It’s
Carers’ Rights Day tomorrow.
In
theory carers have rights specific to the role, but it’s very hard for me to
begin even to discuss them without sounding totally cynical.
I’m
getting this out of my system before resuming a positive attitude - and as I'm always keen to stress, I am one of the lucky ones, a winner in the postcode lottery with access to services and specialist support. But it shouldn't be down to postcodes or being lucky. Carers' rights are human rights, wherever you live.
We
have a right to act on behalf of the person we’re caring for, in their best interests.
We
have a right to be acknowledged for our work.
We
have a right to be recognised for our contribution to the economy.
We
have a right to support from our employers, should we be able to combine
employment with our caring role.
But
-
As unpaid carers for people we love, we fall between the cracks of services and state.
We don’t have the right to claim holiday or sick leave from our caring responsibilities, or the right to any NHS exemptions despite the known effects of caring on health and wellbeing.
We don’t have the right to claim holiday or sick leave from our caring responsibilities, or the right to any NHS exemptions despite the known effects of caring on health and wellbeing.
We
don’t have the right to a living wage or even an allowance in line with Job
Seekers’ Allowance (just let’s not even talk about Universal Credit)
We
don’t have the right to earn more than £120 a week, should we somehow find time
to work alongside our caring role.
We
have a right to an assessment “health check” from the local authority, but most
local authorities lack the capacity to do this, so it doesn't happen.
We
don’t have the right to support services unless we live in the right
area. Even then, we don’t have the right for those services to recognise our
role or make it easier to access their help.
According to a report
by Gov. uk
on carers’ experience in 2016,
“What comes through time and time again is that services are fragmented,
inconsistent and information not helpfully shared between statutory
organisations.”
This report was
designed to feed into a Carers’ Strategy, headed then by a pre-Brexit social
care minister (it scarcely matters whom, as they seem to change before the ink
has dried on the letterhead, yet very little has changed since then to improve the
situation for carers.)
We
should have the right to be heard when we ask the
government for support and solutions in line with social and economic reform, yet they don’t seem to be listening. Caring is still seen as a
“choice”.
Yet
social care, as we all know, is in increasing crisis and for many of us there
is simply no alternative.
I'm frustrated and fed up and angry. Like most other carers I can sound off to anyone who'll listen but find it hard to do much more than that because I'm too involved in the task in hand - yes, the situation badly needs to change but my brother needs me right now and there are only so many hours in a day.
https://petition.parliament.uk/petitions/221220
An
Appeal forChange: https://twitter.com/Appeal4Change