Sight loss and dementia:
From Alzheimer’s Europe
The Dementia and Sight Loss Interest Group
Other causes of sight loss
•Effects of medication: such as blurred vision
•Stroke: including loss of segments of visual field, sometimes
unnoticed by the person but sometimes causing serious loss of vision
Promoting the individuals confidence in their
environment.
Informal and formal carers need to
provide clear, regular communication to promote the persons sense of
orientation and confidence in their environment Techniques such as reality
orientation and validation therapy may help.
Reducing loneliness and isolation
People with dementia and sight loss
would benefit from more one to one contact with paid carers and volunteers
especially if more time could be devoted to maintaining valued pastimes.
Managing threats to independence
People should be supported to pursue
valued activities in a safe environment. Care professionals rather than family
carers should initiate discussion about activities that are no longer
considered safe.
Managing visual hallucinations
Family members need guidance on managing hallucinations –this
might include reassurance and non-confrontation, full explanation and
distraction techniques.
Extra respite resources such as
night carers and more sessions at day centres required. Family carers also
require ready access to information and advice such as that provided by RNIB
and the Alzheimer’s Society.
More services are needed that are
capable of meeting both sight-related and dementia related needs. Day centres,
activities and peer support would benefit people with dementia and sight loss.
Training
Training programmes for vision rehabilitation workers should
include information on working with people with dementia. Joint training of
mental health and sight loss professionals would encourage the exchange of
knowledge and expertise.
Good practice tips: occupation and activity
•Make enjoyed activities accessible -e.g.
•Audio transcription, talking books
•Tactile activities
•Audio labels to sort and locate personal effects
•Provide 1:1 support to explain and describe
•Assess benefits, not just risks
Good practice
tips: eye tests
•Domiciliary tests at home (and in care homes) for those
unable to visit an optometrist
•Appointments that are longer than usual
•Information and training about sight loss and the effect of
interventions is essential for carers (family and paid)
Eye tests and
screening
•People with dementia need regular eye tests and access to
routine interventions, in the same way as any other person
•Optometrists lack experience of dementia
•Paid and family carers may not give priority to eye tests,
spectacle wearing or other interventions
•Eye tests are not enough: information for paid and family
carers is essential
Good practice
tips: occupation and activity
Make enjoyed activities accessible -e.g.
•Audio transcription, talking books
•Tactile activities
•Audio labels to sort and locate personal effects
•Provide 1:1 support to explain and describe
•Assess benefits, not just risks
Good practice
tips: environment
Improve lighting –make it brighter
•Use colour and increase contrast –walls to doors, furniture
to walls
•No clutter –physical or visual
•Reduce glare –shade lamps, blinds
•Support route finding and orientation –use sound, smell,
touch, colour
Improving models
of care
Models of care need respond to both conditions, too often they
may focus on one
•Sight loss should be addressed in dementia resources, and
vice versa
•A sensory model of care is needed
•A network of practice could support staff in different
settings and share good practice
•Care home inspections should address how well services meet
the needs of people with both conditions.
•Regular assessment and diagnosis is essential, with steps to
support follow on action and in particular spectacle wearing.
People with dementia and sight loss –a scoping study of
models of care; Ruth Bartlett and Declan McKeefry. Thomas Pocklington Trust.
2009
This may well help many other like myself understand the problems we struggle with on a daily basis
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I always say that we may have this illness, but we are all so different.
This is my own daily problems, but I would gladly share anyone elses, if they send them in,