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Wesley Study Reveals Family Carers Carry Long-Term Cost


Monday, 14th May 2012 at 1:48 pm
Lina Caneva, Editor
Almost 90 per cent of Australians who have cared for a spouse or relative with mental health issues reported a harmful impact on their own physical and mental health, according to a report by Wesley Mission.

Monday, 14th May 2012
at 1:48 pm
Lina Caneva, Editor


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Wesley Study Reveals Family Carers Carry Long-Term Cost
Monday, 14th May 2012 at 1:48 pm

Almost 90 per cent of Australians who have cared for a spouse or relative with mental health issues reported a harmful impact on their own physical and mental health, according to a report by national welfare organisation, Wesley Mission.

Wesley has released an eight-point plan to help support people caring for relatives with mental health issues after its study of more than 1000 Australians revealed that caring comes at a profound personal cost.

The Wesley Report, Keeping minds well: Caring till it hurts shows that three in four caregivers said their role had adversely affected their relationships with family and friends and 57 per cent said their employment and financial situation had deteriorated.

The CEO of Wesley Mission, the Rev Dr Keith Garner, said the Wesley Report revealed that caregivers too often carried the cost of caring and were the unsung heroes of the community.

“They more often than not sacrifice their time, money and even their careers to ensure that those they support can manage and fulfil their often challenging lives,” Dr Garner said.

“Yet their caring comes at a cost, with an overwhelming number declaring that their caring experience as a child has provided a lasting negative into adult life. The challenge for us as a community is to provide better support these people and to reduce the stigma associated with caring.”

The Wesley Report found that the majority (64 per cent) of carers had been in their caregiving role for more than six years and almost half (43 per cent) indicated they had been caregiving for more than 10 years.

The impact felt by those who started caregiving when they were under 16 is considerably higher than those who were exposed when they were older.

“The role affects their financial status, and mental and physical health,” Dr Garner said.

“They are also more likely to have experienced stigma because of their association with a relative with a mental health issue.”

For many caregivers, stigma remains an enduring concern. Those who had been involved in a caregiving role for longer were more likely to report that stigma had affected their family, them personally and the wellbeing of their relative.

The Wesley Report found that people who were exposed to the caregiving role at an early age were most likely to be afraid to ask for help, despite having positive attitudes toward health services.

“This is a challenge for all mental health providers,” Dr Garner said. “There are significant numbers of young Australians who are caring for a mother, father or sibling but are reluctant to seek help. These young people try to cope on their own. We need to end the stigma around mental health and make it easier for young people to access support services. The long-term cost of not doing so is enormous.”

Most respondents (84 per cent) indicated that their relative’s illness had been formally diagnosed by a health professional such as a GP, psychologist or other mental health professional.

Caregivers use a range of coping mechanisms, preferring things like taking a break, finding comfort in their faith and looking on the positive side to seeking professional help or taking up exercise.  They are less likely to use avoidance strategies such as pretending to others that everything is satisfactory or avoiding discussion.

Age appears to be related to the use of avoidance coping strategies, with younger caregivers being more likely to report using all avoidance strategies than older respondents.
Among the recommendations are a more cohesive, proactive approach among health services, GPs and schools to identifying young carers and ensuring that their needs are met through referrals to relevant services, support and advice.

Wesley Mission also suggests that it be mandatory for teachers to be provided with an understanding of warning signs for children or young people who may be in distress from caregiving.

It also recommends that professionals are not only informed about the experiences of the patient but also about the experiences of the family in the caring role. This could be implemented in the workplace and during the tertiary training of health, teaching and allied professionals, by ensuring a working understanding of appropriate responses.

Frontline service providers should be aware of family and carer needs as they treat a person with a mental health issue and facilitate appropriate support and responses.

“Wesley Mission asks both state and federal governments to ensure the capacity of intervention and respite services so that all carers have access to visible and culturally appropriate support when it is needed,” Dr Garner said.

“We also recommend greater cross-centre information sharing to provide more effective care for both caregivers and those in their care.”

Wesley Mission commissioned research consultants Urbis to undertake the study to provide insight into the experiences, challenges and coping approaches of caregivers who have a family member/partner with mental health issues.

It is the third Wesley Report on mental health and the eleventh overall since 2006.

The report can be downloaded at http://www.wesleymission.org.au/Research/Mental_Health/chrome-images/The%20Wesley%20Report%20May%202012.pdf


Lina Caneva  |  Editor |  @ProBonoNews

Lina Caneva has been a journalist for more than 35 years, and Editor of Pro Bono Australia News since it was founded in 2000.

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One Comment

  • SC SC says:

    I’ve spent the best part of 13 years “shoring up” my partner who suffered major depression. During that time there were many days when it would take me up to four hours just to reassure him enough so he could get out of bed. Other days he would be fine first thing in the morning and I would say a silent hoorah for a good day only to find by mid morning that he’s sitting in a morose state of mind on the sunny spot on our deck. In fact I had to cancel his life insurance policy because I discovered that he was contemplating ending his life and that his insurance would give me enough money to get on with my life. This was a very stressful period for both of us, each caring our own mental anguish – his, severe depression; mine, uncertainty that I was doing enough to keep him safe!

    I’m pleased to say that we found relief through EMDR, an amazing non invasion treatment for a number of conditions. My partner has recovered after 13 long years and I can finally have relaxing days, no longer worried that he may do something from which there was no return.

    But my career is shot. I’m now 60, too old for most employers to consider hiring and what can I say I’ve been doing over the last 13 years that will convince a prospect employer that I have skills they can use. Unless of course, they have some people with depression that need my support. LOL

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