Insights from recent episode analysis
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Insights are generated by CastFox AI using publicly available data, episode content, and proprietary models.
Total monthly reach
Estimated from 1 chart position in 1 market.
By chart position
- 🇦🇺AU · Parenting#1475K to 30K
- Per-Episode Audience
Est. listeners per new episode within ~30 days
2.5K to 15K🎙 Weekly cadence·69 episodes·Last published 1mo ago - Monthly Reach
Unique listeners across all episodes (30 days)
5K to 30K🇦🇺100% - Active Followers
Loyal subscribers who consistently listen
1.5K to 9K
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* Data sourced directly from platform APIs and aggregated hourly across all major podcast directories.
On the show
Recent episodes
In Conversation With Claire: Sitting With Uncertainty
Apr 23, 2026
Unknown duration
In Conversation With Ann-Marie
Mar 16, 2026
Unknown duration
In Conversation With Enny
Mar 16, 2026
Unknown duration
Breaking the Silence with Rachel Kelly (TFMR)
Jan 30, 2025
Unknown duration
The TRIS Project and Its Impact
Jan 28, 2025
Unknown duration
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| Date | Episode | Description | Length | ||||||
|---|---|---|---|---|---|---|---|---|---|
| 4/23/26 | In Conversation With Claire: Sitting With Uncertainty | Claire Rowe bravely speaks of her Trisomy journey with her daughter Loreley. Having already faced a still birth she was devastated to find out her next pregnancy wasn’t to be as she hoped. For more information, visit www.soft.org.ukFor more information about screening, visit: https://www.soft.org.uk/in-pregnancy-copy | — | ||||||
| 3/16/26 | In Conversation With Ann-Marie | In this episode, we hear from Ann-Marie who received a diagnosis of Full Trisomy 18 at 20 weeks pregnant; news that would change the course of her pregnancy and her expectations overnight.She speaks candidly about carrying her son Aangsuke with both uncertainty and fierce love, and what it was like when he defied expectations and survived birth. What followed was a new challenge: advocating for him within a medical system that did not always assume intervention was appropriate.With courage and determination, she shares her experience of fighting for certain surgeries and care decisions, navigating complex conversations with professionals while holding onto hope for her child.This is a story not only of diagnosis and difficulty, but of joy, resilience and the profound love that drives a parent to stand firm for their child. It is an honest reflection on what advocacy looks like when the future is unclear and on the unexpected moments of hope that can unfold along the way. | — | ||||||
| 3/16/26 | In Conversation With Enny | In this episode, we’re joined by Enny, who shares the remarkable journey of her daughter Isabelle, now two years old and living with Full Trisomy 13.Enny speaks openly about receiving Isabelle’s diagnosis, navigating pregnancy with uncertainty, and the mixture of fear, love and determination that shaped those early months. She reflects on celebrating Isabelle’s first birthday, a milestone that once felt unimaginable, and what life looks like today as their family prepares for the next chapter: nursery.This conversation is honest and uplifting in equal measure. Enny shares the realities of medical appointments and advocacy, but also the everyday joys, laughter and personality that define Isabelle far beyond her diagnosis. | — | ||||||
| 1/30/25 | Breaking the Silence with Rachel Kelly (TFMR) | Join us as we speak with Rachel Kelly, mum to Avery and Forest, who both had prenatal diagnoses of trisomy 18. Rachel shares her deeply personal journey, including her living with a rare condition called 'balanced translocation' and her decision to pursue TFMR . Through her openness, Rachel aims to break the silence surrounding these experiences and offer support to others navigating similar paths. | — | ||||||
| 1/28/25 | The TRIS Project and Its Impact | Join us as we speak to Dr Bruns, SOFT UK Professional Advisor, Principal Investigator of the TRIS Project, and Retired Professor in the US. Dr Bruns shares her fascinating journey into the world of rare diseases, her involvement with SOFT UK, and her work on updating the TRIS Project - an important initiative dedicated to cataloguing information about babies and children with trisomy conditions. Interested in enrolling? Visit the TRIS Project enrolment page: https://tris.siu.edu/survey/form/PreEnroll.php To reach out to SOFT UK for support or get in contact, visit: https://www.soft.org.uk/getting-support | — | ||||||
| 1/28/25 | Team SOFT UK: Meet the People Behind the Mission | Go behind the scenes with Shaun, Sonia, Kate, and Sarah as they share what it’s like to be part of Team SOFT UK. In this episode, they discuss their roles in supporting families, reflect on the highlights of their time with the charity, and offer a glimpse into the exciting plans and hopes for SOFT UK's future. Don't miss this inspiring conversation with the heart of our organisation! To reach out to SOFT UK for support or get in contact, visit: https://www.soft.org.uk/getting-support | — | ||||||
| 1/28/25 | Baby Nina’s Incredible Journey | Dive into this amazing family story shared by Shakara, and featuring baby Nina herself! Defying medical predictions, Nina continues to thrive and amaze her family and the medical teams supporting her. From the early stages of testing and her birth to life today, this inspiring journey is one you won’t want to miss.To see the Crowdfund support for Shakara, visit: https://www.gofundme.com/f/support-baby-ninaTo reach out to SOFT UK for support or get in contact, visit: https://www.soft.org.uk/getting-support | — | ||||||
| 1/28/25 | Mark and Ruth Jenner’s Story of Love and Loss | Join us for a moving conversation with the remarkable couple, Mark and Ruth Jenner, as they share their family’s story - honouring their newborn Levi and the children they hope to meet again one day. Their refreshing approach to loss and life offers a unique perspective, with beautifully crafted descriptions that help explain concepts even adults find hard to grasp. Mark and Ruth would be happy to connect with others who feel their stories might intersect. If you’d like to reach out, this can be arranged via SOFT UK. This is truly a one-of-a-kind podcast you won’t want to miss. To reach out to SOFT UK for support or get in contact, visit: https://www.soft.org.uk/getting-support | — | ||||||
| 3/13/24 | In Conversation With Mary: The Frailty of a Butterfly (Bereavement) | In today's podcast we are talking with Mary Wasacz about her journey with Cathy Anne. Mary recounts Cathy Anne's story and her diagnosis of Trisomy 18, and how she and her husband John gave her normalcy and love during her short life. Mary will also be reading an excerpt from her book about Cathy Anne's life: The Frailty of a Butterfly: My Journey Through Newborn Loss. You can find Mary's book here: Amazon: https://www.amazon.co.uk/Frailty-Butterfly-Journey-Through-Newborn/dp/1667891715 Bookshop: https://bookshop.org/p/books/the-frailty-of-a-butterfly-my-journey-through-newborn-loss-mary-wasacz/20141396?ean=9781667891712 About Mary: Mary Wasacz is a family therapist and clinical specialist certified by the American Nurses Association. She was the bereavement and spiritual care coordinator for hospice for over twenty years. Mary and her husband have three children and eight grandchildren. She and her husband are avid travelers who have visited all seven continents. They currently live in New York's suburbs, where they dote on their three parrots. To reach out to SOFT UK visit: www.soft.org.uk To contact us, email: contact@soft.org.uk | — | ||||||
| 10/13/23 | Baby Loss Awareness Week 2023: In Conversation with Kate Sonley | In support of Baby Loss Awareness Week 2023 we are talking with Kate Sonley, mummy to Amber. Kate bravely talks about her story, sharing the ins and outs of her journey. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
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| 9/12/23 | From Past To Present: Reflecting on Demi's Trisomy 18 Journey (Bereavement) | Ahead of the annual Scottish Family Day we interviewed one of our longstanding parents Demi Powell who shared her story about Connor, her baby boy who was diagnosed with Trisomy 18, 22 years ago. It was a great insight to how she has found the family days over the years especially what makes the Scottish family day special. To register please sign up here https://www.eventbrite.co.uk/e/scottish-soft-family-day-2023-tickets-645476015137?aff=oddtdtcreator Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 8/10/23 | Embracing the Extraordinary Journey: Positive about Down syndrome | The podcast today is part of our series, chatting to partner organisations to find out more about what they do. This podcast welcomes Nicola Enoch, joining us from Positive about Down Syndrome and she is their Founder & CEO. As a down's syndrome parent herself she set this charity up for families looking for further support and resources. Found out more: https://downsyndromeuk.co.uk/ Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 7/6/23 | Pregnancy after a trisomy 18 diagnosis (Living with trisomy) | We spoke to Mandy Nelson, mother to Amari, who has Trisomy 18 and who recently became a mother to Dante. In this episode, Mandy shares her heartfelt journey from her pregnancy with Amari, to the present day, where Amari is now a thriving 3.5-year-old, albeit with special educational needs. She also took us through what it's like having a baby after a high risk pregnancy and shared honestly about how it impacted her bonding with her son whilst pregnant. She shares some amazing anecdotes and a wonderful message about the importance of advocating for your child. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 6/29/23 | Leaving the hospital with my Rainbow baby | We spoke to Becky Smith, Mum to Freddie who had trisomy 18 and more recently, she became Mum to Jaxon, her Rainbow baby. Becky opens up about her overwhelming fears and anxiety throughout the pregnancy, revealing how she cautiously began preparing for the arrival of her little one only around the 30-week mark. Step into her world and immerse yourself in a real-life story of pregnancy after loss. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 6/21/23 | A Sibling's Path: From Loss to Strength as a Rainbow Baby | Join us for an insightful episode of the SOFT UK podcast as we speak with Jess Scott, whose life has been profoundly influenced as a rainbow baby after the loss of her sister, Sarah, to Patau syndrome. Listen to her remarkable journey, and how it has shaped her relationships, career, and parenting. Be sure to catch her three important messages at the end, delivering a story of honesty and optimism you won't want to miss. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 6/14/23 | Navigating the Complexities of Genetic Counseling: Insights from a Trainee Genetic Counselor | Join us for an enlightening discussion with Beth Hughes, a trainee Genetic Counselor, as we delve into the fascinating world of genetic testing and ethics. In this episode, we explore a range of intriguing topics, including the cutting-edge advancements like Non-Invasive Prenatal Testing (NIPT), the concept of Mainstreaming, and the roll out of improved newborn screening. Beth shares her firsthand experience working with a family grappling with a diagnosis of balanced translocation trisomy 13, shedding light on the emotional complexities and medical considerations involved. Tune in to gain valuable insights into the world of genetic counseling, you're sure to learn something new! *Correction for Podcast Content* Egg and sperm cells normally have 1 copy of a chromosome and join together to make an embryo with 2 copies. If someone has a balanced translocation, sometimes when their DNA replicates and separates to make an egg or a sperm cell, the cell has 2 copies of a chromosome instead of the normal 1. This means when it joins with an egg or sperm cell with 1 copy, the resulting embryo has 3 copies of a chromosome and has a trisomy. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 5/31/23 | Making a Difference: The Power of Volunteering with SOFT UK | In our latest podcast episode, we had the pleasure of speaking with Tina, one of our dedicated volunteers at SOFT UK. Tina has taken on various roles with us since she first got involved, and in our conversation, she shares what she's learned from volunteering and how she puts those lessons into practice in her everyday life. We also had the opportunity to hear about the individuals who have made a significant contribution to SOFT, and who Tina would like to thank.If you're interested in learning more about volunteering with SOFT UK, this episode is for you. Listen in to discover how you can make a difference and get involved in our mission to support families affected by trisomy 13 and 18. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 5/18/23 | Improve, Inspire, Empower (Bereaved) | Join us for a heartfelt conversation with Raliene and Josh Banks, parents of Faith, a beautiful soul diagnosed with Trisomy 13 in 2022. In this inspiring dialogue, we explore the untold perspective of a grieving father, gain invaluable insights they wish they knew earlier, and witness their incredible resilience in their #JourneyForFaith. Discover more of their touching story at Raliene's blog: https://raebanks.com/journeyforfaith/ Reach out at contact@soft.org.uk For support, contact support@soft.org.uk T o find out more, visit www.soft.org.uk | — | ||||||
| 5/4/23 | The origins and aims of #TFMRAwarenessday | We spoke to Emma Belle, mother of Willow and founder of TFMR Mammas and #TFMRAwarenessDay. She put it beautifully when she told us why TFMR awareness day is so important. She said: “...so that anyone faced with this decision or having gone through this type of loss can go to one place and know that every single resource on there has been checked, is safe, is going to be a soft, loving landing space for their grieving. broken, hearts without any judgement… Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 5/3/23 | Breaking the Silence: Deaf Awareness Week (living with trisomy) | We spoke to Simone Adams, mother to Maebh, who has trisomy 18 and is affected by some of the issues highlighted by Deaf Awareness week. She shares how her daughter's hearing loss was discovered and how it affects Maebh's day-to-day life. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 5/2/23 | In Our Own Little Bubble: Coping with TFMR - Marie's Story | In this episode, we had the privilege of speaking to Marie about her personal journey through TFMR and how she has been coping with the help of her husband. She shared with us some surprising insights she gained from the experience that she hopes will help others going through a similar situation. Tune in to hear Marie's heartfelt story about her baby Heidi and her passion for breaking the silence around TFMR. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 4/6/23 | In Conversation With Richard: A Siblings Journey | We spoke to Richard, Sarah's brother, who passed away from Patau's syndrome (trisomy 13) in 1989. He shared his story and what he could remember as a 3 year old at the time. He also shared a powerful message about mental health and finding acceptance in a situation and looking for the positive in every situation- in this case was bringing the family closer together. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 3/20/23 | In Conversation With Sarah: A Mosaic Pregnancy and Journey (Living with trisomy) | We spoke to Sarah Dowdall, mother to Emilia, with mosaic trisomy 18 about the journey to diagnosis as well as how she copes with the uncertainty of what this will mean for her daughter in the future. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
| 3/20/23 | Working With Eastenders | Listen to the roundtable discussion about what it was like working with EastEnders on the Trisomy 18: Edwards syndrome storyline. We’re joined by some of the people who were directly involved in talking to producers, actors and story researchers. We hope you’ll enjoy this ‘behind the scenes’ look at what went on. Reach out at contact@soft.org.uk For support, contact support@soft.org.uk To find out more, visit www.soft.org.uk | — | ||||||
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Chart Positions
1 placement across 1 market.
Chart Positions
1 placement across 1 market.