This week we have a guest blog from Sam Smethers, Chief Executive of the Fawcett Society, on women and dementia.
Dementia is one of those illnesses that we don’t really like to talk about do we? It’s associated with ageing and while we know that we have an ageing society all the images around us are rather in denial preferring to promote youthful beauty. But it’s also a gender issue because women are more likely than men to be affected.
That is why I am pleased to be speaking at Age UK’s For Later Life conference on this issue in November. In fact I was shocked to learn when researching the subject that dementia is now the biggest cause of death for women in the UK. Women over 60 are twice as likely to develop Alzheimer’s disease than breast cancer. So it would seem reasonable to expect that research in this area would be focussing more heavily on women. But this is not so. Continue reading “Guest blog: Dementia is a women’s issue”
With an ageing population and increasing numbers of us living in to late old age, attitudes to later life have never been more relevant. At the same time, our straitened economic position and pressures on public services to meet financial challenges whilst providing for these growing numbers of over 6os, means the debate often hinges on economic and political issues.
The ‘burden’ of our ageing population is frequently stressed, accompanied by an emphasis on inequalities between generations that incite division.
Yet, one of the strongest messages to come out of a session I chaired last week at Age UK’s For Later Life conference was that the media furore on the ‘burden of ageing’ is not reflected in public attitudes.
Ben Page of Ipsos Mori revealed polling showing that 68% of people aren’t satisfied with the Government’s treatment of older people and that care for the elderly is consistently amongst the top three scoring issues of concern to people of all ages.
I believe this polling strikes at the heart of the debate about attitudes to later life, illustrating the gap between political and media rhetoric and the views of the individual. But why is there such a gap? How do we form our attitudes to later life? And are they showing signs of changing, heralding strains on intergenerational relations? Continue reading “Attitudes to ageing”
Each year, Age UK stands back and takes an overview of how society is meeting the needs of people in later life and sets out our agenda for public policy in the year ahead. In our Agenda for Later Life 2013 report we track changes in a range of key areas including money matters, work and learning and health and social care.
Public attitudes, policies and the economy all impact on people’s experiences of ageing. This year, as the economy bumps along the bottom, it would be all too easy to concentrate on the challenges we face. However, we strongly believe in the need to focus on the opportunities as well.
The publication of a White Paper setting out plans for a new single tier State Pension brings hope of better provision in future for those with low incomes and interrupted working lives. Continue reading “Meeting the challenges of an ageing population”
This blog was contributed by Dr Nick Goodwin a speaker at Age UK’s annual For Later Life conference. Nick is CEO of the International Foundation for Integrated Care and a Senior Fellow at The King’s Fund, London where he leads their programme of research and analysis for improving and integrating care for older people and those with long-term conditions.
When my elderly father was in hospital recently his experience of an uncoordinated, chaotic and impersonal service was both dispiriting and disturbing to both him and his family. Whilst clinical decision-making was good, and as a result his physical health returned through the miracles of blood transfusions and intravenous antibiotics, the experience undoubtedly took a large piece out of his mental wellbeing and future self-confidence.
The underlying problem was a lack of care co-ordination. The lack of information sharing on diagnosis, procedures, results and next steps led to worried waits about the seriousness of his condition and what, as a family, we needed to put in place for home care support. Different and conflicting advice and feedback from doctors and nurses was unhelpful. The lack of communication between wards, and between nurses on the wards, meant that his medication regime for Parkinson’s was often ignored despite constant reminders. No help was given to support discharge, and no plan put in place. Continue reading “Guest blog – Mad as hell: Older people must demand a better care experience”