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- Per-Episode Audience
Est. listeners per new episode within ~30 days
1 - 1,000 - Monthly Reach
Unique listeners across all episodes (30 days)
1 - 5,000 - Active Followers
Loyal subscribers who consistently listen
1 - 500
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On the show
Recent episodes
Living with spinal cord injury, with Emma Murray
Jan 23, 2024
56m 08s
The misunderstandings of miscarriage, with Tahyna MacManus
Jan 16, 2024
38m 30s
SUMMER SERIES : Joh Scully and Georgia Barnes on surrogacy
Jan 9, 2024
1h 07m 50s
SUMMER SERIES: Tiff Hall on Plagiocephaly
Jan 2, 2024
41m 06s
SUMMER SERIES: Ilit Golshevsky on Craniosynostosis
Dec 26, 2023
50m 05s
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| Date | Episode | Description | Length | ||||||
|---|---|---|---|---|---|---|---|---|---|
| 1/23/24 | ![]() Living 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 HERECheck out High Performance Mindfulness HEREFor more information on Dr Golly's sleep program or new book head to drgolly.comSee omnystudio.com/listener for privacy information. | 56m 08s | ||||||
| 1/16/24 | ![]() The 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. LINKSTo watch Misunderstandings of Miscarriage, search on SBS or Apple TV. Check out Tahyna on Instagram @tahynamacmanusVisit The Pink Elephant Support Network website HEREThe Pink Elephants Support Network Instagram @pinkelephantssupport See omnystudio.com/listener for privacy information. | 38m 30s | ||||||
| 1/9/24 | ![]() SUMMER 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. | 1h 07m 50s | ||||||
| 1/2/24 | ![]() SUMMER 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. | 41m 06s | ||||||
| 12/26/23 | ![]() SUMMER 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. LINKShttps://www1.racgp.org.au/ajgp/2022/january-february/paediatric-head-shape-and-craniosynostosisSee omnystudio.com/listener for privacy information. | 50m 05s | ||||||
| 12/19/23 | ![]() SUMMER 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. | 51m 17s | ||||||
| 12/12/23 | ![]() The 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. | 49m 37s | ||||||
| 12/5/23 | ![]() The 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. | 50m 36s | ||||||
| 11/28/23 | ![]() The 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. | 44m 57s | ||||||
| 11/21/23 | ![]() The 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. | 45m 46s | ||||||
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| 11/14/23 | ![]() The 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. | 57m 19s | ||||||
| 11/7/23 | ![]() The many challenges of VACTERL, with Skye and Kieran Burke | Skye and Kieran Burke always thought one child would be enough, yet very quickly the desire for another became stronger and they fell pregnant with their son, Jack. But this pregnancy was nothing like they expected. Jack was diagnosed with VACTERL - a group of birth defects that require multiple major surgeries. This week, Skye and Kieran share how they navigated the many days spent in hospital, why Kieran was urged to seek professional help before Jack was born and how they believe a positive mindset is essential when faced with any diagnosis. LINKS Check out Skye and Kieran’s fundraiser Art Helps Heaps https://arthelpsheaps.com/ Art Helps Heaps Instagram https://www.instagram.com/arthelpsheaps/Check out Skye on Instagram https://www.instagram.com/apatchofskye/ See omnystudio.com/listener for privacy information. | 50m 32s | ||||||
| 10/31/23 | ![]() A complication after four caesareans, with Dr Lisa Chimes | Dr Lisa Chimes is no stranger to a surgical procedure as she has performed many on pets featured on Bondi Vet. But after four children via four caesareans, Dr Lisa found herself on the other end of the scalpel. This week, Dr Lisa shares her experience with a post birth complication, the intense procedures that followed and her long road to recovery. LINKS Check out Dr Lisa on Instagram https://www.instagram.com/drlisachimes/Check out the DOG range by Dr Lisa https://dogbydrlisa.com/ See omnystudio.com/listener for privacy information. | 47m 09s | ||||||
| 10/24/23 | ![]() 3 boys with Level 3 autism, with Kathrine Peereboom | In the early days of raising three young boys with Level 3 Autism, Katherine Peereboom found that access to support was difficult. Determined to make a difference, Kathrine took matters into her own hands. This week, Kathrine shares how she juggles caring for her family, running a world-leading disability organisation and how she is working to build the brightest future possible for her boys. LINKS Check out Kathrine on Instagram https://www.instagram.com/kathrinepeereboom/Kathrine’s website https://www.kathrinepeereboom.com/about Spectrum Support on Instagram https://www.instagram.com/spectrumsupport/Spectrum Support website https://www.spectrumsupport.org/ Autism Spectrum Australia https://www.autismspectrum.org.au/ See omnystudio.com/listener for privacy information. | 59m 20s | ||||||
| 10/17/23 | ![]() Living with the restrictions of Phenylketonuria, with Yolanda Shennan | When Yolanda Shennan fell pregnant with her first born, Hudson, she envisioned all the foods she would get to cook for him. But only days after he was born, Hudson was diagnosed with a rare genetic disorder called phenylketonuria (PKU) leaving him to lead a life on an incredibly restricted diet to survive. This week, Yolanda shares the many challenges of managing Hudson's diet and how she’s raising her son to be the most resilient he can be. LINKS Check out Hudson's food journey on Instagram https://instagram.com/pku_mumma_melbourne?igshid=MzRlODBiNWFlZA==Check out MDDA Australia https://www.instagram.com/mdda_australia/For more information on Phenylketonuria and other metabolic conditions, and how to support families like Yolanda’s, please go to: https://mdda.org.au/ See omnystudio.com/listener for privacy information. | 1h 00m 11s | ||||||
| 10/10/23 | ![]() The silent loss of stillbirth, with Bel and Rory Sloane | At 34 weeks pregnant, Bel Sloane and husband Rory Sloane noticed they hadn’t felt any kicks one day and scheduled in a scan. The couple were given the devastating news that there was no heartbeat. Their son Leo had passed This week Bel and Rory recount their journey from that heart-wrenching day, to where their family stands today, five years later. LINKS Check out Bel on Instagram https://www.instagram.com/bel_sloane/?img_index=6Check out Rory on Instagram https://www.instagram.com/rorysloane/Red Nose Australia Instagram https://www.instagram.com/rednoseaustralia/Red Nose Australia website https://rednose.org.au/ See omnystudio.com/listener for privacy information. | 51m 35s | ||||||
| 10/3/23 | ![]() Understanding Cystic Fibrosis, with Reggie Bird | Two-time Big Brother winner Reggie Bird has always come across as a bit of a tough nut, but that’s because she’s had to be. For fourteen years she’s been battling to keep her son Lucas alive. Lucas was just one month old when he was diagnosed with cystic fibrosis. This week, Reggie shares how she manages Lucas’s condition alongside her own health issues and how she stays her bubbly and positive self through it all. LINKS Check out Reggie on Instagram - https://www.instagram.com/reggiebirdbb/ Cystic Fibrosis Australia Instagram - https://www.instagram.com/cfaustralia/CF Facebook - https://www.facebook.com/CFCCAUST CF Website - https://www.cysticfibrosis.org.au/ See omnystudio.com/listener for privacy information. | 32m 53s | ||||||
| 9/26/23 | ![]() Fighting Cerebral Palsy together, with Youssef Dib | Youssef Dib is a pro boxer who comes from a family of boxing champions. But Youssef’s son, Jibreel, is possibly the toughest in the family. When Jibreel was only 8 months old he was diagnosed with cerebral palsy – a disorder that affects a person's ability to move and maintain balance and posture. This week, Youssef shares his journey from being told that Jibreel would not live long, to being in denial of his son’s diagnosis, to helping him be the fighter he was born to be. LINKS Check out Youssef on Instagram - https://www.instagram.com/uwee_dib/Cerebral Palsy Alliance Instagram - https://www.instagram.com/cpalliance/ Support STEPtember https://www.instagram.com/steptemberau/ Facebook - https://www.facebook.com/cerebralpalsyalliance See omnystudio.com/listener for privacy information. | 45m 58s | ||||||
| 9/19/23 | ![]() Postnatal anxiety in dads, with Michael Brunelli and Martha Kalifatidis | Michael Brunelli has lived with anxiety for a long time, but when he became a father it got much worse. This week, MAFS duo Michael and Martha talk to Dr Golly about how this anxiety has at times come between them, how it has affected the way he fathers and why Michael says he is unlikely to get professional help. LINKS Martha’s Instagram https://www.instagram.com/marthaa__k/Michael’s Instagram https://www.instagram.com/mbrunelli/ SMS 4 Dad’s https://www.sms4dads.com.au/ SMS 4 Dad's Instagram https://www.instagram.com/pandanational PANDA https://panda.org.au/get-support/support-dadsSee omnystudio.com/listener for privacy information. | 40m 55s | ||||||
| 9/12/23 | ![]() Diagnosed with a rare blood cancer at 7, with Samantha Sanfilippo | The word “cancer” strikes fear into the hearts of most... but imagine hearing it applied to your child. A week before his 7th birthday Samantha Sanfilippo’s son, Noah, was diagnosed with a rare blood cancer, anaplastic large cell lymphoma. Today, Samantha shares her story of coming to terms with the life changing diagnosis and how she faced up to the many challenges of supporting a seriously unwell child. LINKS Samantha's Instagram - https://www.instagram.com/samanthasanfilippo4/ Leukaemia Foundation - https://www.leukaemia.org.au/get-involved/blood-cancer-month/ Instagram - https://www.instagram.com/leukaemia_foundation/Facebook https://www.facebook.com/LeukaemiaFoundation See omnystudio.com/listener for privacy information. | 48m 36s | ||||||
| 9/5/23 | ![]() Talking puberty and education, with Yumi Stynes and Dr Melissa Kang | Do you remember learning about puberty and ? What were those conversations like? For Yumi Stynes and Dr Melissa Kang discussions around puberty and were awkward and even unpleasant. They are now on a mission to transform this experience for today's children. Sitting down with Dr Golly, Yumi and Dr. Kang talk about how different puberty is for kids today, and give tips on how we can open up the conversation with our own children. LINKS https://www.instagram.com/yumichild/https://www.booktopia.com.au/welcome-to--melissa-kang/book/9781760509538.html?irclickid=wTIyu6xEaxyPTVzXaV2GGV6VUkFyNFU%3AtXyuwY0&utm_campaign=Yumi%20Stynes&utm_medium=affiliate&utm_source=Impact&bk_source=1431742&bk_source_id=1431742&irgwc=1 See omnystudio.com/listener for privacy information. | 42m 20s | ||||||
| 8/29/23 | ![]() The gift of life via surrogacy, with Joh Scully and Georgia Barnes | Joh Scully had tried every possible way to fall pregnant when she decided that surrogacy was her last chance. In Australia, surrogacy has to be altruistic. That is - you can only attempt surrogacy if someone is willing to carry your child out of the goodness of their heart. For Joh that “someone” turned out to be her good friend, Georgia Barnes. This week Georgia and Joh share their experience of surrogacy with all its emotional challenges, and how together they made what felt impossible, possible. LINKS https://www.betterhealth.vic.gov.au/health/healthyliving/surrogacy https://www.surrogacyaustralia.org/ See omnystudio.com/listener for privacy information. | 1h 08m 30s | ||||||
| 8/22/23 | ![]() Unfiltered: Living with Tourette Syndrome, with Mandy Maysey | How would you cope if your child sporadically swore at strangers or made obscene gestures at family dinners? Mandy Maysey is a mum who understands how challenging it can be to raise a child with Tourette’s Syndrome. She has three children with the syndrome and is President of Tourette Syndrome Association of Australia (TSAA), This week, Mandy explains what it’s like to live with three kids with different presentations of Tourette’s Syndrome and reveals the unique perspectives she's gained through her roles as both a parent and an advocate. LINKShttps://www.instagram.com/tsassociation_australia/ https://tourette.org.au/ See omnystudio.com/listener for privacy information. | 41m 00s | ||||||
| 8/15/23 | ![]() Snoring babies and sleep apnoea, with Kylie and Jonathan Brown. | In the beginning, Kylie and Jonathan Brown thought it was cute that their youngest and smallest child, Macy, was a loud snorer. But snoring in children can be serious, leading to sleepless nights, trouble breathing, gut issues and in their daughter’s case, intrusive surgery to fix it. Today, the couple sit down with Dr Golly (the Brown’s very own paediatrician) to talk about the signs to look out for in snoring babies. LINKS https://www.rch.org.au/kidsinfo/fact_sheets/childhood_obstructive_sleep_apnoea_osa/https://www.instagram.com/kylie_m_brown/ https://www.instagram.com/jonathan16brown/ See omnystudio.com/listener for privacy information. | 37m 22s | ||||||
| 8/8/23 | ![]() Miller-Dieker syndrome and celebrating the life of Lily, with Priyanka Saha | When Priyanka Saha attended her final pregnancy scan, she was told that her baby wouldn’t live very long. Lily was diagnosed with Miller Dieker Syndrome - a rare disorder that causes the outer part of a child's brain (the cerebral cortex) to be smooth causing severe developmental issues. Despite the heart-wrenching prognosis and knowing that Lily only had a limited time on earth, Priyanka and her husband made it their mission to make every day special. LINKS https://www.instagram.com/the_lilyflower/ https://lilycalvert.com/ https://www.vsk.org.au/ https://www.instagram.com/veryspecialkids/?hl=en See omnystudio.com/listener for privacy information. | 52m 27s | ||||||
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Chart Positions
4 placements across 2 markets.
Chart Positions
4 placements across 2 markets.


























