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Respite Care & Carers
The Unsung Heroes
BY PHILLIPA SAXTON
One in eight people in NSW are carers.
In 1998 there were almost 800 000 carers or
13% of the population. This figure is now
estimated at one million. Of this group 20% are
primary carers and 75% are workforce age.
Women aged 45-53 years are the largest single
group of carers. Caring tends to be a long term
commitment, 40% of primary carers report that
they have been caring for at least 10 years, and
a further 29% for a least 5 years. 79% of primary
carers live with the person they care for, and of
this group, 44% report they provide on average,
40 hours or more care per week.
AUSTRALIAN BUREAU OF STATS (ABS) 1998 DATA. |
Carers of the
elderly and sick
are the unsung
heroes of the
community. They
save the tax
payer dollars,
they free-up
hospital and nursing home beds, they take the
pressure off other family members and more
importantly, they provide a loving home environment
for aged parents, friends and relatives.
Peace of Mind looks at the lives and
responsibilities of carers, the assistance
offered to carers by the community and government
(both financial and psychological)
and what choices are available for these special
people to take a well-earned break.
Carers of the sick and elderly are usually
family members or friends who provide support
to children or adults who have a disability,
mental illness, chronic condition or who are
frail aged. Carers can be parents, partners,
brother, sister, friends or children of any age.
Carers may care for a few hours a week, or all
day every day.
Care recipients can fall into many categories,
from the mildly needy to totally dependent.

Care recipients can have a clear mind,
but be physically handicapped to some extent,
physically incapacitated due to minor strokes
or post-operative effects, or they can
be suffering from the increasingly debilitating
effects of an illness such
as dementia or Alzheimer’s.
Care recipients
can be cheerful and positive or frustrated at
the loss of their independence and dignity.
Carers sometimes have to distinguish
between doing what is necessary and doing
too much. Doing too much is often the result
of outside pressure or simply because it is
quicker than getting the care recipient (patient)
to do something for themselves. A carer doing
more than necessary can lead
to a patient becoming needlessly sedentary
and ultimately to a speedy downturn in their
general health.
Keeping busy, feeling useful and being
involved to the best of one’s abilities are the
good ways to maintain or possibly create positive
thoughts and, in some cases, even
improve physical health.
If a person is still capable of peeling and
chopping vegetables, doing the washing up,
taking out the compost, brushing the dog or
cat – let them.
Sure it might take a lot longer
but the benefits to the patient are great and
ultimately the carer will feel less like a martyr
as time goes on.
If the patient is ambulatory to any extent,
don’t jump up to pass them something from
the other side of the room. Let them get it
themselves – if they can get themselves to the
toilet, they can get anywhere else in the house.

They maybe slow and frail, but they are still
capable and quite often the more exercise they
get, no matter how little or mundane, the
more they will be able to achieve on their own
and feel more independent.
Stress on a carer, especially a full-time
carer, can go beyond the obvious physical
effects.
Most elderly people suffer loss of
short-term memory, while retaining a crystal
clear long-term memory. Hearing the same
story told over and over or having to
constantly reiterate something can be taxing for the most patient carer.
For carers dealing with serious disabilities
such as dementia, Alzheimer’s and wheelchair
or bed-ridden recipients, these scenarios
and others are significantly increased.
There are many publications and associations
that deal with the special needs of these
more serious cases. Professional advice and
support for carers can be sought through
Carer Resource centres, Carer Respite centres,
community groups or specific associations.
Carers Need to Take Care of
Themselves
As any airline will tell you, if there is an emergency
and oxygen levels drop in the cabin, put
your own mask on first before dealing with
others.
The premise of this is obvious – if you
are not in a position of strength, you are not
going to be any use to anybody when they
need it most.
Carers need to take breaks,
they need time on their own and they need
other outlets in their lives if they are going to
be effective over time. Organise respite as far
in advance as possible.
Except in emergencies, try not to wait until
a break is essential. Sometimes a care recipient
may be reluctant to accept that you need
a break, so time is required for them to get
used to the idea. They might need to meet or
see, well in advance, the person who will be
caring for them in your absence or to visit a
residential or day care centre.
Taking a break can also benefit the care recipient. When their normal carer is away they have the opportunity to interact with other
people, have new experiences, garner fresh
stories to tell, have a fresh audience for much told anecdotes and a whole set of memories unrelated to the person they live with day in and day out.
There are a number of personal issues a
carer needs to address, such as keeping
healthy (exercising, getting enough sleep and eating well), staying in touch with friends, taking regular and planned breaks and putting
aside some time for relaxation – every day!
Another problem for carers is one of stubbornness
on the part of the care recipient. It is
usually very difficult for an aging person to
admit they are not as strong and capable as
they once were and many, even those weakened
by strokes, will steadfastly refuse to use
a walking stick or frame.
For their safety and your peace of mind it is
imperative that you be firm on this point. “But
I don’t need one,” is often the response. Try, “I understand your reluctance to use one but
for my sake, please do it. I need to you use
one.” Tell them you need to relax a bit, to be
less concerned all the time. If that doesn’t
work, be ‘mean’, get a little cross, “Look, I can’t
be with you all the time and it will give you
more independence. I can’t even leave you
browsing in a shop in case you lose your balance,” etc.
At the start you may to be forever
reminding them, “Where’s your stick?” But
eventually it will become a habit and it will
make the world of difference to both your
lives.
Getting Away
While getting away on your own for a few
hours, days or even taking a
holiday is all important, the stress of caring can
also be lessened by taking a break with the
care recipient, preferably also with other family
members. They say that a change is as
good as a holiday, but if finances permit, a real
holiday is a wonderful way to unwind and
recharge batteries for both carer and recipient.
If it is possible to get away with family members
or friends, the onus of care is shared and
it is often found that the care recipient’s mental
and physical condition improves with the
extra stimulus and physical exertion.
If the
patient’s condition allows, even marginally, a
campervan is a wonderful way to travel as it is
less crowded than a car, a wheelchair (for longer
forays than the person can manage on foot) can
be transported with ease and outside school holidays
overnight stops can be taken without the
need to book ahead.
Elderly people are often quite set in their
ways and like to know where everything is –
a campervan can become a little home-away
from home without the need to acquaint themselves
with new surroundings each night.
Providing the van’s facilities are checked out
in detail and camping grounds are selected
according to the specific needs of the travellers
eg handicapped facilities and bathroom rails,
it can be a virtually stress-free and fun time
away.
People and Facilities
to Meet Your Needs
The Australian Government Carer Resource
Centre and Respite Centres, provides support
to carers. Similar services are available in
New Zealand. The Carer Associations listed on
this page also have information on respite services
and it is important to note that there are
different kinds of respite available and not all
are provided through respite centres.
Respite services provide emotional support
and counselling for carers as well as look after themselves, but are frail and not up
to living entirely on their own 24 hours a day,
there are many excellent electronic monitoring
services available.
These privately owned companies provide
a variety of home safety monitors which are
linked directly back to base. The service is
checked daily – generally a phone call is
made to ensure the facility is working and if an
emergency occurs, such as a fall, the patient
just has to use a buzzer to call for assistance.
To guard against false alarms, when the buzzer
is pressed, the base will phone the recipient’s
home. If the call is not answered, an ambulance
is immediately dispatched to the premises.
In Australia these companies can be found
under Alerting Systems in your local yellow
pages and in New Zealand under, Medical
Alarms.
The information supplied above has come out
of the Carers NSW Submission for State
Budget 2004-5 and can be accessed along
with further information through their website:
www.carersnsw.asn.au
| CONTACTS |
Carers Australia
PO Box 73, Deakin West 2600 ACT
Unit 2, 43-49 Geils Court,
Deakin 2600 ACT
Phone: (02) 6282 7886
Fax: (02) 6282 7885
www.health.gov.au/acc/carers/respite/
www.centrelink.gov.au
www.carers.asn.au
Commonwealth Carer Resource Centres
Freecall*: 1800 242 636
Carer Respite Centres
Freecall*: 1800 059 059
*Freecall from local phones.
*Mobile calls at mobile rates. |
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