Inside the heartbreaking epidemic killing 100 people an hour
She was in her twenties, educated, working, constantly texting, constantly posting. She had the kind of social life that looks, from the outside, like a shield against despair.
And yet she felt adrift in a sea of surface-level connection that never quite touched her.
'I don't know if anyone really knows me,' she told an interviewer. 'I don't even know how to start that conversation.'
Her loneliness wasn't about being alone. It was about invisibility.
She is not unique. She is the chorus.
It's the unspoken epidemic: young Australians, more connected than ever, but somehow more isolated, more adrift, more quietly undone.
Last week, the World Health Organisation declared loneliness a public health threat on the scale of smoking or obesity.
The numbers are staggering: one in six people on Earth now feels profoundly alone .
The World Health Organisation estimates that it is responsible for more than 100 deaths every hour. That's nearly 900,000 a year.
\We often talk about climate change as the defining crisis of our age. But maybe the real climate crisis is emotional.
A spiritual drought. A generation raised online, surrounded by noise but starved of closeness, absorbing highlight reels while silencing their own pain.
We are living through a global emergency. But it's not broadcast with sirens or televised briefings. It creeps quietly, almost politely, into bedrooms and buses, classrooms and cafes.
What do you do with a crisis that doesn't announce itself?
Loneliness doesn't show up on a scale or an X-ray. It masquerades behind smiles. It haunts crowded rooms. It whispers, 'You're the only one.'
But the truth is, it's all of us. We are a world full of people scrolling past each other in search of something we can't name. Among teenagers, it's even worse.
For millions of young people, the defining feeling of modern life is not excitement or hope, it is disconnection. Australia is no exception.
One in four young Australians report struggling with loneliness. They are not alone, and yet they feel they are. They live with full inboxes and empty hearts, scrolling past curated perfection while wondering why the silence won't let go.
Loneliness is not a mood. It's a wound.
One that festers quietly in bedrooms and lecture halls and office cubicles. It disguises itself well, in jokes, in parties, in social media profiles and it grows in the absence of language.
You can say you're stressed. You can say you're burnt out. But say you're lonely? That's different. That feels like admitting failure.
This young generation was the first to grow up online. And in that great leap forward nto connectivity, into information, into self-expression we lost something primal. The quiet, nourishing texture of presence. Of being seen. Not just liked.
We often talk about mental health in terms of brains and biochemistry. But loneliness attacks the soul.
It leaves people doubting whether they matter. Whether their absence would be noticed. Whether they are, at core, lovable. And that kind of pain doesn't just sit in the mind. It shows up in the body.
In inflammation. In heart disease. In diabetes. In early death. I recently spoke to a young woman who, on the surface, had it all: friends, followers, a steady job.
And yet she said the most honest thing I've heard in years: 'I don't know if anyone really knows me. I don't even know how to start that conversation.'
Her loneliness wasn't about absence—it was about invisibility.
One study found that loneliness is as bad for your health as smoking 15 cigarettes a day.
And yet, where is the national outcry? The emergency summit? The hotline?
We are a country that prides itself on mateship. But mateship is not just a beer after work.
It's what we do when someone in the group hasn't spoken in a while. It's what we say when someone admits they don't want to be here anymore. It's the way a society tells its members: you matter.
Right now, too many Australians aren't hearing that.
They are students on campuses full of people, yet without a single confidante. They are teenagers with group chats but no real conversation. They are elderly neighbours we used to wave to, now seen only through a window.
They are all around us. They are us. And what makes loneliness so dangerous is that it doesn't just cause pain, it changes behaviour.
It makes people suspicious. It makes them angry. It drives them toward echo chambers, where belonging is offered in exchange for bitterness.
In that sense, loneliness isn't just a health risk. It's a civic one. It corrodes trust. It hollows out empathy. So what do we do?
Start small. We do not need a billion-dollar task force to start saying hello to strangers. To invite someone for a walk.
To text the friend who's gone quiet. We need churches, mosques, and synagogues to be open even when there's no service. We need schools to teach not just math and science but connection. We need workplaces where small talk is not a sin but a lifeline.
We need to stop pretending that connection will come through bandwidth alone.
And we need to hear from people like Amaleed. Not just because her story is brave but because it's common.
Because every silent commuter, every crowded party, every unread message may be carrying someone through a storm they can't name.
The WHO has sounded the alarm. Now it's our turn to listen.
We will not fix this with hashtags. But we can start to fix it with each other.
Australia is not the loneliest country. But right now, we are lonelier than we admit.
And the most urgent thing we can say to each other may be the simplest: I see you. I'm here.
Let's talk.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles

ABC News
an hour ago
- ABC News
20th Anniversary Collection: How power and fear play out in the dentist's chair
Sharonne Zaks grew up in a family of dentists, and when she too became a dentist, she developed an empathetic relationship with her patients, never judging them even if they'd avoided the dentist for years. A patient named Anna profoundly changed Sharonne's understanding of a patient's experience in the dentist's chair. Sharonne realised that for those who have been through a sexual assault or trauma, the extreme powerlessness of being treated at the dentist can be highly triggering. Sharonne undertook study into the area, and began a new regime to treat survivors in her own practice. She then began explaining what she'd found about the power dynamic between dentist and patient, to her own colleagues. Further information 2025 update: Sharonne regularly presents on trauma-informed care to groups across the dental profession and beyond, including lawyers, nurses, doctors and carers. Trauma-informed dental knowledge and skills have recently been made core competencies for all newly qualified dentists by the Australian Dental Council. You can read all about the Conversations origin story on the ABC News website.

News.com.au
2 hours ago
- News.com.au
Assistive tech targets market growth while improving lives
Demand for assistive technologies on the rise with growing global ageing population and awareness of disability inclusion Cochlear one of most high-profile ASX assistive technologies companies with legacy spanning more than 40 years Control Bionics helping thousands around the world communicate and connect in ways once thought impossible With a rising global ageing population and awareness of disability inclusion growing, demand is increasing for technologies that help people maintain independence and improve quality of life. Assistive technologies go beyond medical diagnostics or treatment by directly enabling individuals to hear, see, communicate and perform daily activities they might otherwise struggle to do. And while assistive technology delivers clear social benefits and aligns with ESG goals, it's also targeting a rapidly expanding market. Globally the assistive tech market was valued at ~US$22.9 billion in 2023 and is projected to reach US%36.6 bn by 2033, reflecting a compound annual growth rate (CAGR) of 4.8% throughout the decade. In Australia, the assistive technology sector is projected to expand from ~US$720 million in 2023 to more than US$1.7bn by 2030, driven by demographic shifts such as an ageing population and rising prevalence of long-term disabilities. Australia's substantial healthcare expenditure is also considered a pivotal driver for demand in the Australian disabled and elderly assistive device market. Global pioneer in hearing implant technology From restoring communication for those with severe disabilities to preserving vision and enhancing hearing, Australian companies have a proud history in assistive technologies with ASX blue-chip Cochlear (ASX:COH) one of the most high profile. Cochlear stands as one of the world's foremost innovators in assistive hearing technology with a legacy spanning more than 40 years. Cochlear implants and bone conduction devices are life-changing products, which have enabled hundreds of thousands of people globally across all ages to hear and communicate more effectively. Cochlear CEO and president Dig Howitt told Stockhead the organisation continued to progress new technology and care models, having recently launched the Cochlear Nucleus Nexa System, the world's first and only smart implant system. "The Nucleus Nexa Implant is the outcome of a 20 year investment in R&D and is the first cochlear implant to run its own firmware," he said. Howitt said similar to smartphones, the implant firmware could be updated to enable new features and access future innovations. "Recipients will now have access to a better hearing experience with both implant and sound processor updates," he said. "The Nucleus Nexa System builds upon Cochlear's industry-leading portfolio of electrodes, which are designed to optimise the electrode-neural interface and protect cochlea health and opens the door to even greater hearing potential for patients into the future." Enhancing sound in real-world situations While Cochlear may dominate the implantable hearing device market Brisbane-based Audeara (ASX:AUA) is carving out its own space in personalised listening solutions that sit between consumer audio products and clinical hearing aids. The flagship Audeara headphones and TV bundles the company started with use built-in hearing checks to create tailored sound profiles, ensuring clearer, enhanced listening experiences. Audeara managing director James Fielding told Stockhead the features made the devices valuable for those with mild to moderate hearing loss, or for people using cochlear implants and hearing aids who got an incredible entertainment experience when the sound was tailored to their needs. Building its portfolio Audeara launched Buds into its clinic networks this year. Unlike conventional hearing aids, Buds focus on enhancing the sound in real world situations like a busy cafe while also staying true to their entertainment focus, enhancing calls, TV and music. "We believe assistive technology should enhance the human experience without compromise," Fielding said. "At Audeara, our personalised hearing solutions empower people to connect more deeply with music, conversations and entertainment, regardless of their hearing ability." The technology also supports accessibility through government funding programs including NDIS, DVA and the Hearing Services Program, broadening its reach and affordability. With distribution in 1,500 clinics across Australia and more than 3,000 globally, including partnerships with major networks like Specsavers and Amplifon, Audeara is well positioned to capture growth in a market that's both socially impactful and commercially attractive. "The future of assistive technology is about inclusion, not limitation," Fielding said. "Audeara's mission is to ensure that hearing health solutions are seamlessly integrated into everyday life, combining clinical credibility with consumer-level accessibility." 'Giving communication back for more than two decades' Control Bionics (ASX:CBL) CEO Jeremy Steele describes the assistive technology medical device company as "sitting at the intersection of neuroscience and accessibility". "For more than 20 years, Control Bionics has been at the forefront of assistive technology innovation, helping thousands of people around the world communicate and connect in ways once thought impossible," Steele told Stockhead. Control Bionics has developed the NeuroNode – a wearable, watch-like, wireless non-invasive electromyography (EMG) and spatial sensor device to assist cognitive people with physical disabilities perform everyday functions. He said NeuroNode was globally unique as the only augmentative and alternative communication (AAC) technology of its kind that combined movement and EMG signals into a single platform. "Recognition by the US Centers for Medicare & Medicaid Services, awarding NeuroNode the first HCPCS code for an AAC device in 13 years, validates both the technology and the profound impact it delivers," he said. "We're proud to be a pioneer in the fast-emerging neurotechnology space, empowering people living with conditions like ALS, cerebral palsy and spinal cord injury to reclaim their voice and their independence." Steele said the company's objective was simple but ambitious – to expand global access to the most advanced, intuitive and life-changing assistive technologies available today. "The NeuroNode isn't just a device, it's a lifeline to communication, control and connection," he said. "We believe that every person – regardless of physical ability — deserves a way to engage with the world. "Our team's work over two decades reflects a deep commitment to designing technologies that break through barriers and restore possibility."

News.com.au
2 hours ago
- News.com.au
How Australia is failing dying children
EXCLUSIVE Warning: This story discusses the death of a child and paediatric palliative care Looking back now, 51-year-old Alix can see the signs that her irreverent, curious youngest child, Sofia, was seriously ill much earlier than anyone realised. In early 2018, the six-year-old was getting headaches. Somewhat inexplicably – given Sofia's happy and relaxed family and school life – the doctors put the issue down to 'stress'. Only when Alix, her husband and their eldest daughter holidayed with Sofia in Bali later that year did things become impossible to ignore. To Alix, Sofia seemed unusually thin, and her stomach was swollen. On their return to Australia, an ultrasound revealed the devastating truth. 'That's when our lives changed, you know? The doctor phoned me to say I had to come to the clinic immediately. Sofia had a tumour in her tummy, in her liver,' Alix told The diagnosis was angiosarcoma, a rare and aggressive cancer usually seen in adults, not young children. The prognosis was grim. Sofia's story is far from unique. In Australia, approximately 32,000 children live with life-limiting conditions. Yet, according to the Australian Institute of Health and Welfare, in 2021 alone, an estimated 654 children died from these conditions, and less than half received specialist paediatric palliative care. Palliative care is specialised medical support for people with life-limiting illnesses, focused on improving quality of life rather than prolonging it. Yet despite its benefits, many families of critically ill children are never offered this care — a gap experts say must urgently be addressed. In the wake of Sofia's diagnosis, what followed were months of surgeries, chemotherapy, radiotherapy, and unrelenting uncertainty. At one stage, doctors removed a vertebra from Sofia's spine and replaced it with titanium. The young girl, once so lively and full of energy, woke from surgery unable to walk, plagued by burning sensations and neurological issues. 'When you talk about the treatment, that's what hurts the most,' Alix says, her voice faltering with grief as she recalls the needles, the fever, the feeding tube. 'That is the part that becomes difficult.' For a while, Sofia returned to school. But the cancer came back, this time in her foot and hip. The doctors understood Sofia would not survive. 'They knew she would die but they didn't tell us: 'This is the path.' 'Communication was absent,' Alix explained. Instead, a cycle of vague suggestions for further chemotherapy and radiotherapy continued, even after it was clear Sofia's cancer was terminal. Alix remembers the moment she and her husband were encouraged to consider yet more treatment. 'We couldn't understand. If she's going to die and the cancer is going to keep growing, why are you offering her chemo and radio,' she said. The family had reached breaking point. 'We didn't want to be disrespectful, but we wanted to scream at the doctor and say: 'Are you stupid? Why do you want her to have that?' So, she's going to last six more months and she will die, vomiting, bald, not eating and with a tube. Horrible!' In that moment, Alix did something many parents never feel empowered to do. She took a deep breath and asked for something radically different. 'I said, 'When the time comes, can you help her to die well? I don't want her to suffer.'' Only then, after Alix specifically requested it, was Sofia referred to specialist palliative care services. This delay is heartbreakingly common, according to experts like Sara Fleming, an Adelaide-based nurse practitioner with nearly 25 years' experience in paediatric palliative care. 'The most heartbreaking thing that used to happen, and sometimes still does, is when referrals come late, and a family would sit there asking, 'Where have you been? Why didn't we meet you before?'' Sara recalls her early days in the sector when families with dying children were left isolated, afraid, and unsupported. 'There was a level of suffering that didn't need to be there, just because of a lack of knowledge and a lack of outreach from health professionals.' In the wider community, families face social isolation too. Friends, neighbours and acquaintances often don't know how to cope, so they simply disappear. 'You represent the unthinkable,' Sara says. 'These diagnoses, these things that kill people's kids … it's generally just a s**tful roll of the dice. And so, you reflect, 'There by the grace of God, goes me.'' Alix experienced this first-hand. 'When a kid gets sick, everyone is so panicked, and people don't talk to you anymore because they don't know how to manage,' she explained. Yet, as Alix and experts like Sara argue, early, honest conversations about prognosis, treatment options, and palliative care could dramatically change families' experiences. Sara believes paediatric palliative care is fundamentally different from end-of-life care for adults. Children often live with life-limiting conditions for years, while still navigating normal developmental challenges like puberty, friendships and schooling. 'We're stepping into working alongside a family where their child has been diagnosed with a life-limiting illness or disease,' she said, 'However, in the meantime, what matters is the living of that life. For children, it's also about what happens after they die. 'What memories or mark will they leave behind? For kids, it's important that we have these conversations about what's their legacy.' Alix's daughter Sofia was a perfect example of this. 'She was always laughing, even since she was four months old. She was so much fun, and even when she grew up, she was always cheeky.' Sofia loved to paint, read, and collect rocks. Her bedroom is still filled with soft toys, books, and her framed artwork. 'Rocks?' I ask Alix, surprised. Alix nods, laughing softly through tears. 'She used to pick them up and bring them to the house. And I used to throw them away so much! She was a different [type of] person, and she would speak up her mind.' In Sofia's final months, Alix kept her promise: no more needles, no more invasive treatments. Her pain was managed, and she was surrounded by loved ones. The night before she died, Sofia's family gathered for a prayer. Alix whispered gently to her: 'When you dream, just follow the light, because you're going to be happy again. You're going to run again.' Sofia died at home on June 7, 2020. For Alix, one of the most painful parts of the experience remains the absence of clear, compassionate conversations from medical professionals early in Sofia's diagnosis. 'Don't make people suffer because you don't want people to die. It's not your job to save everyone,' she said. Her message echoes what advocates have been fighting for decades to achieve: a health system where families like hers aren't left to fend for themselves, and where palliative care is offered early, not as a last resort. A national first for Australia, the Paediatric Palliative Care National Action Plan is aiming to shift that reality. Released in 2023 by Palliative Care Australia (PCA) after years of research and consultation, the Plan marks a significant step forward for Australian families and health professionals. Now in its second stage, PCA is working on nationwide awareness and implementation. 'This is a really important step for paediatric palliative care in Australia,' Annette Vickery, Projects Manager at PCA, told 'Having a national plan and clear guidelines means families and clinicians will finally have more consistency and support. I hope it makes a real difference in everyday practice — helping teams feel more confident and better equipped to care for children, wherever they are.' The Plan has also led to the development of Australia's first paediatric palliative care clinical guidelines – which will be made public by the end of this year – as well as the nation's first Paediatric End-of-Life Care Communication course for health professionals. This whole suite of work was co-designed with bereaved parents. 'Talking and communicating a terminal diagnosis is difficult and especially so when it involves children and young people,' Annette explained. 'It was very important that we equip and empower our health professionals with the right skills and tools to communicate meaningfully across different stages of the care journey and across diverse cultures.' But Annette is clear: there is still a long way to go. 'Too many children who could benefit from paediatric palliative care are not referred early enough,' she said. 'Systemic barriers like workforce shortages, lack of community-based services, lack of connections between specialists, and the stigma attached to the term 'palliative care' often delay or limit access.' The Plan specifically acknowledges the inequities faced by families outside major cities, those from disadvantaged backgrounds, and children with non-cancer conditions — groups who often miss out on timely care altogether. To tackle this, the Plan recommends workforce training, culturally safe care, and expanding outreach services, including for families in rural and remote areas. Annette also believes it's about reframing how society understands palliative care. 'When palliative care is seen only as end-of-life care, families and health professionals often delay referrals, fearing it means giving up hope,' she explained. 'What's lost is the chance to make memories, and spend the last days, months or years doing what matters most with your loved ones.' For Sara, it's time for the health workforce to face the uncomfortable truth. 'It's about the clinician saying, 'This is not a failure.' It's not a failure to acknowledge that maybe time might be short.' Her hope, like Alix's, is for a cultural shift — one that finally brings children's palliative care out of the shadows. 'If we start teaching kids about death, since they are little, they will take it as natural from childhood into adulthood,' Alix added. And, perhaps, families like hers will no longer have to navigate the unimaginable alone. For anyone seeking further information and resources about paediatric palliative care, start here.