рдЗрд╕ рдкреЙрдбрдХрд╛рд╕реНрдЯ рдХреА рдЬрд╛рдирдХрд╛рд░реА 🔗

рд╣реЛрд╕реНрдЯ:
рдЕрджреНрдпрддрди рдЖрд╡реГрддреНрддрд┐:
every 10 days
рдФрд╕рдд рдСрдбрд┐рдпреЛ рд▓рдВрдмрд╛рдИ:
40 minutes
рдЕрддрд┐рдерд┐ рд╕рд╛рдХреНрд╖рд╛рддреНрдХрд╛рд░
рдЕрдВрдЧреНрд░реЗрдЬрд╝реА
рд╕рдВрдпреБрдХреНрдд рд░рд╛рдЬреНрдп рдЕрдорд░реАрдХрд╛
90 рдПрдкрд┐рд╕реЛрдб
3 рдЕрдХреНрдЯреВрдмрд░ 2023
episodic

рдирд╡реАрдирддрдо рдПрдкрд┐рд╕реЛрдб 🔗

Let's Talk MND - Peta Harding, OT

· рдЕрдиреБрд▓рд┐рдкрд┐
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.

рдкрд┐рдЫрд▓реЗ рдПрдкрд┐рд╕реЛрдбреНрд╕ рдЦреЛрдЬреЗрдВ

Let's Talk MND рдХреЗ рдкрд┐рдЫрд▓реЗ рдПрдкрд┐рд╕реЛрдб рдЦреЛрдЬреЗрдВред

рдкрд┐рдЫрд▓реЗ рдПрдкрд┐рд╕реЛрдб

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 oтАж
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 theyтАЩve learned alongтАж
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 тАФ not just for you, but for your family and future generations. He talks about genetic testing and counselling, navigating converтАж
In this episode, IтАЩm joined by Sarah Shuttlewood, who shares her familyтАЩs journey following her father PeterтАЩs diagnosis with MND. Sarah speaks openly about navigating MND from a daughterтАЩs perspective тАФ the shock of diagnosis, supporting her children through their grandfatherтАЩs illness, and the cтАж
Professor Tom Oxley In this episode, IтАЩm joined by Professor Tom Oxley, CEO and co-founder of Synchron, a company pioneering brain-computer interface technology. We discuss how SynchronтАЩs Brain Computer Implant is helping people living with Motor Neurone Disease regain independence by enabling theтАж

Let's Talk MND - Marlene Answer-Lewis & Nicole Answer

In this episode, IтАЩm 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 challeтАж
Professor Tom Oxley In this episode, IтАЩm joined by Professor Tom Oxley, CEO and co-founder of Synchron, a company pioneering brain-computer interface technology. We discuss how SynchronтАЩs Brain Computer Implant is helping people living with Motor Neurone Disease regain independence by enabling theтАж
Tom Oxley In this episode, IтАЩm joined by Professor Tom Oxley, CEO and co-founder of Synchron, a company pioneering brain-computer interface technology. We discuss how SynchronтАЩs Brain Computer Implant is helping people living with Motor Neurone Disease regain independence by enabling them to contrтАж
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 coтАж
рдЕрд╕реНрд╡реАрдХрд░рдг: рдЗрд╕ рдкреГрд╖реНрда рдкрд░ рдПрдореНрдмреЗрдбреЗрдб рдкреЙрдбрдХрд╛рд╕реНрдЯ рдФрд░ рдХрд▓рд╛рдХреГрддрд┐ Jane Simpson рд╕реЗ рд╣реИрдВ, рдЬреЛ рдЗрд╕рдХреЗ рдорд╛рд▓рд┐рдХ рдХреА рд╕рдВрдкрддреНрддрд┐ рд╣реИ рдФрд░ Listen Notes, Inc. рд╕реЗ рд╕рдВрдмрджреНрдз рдпрд╛ рд╕рдорд░реНрдерд┐рдд рдирд╣реАрдВ рд╣реИред