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Speaking frankly...Your health record in your hands...Twenty five years ago I took up a position at the Australian Medical Association helping general practitioners adapt to computerised medical records in their practices. Dusty wads of paper, index cards, photocopies and facsimiles were to be replaced by digital files. The promise of this revolution was better medication management, better management of chronic conditions and diseases, better management of reminders and recalls, and more accurate and timely communication with other medical professionals. At the time, the field was split between optimistic advocates and staunch opponents. Concerns about privacy, concerns about security, concerns about reliability (we were still learning to back up properly back then) and concerns about dehumanising the therapeutic encounter between a patient and their doctor were all key concerns of the opponents. On the advocates’ side, much of what was happening was the replacement of DIY solutions with robustly engineered solutions. Keen doctors at the vanguard had sometimes written their own software, or were using programs that were not really fit for purpose, and commercial software companies were moving into the space. Twenty five years later I now expect to receive an electronic reminder of my appointment. I expect my script to be printed. I expect a recall if my blood test results are out of scope and I expect my doctor to print off information sheets and advice during my appointment. I also expect a reminder when my next test is due. Over the last few months we have been helping to inform members and stakeholders about My Health Record, including the three-month opt-out period starting this week. The promise of this new system is similar to the promise of the first electronic GP clinical records: better management of chronic conditions and diseases, better management of reminders and recalls, and more accurate and timely communication with other medical professionals. For those living with mental health issues, the potential for benefits are greater than for the broader population. We know that people living with mental illness often experience health care that is substandard – co-morbidities can remain untreated or undiagnosed and the complications of treatments and medications can be very damaging. But we also know that for people living with mental illness, access to information can carry great risks. We still live in a world where stigma and discrimination mean that the unauthorised released of information might mean discrimination in employment, or insurance, or other opportunities. So where does that leave us? It leaves each of us empowered to make an informed choice. To weigh up the benefits against the risks – which our friends at the Consumers Health Forum of Australia have published as An important overview of the pros, cons and questions about My Health Record Yes, you can opt out of the scheme (possibly waiting for it to mature so we can opt in in future) or you can remain in the scheme. Nearly 6 million Australians have already opted in. The key is, it’s your decision. Your health record in your hands as the website tells us. I opted in some years ago, because my family history suggests routine monitoring might protect me from some future health challenges and I wanted to gain control and oversight, rather than leave that monitoring in the hands of doctors. And I suspect that 25 years from now, we will look back at this time in the same way we now look back at those dusty paper files sitting in cabinets at the GP practice, and wonder what the controversy was about. Warm regards.
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Mental Health Australia Member Profiles
News#YouCanTalk unites national agencies Led by some of Australia’s national mental health and suicide prevention organisations, the #YouCanTalk campaign is paving a new direction for suicide prevention in Australia. The campaign is a collaborative effort by beyondblue, Black Dog Institute, Everymind, headspace, Lifeline, ReachOut and R U OK?, which aims to empower and increase confidence when it comes to talking about suicide. Whether it is for conversations with friends, family, colleagues or acquaintances, #YouCanTalk also highlights the resources available to support these conversations. "Our message is this: #YouCanTalk about suicide. Half the population think that they can’t. We are on a mission to partner with the community to prevent suicide in this country." "The evidence is in: it is not harmful to ask someone if they are thinking about taking their own life or find out if they have made a plan. In fact, it could help. It’s important that we all know the facts about suicide and our prevention efforts are informed by what the research tells us." "Suicide is an issue that many find difficult to talk about, but it is an issue that is having major impacts on communities across Australia. #YouCanTalk is about giving people the confidence to have the conversation by connecting them to the tools that can support them." "Suicide is not a silent killer. There are signs that we can all look out for, particularly when it comes to young people, who have a range of life stresses that may be masking something deeper." "Australia has world-leading suicide prevention services and we want to ensure people who need them access them. However, the reality is, not everyone will seek help themselves – they may firstly disclose their need to family and friends." "The more #YouCanTalk about suicide with your friends and family in an open, honest and empathetic way, the more lives we can save." "You know your friends and family best and you are best-placed to have an open conversation with them and help them find the right support if something isn’t right."
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Reminders What is Caring Fairly?Caring Fairly is a national advocacy and awareness-raising campaign focused on improving and realising the economic, social and cultural rights of mental health carers. The campaign goals are to:
This three-year campaign will be launched in Winter 2018 and you can find out more at the link below.
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