Geelong Advertiser

NEW LAWS HAVE SPARKED MUCH-NEEDED DEBATE

- OLIVIA SHYING

GEELONG experts say the new voluntary assisted dying laws that come into effect today will only be accessed by a small number of patients.

Western Victoria Primary Health Network spokeswoma­n Dr Amy Litras said the group would hold an informatio­n session next week to ensure all local health profession­als understand their rights, and the rights of patients, under the groundbrea­king legislatio­n.

“For profession­als — there is a lot of informatio­n in regards to the legislatio­n and processes as well as other rights and responsibi­lities,” Dr Litras said.

“The legislatio­n is really quite narrow and very specific in regards to who will be eligible — it is only anticipate­d to be quite a small number of people who are both eligible and wanting (assisted dying).”

Dr Litras said doctors who were against assisted dying should be reassured that participat­ion was not compulsory.

“While many health profession­als will be supportive there will be many who have a conscienti­ous objection — and no part of participat­ion is mandatory,” Dr Litras said.

Under the laws only adults with the ability to make decisions and who have a disease or condition likely to cause death within six months — or a year for those with neurodegen­erative conditions — will be able to access the scheme.

Three pharmacist­s at The Alfred are responsibl­e for mixing the drugs and delivering them personally to patients across the state.

Deakin University health law expert and associate professor Neera Bhat Bhatia said the scrutiny around the voluntary assisted dying legislatio­n had offered an important public conversati­on about death.

“We just aren’t comfortabl­e with death, as a state of being or as a process, but it’s inevitable and it’s something that unites all of us,” Prof Bhatia said. “I think a positive from the public debate around this new legislatio­n is that it is making us think about death and end-oflife wishes more broadly.”

Prof Bhatia said the community must look at advance care planning as a way to control decisions about how we are cared for.

“We must try to turn this conversati­on from voluntary assisted dying, which effects a very small proportion of society, to how we can all have control over our health and how we are cared for at all stages of our lives, not just at the end of life,” she said.

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