[1] Alzheimer Europe. National Dementia Plans: A Snapshot of the Status of National Dementia Strategies around Europe. 2013.
http://www.alzheimer-europe.org/Policy-in-Practice2/National-Dementia-Plans
[2] Skladzien, E., Bowditch, K. and Rees, G. (2011) National Strategies to Address Dementia: A Report by Alzheimer’s Australia. Alzheimer’s Australia, Australia.
[3] United Kingdom Department of Health (2009) Living Well with Dementia: A National Dementia Strategy. Department of Health, England.
[4] National Health Service England (2013) Enhanced Service Specification: Facilitating Timely Diagnosis and Support for People with Dementia. NHS, England.
[5] Australian Health Ministers Advisory Council (2015) National Framework for Action on Dementia 2015-2019. Department of Social Services, Australia.
[6] De Lepeleire, J., et al. (2008) The Primary Care Diagnosis of Dementia in Europe: An Analysis Using Multidisciplinary, Multinational Expert Groups. Aging & Mental Health, 12, 568-576.
https://doi.org/10.1080/13607860802343043
[7] Prince, M., Bryce, R. and Ferri, C. (2011) World Alzheimer Report 2011 Benefits of Early Diagnosis and Intervention. Alzheimer’s Disease International.
[8] Mate, K.E., et al. (2012) Diagnosis and Disclosure of a Memory Problem Is Associated with Quality of Life in Community Based Older Australians with Dementia. International Psychogeriatrics, 24, 1962-1971.
https://doi.org/10.1017/S1041610212001111
[9] Belle, H., et al. (2006) Ehancing the Quality of Life of Dementia Caregivers from Different Ethic or Racial Groups. Annals of Internal Medicine, 145, 727-738.
https://doi.org/10.7326/0003-4819-145-10-200611210-00005
[10] Gaugler, J.E., Zarit, S.H. and Pearlin, L.I. (2003) The Onset of Dementia Caregiving and Its Longitudinal Implications. Psychology and Aging, 18, 171-180.
https://doi.org/10.1037/0882-7974.18.2.171
[11] de Vugt, M.E. and Verhey, F.R. (2013) The Impact of Early Dementia Diagnosis and Intervention on Informal Caregivers. Progress in Neurobiology, 110, 54-62.
https://doi.org/10.1016/j.pneurobio.2013.04.005
[12] Australian Bureau of Statistics (2014) Caring in the Community, Australia: Summary of Findings, 2012. ABS Cat. No. 4436.0. Canberra ABS.
abs.gov.au/AUSSTATS/abs@.nsf/mf/4436.0
[13] AIHW (2012) Dementia in Australia. Cat. No. Age 70. Australian Institute of Health and Welfare, Canberra.
[14] Australian Institue of Health and Welfare (2015) Dementia.
http://www.aihw.gov.au/dementia
[15] Brodaty, H. and Donkin, M. (2009) Family Caregivers of People with Dementia. Dialogues in Clinical Neuroscience, 11, 217-228.
[16] Baiardi, J.M. (1997) The Influence of Health Status, Burden, and Degree of Cognitive Impairment on the Self-Care Agency and Dependent-Care Agency of Caregivers of Elders. Wayne State University, Detroit, 220 p.
[17] Raccichini, A., Castellani, S., Civerchia, P., Fioravanti, P. and Scarpino, O. (2009) The Caregiver’s Burden of Alzheimer Patients: Differences between Live-In and Non-Live-In. American Journal of Alzheimer’s Disease and Other Dementias, 24, 377-383.
http://dx.doi.org/10.1177/1533317509340025
[18] Holland, J.M., et al. (2011) Cortisol Outcomes among Caucasian and Latina/Hispanic Women Caring for a Family Member with Dementia: A Preliminary Examination of Psychosocial Predictors and Effects of a Psychoeducational Intervention. Stress & Health, 27, 334-346. http://dx.doi.org/10.1002/smi.1375
[19] Stokes, L.A., Combes, H. and Stokes, G. (2014) Understanding the Dementia Diagnosis: The Impact on the Caregiving Experience. Dementia, 13, 59-78.
http://dx.doi.org/10.1177/1471301212447157
[20] Abley, C., et al. (2013) Patients’ and Carers’ Views on Communication and Information Provision When Undergoing Assessments in Memory Services. Journal of Health Services Research & Policy, 18, 167-173.
http://dx.doi.org/10.1177/1355819613479945
[21] Innes, A., Szymczynska, P. and Stark, C. (2014) Dementia Diagnosis and Post-Diagnostic Support in Scottish Rural Communities: Experiences of People with Dementia and Their Families. Dementia, 13, 233-247.
http://dx.doi.org/10.1177/1471301212460608
[22] Manthorpe, J., et al. (2013) From Forget-fulness to Dementia: Clinical and Commissioning Implications of Diagnostic Experiences. British Journal of General Practice, 63, e69-e75.
http://dx.doi.org/10.3399/bjgp13x660805
[23] Karnieli-Miller, O., Werner, P., Aharon-Peretz, J., Sinoff, G. and Eidelman, S. (2012) Expectations, Experiences, and Tensions in the Memory Clinic: The Process of Diagnosis Disclosure of Dementia within a Triad. International Psychogeriatrics, 24, 1756-1770.
http://dx.doi.org/10.1017/S1041610212000841
[24] Morgan, D.G., et al. (2014) Informal Caregivers’ Hopes and Expectations of a Referral to a Memory Clinic. Social Science & Medicine, 102, 111-118.
http://dx.doi.org/10.1016/j.socscimed.2013.11.023
[25] Boots, L.M.M., Wolfs, C.A.G., Verhey, F.R.J., Kempen, G.I.J.M. and de Vugt, M.E. (2015) Qualitative Study on Needs and Wishes of Early-Stage Dementia Caregivers: The Paradox between Needing and Accepting Help. International Psychogeriatrics, 27, 927-936.
http://dx.doi.org/10.1017/S1041610214002804
[26] Brooker, D., La Fontaine, J., Evans, S., Bray, J. and Saad, K. (2014) Public Health Guidance to Facilitate Timely Diagnosis of Dementia: ALzheimer’s Cooperative Valuation in Europe Recommendations. International Journal of Geriatric Psychiatry, 29, 682-693.
http://dx.doi.org/10.1002/gps.4066
[27] Farmer, T., Robinson, K., Elliott, S.J. and Eyles, J. (2006) Developing and Implementing a Triangulation Protocol for Qualitative Health Research. Qualitative Health Research, 16, 377-394.
http://dx.doi.org/10.1177/1049732305285708
[28] Buckner, S. (2005) Taking the Debate on Reflexivity Further. Journal of Social Work Practice, 19, 59-72.
http://dx.doi.org/10.1080/02650530500071969