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Notice
of Motion for Full Council
That
this Council adopts the Motor Neurone Disease (MND) charter and
thereby supports achieving quality of life, dignity and respect for
people with MND and their carers.
Council
notes that over 60 councils across the country have signed up to the
Motor Neurone Disease (MND) Charter
The
Charter is made up of 5 points:
1.
People with MND have the right to an early diagnosis and information
2.
People with MND have the right to access quality care and treatments
3.
People with MND have the right to be treated as individuals and with
dignity and respect
4.
People with MND have the right to maximise their quality of life
5.
Carers of people with MND have the right to be valued, respected,
listened to and well supported
Motion
to be moved by Councillor Julian Ware-Lane
Seconded
by Councillor Tony Cox
Background:
The
Motor Neurone Disease (MND) Association, five-point MND Charter sets
out the rights of people with MND and their carers and the pillars of
good care and support. Five people a day die in the UK from MND. It
is a rapidly progressive, fatal disease that can affect any adult at
any time. The disease leaves people unable to walk, talk or feed
themselves. The cause of MND is unknown and there is no cure.
*
MND is a fatal, neurological disease for which there is no effective
treatment and no cure.
*
MND kills five people in the UK every day.
*
Today there are 5,000 people living with MND in the UK. Life
expectancy from diagnosis is two to five years
*
It can affect any adult at any age. Imagine being trapped inside a
body that can’t move.
*
MND attacks the nerves that control movement; people with MND can
still think and feel, but their muscles refuse to work. As these
nerves die, the muscles weaken and waste, leaving people locked in a
failing body, unable to move, walk or talk.
Why
should councils adopt the charter?
Many
decisions about services used by people with MND, such as social
care, housing adaptations and support for carers, are made at the
local level by councillors. Currently, there are significant
differences in the quality of services available to people with MND
locally, depending on where they happen to live. As such, it is
important that councillors, and all those working for and with the
council, understand the needs of people with MND and their carers.
While councils aren’t responsible for everything outlined in the
MND Charter, they are a significant part of the jigsaw. When services
such as social care and housing are provided in a timely
person-centred way, this has a huge impact on the person with MND and
their family.MND is a devastating, complex disease and particularly
difficult to manage. If a council can get it right for MND, it can
get it right for residents with other neurological conditions and
disabilities too.
*
The MND Association is the only national charity in England, Wales
and Northern Ireland that funds and promotes global research into the
disease and provides care and support for people affected by MND.
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