Better health and ageing for all Australians

Publications

Feelings

Information sheet for carers on the demands of caring and how the many changes in family life may bring about a range of feelings and emotions.

In this section:

You may download this document in PDF format:

PDF printable version of Feelings (PDF 283 KB)

Carers 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 may be parents, partners, brothers, sisters, friends or children of any age.

Carers may care for a few hours a week or all day every day. Some carers are eligible for government benefits, while others are employed or have a private income.

The constant demands of caring and the many changes in family life may bring about a range of feelings and emotions. Some people may feel a sense of satisfaction about being a carer. Others may feel angry and overwhelmed at times. These emotions can be difficult to cope with.

Different feelings

Carers may experience a range of different feelings, which surface from time to time. There are no right or wrong feelings. These feelings are a natural and normal reaction to caring.

All carers respond to the demands of caring in their own way. Feelings are always individual and everyone will react differently. Regard your feelings as signposts. They will tell you when things are not going well and need your attention.

Below are some of the feelings carers often say they experience.

Feeling Overwhelmed, Confused and Shocked by:

  • the diagnosis of illness or disability, especially at first; and
  • finding yourself caring and realising the changes this will bring to your life.
‘I never expected this to happen. I didn’t know what had hit me’.

Feeling Guilty for:

  • believing you bear some responsibility for the disability or illness;
  • not wanting to be a carer;
  • lost tempers and harsh words;
  • being embarrassed by the person you care for;
  • not being perfect;
  • not doing enough;
  • needing a break from caring; or
  • placing the person you care for in residential care.

Feeling Love and Commitment for:

  • the person you are caring for and the relationship you once had; or
  • caring for someone you love.

Feeling Frustration and Anger at:

  • having to be the carer;
  • others in the family who don’t do their fair share;
  • the person being cared for;
  • stigma that may surround the illness or disability;
  • friends who don’t make contact anymore;
  • support services which don’t provide enough help;
  • the loneliness and isolation; or
  • the focus always being on the person you care for.
‘As much as I love him and care for him, sometimes I feel physically run down myself’.

Feeling Afraid about:

  • what will happen if you don’t cope;
  • picking up your life after the caring role ends;
  • what will happen if you die; or
  • needing to learn new skills.

Feeling Sadness for:

  • loss of a relationship – the parent, husband or wife, or child you once knew;
  • loss of the life you used to know and the sense of who you are;
  • loss of the life you planned;
  • loss of a sexual relationship with your partner; or
  • loss of opportunities for the person you care for.
‘I love my child dearly – it’s a matter of coping and sometimes it’s very hard’.

Grief is the emotional pain that comes about as a result of a loss or a number of losses. It may be one of the strongest feelings experienced by carers and often causes great distress. Grief can go unrecognised because there has been no death.

Recognising your grief and talking to someone about how you are feeling can help. If feelings of sadness persist for a long time, or affect your life to a great extent, contact your family doctor or community health centre.

‘You have grief all your life whether you recognise it or not. All the expectations you have for your child have to be adjusted’.
Top of page

Feeling Stressed

Stress is a part of our daily lives but too much stress can lead to physical and emotional exhaustion. Caring may mean being cut off from others and facing high stress over a very long period of time. Carers are very vulnerable to stress because of the demands of caring. Stress may bring physical symptoms such as headaches or difficulty sleeping. Some people become very emotional or anxious. Others report feeling persistently tired and chronically unwell.

We can’t always do something about the causes of stress in our lives so it’s important to learn to recognise stress and to try new ways of coping with it. Try some of the tips for taking good care of yourself listed at the end of this fact sheet or contact your Commonwealth Respite and Carelink Centre on 1800 052 222* for information on techniques or courses for dealing with stress.

Feeling Depressed

Sometimes being a carer may feel like an endless grind. Over time you may stop feeling angry or sad about your situation and instead just feel numb. Even happy times don’t seem to lift you and the simplest tasks seem to take too much energy. You may find you are sleeping too much or waking early or during the night. You might feel worthless or agitated most of the time and have difficulty making decisions.

These changes may be signs you are suffering from depression. Depression is a serious illness but is often overlooked. It is common and treatable. Talk to your doctor, who will help you find the treatment that works best for you.

How can I deal with difficult feelings?

Feelings may become overwhelming and lead you to act in ways you don’t like. It may become hard to think clearly about important decisions.

Just as feelings are individual so are ways of dealing with them. However, there is a way to deal with difficult feelings that many carers say is extremely helpful – talking to someone. Talking about problems can help, either to family and friends, to other carers in a support group or to a counsellor.

‘I’m a very independent person, always have been. So asking for help was a really hard thing for me. Now I know there are people out there who will just listen to what I have to say’.

Support groups

Why join a support group?
  • To meet others in a similar position.
  • To have a break.
  • To get information.
  • For support.
Sharing ideas, feelings, worries, information and problems can help you feel less isolated. Sometimes family and friends don’t understand the condition of the person you care for. People in the support group will understand.

Support groups bring together carers in local areas sometimes under the guidance of a facilitator. Often other carers or workers are invited to present information and training.

Your Commonwealth Respite and Carelink Centre can help put you in touch with carer support groups in your area. Contact them on 1800 052 222*.
Top of page

Counselling

Counselling involves talking to someone who understands and can work with you to give you the encouragement, support and ideas to improve your situation. It may be a way to assist with the many changes in your relationships and roles as well as dealing with the strong feelings associated with caring.

Counselling may involve just you and the counsellor, either face-to-face or over the telephone, so it’s important you feel comfortable with the counsellor you choose. Anything said is completely confidential, so it’s a good chance to talk about those things you may feel you can’t raise with family or friends.

Counselling usually involves a limited number of sessions but will vary according to your needs. Some counselling services are free. Private counsellors charge a fee although many are willing to negotiate their costs.

Your local doctor, community health centre, council or service provider may be able to assist.

Condition-specific Associations

There are many organisations that specialise in support for specific conditions. You may like to talk to workers in these associations as they will understand the condition of the person you care for and the demands it makes on you. Many associations publish regular newsletters. Reading these may be another good way to get information and support.

How can I find out what services can help me with my difficult feelings?

  • Commonwealth Respite and Carelink Centre - 1800 052 222*
  • Relationships Australia - 1300 364 277*
  • Lifeline - 13 11 14*
  • Kids Helpline - 1800 551 800*
  • Dementia Helpline - 1800 100 500*

Take care of yourself

Planning for breaks

You cannot care constantly without a break. It can be difficult so ask for help. Ask family and friends and respite care services but make sure the breaks are regular and frequent. Contact your local Commonwealth Respite and Carelink Centre on 1800 052 222* to discuss what respite options are available for you and for the person you care for. For emergency respite support outside standard business hours, call 1800 059 059*.

Planning for health

Regular exercise, rest and nutritious food are all necessary in order to withstand stress. Try to plan your day so you get all three.
  • Walking, swimming, yoga, gardening or dancing are good ways to get some gentle exercise.
  • Learning to relax by listening to pleasant music, meditating or specific relaxation exercises can help you sleep better.
  • Trying new vegetables or fruit, eating at regular times and looking for new recipes are good ways of making eating well easier.
‘You need a sense of humour. Sometimes a laugh helps relieve the stress’.

Planning to keep friendships and interests

Try to relax and enjoy yourself. Maintain an identity of your own separate from the person you care for. Keep your links to the world outside. Absorbing interests, having fun and relaxation are all good for your physical and mental health.

Where can I get more information?

There is a lot more information for carers available on a range of topics. Commonwealth Respite and Carelink Centres in each state and territory provide carers with referral to services and practical written information to support them in their caring role. Contact your Commonwealth Respite and Carelink Centre on 1800 052 222*. Alternatively, carers may use the services provided by the carer association in each state or territory. More information on these services can be found by contacting 1800 242 636*.

The Translating and Interpreting Service (TIS) can help you if you need assistance with a language other than English. TIS can be contacted on 13 14 50#.

Commonwealth Respite and Carelink Centre 1800 052 222*

*Free call from local phones, mobile calls at mobile rates
#Local call from local phones, mobile calls at mobile rates
Top of page

Help with accessing large documents

When accessing large documents (over 500 KB in size), it is recommended that the following procedure be used:

  1. Click the link with the RIGHT mouse button
  2. Choose "Save Target As.../Save Link As..." depending on your browser
  3. Select an appropriate folder on a local drive to place the downloaded file

Attempting to open large documents within the browser window (by left-clicking) may inhibit your ability to continue browsing while the document is opening and/or lead to system problems.

Help with accessing PDF documents

To view PDF (Portable Document Format) documents, you will need to have a PDF reader installed on your computer. A number of PDF readers are available through the Australian Government Information Management Office (AGIMO) Web Guide website.