Dr Golly and the Experts - podcast cover

Dr Golly and the Experts

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
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Episodes

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 HERE Check out High Performance Mindfulness HERE For more information on Dr Golly's sleep program or new book head to drgolly.com See omnystudio.com/listener for priva...

Jan 23, 202456 minEp. 20

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. LINKS To watch Misunderstandings of Miscarriage, search on SBS or Apple TV. Check out Tahyna on Instagram @tahynamacmanus Visit The Pink ...

Jan 16, 202439 minEp. 19

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....

Jan 09, 20241 hr 8 minEp. 18

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...

Jan 02, 202441 minEp. 17

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. LINKS https://www1.racgp.org.au/ajgp/2022/january-february/paediatric-head-shape-and-craniosynostosis See omnystudio.com/listener for privacy information....

Dec 26, 202350 minEp. 16

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....

Dec 19, 202351 minEp. 15

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 website See omnystudio.com/listener for privacy informa...

Dec 12, 202350 minEp. 14

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...

Dec 05, 202351 minEp. 13

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/nofa...

Nov 28, 202345 minEp. 12

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/sanfilippochildr...

Nov 21, 202346 minEp. 11

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 creat...

Nov 14, 202357 minEp. 10

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 m...

Nov 07, 202351 minEp. 9

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 omnystu...

Oct 31, 202347 minEp. 8

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 ht...

Oct 24, 202359 minEp. 7

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 htt...

Oct 17, 20231 hrEp. 6

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=6 Check out Rory on Instagram https://www.instagram.com/rorysloane/...

Oct 10, 202352 minEp. 5

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/ Cys...

Oct 03, 202333 minEp. 4

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 Youss...

Sep 26, 202346 minEp. 3

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 h...

Sep 19, 202341 minEp. 2

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 Found...

Sep 12, 202349 minEp. 1

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.co...

Sep 05, 202342 minEp. 20

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, possib...

Aug 29, 20231 hr 9 minEp. 19

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 throug...

Aug 22, 202341 minEp. 18

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...

Aug 15, 202337 minEp. 17

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_lilyflo...

Aug 08, 202352 minEp. 16

Plagiocephaly and helmet-wearing babies, with Tiff Hall

Renowned fitness instructor, podcaster and author Tiffiny Hall was told not to worry about her daughter's flat head and that she would grow into it. Tiff’s intuition said otherwise and led to a journey with her daughter being diagnosed with plagiocephaly. For the first time, Tiffiny opens up about the challenges she faced while navigating this condition, shedding light on the importance of early detection and to always follow your “Mum gut”. LINKS https://raisingchildren.net.au/newborns/health-d...

Aug 01, 202342 minEp. 15

Coping with Sudden Infant Death Syndrome, with Keren Ludski

Keren Ludski is the CEO of Red Nose, Australia’s leading authority on safe sleep and safer pregnancy advice, and bereavement support for anyone affected by miscarriage or the death of a baby or child. In this episode, Keren shares her personal story, the story that led her to become involved with Red Nose, and to help other families. LINKS: https://rednose.org.au/ See omnystudio.com/listener for privacy information....

Jul 25, 20231 hr 1 minEp. 14

The Autism Spectrum and juggling siblings, with Christie Hayes

Christie Hayes is an actress and radio host who makes her living talking. But when her son Hendrix was still very small, she learned that communication was going to look different for him. Hendrix was diagnosed with Level 2 Autism at 18 months old. Opening up to Dr Golly, Christie talks about how she stopped being scared by the word ‘autism’ and why she decided to be so public about his diagnosis. LINKS: https://www.instagram.com/christiehayes_/ https://www.amaze.org.au/ https://www.autismspectr...

Jul 18, 202350 minEp. 13

Traumatic brain injury and recovery, with Dr Norman Swan

Seven years ago, broadcaster and investigative journalist Dr Norman Swan, along with his family, took a holiday to Italy. Little did he know that this trip would take an unexpected turn, as one of his children suffered a severe head injury and ended up in the hospital. Norman's daughter, Anna, had been riding her bike without a helmet when she was in an accident. Norman shares the challenges he faced while dealing with his daughter's injury in a foreign country, ensuring her safe return to Austr...

Jul 11, 202329 minEp. 12

Craniosynostosis: Dealing with serious surgery for your baby, with Ilit Golshevsky

Today’s episode is one close to Dr Golly’s heart. His third child Olympia was born with a condition called Craniosynostosis. This meant that the bones in her skull weren’t developing as they should, and that Pia would need to have serious, intensive surgery. In this unique and introspective episode, Dr. Golly invites his wife Ilit Golshevsky onto the show. Together they open up about their individual struggles and for the first time, candidly reflect on the impact this experience had on their re...

Jul 04, 202352 minEp. 11
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