Search results for ‘Subject term:"carers"’ Sort:
Results 1 - 10 of 164
Make connections, get support: recognising ourselves and others as carers
- Author:
- CARERS UK
- Publisher:
- Carers UK
- Publication year:
- 2017
- Pagination:
- 11
- Place of publication:
- London
Drawing on findings of an online survey of 4511 adults, this study explores the levels of public awareness and recognition of carers in families, circles of friends and the workplace; and the extent to which people have confidence in their ability to help carers find support. The study shows that more than half of respondents believe they don’t know a single family member or friend who cares, whilst as many as 3 in 5 workers believe they don’t know ‘any work colleagues’ who help look after a loved one. This despite the fact that 1 in 10 people in the UK are carers and 1 in 9 people in the workforce are juggling their paid job with unpaid caring. Amongst those members of the public who did manage to recognise that a friend or family member looked after someone, as many as 3 in 5 did not ‘suggest where to find further information on caring’ and the number rose to 65% amongst those who knew carers in the workplace. Amongst all of those polled, including those that had not recognised carers in their social circles or at work, two thirds said they would feel confident providing ‘emotional support’ to a new carer. Yet, only 2 in 5 would feel confident pointing people in the direction of information about caring. The findings also revealed differences amongst men and women, carers, and non-carers, and those of different ages: women are more likely to say they know a friend, a family member or a colleague who is a carer compared with men and to have suggested sources of information and support; those aged 45-54 are only slightly more likely to say they have any family or friends that are carers compared with the wider public; and those who have never had an unpaid caring role are more likely to say they don’t have any friends or family who care. (Edited publisher abstract)
Use of the internet by informal caregivers assisting people with multiple sclerosis
- Authors:
- BUCHANAN Robert J., HUANG Chunfeng, CRUDDEN Adele
- Journal article citation:
- Journal of Technology in Human Services, 30(2), April 2012, pp.72-93.
- Publisher:
- Taylor and Francis
- Place of publication:
- Philadelphia, USA
Multiple sclerosis (MS) is the most common neurological disease disabling younger adults in the United States. About 30% of people with MS in the US require support and assistance at home, with an estimated 80% of that care provided by informal caregivers, usually family members. Previous studies have identified that the internet is used to help informal caregivers provide assistance to people with chronic illness and disability. The aim of this study was to identify characteristics of informal caregivers, caregiving, and people with MS receiving their assistance that are associated with caregiver use of the internet. A sample of 530 informal caregivers assisting people with MS was recruited using the Registry of the North American Research Committee on Multiple Sclerosis (NARCOMS). Factors associated with internet use were identified using a logistic regression model. Duration of MS in the person receiving care and caregiver age predicted lower internet use. More hours per week providing care and higher caregiver educational level increased odds of internet use. The internet can be a low-cost service delivery option to provide education and support to caregivers assisting people with MS.
In the know: the importance of information for carers
- Author:
- CARERS UK
- Publisher:
- Carers UK
- Publication year:
- 2006
- Pagination:
- 21p.
- Place of publication:
- London
... that they had not missed out on benefits, many did. Of those who did, a staggering 58% had missed out for over 3 years. A similar proportion of carers felt they missed out on practical support. Of those who felt they had missed out, 68% had missed out for over 3 years. Earlier work by Carers UK demonstrated that an estimated £740 million a year in carers’ benefits alone could be going unclaimed every year. The research, based on a survey of carers’ experiences highlights the cost to carers who remain hidden. It also shows the difference that claiming benefits made to carers’ lives. Some bought in extra help, some adapted their homes, others had a bit of extra cash so they could go out, rather than being trapped indoors because they could not afford to take a simple trip out. It is clear that carers use the extra money for vital things to improve their quality of life. If carers do not get the financial and practical support they need they are vulnerable to a poor quality of life, cutting back and having their health and well-being seriously affected. Yet reaching these new carers is a difficult task and compounded by the high rate of turnover of carers. This research also includes a fresh analysis
The carer's handbook: what to do and who to turn to
- Author:
- LEWYCKA Marina
- Publisher:
- Age Concern
- Publication year:
- 2004
- Pagination:
- 127p.
- Place of publication:
- London
At some point in their lives, millions of people find themselves unexpectedly responsible for organising the care of an older person facing a crisis. All too often, such carers have no idea what services are available or who can be approached for support. This book aims to help people through the first hours and days of an emergency. It is a practical book packed full of advice and information.
Family caregiver self-identification: implications for healthcare and social services professionals
- Authors:
- DOBROF Judith, EBENSTEIN Helene
- Journal article citation:
- Generations, 27(4), Winter 2003, pp.33-38.
- Publisher:
- American Society on Aging
Discusses the problem of providing support to family caregivers, who may not recognise themselves as caregivers, or who do not know support services exist. Describes an American programme that aims to reach out to caregivers, self-identified or not. The service, the Caregivers and Professionals Partnership, provides a resource centre, and an educational programme for caregivers and professionals.
Low benefits take-up is barrier to a better quality of life for carers
- Author:
- TAYLOR Amy
- Journal article citation:
- Community Care, 11.12.03, 2003, pp.18-19.
- Publisher:
- Reed Business Information
Discusses how lack of awareness of carers' rights among professionals, the public and carers themselves has stalled progress on carers claiming carers allowances.
Scottish Government response to 'Carers legislation: consultation proposals: January 2014'
- Author:
- SCOTLAND. Scottish Government
- Publisher:
- Scotland. Scottish Government
- Publication year:
- 2015
- Pagination:
- 31
This government response sets out how Scottish Ministers have considered the findings of the consultation exercise on carers legislation and feedback from other engagement activity, and outlines what will be included in the Carers Bill. The response covers: the carer's assessment, now adult carer support plan (ACSP) and the young carer statement (YCS); information and advice; support to carers (other than information and advice); stages and transitions; carer involvement; local carer strategies; identification of carers and young carers; carer and cared-for person(s) in different local authority areas; links between ACSP/YCS and cared-for person's assessment. (Edited publisher abstract)
Carers legislation: analysis of consultation responses
- Authors:
- GRANVILLE Sue, MULHOLLAND Shona, FAWCETT Jo
- Publisher:
- Scotland. Scottish Government Social Research
- Publication year:
- 2015
- Pagination:
- 98
- Place of publication:
- Edinburgh
Report of the independent analysis of the responses to the Carers Legislation public consultation. The consultation sought views on a number of matters for carers and young carers. These included renaming carer assessments 'Carers Support Plans' and removal of the substantial and regular test as eligibility for assessment. Questions were included on support for carers, including information and advice and short breaks; carers/young carers involvement in the planning of services and identification of carer by public services. There were 165 responses from organisations and individuals and 1,422 generated by surveys distributed by two stakeholder organisations submitted to the Scottish Government. This report contains analysis of the views from the consultation responses. (Edited publisher abstract)
Caring for someone with dementia: a practical guide to help you
- Author:
- AGE UK
- Publisher:
- Age UK
- Publication year:
- 2014
- Pagination:
- 48
- Place of publication:
- London
This is a guide for carers of people with dementia, providing practical information on a broad range of aspects, from getting a referral to a memory clinic, through talking to family and friends about the diagnosis, joining a carers’ group, sorting out legal affairs, getting help from social services and more. Throughout this guide carers will find suggestions for organisations that can offer (Edited publisher abstract)
Malnutrition and caring: the hidden cost for families
- Author:
- CARERS UK
- Publisher:
- Carers UK
- Publication year:
- 2012
- Pagination:
- 8p.
- Place of publication:
- London
For those caring for a relative or friend, the diet of that person is often the carer’s responsibility. This research survey from Carers UK and Nutricia shows 60% of carers worry about the nutrition of the person they care for, because their condition makes eating or taking on nutrition difficult. As a result many families are struggling to cope with the consequences of malnutrition without advice, information and support. This report explores the research findings, family case studies and gives recommendations to tackle malnutrition. It calls for access to basic training and information on nutrition and recognising the signs of malnutrition, access to experts who can support carers in giving good nutrition through existing healthcare channels and NHS Direct, and suggests that all