이 팟캐스트 소개 🔗
🎙️ Let's Talk MND Hosted by Jane Simpson | #EndMND 💙 Hosted by Jane Simpson, whose late husband Robert fought MND for 10 months, Let's Talk MND shares the real stories of those affected by Motor Neurone Disease. Through heartfelt conversations with people living with MND, their families, carers, and leading experts, the podcast brings together a community of strength, understanding, and hope — proving that even in the darkest times, love and courage shine through.
진행자:
업데이트 빈도:
every 10 days
평균 오디오 길이:
40 minutes
게스트 인터뷰
영어
미국
에피소드 90 개
2023년 10월 3일부터
episodic
최신 에피소드 🔗
In this episode, Peta Hardy, an Occupational Therapist who specialises in MND, and shares insights on how occupational therapy supports individuals with MND.
She discusses assistive technology, home safety, and the importance of a multidisciplinary team to improve quality of life.
이전 에피소드 🔗
In this mind blowing episode, Dr. Amanda Wright and Dr. Lyndal Henden discuss their recent research findings that MND has a 7 times higher prevalence in areas of in Western NSW, compared with the rest of the world!
We explore incidence rates, genetics and environmental factors, and the challenges o…
What happens when you live with MND far longer than expected?
In this special episode, Phil Camden, John Hanley, Matt Stickland and Peter Chambers come together to share their experiences of living with MND over many years.
They talk openly about what keeps them going, what they’ve learned along…
Adam Dowling is living with SOD1 MND, a rare genetic form of motor neurone disease.
In this episode, Adam shares what it means to discover your MND has a genetic cause — not just for you, but for your family and future generations.
He talks about genetic testing and counselling, navigating conver…
In this episode, I’m joined by Sarah Shuttlewood, who shares her family’s journey following her father Peter’s diagnosis with MND.
Sarah speaks openly about navigating MND from a daughter’s perspective — the shock of diagnosis, supporting her children through their grandfather’s illness, and the c…
Professor Tom Oxley
In this episode, I’m joined by Professor Tom Oxley, CEO and co-founder of Synchron, a company pioneering brain-computer interface technology.
We discuss how Synchron’s Brain Computer Implant is helping people living with Motor Neurone Disease regain independence by enabling the…
In this episode, I’m joined by Marlene Lewis and her daughter Nicole to share the story of their husband and father, Shane Lewis, who lived with MND.
Together, they speak candidly about the realities of living with MND in regional Australia, where accessing specialist care can be incredibly challe…
Professor Tom Oxley
In this episode, I’m joined by Professor Tom Oxley, CEO and co-founder of Synchron, a company pioneering brain-computer interface technology.
We discuss how Synchron’s Brain Computer Implant is helping people living with Motor Neurone Disease regain independence by enabling the…
Tom Oxley
In this episode, I’m joined by Professor Tom Oxley, CEO and co-founder of Synchron, a company pioneering brain-computer interface technology.
We discuss how Synchron’s Brain Computer Implant is helping people living with Motor Neurone Disease regain independence by enabling them to contr…
In this episode, Todd Johnson shares his personal journey with MND, the challenges of diagnosis, and his passionate advocacy for improved care and innovation in the sector.
Todd is also the Chair on MND Victoria
Discover insights on care gaps, technological opportunities, and how community and co…
면책 조항: 이 페이지에 포함된 팟캐스트와 작품은 Jane Simpson에서 가져온 것입니다. 이 팟캐스트는 소유자의 재산이며 Listen Notes, Inc.와 제휴하거나 보증하지 않습니다.
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