, “An Analysis of Social Support Exchanges in Online HIV/AIDS Self-Help Groups,” Computers in Human Behavior, Vol. 25, No. 4, 2009, pp. 911-918. http://dx.doi.org/10.1016/j.chb.2009.03.006
 E. G. Benzein and A. C. Berg, “The Level of and Relation between Hope, Hopelessness and Fatigue in Patients and Family Members in Palliative Care,” Palliative Medicine, Vol. 19, 2005, pp. 234-240.
 M. Sanbrook and A. Harris, “Origins of Early Intervention in First-Episode Psychosis,” Australasian Psychiatry, Vol. 11, No. 2, 2003, pp. 215-219.
 R. H. Moos, “Depressed Outpatients’ Life Contexts, Amount of Treatment, and Treatment Outcome,” Journal of Nervous and Mental Disease, Vol. 178, No. 2, 1990, pp. 105-112.
 L. Hansson, S. Stjernsward and B. Svensson, “Perceived and Anticipated Discrimination in People with Mental Illness—An Interview Study,” Nordic Journal of Psychiatry, 2013, pp. 1-7.
 Ministry of Health and Social Affairs, “Nationell IT-Strategi for vard och omsorg. Var starviidag?” Lagesrapport, 2007.
 H. Bragadottir, “Computer-Mediated Support Group Intervention for Parents,” Journal of Nursing Scholarship, Vol. 40, No. 1, 2008, pp. 32-38.
 B. R. Shaw, F. McTavish, R. Hawkins, D. H. Gustafson and S. Pingree, “Experiences of Women with Breast Cancer: Exchanging Social Support over the CHESS Computer Network,” Journal of Health Communication, Vol. 5, No. 2, 2000, pp. 135-159.
 K. M. Griffiths, A. L. Calear and M. Banfield, “Systematic Review on Internet Support Groups (ISGs) and Depression (1): Do ISGs Reduce Depressive Symptoms?” Journal of Medical Internet Research, Vol. 11, No. 3, 2009.