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Hero doctor's devastating health update after terminal diagnosis

Hero doctor's devastating health update after terminal diagnosis

Perth Now20-05-2025

Acclaimed melanoma expert and former Australian of the Year Professor Richard Scolyer has shared a heartbreaking update on his battle with brain cancer – revealing the disease is advancing again.
Professor Scolyer, 58, was diagnosed with the aggressive and incurable glioblastoma in 2023 and initially given just eight months to live. However, after undergoing experimental immunotherapy based on melanoma research, his cancer remained at bay for 18 months.
In a social media post on Monday, Professor Scolyer confirmed a recent MRI scan had shown further progression of the tumour on the left side of his brain.
'While this may not be the best direction to be heading with my changes, amazingly (to me), I still seem keen to keep living, loving and having fun, whenever possible,' he wrote on social media.
'I feel like there are quite a few people on my team (including my family & friends) and they make me happy and proud.'
The prominent cancer researcher, jointly named Australian of the Year in 2024 alongside fellow Melanoma Institute Australia co-director Professor Georgina Long, has remained remarkably candid and optimistic throughout his treatment journey. Professor Scolyer credited his friends and family, saying they make him 'happy and proud'. Credit: Supplied
In February, Professor Scolyer announced the cancer had returned, prompting him to undergo surgery in March to remove as much of the tumour as possible.
He later explained that while the procedure successfully removed a significant portion of the mass, 'little tentacles' remained and would require additional treatment to 'mop up' the remaining cancer cells.
'Depending on what the scan shows … that will help choose what are the next forms of therapy that I can have to see where we need to go from here,' he said at the time. A recent MRI scan showed, in the left side of his brain, further progress of his tumour. Credit: Supplied
He also acknowledged the emotional and physical toll of ongoing treatment, admitting he had been feeling 'a little up and down' due to side effects, though he continued to cherish time spent with his wife Katie and their children.
'Sometimes I'm happy to have fun, but some of the therapies have knocked me around a bit, so I can't do some of the things I love doing,' he said.
'I'm still having a fun time at home with my kids, they've been very kind, as well as my beautiful wife Katie has, who's been using her incredible intellect to help me speak to different doctors about various options that are available.'
Professor Scolyer said he expects to undergo another operation and remains hopeful about future treatments.
'Fingers crossed this operation isn't so bad and we can move forward with the next form of therapy and hopefully push things along faster to try and get things open up for many, many patients who have got glioblastoma,' he said. Professor Georgina Long AO Professor Richard Scolyer AO (NSW) at the 2024 Australian of the year awards. Credit: News Corp Australia

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Could a scan seven years ago have found the sleeping killer in a WA girl's head?
Could a scan seven years ago have found the sleeping killer in a WA girl's head?

The Age

time17 hours ago

  • The Age

Could a scan seven years ago have found the sleeping killer in a WA girl's head?

After her birth in the Kimberley in July 2014, Jane* was given a year to live owing to a rare, widespread congenital syndrome that impacted her brain development and ability to see, hear, walk and talk. But 10 years on, with the help of her foster mum, Sharyn Morris, she defied the odds and flourished into a bright little girl who loved the solar system and Elmo. Jane captured the hearts of anyone who met her – including Health Minister Meredith Hammat. This incredible progress was cut short in August last year, when Jane died unexpectedly from a brain bleed. 'She just was developing so well, and there was no reason to believe that anything was going to happen to her,' Morris says. The bleed was thought to have been caused by a blood vessel abnormality hidden in her brain. It was a condition that doctors consistently assured Morris that Jane did not have, and recommended against scans that would have identified it. This was despite years of medical documents that said otherwise, which has led Morris to demand a coronial inquest into her foster daughter's death. Loading In echoes of previous cases of parents' concerns being ignored at WA hospital – such as those of Aishwarya Aswath and Sandipan Dhar – Morris says Jane's death could have been prevented if her requests for more rigorous scans years ago had been acted on. 'She would say to me, '[Jane], grow up to be a big girl' and I'd say, 'Yes, honey, mum promises you, you'll grow up to be a big girl',' Morris says. 'She just never got that opportunity. They took everything away from her and took her away from us. They destroyed our lives as well. It's not right.' Shock death There were only four children in the world with Jane's condition in 2019. Under that she had a multitude of other conditions, including dark skin lesions covering her head and body, tumours on her brain and in her eyes, rickets, autism, and epilepsy. Morris, 61, fostered Jane 10 days after her birth at the request of her biological mother, and was eventually given a special guardianship order, granting her total parental responsibility. Despite obtaining permission from Morris to write this story, this masthead cannot reveal the girl's real name – Jane is a pseudonym – nor show pictures of her because the Department of Communities retains control over publication of information about her. The department refused to allow the publication of her name or images of her on the request of her biological family for cultural reasons. Jane's conditions meant she was a regular visitor to Perth Children's Hospital, but despite this, in recent years her speech and walking were advancing in leaps and bounds thanks to a new medication regimen. Morris says her foster daughter was doing so well, Jane would have probably outlived her, which is why her rapid deterioration last year came as such a shock. Morris had taken Jane to PCH in February and April 2024, complaining of headaches and 'whipper snipper' noises in her head. She was given an MRI during that visit, but doctors found no issues or bleeding. By August, Jane had deteriorated to the point she was no longer walking. 'It would appear that four years after Aishwarya's death that nothing has changed.' Family advocate Suresh Rajan On August 22, Jane suddenly collapsed on the kitchen floor of her Marangaroo home and was rushed to hospital by ambulance. That afternoon was the last time Morris saw her daughter conscious. Doctors reported her seizing, but Morris repeatedly told them they were not like her regular seizures. She says that evening she pleaded with doctors for a CT scan, but it did not happen until early morning the next day. The scan found the bleed. In a clinical incident report known as a SAC1 report, seen by this masthead, doctors noted Jane had to be stabilised before they could do the scan. Jane was eventually found to have had a massive brain bleed, and surgery to drain it was unsuccessful. Morris and her daughters, who had travelled from across the state to see Jane, switched off her life support at 5.55pm on August 24 in time for sunset, which Morris says was her favourite time of day. Ten months on, Morris is yet to receive Jane's official cause of death, but the SAC1 report and her discharge summary both note a blood vessel deformity known as an arteriovenous malformation (AVM) found in her brain after her death may have been the source of the bleed. Conflicting reports AVMs are a tangling of arteries and veins that can disrupt the flow of blood and cause internal bleeding. According to the Sydney Children's Hospital, AVMs usually form during development or shortly after birth. They are often only found if they start bleeding, but can be detected using medical imaging techniques like MRIs, CT scans and angiograms. Loading Angiograms are considered the gold standard of diagnosing AVMs, which are treatable through surgery, radiosurgery or endovascular treatment. Jane's medical documents from 2017 onwards show conflicting reports about the presence of an AVM, and that Morris' repeated requests for an angiogram did not eventuate. In a 2017 letter between neurologists and PCH, obtained by Morris under Freedom of Information laws, it was revealed an MRI taken found a possible AVM, but it was not conclusive and would require an angiogram. The doctor said there was a risk associated with the angiogram, and they had discussed whether they outweighed the risk of the AVM haemorrhaging. That same letter noted Morris was 'very keen' to do the angiogram and the doctor agreed to do it if the Neurological Intervention and Imaging Service of WA supported the move. In a separate letter from December 2018, NIISWA found there was 'no evidence' of an AVM after an enhanced MRI scan. Jane never received an angiogram, and in all her annual care plans until her death, it was noted a brain lesion spotted in the past MRI was 'not an AVM'. 'No further investigation, surgery or intervention is required from NIISWA point of view,' it said. However, discharge summaries from several hospital visits from March 2020 until her final visit, seen by this masthead, clearly stated she did have an AVM. Jane's final discharge notice notes her brain bleed was thought to be caused by a small AVM, which was 'noted on previous MRI image series'. This conflicts with the SAC1 report, where a panel found previous scans 'did not demonstrate an AVM or other vascular lesion for which prior neurological intervention would have indicated.' Morris says she only noticed mentions of the AVM on Jane's discharge summaries after her death. She says had she been alerted sooner, she would have pushed harder for more scans and treatment. 'I'm of the understanding that she doesn't have one. I'm her primary carer. I have a special guardianship order for this child, she's my child. I'm raising her, and I'm told by doctors she doesn't have one,' she says. Morris claims Jane's Indigenous background and disabilities may have been a factor in her struggle to get her properly diagnosed. 'In seven years why did they not do it? Because she's Indigenous, because she was special needs? What are their answers?' she said. 'No faith' in Aishwarya's CARE call During Jane's final days in hospital, Morris did not activate the Aishwarya CARE call system – the system implemented in WA hospitals after Aishwarya Aswath's death in 2021 to help parents escalate their concerns. Both Morris and the clinical incident report concede Morris had made her concerns heard enough to have senior medical staff in the room, but Morris says she had no faith in the system. 'Why would I? I already have [senior doctors] treating my child, and they won't listen to me. Who is going to take notice of me at 10 o'clock at night?' she says. Morris' concerns around the Aishwarya CARE call system concerned family advocate Suresh Rajan, who also helped Aishwarya's parents in the aftermath of their daughter's death. 'When the Aishwarya CARE call was implemented, the then-health minister, now premier, wrote to us to advise that the system was to 'change the culture of the WA Health Service so that patients and caregivers were listened to',' he says. 'It would appear that four years after Aishwarya's death that nothing has changed.' What needs to change Morris is furious at the handling of Jane's care and subsequent investigations, including the SAC1 report, which suggested her death was not preventable. She says she did not have the opportunity to address the panel conducting the report, nor respond to its findings. She wants Hammat's support to launch a coronial inquest into her daughter's care and death and is demanding a raft of changes in hospital accountability. These include more accountability of individual doctor decision-making, laws to force doctors to act on observations and concerns of parents, establishing an independent medical investigation body and more transparency around investigations. 'Parents are right' Health Minister Meredith Hammat, who attended Jane's funeral, confirmed she would reach out to Morris to discuss her concerns, but would not say whether she supported her request for a coronial inquest. '[Jane] was an incredible little girl and loved by many people in our community,' she said. 'I've spoken with Sharyn many times over the years, most recently just a few weeks ago. Sharyn is a strong woman and a fearless advocate, and I'm sorry for her loss. 'I won't discuss the details of our meetings, but it is my firm view that parents and guardians should be listened to. They know their child best. 'Our conversations are ongoing, and I will continue to support Sharyn as both her local member and Minister for Health to ensure she gets the answers she needs.' A Child and Adolescent Health Service spokesman said they could not discuss confidential patient details.

Could a scan seven years ago have found the sleeping killer in a WA girl's head?
Could a scan seven years ago have found the sleeping killer in a WA girl's head?

Sydney Morning Herald

time17 hours ago

  • Sydney Morning Herald

Could a scan seven years ago have found the sleeping killer in a WA girl's head?

After her birth in the Kimberley in July 2014, Jane* was given a year to live owing to a rare, widespread congenital syndrome that impacted her brain development and ability to see, hear, walk and talk. But 10 years on, with the help of her foster mum, Sharyn Morris, she defied the odds and flourished into a bright little girl who loved the solar system and Elmo. Jane captured the hearts of anyone who met her – including Health Minister Meredith Hammat. This incredible progress was cut short in August last year, when Jane died unexpectedly from a brain bleed. 'She just was developing so well, and there was no reason to believe that anything was going to happen to her,' Morris says. The bleed was thought to have been caused by a blood vessel abnormality hidden in her brain. It was a condition that doctors consistently assured Morris that Jane did not have, and recommended against scans that would have identified it. This was despite years of medical documents that said otherwise, which has led Morris to demand a coronial inquest into her foster daughter's death. Loading In echoes of previous cases of parents' concerns being ignored at WA hospital – such as those of Aishwarya Aswath and Sandipan Dhar – Morris says Jane's death could have been prevented if her requests for more rigorous scans years ago had been acted on. 'She would say to me, '[Jane], grow up to be a big girl' and I'd say, 'Yes, honey, mum promises you, you'll grow up to be a big girl',' Morris says. 'She just never got that opportunity. They took everything away from her and took her away from us. They destroyed our lives as well. It's not right.' Shock death There were only four children in the world with Jane's condition in 2019. Under that she had a multitude of other conditions, including dark skin lesions covering her head and body, tumours on her brain and in her eyes, rickets, autism, and epilepsy. Morris, 61, fostered Jane 10 days after her birth at the request of her biological mother, and was eventually given a special guardianship order, granting her total parental responsibility. Despite obtaining permission from Morris to write this story, this masthead cannot reveal the girl's real name – Jane is a pseudonym – nor show pictures of her because the Department of Communities retains control over publication of information about her. The department refused to allow the publication of her name or images of her on the request of her biological family for cultural reasons. Jane's conditions meant she was a regular visitor to Perth Children's Hospital, but despite this, in recent years her speech and walking were advancing in leaps and bounds thanks to a new medication regimen. Morris says her foster daughter was doing so well, Jane would have probably outlived her, which is why her rapid deterioration last year came as such a shock. Morris had taken Jane to PCH in February and April 2024, complaining of headaches and 'whipper snipper' noises in her head. She was given an MRI during that visit, but doctors found no issues or bleeding. By August, Jane had deteriorated to the point she was no longer walking. 'It would appear that four years after Aishwarya's death that nothing has changed.' Family advocate Suresh Rajan On August 22, Jane suddenly collapsed on the kitchen floor of her Marangaroo home and was rushed to hospital by ambulance. That afternoon was the last time Morris saw her daughter conscious. Doctors reported her seizing, but Morris repeatedly told them they were not like her regular seizures. She says that evening she pleaded with doctors for a CT scan, but it did not happen until early morning the next day. The scan found the bleed. In a clinical incident report known as a SAC1 report, seen by this masthead, doctors noted Jane had to be stabilised before they could do the scan. Jane was eventually found to have had a massive brain bleed, and surgery to drain it was unsuccessful. Morris and her daughters, who had travelled from across the state to see Jane, switched off her life support at 5.55pm on August 24 in time for sunset, which Morris says was her favourite time of day. Ten months on, Morris is yet to receive Jane's official cause of death, but the SAC1 report and her discharge summary both note a blood vessel deformity known as an arteriovenous malformation (AVM) found in her brain after her death may have been the source of the bleed. Conflicting reports AVMs are a tangling of arteries and veins that can disrupt the flow of blood and cause internal bleeding. According to the Sydney Children's Hospital, AVMs usually form during development or shortly after birth. They are often only found if they start bleeding, but can be detected using medical imaging techniques like MRIs, CT scans and angiograms. Loading Angiograms are considered the gold standard of diagnosing AVMs, which are treatable through surgery, radiosurgery or endovascular treatment. Jane's medical documents from 2017 onwards show conflicting reports about the presence of an AVM, and that Morris' repeated requests for an angiogram did not eventuate. In a 2017 letter between neurologists and PCH, obtained by Morris under Freedom of Information laws, it was revealed an MRI taken found a possible AVM, but it was not conclusive and would require an angiogram. The doctor said there was a risk associated with the angiogram, and they had discussed whether they outweighed the risk of the AVM haemorrhaging. That same letter noted Morris was 'very keen' to do the angiogram and the doctor agreed to do it if the Neurological Intervention and Imaging Service of WA supported the move. In a separate letter from December 2018, NIISWA found there was 'no evidence' of an AVM after an enhanced MRI scan. Jane never received an angiogram, and in all her annual care plans until her death, it was noted a brain lesion spotted in the past MRI was 'not an AVM'. 'No further investigation, surgery or intervention is required from NIISWA point of view,' it said. However, discharge summaries from several hospital visits from March 2020 until her final visit, seen by this masthead, clearly stated she did have an AVM. Jane's final discharge notice notes her brain bleed was thought to be caused by a small AVM, which was 'noted on previous MRI image series'. This conflicts with the SAC1 report, where a panel found previous scans 'did not demonstrate an AVM or other vascular lesion for which prior neurological intervention would have indicated.' Morris says she only noticed mentions of the AVM on Jane's discharge summaries after her death. She says had she been alerted sooner, she would have pushed harder for more scans and treatment. 'I'm of the understanding that she doesn't have one. I'm her primary carer. I have a special guardianship order for this child, she's my child. I'm raising her, and I'm told by doctors she doesn't have one,' she says. Morris claims Jane's Indigenous background and disabilities may have been a factor in her struggle to get her properly diagnosed. 'In seven years why did they not do it? Because she's Indigenous, because she was special needs? What are their answers?' she said. 'No faith' in Aishwarya's CARE call During Jane's final days in hospital, Morris did not activate the Aishwarya CARE call system – the system implemented in WA hospitals after Aishwarya Aswath's death in 2021 to help parents escalate their concerns. Both Morris and the clinical incident report concede Morris had made her concerns heard enough to have senior medical staff in the room, but Morris says she had no faith in the system. 'Why would I? I already have [senior doctors] treating my child, and they won't listen to me. Who is going to take notice of me at 10 o'clock at night?' she says. Morris' concerns around the Aishwarya CARE call system concerned family advocate Suresh Rajan, who also helped Aishwarya's parents in the aftermath of their daughter's death. 'When the Aishwarya CARE call was implemented, the then-health minister, now premier, wrote to us to advise that the system was to 'change the culture of the WA Health Service so that patients and caregivers were listened to',' he says. 'It would appear that four years after Aishwarya's death that nothing has changed.' What needs to change Morris is furious at the handling of Jane's care and subsequent investigations, including the SAC1 report, which suggested her death was not preventable. She says she did not have the opportunity to address the panel conducting the report, nor respond to its findings. She wants Hammat's support to launch a coronial inquest into her daughter's care and death and is demanding a raft of changes in hospital accountability. These include more accountability of individual doctor decision-making, laws to force doctors to act on observations and concerns of parents, establishing an independent medical investigation body and more transparency around investigations. 'Parents are right' Health Minister Meredith Hammat, who attended Jane's funeral, confirmed she would reach out to Morris to discuss her concerns, but would not say whether she supported her request for a coronial inquest. '[Jane] was an incredible little girl and loved by many people in our community,' she said. 'I've spoken with Sharyn many times over the years, most recently just a few weeks ago. Sharyn is a strong woman and a fearless advocate, and I'm sorry for her loss. 'I won't discuss the details of our meetings, but it is my firm view that parents and guardians should be listened to. They know their child best. 'Our conversations are ongoing, and I will continue to support Sharyn as both her local member and Minister for Health to ensure she gets the answers she needs.' A Child and Adolescent Health Service spokesman said they could not discuss confidential patient details.

Burnt-out cops' astonishing compo payout
Burnt-out cops' astonishing compo payout

Perth Now

time2 days ago

  • Perth Now

Burnt-out cops' astonishing compo payout

The NSW Auditor-General has revealed NSW Police officers suffering psychological injuries received $1.75bn in compensation payments between 2019 and 2024. A new report titled The Mental Health and Wellbeing of NSW Police released by the Auditor-General's office examined whether the force had effectively managed the psychological wellbeing of its workforce. It found the number of psychological injury claims, compensation payments and medical exits from the police force escalated in five years from 2019. There were more than 1200 psychological injury claims from NSW Police officers in 2023-24, and of those who left the force, more than half cited medical reasons. The number of psychological injury claims from NSW Police officers has escalated. Tom Parrish Credit: News Corp Australia Psychological injuries were the most common, accounting for 769 officers leaving in 2023-24. Mental stress, exposure to workplace violence and work pressure were the main reasons for quitting. In February last year, 1261 officers were on long-term sick leave with active workers compensation claims for a psychological injury, which 536 employees attributed to post-traumatic stress disorder. The NSW Police Force is Australia's largest law enforcement agency, with more than 16,200 sworn officers and 4294 civilian officers serving 8.5 million people. Like other NSW public sector departments, the number of police psychological injury claims had been increasing until a significant investment in October last year of tens of millions of dollars to better support police. More than $1.7bn in compensation payments have been paid out to police between 2019 and 2024. NewsWire/ Gaye Gerard Credit: News Corp Australia But the Auditor-General found that while the NSW Police Force monitored psychological injuries, it had not analysed the root cause to effectively prevent future harm in its workforce. The Auditor-General found that improved risk reporting had not been implemented and initiatives to improve wellbeing within the workforce had been done without proper analysis of the cause of psychological injuries. 'The new initiatives provide counselling and support for police after traumatic incidents but do not address other psychological risk factors such as role overload, fatigue or burnout,' the report stated. 'There has been limited evaluation of initiative outcomes to date, and their effectiveness has not been determined. 'In the absence of data about the causes of psychological injury, or evaluations of wellbeing services, the NSW Police Force was unable to demonstrate the efficiency or effectiveness of its wellbeing investment.' Psychological injury is a common trait among police. Picture Thomas Lisson Credit: News Corp Australia Recommendations were made for police to allocate officers that matched workloads in command areas and to implement systems to better understand factors that led to psychological injury claims. A NSW Police spokesman told NewsWire that policing was a challenging and rewarding job that exposed officers to traumatic incidents. 'The psychological wellbeing of our people is vitally important, and we will continue to improve the support programs at all levels that enable our officers to do the job that they love,' the spokesman said. 'We welcome the report and the work of the Audit Office of NSW, and it is important that we acknowledge the challenges and opportunities recognised in the report. 'We are well on the way to doing better and have made significant improvements over the past three years to improve our awareness, training, education and support of all our people.'

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