Dr Golly

Dr Golly and the Experts

Kids EN ↓ 41 episodios

We all go into parenting as beginners. But imagine the learning curve when things don’t go to plan. Dr Golly delves into the hard-earned wisdom of parents who have faced tough times and come out the other side as… the Experts. For more info about Dr Golly check out his website: drgolly.com

Autor

Dr Golly

Categoría

Kids

Web del podcast

admin6wc.podbean.com

Último episodio

23 de ene. de 2024

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Episodios

Living with spinal cord injury, with Emma Murray 23.01.2024

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 inform...

The misunderstandings of miscarriage, with Tahyna MacManus 16.01.2024

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...

SUMMER SERIES : Joh Scully and Georgia Barnes on surrogacy 09.01.2024

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...

SUMMER SERIES: Tiff Hall on Plagiocephaly 02.01.2024

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/...

SUMMER SERIES: Ilit Golshevsky on Craniosynostosis 26.12.2023

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/paediat...

SUMMER SERIES: Hamish McLachlan on West Syndrome 19.12.2023

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.

The unique challenge of childhood stroke, with Denton Pugh 12.12.2023

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...

The harsh assumptions around Down Syndrome, with Julie Mathers 05.12.2023

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/ju...

The invisible disability of foetal alcohol spectrum disorder (FASD), with Sophie 28.11.2023

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 d...

The road to diagnosis of Sanfilippo Syndrome, with Sarah Warden 21.11.2023

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...

The reality of severe eczema and anaphylaxis, with Alexis Bree 14.11.2023

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...

The many challenges of VACTERL, with Skye and Kieran Burke 07.11.2023

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,...

A complication after four caesareans, with Dr Lisa Chimes 31.10.2023

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:/...

3 boys with Level 3 autism, with Kathrine Peereboom 24.10.2023

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.  L...

Living with the restrictions of Phenylketonuria, with Yolanda Shennan 17.10.2023

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 raisi...

The silent loss of stillbirth, with Bel and Rory Sloane 10.10.2023

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....

Understanding Cystic Fibrosis, with Reggie Bird 03.10.2023

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 se...

Fighting Cerebral Palsy together, with Youssef Dib 26.09.2023

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...

Postnatal anxiety in dads, with Michael Brunelli and Martha Kalifatidis 19.09.2023

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 Instag...

Diagnosed with a rare blood cancer at 7, with Samantha Sanfilippo 12.09.2023

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 unwe...

Talking puberty and education, with Yumi Stynes and Dr Melissa Kang 05.09.2023

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 co...

The gift of life via surrogacy, with Joh Scully and Georgia Barnes 29.08.2023

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 o...

Unfiltered: Living with Tourette Syndrome, with Mandy Maysey 22.08.2023

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 d...

Snoring babies and sleep apnoea, with Kylie and Jonathan Brown. 15.08.2023

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...

Miller-Dieker syndrome and celebrating the life of Lily, with Priyanka Saha 08.08.2023

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...

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