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Has it made a difference?
Juliet Cheetham, writing in Community Care in 1999, said
the Act had raised hopes amongst carers but has not always
delivered its potential. Cheetham identified a number of barriers
to using the Act effectively:
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Carers simply aren't always
aware of their statutory
rights. They don't ask
for an assessment because they don't know they are entitled
to one!
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Many people are
hesitant to define themselves as carer's.
People see themselves as parents, husbands or wives, families
or friend caring for and about loved ones.
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People are sceptical
about the practical value
of an assessment.
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Workers own ignorance
or ambivalence about the legislation. Many staff are not
aware either and carers do not get offered them
Some important research on the effectiveness of the Carers
Recognition Act for families of people with learning disabilities
has been undertaken by the Norah Fry research Centre in Bristol.
The study, 'In their Own right' concluded that family carers
of people with learning disabilities were not well served
by the Act. Many families had either not been offered a carer
assessment, or where not sure, when asked, if they had had
one! The process was not clear to people and they did not
feel informed.
Where assessments had been undertaken there was a concern
that the vital aspects of the carer's situation had not been
assessed. This included the carer's own health and the fact
they often have multiple caring responsibilities, older parents,
younger grandchildren as well as caring for a learning disabled
son or daughter. Even more worryingly, the small number who
had a Carer's assessment carried out were visited a year later
and for the majority, nothing had changed as a result of the
assessment. Assessment should never be seen as an end in itself,
but as apart of a process of targeting and focussing the right
level of support for families. It should make a difference
in people's lives.
Another limitation of the Carers (Recognition and Services)
Act was that the carers right to assessment are linked integrally
to the Community Care Assessment of the 'cared' for person.
If that person refuses to have an assessment then their carer
has no right to one in their own right. Even if their role
as carer is having a major impact on their life.
This piece of legislation was undoubtedly a step in the
right direction but it did not go far enough. The Carers'
campaigning lobby has been advocating for an extension of
carers rights for some time. This has been more fully realised
in the last few years with first, the publication of the Carers
National Strategy: Caring for the Carers and the passing of
the Carers and Disabled Children Act 2000, which came into
effect in April 2001.
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