- 56 minutes 8 secondsLiving with spinal cord injury, with Emma Murray
Seven years ago mindfulness coach Emma Murray had to put her training to the test when her eldest son, Will, had an accident that left him paralysed from the chest down.
This week, Emma shares the story of that fateful day and how she must continually master the art of acceptance to keep on going.LINKS
Check out Emma on Instagram HERE
Check out High Performance Mindfulness HERE
For more information on Dr Golly's sleep program or new book head to drgolly.comSee omnystudio.com/listener for privacy information.
23 January 2024, 6:00 pm - 38 minutes 30 secondsThe misunderstandings of miscarriage, with Tahyna MacManus
When Tahyna MacManus experienced her first miscarriage, she was shocked to find out how common it was. After her second miscarriage, she decided to make a documentary.
This week, Tahyna shares the story of her three miscarriages, the insights that she gained from conversations with other women during the making of her documentary and where her family is today.LINKS
To watch Misunderstandings of Miscarriage, search on SBS or Apple TV.
Check out Tahyna on Instagram @tahynamacmanus
Visit The Pink Elephant Support Network website HERE
The Pink Elephants Support Network Instagram @pinkelephantssupportSee omnystudio.com/listener for privacy information.
16 January 2024, 7:00 pm - 1 hour 7 minutesSUMMER SERIES : Joh Scully and Georgia Barnes on surrogacy
Happy holidays and welcome to our Summer Series! Whilst we're on break, we've handpicked some of our favourite episodes for your summer holiday listening.
This episode features Joh Scully and her best friend AND surrogate, Georgia Barns. This is the story of how together they were able to make Joh’s dream of being a mother come true.
LINKS
https://www.betterhealth.vic.gov.au/health/healthyliving/surrogacy
https://www.surrogacyaustralia.org/See omnystudio.com/listener for privacy information.
9 January 2024, 7:00 pm - 41 minutes 6 secondsSUMMER SERIES: Tiff Hall on Plagiocephaly
Happy holidays and welcome to our Summer Series! Whilst we're on break, we've handpicked some of our favourite episodes for your summer holiday listening.
This week's episode features fitness instructor extraordinaire, Tiffany Hall. Here, Tiff shares what happened when her daughter Vada was born with Plagiocephaly - which in simple terms it means ‘flat head.'
LINKS
https://raisingchildren.net.au/newborns/health-daily-care/health-concerns/plagiocephaly
https://mytxo.com/
https://www.instagram.com/tiffhall_xo/See omnystudio.com/listener for privacy information.
2 January 2024, 7:00 pm - 50 minutes 5 secondsSUMMER SERIES: Ilit Golshevsky on Craniosynostosis
Happy holidays and welcome to our Summer Series! Whilst we're on break, we've handpicked some of our favourite episodes for your summer holiday listening.
This episode features Dr Golly's wife, Ilit Golshevsky. Together, they share the story of their youngest daughter, Pia, who was born with a birth defect called Craniosynostosis.
LINKS
https://www1.racgp.org.au/ajgp/2022/january-february/paediatric-head-shape-and-craniosynostosisSee omnystudio.com/listener for privacy information.
26 December 2023, 7:00 pm - 51 minutes 17 secondsSUMMER SERIES: Hamish McLachlan on West Syndrome
Happy holidays and welcome to our Summer Series! Whilst we're on break, we've handpicked some of our favourite episodes for your summer holiday listening.
This episode features sports broadcaster, Hamish McLachlan whose daughter Milla was diagnosed with West Syndrome.
LINKS:
https://rarediseases.org/rare-diseases/west-syndrome/See omnystudio.com/listener for privacy information.
19 December 2023, 7:00 pm - 49 minutes 37 secondsThe unique challenge of childhood stroke, with Denton Pugh
Denton Pugh was in the middle of an important presentation when he received a message from his wife to say their four-year-old son, Rocky, had a lump in his brain. Further investigation revealed that Rocky had in fact suffered multiple childhood strokes.
This week, Denton shares what happened that fateful day, the heartbreaking reality of Rocky’s future and how the family are doing today.LINKS
For more info, check out the Stroke Foundation websiteSee omnystudio.com/listener for privacy information.
12 December 2023, 7:00 pm - 50 minutes 36 secondsThe harsh assumptions around Down Syndrome, with Julie Mathers
Julie Mathers was 12 weeks pregnant with her first son, Woody, when she and her husband were told that he had Down Syndrome. The same day, they were confronted with the option to terminate the pregnancy. This week, Julie opens up about the process of making the decision to go forward and how 5 years later they have never looked back.
LINKS
Check out Julie on Instagram https://www.instagram.com/juliemathers/
Check out Snuggle Hunny https://www.instagram.com/snugglehunnykids/
For more info on Down Syndrome, visit Down Syndrome Australia https://www.downsyndrome.org.au/
See omnystudio.com/listener for privacy information.
5 December 2023, 7:00 pm - 44 minutes 57 secondsThe invisible disability of foetal alcohol spectrum disorder (FASD), with Sophie
When Sophie discovered she was pregnant, she was filled with joy but also concern as she thought back to the nights that she had enjoyed a glass of wine before knowing she was expecting. Fourteen years later, her son was diagnosed with foetal alcohol spectrum disorder (FASD). This week, Sophie shares the struggles her son faces, how she and her husband have supported him and her passion to break down the stigmas surrounding FASD.
LINKS
Check out NOFASD on Instagram https://www.instagram.com/nofasd.australia/
For more information on FASD check out https://www.nofasd.org.au/
For the FASD free helpline call 1-800-860-6113
Check out Every Moment Matters website https://everymomentmatters.org.au/See omnystudio.com/listener for privacy information.
28 November 2023, 7:00 pm - 45 minutes 46 secondsThe road to diagnosis of Sanfilippo Syndrome, with Sarah Warden
Sarah Warden knew that her son, Callum wasn’t progressing as he should, but she could never have predicted what was causing the delays. Callum’s final diagnosis was Sanfilippo Syndrome, a rare genetic condition described as ‘childhood dementia’. This week, Sarah talks about how she had to persevere to get the right diagnosis, and what this rare condition means for her life and her family.
LINKS
Check out the Sanfilippo Children’s Foundation on Instagram https://www.instagram.com/sanfilippochildrensfoundation/
To visit the Sanfilippo Children’s Foundation website click HERE
To donate to Sarah’s fundraiser click HERESee omnystudio.com/listener for privacy information.
21 November 2023, 7:00 pm - 57 minutes 19 secondsThe reality of severe eczema and anaphylaxis, with Alexis Bree
For the past six years, Alexis Bree has faced the relentless challenges that come with her son's severe eczema and severe anaphylaxis. These conditions have led to countless sleepless nights, heightened vigilance in everyday environments, and the constant feeling of being an overprotective parent.
This week, Alexis shares how she has embraced being a pedantic parent, the extra precautions she must take to keep her son safe and how other parents with young children can help do their part in creating a safe environment for all.LINKS
Check out Alexis on Instagram https://www.instagram.com/alexis_bree/
Allergic Australia Instagram https://www.instagram.com/allergicaustralia/
Allergic Australia https://allergyfacts.org.au/
Ezcema Aus Instagram https://www.instagram.com/eczemaau/
Ezcema Aus website https://www.eczema.org.au/See omnystudio.com/listener for privacy information.
14 November 2023, 9:42 pm - More Episodes? Get the App