
Eminent pathologist Richard Scolyer reveals heartbreaking cancer update months after experimental immunotherapy
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.
Acclaimed melanoma expert and former Australian of the Year Professor Richard Scolyer, 58, has shared a heartbreaking update that his cancer has advanced once more.
X /@ProfRAScolyer
'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.
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.
Scolyer was diagnosed with incurable glioblastoma in 2023 and initially given just eight months to live but under experimental immunotherapy, his cancer remained at bay for 18 months.
X /@ProfRAScolyer
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.

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New York Post
23 minutes ago
- New York Post
I had breast cancer at 24 — now I'm already going through menopause
Mood swings. Hot flashes. Night sweats. They're symptoms most women expect in middle age, not when you're barely old enough to rent a car. But Alexis Klimpl was just 25 when the brutal reality of premature menopause struck. A year ago, though, she faced an even tougher battle — and was unsure if she'd live long enough to go through the so-called 'change of life' at all. Advertisement 9 Alexis Klimpl is a publicist based in San Diego, Calif. Courtesy Alexis Klimpl A lump and a life-changing call Lying in bed at home in San Diego one night last July, Klimpl reached down to scratch an itch — but her hand froze as her fingers brushed against a small, hard lump on her right breast. 'I shot up and looked over at my boyfriend, and my face just dropped,' she told The Post. Advertisement Her mind ran through the possibilities: fibrous tissue, a cyst, maybe even a benign tumor. But lurking in the back of her mind was a thought she couldn't shake: breast cancer. In 2025, the American Cancer Society estimates that 316,950 women in the US will be diagnosed with the disease — yet only a small fraction of these cases occur in women under 45. Even fewer are as young as Klimpl, then just 24. Her thoughts quickly turned to her father, who had died of bile duct cancer at 67. 9 Klimpl credits the support of her family and friends as a major bright spot in her cancer journey. Courtesy Alexis Klimpl Advertisement But Klimpl didn't get it checked out immediately. Days later, she left for a three-week surfing trip to Indonesia to chase waves her father had introduced her to as a young girl. 'I wasn't going to cancel that for anything,' she said. The lump was the size of a Skittle when she left. When she returned less than a month later, it had grown to the size of a grape. 'We always think that we're going to be young and healthy forever, and that's just not the case.' Alexis Klimpl Advertisement Alarmed, her doctor ordered a mammogram and biopsy. She then got a call asking her to come in the next day to discuss the results, sending her into a panic. 'I was spiraling,' she recalled. 'What if it's terminal? What if it's growing faster than we can start chemo? What am I going to do about work? Oh god, am I going to be able to have kids one day?' The next morning, her worst fears were confirmed: The lump was Stage 1 triple positive breast cancer. Two weeks later, an MRI showed it had advanced to Stage 2. 9 Concerned about chemotherapy negatively affecting her fertility, Klimpl froze her eggs before starting treatments. Courtesy Alexis Klimpl Facing the future Doctors warned her that chemotherapy could threatened her ability to have children naturally — and hormone injections to stave off future cancer could send her into early menopause — so she met with a fertility specialist who recommended freezing her eggs. 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Advertisement 'I remember always thinking, this time I'm going to be strong, but then [the cap] touches you, and like a flip of a switch, you just absolutely lose it in front of a room full of strangers,' she said. 'It was hard seeing people my age going out and having fun, meeting new people. My life was on pause.' Alexis Klimpl She ended up losing about 30% of her hair — and though she wondered if she'd have been better off shaving her head, she knew being bald, on top of everything else, 'probably would have broken me.' The rest of Klimpl's chemo was milder than expected, with fatigue, body aches and a rash — though the queasiness tested her. Advertisement 9 Cold capping, also known as scalp cooling, helped Klimpl preserve most of her hair while going through chemotherapy. Courtesy Alexis Klimpl 'This nausea was in my bones,' Klimpl recalled. 'I felt it all over my body. It was always there, every single day, for 4½ months.' But the hardest part was being cut off from the ocean — her main source of stress relief — since the salt water could interfere with her cold cap treatments. Advertisement 'My dad was the person who taught me how to surf, and that's how I've always felt most connected to him, so it was pretty emotionally dark for me,' Klimpl said. She also felt isolated. The young survivor group at her hospital mostly included women in their 40s and 50s, many married with kids. 'It was hard seeing people my age going out and having fun, meeting new people,' she said. 'My life was on pause.' 9 Klimpl is a lifelong surfer, and the hope of returning to the ocean kept her motivated through her treatments. Courtesy Alexis Klimpl Surgery, sacrifice and survival Klimpl finished chemotherapy in December. Her tumor had shrunk significantly. Soon after, she faced a tough series of surgeries: tumor removal in late January, a double mastectomy a week later and breast reconstruction in May. 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New York Post
19 hours ago
- New York Post
Mom's brain tumor caused her to ‘forget' she had a son: ‘That was heartbreaking'
A UK woman says her brain tumor made her 'forget' she was a mom — after flashing lights and rainbow-like patterns in her vision led to her diagnosis. Clare Smerdon, 37, was diagnosed with a grade 4 astrocytoma — just weeks after her son Teddy turned 13 months. Advertisement Doctors told her the aggressive tumor was life-limiting, and Clare feared she would never get to watch Teddy grow up. While waiting for surgery to remove the tumor she says she was 'acting completely out of character' and 'forgot I was a mum.' 5 UK mom Clare Smerdon was diagnosed with a brain tumor just 13 months after giving brith to her son Teddy. Brain Tumour Research / SWNS But two years on, she has defied the odds and proudly watched her son, now four, put on his uniform and walk through the gates of Barton Hill Academy for his first day of school. Advertisement Clare from Torquay, Devon, said: 'When I received my diagnosis, I didn't think I'd be alive today to see Teddy start school. 'This is such a huge milestone for us. 'I no longer feel like I am dying and feel incredibly lucky, but I know others may not get the same chance.' 5 Clare's scar from her brain tumor surgery. Brain Tumour Research / SWNS Advertisement Clare's symptoms first appeared in early 2022, when she began experiencing flashing lights and rainbow-like patterns across her vision. She said: 'I felt as though people didn't understand what I was going through. I was desperate to find out what was causing the immense pain in my head and changes in my vision.' Clare had an MRI scan at Derriford Hospital in Plymouth which revealed a 2.75 inch brain tumor in July 2022. She said: 'When I got the diagnosis I remember thinking that I'd just had a baby, and I wanted to be around to watch my son grow up for as long as I could. Advertisement 5 The tumor caused Clare to see flashing lights and even forget that she was a mother. Brain Tumour Research / SWNS 'Then the wait for surgery was horrendous. I was losing myself and acting completely out of character. 'I even forgot I was a mum. Teddy spent more time with his dad, and we drifted apart. That was heartbreaking.' In August 2022, Clare underwent a six-hour operation to remove the tumor followed by six weeks of radiotherapy and chemotherapy. She said: 'Two weeks after surgery I returned home, and doctors confirmed I had a grade 4 astrocytoma which is also classified as a glioblastoma. 'On hearing the pathology results I knew my life was over. The treatment made me sick, and I could only stomach a meal in the evening. 5 Clare was told in 2023 that she would only have two to three years to live. Brain Tumour Research / SWNS 'At the same time, I got to spend more time with Teddy, and we were both getting to know each other again.' Advertisement A routine scan in August 2023 revealed she had just two to three years to live. Clare said: 'The thought of not being here to watch Teddy grow is destroying. I'm not sure if another operation is something I want due to the implications that comes with it. 'My eyesight is already compromised, and my speech has been impacted, so now I just watch and wait. 'There are so few treatment options for brain tumor patients, and the ones we do have are invasive and often life changing. Advertisement 5 Clare participating in a charity walk to raise money for brain tumor research. Brain Tumour Research / SWNS 'I've looked into clinical trials abroad, but for most working-class families, the cost is impossible. I'm angry and frustrated at how little support and research funding there is.' Clare is now working with Brain Tumour Research and will take part in the charity's Walk of Hope in September. She said: 'I want to do everything I can to help fund the research that will lead to better treatments and, ultimately, a cure. Advertisement Start your day with all you need to know Morning Report delivers the latest news, videos, photos and more. Thanks for signing up! Enter your email address Please provide a valid email address. By clicking above you agree to the Terms of Use and Privacy Policy. Never miss a story. Check out more newsletters 'If sharing my story and taking part in fundraising encourages even one more person to join the cause, it will be worth it. 'That's why I'm calling on the government to increase funding for research into brain cancer, more must be done.' Letty Greenfield, community development manager at Brain Tumour Research, said: 'Clare's story is a powerful reminder of both the personal impact of a brain tumor diagnosis and the urgent need for change. Advertisement 'We are so inspired by her strength and determination. Brain Tumour Research is committed to funding sustainable research at our dedicated Centres of Excellence, but we also campaign for the government to increase funding. 'It's only through increased investment that we can accelerate new treatments and, ultimately, find a cure.' Brain Tumour Research is calling for a national annual spend of $47.2 million to bring brain cancer funding in line with other cancers such as breast cancer and leukemia. A JustGiving page has been set up by Clare to help raise money for Brain Tumour Research ahead of the Walk of Hope in September.
Yahoo
2 days ago
- Yahoo
Prenatal Pesticide Exposure Alters Children's Brain Development, Impairing Motor Skills
Exposure during pregnancy to chlorpyrifos, a widely used pesticide, causes lasting changes in children's brains and motor function impairments. LOS ANGELES, August 18, 2025--(BUSINESS WIRE)--A joint observational study by Children's Hospital Los Angeles (CHLA) and Columbia University has found that prenatal exposure to a common pesticide also used as an insecticide could impair children's brain development and motor function for years to come. In this long-term study of children between 6 and 14 years old, followed since birth, prenatal exposure to the pesticide chlorpyrifos (CPF) was associated with alterations in brain structure and impairments in motor function. This is the first study to show that prenatal exposure to a pesticide produces enduring and widespread molecular, cellular, and metabolic effects in the brain. The results were published in JAMA Neurology. "More CPF exposure led to more thickening of the cerebral cortex—the area of the brain that directs functions like thinking, memory and movement," says Bradley Peterson, MD, first author on the study and Chief of the Division of Child & Adolescent Psychiatry at Children's Hospital, where he also leads the Brain Imaging Lab. "We don't know the consequences of these brain effects, but we found that CPF exposure most impairs motor functioning." Fetal exposure to CPF affects neurological development Between January 1998 and July 2005, the team conducted behavioral assessments and MRI scans of the brains of 270 youths in upper Manhattan whose mothers had been exposed to CPF during pregnancy when their apartments were fumigated. The researchers from CHLA and the Columbia University Mailman School of Public Health also accessed behavioral exposure information from umbilical cord samples from each child at delivery as well as samples of their mothers' blood collected the day after birth. The MRI scans found: Thickening of the brain cortex Alterations in white matter, which could affect brain function Changes in the internal capsule, the structure that governs communication between the cortex and subcortical areas, affect motor and sensory pathways Fewer neurons in white matter could signal impaired development Abnormalities in brain pathways that support motor control Impaired nerve insulation (myelination), which can affect function Reduced blood flow, indicating less energy use, throughout the brain "Current widespread exposures, at levels comparable to those experienced in this sample, continue to place farm workers, pregnant women, and unborn children in harm's way. It is vitally important that we continue to monitor the levels of exposure in potentially vulnerable populations, especially in pregnant women in agricultural communities, as their infants continue to be at risk," said Virginia Rauh, ScD, senior author on the study and the Jane and Alan Batkin Professor of Population and Family Health at Columbia Mailman School. The data strongly suggest that one of the fundamental problems of CPF exposure is altered differentiation of neuronal tissue, says Dr. Peterson. "That happens early in pregnancy, when neurons develop in the cortex and differentiate into cortical gray matter—densely packed nerve cells which process information—and underlying white matter—which is mostly nerve fibers that connect neurons," he says. "All these abnormalities can contribute to poor motor function in these kids. The contributing mechanisms seem to be the inflammation and oxidative stress that CPF and other pesticides produce." The researchers also found a dramatic and global reduction in brain blood flow. "To me, this is the most profound finding because it's so powerful and very rare to see something like this," says Dr. Peterson. "Blood flow is an important indicator of underlying metabolism—the energy used by brain tissue. In my opinion, it's maybe the most important finding of the paper, because it says that globally there's a problem with brain metabolism in direct proportion to how much CPF exposure they had." While this current paper reports results on children up to age 14, the researchers have now collected MRI scans of adolescents up to age 19 and are analyzing the data in preparation for the next release of results from this ongoing study. CPF is in the food chain CPF is an organophosphate pesticide—in the same chemical family as nerve gas–that disrupts nerve signaling. In pregnancy, it can cross the placenta to the fetus, easily traversing the fetal blood-brain barrier. Prior studies by other groups have linked maternal CPF exposure to lower birth weight, smaller head size, abnormal newborn reflexes, and neurodevelopmental issues in toddlers—including autism, inattention, and lower intelligence. CPF was banned from home use in the U.S. in 2001, but it is still used as an agricultural pesticide. A 2020 ban on food crops was reversed in 2023. The EPA wants to continue to allow CPF residues in certain food crops, including apples, strawberries, asparagus, tart cherries, citrus, and peaches. "It's in our food supply," cautions Dr. Peterson. "And other chemicals used in the home act in similar ways and almost certainly increase inflammation and oxidative stress. This is why it is important to do these studies about the chemicals in our environment to protect children's health." Editor's note: An embargoed copy of the study can be obtained from JAMA Neurology (mediarelations@ or CHLA can provide a copy. About Children's Hospital Los Angeles Children's Hospital Los Angeles is at the forefront of pediatric medicine and is the largest provider of hospital care for children in California. Since its founding in 1901, CHLA has delivered a level of pediatric care that is among the best in the world. Ranked one of the top 10 children's hospitals in the nation by U.S. News & World Report, Children's Hospital Los Angeles provides comprehensive and compassionate care to one of the largest and most diverse pediatric patient populations in the country. The hospital is the top-ranked children's hospital in California and the Pacific U.S. region for 2024-25. A leader in pediatric research, CHLA is among the top 10 children's hospitals for research funding from the National Institutes of Health. The Saban Research Institute of Children's Hospital Los Angeles supports the full continuum of research, translating scientific discoveries into life-changing treatments for patients around the globe. As a pediatric academic medical center, CHLA is also home to one of the largest graduate education programs for pediatricians in the United States. The hospital's commitment to building stronger, healthier communities is evident in CHLA's efforts to enhance health education and literacy, introduce more people to careers in health care, and fight food insecurity. To learn more, follow CHLA on Facebook, Instagram, LinkedIn, YouTube, and X, and visit View source version on Contacts CHLA Contact: Lorenzo Benet e: lbenet@ Sign in to access your portfolio