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New Models of Care. The Social Club Model. Presented by Mary Bolger, Services Manager (Kildare/West Wicklow) Alzheimer Society of Ireland. Presentation outline. Examine the origin of the social clubs Outline the study design and procedure Present the literature supporting the social clubs
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New Models of Care The Social Club Model Presented by Mary Bolger, Services Manager (Kildare/West Wicklow) Alzheimer Society of Ireland
Presentation outline • Examine the origin of the social clubs • Outline the study design and procedure • Present the literature supporting the social clubs • Present the core elements of what makes the model ‘unique’ • Reflect staff and members’ experience • Discuss future developments and implications for policy and practice
Social Club’s Origin • Identification of unmet need • No service for both PWD and spouse/carer • Carers’ socially isolated • The Social Club • Meeting once a week • Outing every second week • Informal and loose structure
Study Design and Procedure • Small scale –mixed quantitative and qualitative • Postal survey to members and staff • Feedback of themes to one club • Interviews with key stakeholders • Analysed for themes
Supporting Literature • Dementia and effect on caregiver • Increased rate of stress/depression • More socially isolated • Requires continuous adaptation to change • Loss of confidant • Social Support and Caring • ‘stress buffering’ qualities • More significant in the elderly
Supporting Literature • Alzheimer Café Model • Underlying vision of ‘living with dementia’ • Meeting places for PWD and their families, carers • Social and educational • Couple Identity and Couplehood
Couple Identity and Couplehood • Couple Identity • “being part of a couple as being part of one’s identity” (Beeson, 2003) • Losing this identity is a real threat – to carer and to person with dementia • Celebrating personhood may require the celebration of couplehood • ‘Doing things together’ – couple receives recognition; carer receives support
Unique Elements of Social Clubs • Embrace couplehood • Informal structure • ‘Worry-free socialising’ • Outings • ‘Members’ as opposed to ‘Service-Users’ • Sense of belonging
Reflections – members of the club “it makes you realise you’re not on your own” “as a couple it allows us to meet others with similar interests” “outings with security of knowing support and help is at hand”
Reflections – facilitators of the club “Forget the formal stuff. People are lonely and they want to talk to others in the same boat” “The person with dementia…..have a contribution to make from a social point of view….very important for self-esteem” “great friendships have been born and we as a group have shared some very happy and emotional days together”
Future Developments • Expansion of social club model to other regions • Without losing uniqueness of each group to function as their members desire • Multiple benefits, value for money • Investing in staff and resources
Implications for Practice • Some Questions • Should service models continue to separate the couple? • Which is more beneficial for spouse – a break away from PWD or a break with them, with no responsibility for care needs? • By having spouse involved – do we share the duty of care? • Are the club and traditional service models mutually exclusive or mutually beneficial?
Implications for Policy • Traditional approach needs to be critically analysed • Policy shift from providing services ‘onto’ to ‘in conjunction with’ • Maintaining couple as central to all discussions regarding care • Re-examine models and further research into emerging models
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