BirgerssonAMBEdbergAK (2004) Being in the light or in the shade: Persons with Parkinson’s disease and their partners’ experience of support. International Journal of Nursing Studies41(6): 621–630.
2.
GruffyddERandleJ (2006) Alzheimer’s disease and the psychosocial burden for caregivers. Community Practitioner79(1): 15–18.
3.
Kanwar S and Whomsley S (2011) Working with Pakistani service users and their families: A practitioner’s guide. Retrieved from www.cpft.nhs.uk (accessed 24 October 2018).
4.
LawsonRACollertonDTaylorJP, et al.(2018) Coping with cognitive impairment in people with Parkinson’s disease and their carers: A qualitative study. Parkinson’s Disease1362053: 1–10.
5.
MeyerOLNguyenKHDaoTN, et al.(2017) The sociocultural context of caregiving experiences for Vietnamese dementia family caregivers. Asian American Journal of Psychology6(3): 263.
6.
parkinsons.org.uk (2018) What is Parkinson’s? Available at: www.parkinsons.org.uk (accessed 24 October 2018).
7.
RobinsonLGemskiAAbleyC (2011) The transition to dementia – individual and family experiences of receiving a diagnosis: A review. International Psychogeriatrics23(7): 1026–1043.