Empowering yourself as a patient
“I’m a big fan of digital. It’s just the way to go these days as far as monitoring your health,” says Russell Winwood, a triathlete who’s had a severe lung condition for over a decade. He shares ...
“I’m a big fan of digital. It’s just the way to go these days as far as monitoring your health,” says Russell Winwood, a triathlete who’s ...
by Karen Finn Chronic Conditions“I’m a big fan of digital. It’s just the way to go these days as far as monitoring your health,” says Russell Winwood, a triathlete who’s had a severe lung condition for over a decade. He shares ...
• by Karen Finn
Pritpal Kaur was a healthy and active 72-year-old when she suddenly started experiencing pain across her ribs. It was the first in a series of symptoms that led to an unexpected cancer diagnosis. She shares her story below to raise ...
• by Karen Finn
Rachel Murray has seen many advances in asthma treatment over the years, but her biggest hope is that people will understand how serious the condition is. She shares her story with This Is MedTech on World Asthma Day. “I’d ...
• by Karen Finn
Picture by Caroline White When Katie Grant started having hearing difficulties in her early 50s, she was in denial. She reluctantly got hearing aids and was amazed at the transformation that followed. To raise awareness on World Hearing Day, she ...
• by Karen Finn
It’s been a long but rewarding journey for Iuliana Dumitriu, whose 9-year-old son Victor has a rare genetic disorder called Coffin-Lowry syndrome. Now she’s helping other families by connecting them and raising awareness around the world. “When Victor ...
• by Karen Finn
The challenges that Natasha Price has faced over the past 15 years would be insurmountable for most people, but becoming blind and paralysed has only made her stronger. On International Day of Persons with Disabilities, she tells This Is MedTech about ...
• by Karen Finn
Having lived with the HIV her whole life, Doreen Moraa Moracha is determined to educate the public and stop the stigma attached to the viral infection. Her hope is that this will lead to more people taking preventive measures, getting ...
• by Karen Finn
Tim Buckinx was just a teenager when he was diagnosed with a rare blood disorder that changed the trajectory of his life. Now he’s on a mission to help other people with a medical condition to live their best ...
• by Karen Finn
It’s hard to imagine that your watch could save your life, but that’s exactly what happened to Joe Plumb, who was diagnosed with type 1 diabetes as a child. To mark World Patient Safety Day, he shares his story ...
• by Karen Finn
“One minute you wake up fine and you’re ready to start the day and then within the next hour you may have to cancel everything.” This is what every day is like when you live with Sickle Cell Disease, ...
• by Karen Finn
Sam Renke has been challenging misconceptions about disability since she was diagnosed with a rare genetic condition called Osteogenesis Imperfecta (OI), or brittle bone condition, shortly after her birth. “I was born with multiple fractures and I actually fractured in ...
• by Karen Finn
Karen Hoyt had no idea that there was anything wrong with her liver when her feet started swelling one day while she was riding her bike. A high school teacher, adjunct professor and community volunteer with many active hobbies, Karen ...
• by Comms Team
Khadija Stewart-Brown accepted daily insulin injections and finger-prick tests as part of normal life, but then she reached her teens. “I saw the difference between me and my peers and it got annoying,” she says. Khadija has always had to ...
• by Comms Team
Kevin Wake’s mother taught him to become a Sickle Cell Disease expert from a young age. Today, the seasoned patient advocate shares his story with This Is MedTech to mark World Sickle Cell Day. “I was diagnosed when I ...
• by Karen Finn
“They knew I had thalassemia even before I was born, and they knew it was major,” says Amit Ghelani. But with an effective treatment plan, including regular blood transfusions and routine monitoring, Amit, now 35, lives what he happily describes as ...
• by Comms Team
At 43, health researcher Nicola McMeekin was blissfully unaware of her hypertension until she had a life-threatening heart injury. “There was no warning. I was sitting at my desk writing an email when I suddenly had pains in my chest, down ...
• by Karen Finn
“Haemophilia shouldn’t limit what people do,” says Clive Smith, qualified barrister, prominent haemophilia patient advocate and keen sportsman. As if to reinforce his point, Clive has not only competed for Great Britain in the European duathlon championships but is ...
• by Comms Team
“With or without diabetes, there’s nothing you can’t be,” says German field hockey Olympic champion and orthopaedic surgeon Carsten Fischer. But there was a time when Carsten – nicknamed The Man With the Hammer for his ferocious penalty corners – ...
• by Comms Team
Andy Braybrook’s life changed after a near-fatal accident left him permanently paralysed. Three years after his road collision, he is now back on the road and setting his sights even higher. Andy’s story started on the first fine ...
• by Comms Team
Mike Rolls says his golf game is stronger as a bilateral amputee than it ever was when he had both his legs. The 37-year-old Australian has come a long way since a deadly infection called meningococcal septicaemia changed the trajectory ...
• by Karen Finn
Lara Chappell was in complete shock when her one-year-old son Pierre was diagnosed with a rare genetic disorder called Angelman Syndrome. She’d been expressing concerns to multiple health professionals about her baby’s delayed development from the time he ...
• by Comms Team
One phone call from her daughter’s school changed Csilla’s life forever. “The school said that my little girl was feeling ill, so I quickly finished a couple of things at work and rushed to the doctor with my ...
• by Comms Team
Ami Ireland thought her hearing difficulties were just the remnants of a cold. At the time, she didn’t know this was the first in a series of symptoms that would leave her with permanent disabilities and change her life ...
• by Karen Finn
On World AIDS Day, author and Emmy Award winning AIDS activist Rae Lewis-Thornton talks about her decades-long journey with the disease and how medtech innovations have supported her. “I believe I was infected with HIV in 1983,” says Rae. “In the ...
• by Karen Finn
On World Obesity Day, Stefanie Wirtz opens up about her personal struggle with obesity and the turning point that led her to undergo bariatric surgery. “I’ve lived with obesity since childhood, and like most of those affected, I’ve ...
• by Comms Team
As we stride into September marking a new Sickle Cell Awareness Month, Jemela Williams discusses the disease she’s lived with her whole life and shares her hopes for a future world that better understands it. When Jemela was just ...
• by Comms Team
After being hooked up to an antibiotics drip in hospital for three weeks, David John Watson had had enough. However, the life-threatening blood poisoning that he’d developed meant another few weeks of intravenous (IV) antibiotic treatment was necessary. It ...
• by Comms Team
Kim Opszala thought her eczema had returned when a rash appeared on her face, but it was a disease called lupus. She’d been travelling around Australia before starting university in 2005/06 and upon her return Kim noticed the butterfly-shaped rash ...
• by Karen Finn
British author and disability advocate Alice Barker is keen to express her gratitude for the healthcare and medtech “that have enabled me to lead a rich and blessed life.” As someone who has relied heavily on specialised medical care and ...
• by Karen Finn
Gunnar Esiason just celebrated a major milestone: his good health. When you have cystic fibrosis (CF) – a rare genetic disease that creates a build-up of thick sticky mucus in the lungs, digestive system and other organs that can lead to ...
• by Karen Finn
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