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
Tue, January 23, 2024
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 privacy information.
Tue, January 16, 2024
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 Elephant Support Network website HERE The Pink Elephants Support Network Instagram @pinkelephantssupport See omnystudio.com/listener for privacy information.
Tue, January 09, 2024
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.
Tue, January 02, 2024
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.
Tue, December 26, 2023
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.
Tue, December 19, 2023
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.
Tue, December 12, 2023
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 information.
Tue, December 05, 2023
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.
Tue, November 28, 2023
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.
Tue, November 21, 2023
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 HERE See omnystudio.com/listener for privacy information.
Tue, November 14, 2023
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.
Tue, November 07, 2023
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.
Tue, October 31, 2023
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.
Tue, October 24, 2023
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.
Tue, October 17, 2023
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.
Tue, October 10, 2023
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/ Red Nose Australia Instagram https://www.instagram.com/rednoseaustralia/ Red Nose Australia website https://rednose.org.au/ See omnystudio.com/listener for privacy information.
Tue, October 03, 2023
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.
Tue, September 26, 2023
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.
Tue, September 19, 2023
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-dads See omnystudio.com/listener for privacy information.
Tue, September 12, 2023
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.
Tue, September 05, 2023
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.
Tue, August 29, 2023
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.
Tue, August 22, 2023
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. LINKS https://www.instagram.com/tsassociation_australia/ https://tourette.org.au/ See omnystudio.com/listener for privacy information.
Tue, August 15, 2023
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.
Tue, August 08, 2023
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.
Tue, August 01, 2023
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-daily-care/health-concerns/plagiocephaly https://mytxo.com/ https://www.instagram.com/tiffhall_xo/ See omnystudio.com/listener for privacy information.
Tue, July 25, 2023
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.
Tue, July 18, 2023
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.autismspectrum.org.au/ https://www.healthdirect.gov.au/autism See omnystudio.com/listener for privacy information.
Tue, July 11, 2023
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 Australia, and the difficulties he experienced as both a parent and a doctor. LINKS: https://www.braininjuryaustralia.org.au/ See omnystudio.com/listener for privacy information.
Tue, July 04, 2023
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 relationship and how it has shaped their family LINKS https://www1.racgp.org.au/ajgp/2022/january-february/paediatric-head-shape-and-craniosynostosis See omnystudio.com/listener for privacy information.
Tue, June 27, 2023
Step parenting and blended families, with Melissa Ambrosini
Best-selling author and podcaster Melissa Ambrosini was not thinking about blended families when she met the love of her life. But that became her reality once she married Nick Broadhurst (a founding member of Sneaky Sound System) who already had a son from a previous marriage. In this candid conversation, Melissa shares her personal journey and reveals invaluable insights gained from her own experience as a step-parent. LINKS https://melissaambrosini.com/ https://www.instagram.com/melissaambrosini/ https://www.timemagic.me/ See omnystudio.com/listener for privacy information.
Tue, June 20, 2023
Embracing neurospicy brains and being a nonconforming ADHD-er, with Em Rusciano
Em Rusciano doesn’t want to be called an advocate, but she does want you to know that the systems in place for neurodivergent girls and women aren’t good enough. Em was diagnosed with ADHD after her son went through the diagnostic process. Since then her eldest daughter Odette has also been diagnosed. Em explains to Dr Golly why she thinks occupational therapy skates too close to conversion therapy, and how she’d change the way we help neurodivergent kids. LINKS: www.emrusciano.com Em’s National Press Club Speech https://www.youtube.com/watch?v=4v88Wd20GiU Em’s podcast https://www.instagram.com/emsolationpodcast/ and Insta https://www.instagram.com/emrusciano/ AUTISM LINKS: https://www.amaze.org.au/ https://www.healthdirect.gov.au/attention-deficit-disorder-add-or-adhd https://www.rch.org.au/kidsinfo/fact_sheets/Autism_spectrum_disorder/ See omnystudio.com/listener for privacy information.
Tue, June 13, 2023
Explaining serious illness, separation and loss, with Erin Molan
When Erin Molan and her ex-partner Sean Ogilvy decided to separate, they moved into the same apartment building for the first six months to ensure their daughter Eliza would be okay. And while they both put Eliza first, the challenge of single parenting hit Erin hardest when Eliza became dangerously unwell one night. Erin talks to Dr Golly about how she has handled the hurdles she’s faced as a single parent, including the loss of her beloved dad. See omnystudio.com/listener for privacy information.
Tue, June 06, 2023
Sleep deprivation when you’re an elite athlete, with Jordan Lewis and Jarryd Roughead
Most parents struggle to get through a normal day after a night tending to a crying baby, but imagine if your job relied on elite athletic performance! Former AFL stars Jordan Lewis and Jarryd Roughead open up to Dr Golly about the impact having children had on their sporting careers. LINK: https://www.sms4dads.com.au/ See omnystudio.com/listener for privacy information.
Tue, May 30, 2023
Dealing with a double diagnosis post birth, with Jacqueline Alwill
Nutritionist Jacqueline Alwill’s world turned upside down when her daughter Amelie was diagnosed with hip dysplasia, requiring an immediate brace to be applied. While navigating the challenge of managing her in a brace, incredibly - Jacqueline herself was diagnosed with the exact same condition - missed in her own childhood. Currently recovering from a double hip replacement surgery, Jacqueline opens up to Dr Golly about the challenges of getting the same diagnosis as her baby, and how she managed both recoveries. LINKS: https://www.instagram.com/brownpapernutrition/ https://www.pregnancybirthbaby.org.au/hip-dysplasia-in-babies See omnystudio.com/listener for privacy information.
Tue, May 23, 2023
The secret life of stay-at-home dads, with Steph Claire Smith and Josh Miller
Entrepreneur and co-host of KICPOD and KICBUMP Steph Claire Smith always knew she would go back to work after she had her first child. It made sense to her and her husband, Josh Miller, that he would become the stay-at-home parent. Steph and Josh talk to Dr Golly about how their non-traditional family dynamic still cops flak, and how they make it work for their little family. LINKS: https://www.instagram.com/stephclairesmith/?hl=en https://www.instagram.com/itsjoshmiller/ See omnystudio.com/listener for privacy information.
Tue, May 16, 2023
Navigating the pitfalls of social media, with Rachael Finch
Social media star and model Rachael Finch knows how cutting online criticism can get. She’s copped her fair share of comments over the years, but she says that when trolls target her children, it cuts even deeper. Rachael talks to Dr Golly about how she and her husband Michael manage trolls, why she continues to post on social media and why she’s super vigilant with her own children when they go online. LINKS: https://www.instagram.com/rachael_finch/ https://www.esafety.gov.au/parents/issues-and-advice/are-they-old-enough See omnystudio.com/listener for privacy information.
Tue, May 09, 2023
Surviving peri and post-natal depression, with Sophie Pearce and Jayde Couldwell
Popular podcasters from Beyond the Bump Sophie Pearce and Jayde Couldwell might look like they have it all together but both had to overcome significant challenges in their pregnancies. Anxiety, depression and the overwhelming impact of hyperemesis gravidarum (HG) made pregnancy and juggling childcare extremely difficult. Sophie and Jayde open up to Dr Golly about their experiences and how their friendship helped them survive it all. LINKS: https://panda.org.au/ https://www.pregnancybirthbaby.org.au/severe-vomiting-during-pregnancy-hyperemesis-gravidarum See omnystudio.com/listener for privacy information.
Tue, May 02, 2023
How childhood trauma can impact birth, with Moana Hope and Isabella Carlstrom
There aren’t many couples who can say they both know what it’s like to give birth. Former AFLW player, Survivor contestant and author Moana Hope and her wife model Isabella Carlstrom have each been through pregnancy and birth, though they were very different experiences. Moana and Isabella talk to Dr Golly about the impact of childhood trauma on their lives as parents, and how their unique understanding of birth helped them overcome it. LINKS: https://www.rch.org.au/kidsinfo/fact_sheets/Bronchiolitis/ https://birthtrauma.org.au/ See omnystudio.com/listener for privacy information.
Tue, April 25, 2023
Hamish McLachlan and his miracle daughter
At just six months old McLachlan’s daughter Milla started having seizures. What McLachlan and his wife referred to as “twitches” turned out to be West Syndrome, a rare form of epilepsy. McLachlan was told that Milla had a 10% chance of dying in the hospital, 80% chance of having brain damage for life, and just 10% chance of being unscathed. LINKS: https://rarediseases.org/rare-diseases/west-syndrome/ https://drgolly.com/ See omnystudio.com/listener for privacy information.
Tue, April 18, 2023
Dr Golly and The Experts – launches April 26
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. * Launches 26th April, new episode every week! See omnystudio.com/listener for privacy information.
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