Trisomy Family Stories artwork

Trisomy Family Stories

98 episodes - English - Latest episode: about 1 month ago -

A collection of stories and experiences from families dealing with Trisomy 13 and 18.

Parenting Kids & Family
Homepage Apple Podcasts Google Podcasts Overcast Castro Pocket Casts RSS feed

Episodes

In Conversation With Mary: The Frailty of a Butterfly

March 13, 2024 13:23 - 44 minutes - 40.3 MB

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...

Baby Loss Awareness Week 2023: In Conversation with Kate Sonley

October 13, 2023 09:59 - 30 minutes - 28.3 MB

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 [email protected] For support, contact [email protected] To find out more, visit www.soft.org.uk

From Past To Present: Reflecting on Demi's Trisomy 18 Journey

September 12, 2023 11:42 - 32 minutes - 29.4 MB

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 [email protected]...

Embracing the Extraordinary Journey: Positive about Down syndrome

August 10, 2023 12:49 - 27 minutes - 50.5 MB

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 [email protected] For support, contact [email protected] To find out more, visit www.so...

Pregnancy after a Trisomy 18 diagnosis

July 06, 2023 11:40 - 42 minutes - 78.5 MB

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...

Leaving the hospital with my Rainbow baby

June 29, 2023 12:01 - 23 minutes - 44.5 MB

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 [email protected] For support, contact [email protected] To find out more, vi...

A Sibling's Path: From Loss to Strength as a Rainbow Baby

June 21, 2023 10:29 - 21 minutes - 39.4 MB

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 [email protected] For support, contact [email protected]...

Navigating the Complexities of Genetic Counseling: Insights from a Trainee Genetic Counselor

June 14, 2023 13:56 - 36 minutes - 67.9 MB

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 1...

Making a Difference: The Power of Volunteering with SOFT UK

May 31, 2023 02:36 - 11 minutes - 20.8 MB

 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 l...

Improve, Inspire, Empower (Bereaved)

May 18, 2023 13:14 - 41 minutes - 76.7 MB

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 [email protected] For support, contact su...

Improve, Inspire, Empower (Bereaved)

May 18, 2023 13:14 - 41 minutes - 76.7 MB

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 [email protected] For support, contact su...

The origins and aims of #TFMRAwarenessday

May 04, 2023 10:18 - 20 minutes - 38.1 MB

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 [email protected] F...

Breaking the Silence: Deaf Awareness Week (living with trisomy)

May 03, 2023 11:10 - 15 minutes - 29.4 MB

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 [email protected] For support, contact [email protected] To find out more, visit www.soft.org.uk

Breaking the Silence: Deaf Awareness Week and Trisomy 18

May 03, 2023 11:10 - 15 minutes - 29.4 MB

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 [email protected] For support, contact [email protected] To find out more, visit www.soft.org.uk

In Our Own Little Bubble: Coping with TFMR - Marie's Story

May 02, 2023 10:49 - 27 minutes - 50.7 MB

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 [email protected] For support, contact [email protected] To f...

In Conversation With Richard: A Siblings Journey

April 06, 2023 11:25 - 16 minutes - 31.3 MB

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 [email protected] For support, contact [email protected] To find out more, visit www.soft.org.uk

In Conversation With Sarah: A Mosaic Pregnancy and Journey (Living with trisomy)

March 20, 2023 14:18 - 21 minutes - 39.7 MB

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 [email protected] For support, contact [email protected] To find out more, visit www.soft.org.uk

In Conversation With Sarah: A Mosaic Pregnancy and Journey

March 20, 2023 14:18 - 21 minutes - 39.7 MB

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 [email protected] For support, contact [email protected] To find out more, visit www.soft.org.uk

Working With Eastenders

March 20, 2023 09:56 - 30 minutes - 56.7 MB

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 [email protected] For support, contact [email protected] To find out more, visit www.soft.org.uk

With The Benefits of Hindsight (Bereavement)

March 15, 2023 14:46 - 26 minutes - 48.4 MB

We had a great chat with Chris O' Toole about his daughter Maria's story and what he has learnt 30 one years later. His perspective as a Dad, urging people to reach out for support was really touching. Reach out at [email protected] For support, contact [email protected] To find out more, visit www.soft.org.uk

With The Benefits of Hindsight

March 15, 2023 14:46 - 26 minutes - 48.4 MB

We had a great chat with Chris O' Toole about his daughter Maria's story and what he has learnt 30 one years later. His perspective as a Dad, urging people to reach out for support was really touching. Reach out at [email protected] For support, contact [email protected] To find out more, visit www.soft.org.uk

Introducing Sarah: SOFT UK Trisomy Advocate

March 14, 2023 12:58 - 11 minutes - 21.9 MB

We spoke to our new Trisomy Advocate, Sarah Bowell, about her career background and what attracted her to the role at SOFT. To hear how she hopes to support families and what she is already working on, tune in! Reach out at [email protected] For support, contact [email protected] To find out more, visit www.soft.org.uk

SOFT UK: Royal Parks Half Marathon Discussion

March 08, 2023 13:14 - 10 minutes - 19.2 MB

Join SOFT UK and the team as they discuss their upcoming fundraiser. They will be taking part in the Royal Parks Half Marathon and their training begins today! Check out our fundraising page here: https://www.justgiving.com/campaign/royalparkssoftuk

SOFT UK: Royal Parks Half Marathon Discussion (Fundraising)

March 08, 2023 13:14 - 10 minutes - 19.2 MB

Join SOFT UK and the team as they discuss their upcoming fundraiser. They will be taking part in the Royal Parks Half Marathon and their training begins today! Check out our fundraising page here: https://www.justgiving.com/campaign/royalparkssoftuk

Can HIV Cause Trisomy 18 Edwards Syndrome

March 06, 2023 16:53 - 11 minutes - 21.5 MB

Following the recent storyline in Eastenders, where a couple have received a diagnosis of Trisomy 18, we wanted to answer a question that may arise from this. Can HIV cause Trisomy 13 or Trisomy 18?   In the story, the mothers partner has been diagnosed with HIV, and there have been questions regarding whether it could be a cause Trisomy 13 or Trisomy 18. In light of this, we wanted to reach out to our professional adviser for comment and also speak with one of our support volunteers regard...

Fiona’s Story

March 06, 2023 15:35 - 30 minutes - 56.2 MB

We chatted with Brandon Huxhold, Fiona’s Dad, from Illinois in the US. He told us the extraordinary story about their daughter who has mosaic trisomy 18 and turns 2 in a few weeks. He describes her as a loving child whose siblings adore her. He explains  that she achieves everything in two thirds of the time it takes typical toddlers to do it. Listen to this lovely story as told by a very proud father. To share your story, get in touch at: [email protected] To reach out to our support te...

Fiona’s Story (Living with trisomy)

March 06, 2023 15:35 - 30 minutes - 56.2 MB

We chatted with Brandon Huxhold, Fiona’s Dad, from Illinois in the US. He told us the extraordinary story about their daughter who has mosaic trisomy 18 and turns 2 in a few weeks. He describes her as a loving child whose siblings adore her. He explains  that she achieves everything in two thirds of the time it takes typical toddlers to do it. Listen to this lovely story as told by a very proud father. To share your story, get in touch at: [email protected] To reach out to our support te...

What is Rare Disease day?

February 27, 2023 13:53 - 16 minutes - 30.4 MB

We chat to Sophie Peet from Genetic Alliance to hear more about what their charity does and about the Rare Disease day, celebrated on the last day of February. Listen to this conversation as she explains this year's theme and what they hope to achieve in 2023. To find out more about Genetic Alliance, visit: https://geneticalliance.org.uk/ If you want to get in contact with SOFT UK please email us at [email protected] Song: Mellow Music by: CreatorMix.com

Introduction to a Professional Advisor: Jenny Hudson

December 07, 2022 13:29 - 15 minutes - 28.7 MB

We speak to our newest Professional Advisor, Jenny Hudson. She is a chiropractor with an interest in breastfeeding support about we hear how she came to be involved with SOFT and how she hopes to make a difference to the charity. To share your story or get involved get in touch: [email protected]

Introduction to a Professional Advisor: Jenny Hudson

December 07, 2022 13:24 - 15 minutes - 14.2 MB

We speak to our newest Professional Advisor, Jenny Hudson. She is a chiropractor with an interest in breastfeeding support about we hear how she came to be involved with SOFT and how she hopes to make a difference to the charity.

In Conversation With Charlotte Pt 2: Rainbow Baby

August 04, 2022 18:06 - 33 minutes - 61.4 MB

Some define a rainbow baby as a baby that is born after a loss. This podcast revisits Charlotte Clark's journey who currently is expecting her rainbow baby at 34 weeks. She shares life after Blaze and anwsers some interesting questions for those families trying or thinking about trying for a rainbow baby and/or expecting themselves. If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SOFT UK, please visit our ...

In Conversation With Becky: After a Loss

July 29, 2022 07:53 - 19 minutes - 37 MB

In this continuation of our conversation, Becky tells us about Heidi’s funeral, what bereavement felt like for her and why she became a SOFT trustee. If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SOFT UK, please visit our pages: Website: www.soft.org.uk Facebook:  http://www.facebook.com/SOFTUK Instagram: https://www.instagram.com/soft_uk/ Twitter:  http://twitter.com/soft_uk Music: Precious Memorie...

In Conversation With Becky: After a Loss (Bereavement)

July 29, 2022 07:53 - 19 minutes - 37 MB

In this continuation of our conversation, Becky tells us about Heidi’s funeral, what bereavement felt like for her and why she became a SOFT trustee. If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SOFT UK, please visit our pages: Website: www.soft.org.uk Facebook:  http://www.facebook.com/SOFTUK Instagram: https://www.instagram.com/soft_uk/ Twitter:  http://twitter.com/soft_uk Music: Precious Memorie...

In Conversation With Charlotte

July 21, 2022 22:29 - 22 minutes - 41 MB

Charlotte Clark shares her amazing journey about her beautiful baby Blaze, who was diagnosed with Trisomy 18 during the pregnancy. Charlotte bravely shares the challenges and concerns she faced during this time. If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SOFT UK, please visit our pages: Website: www.soft.org.uk Facebook:  http://www.facebook.com/SOFTUK Instagram: https://www.instagram.com/soft_uk/ ...

In Conversation With Charlotte (Bereavement)

July 21, 2022 22:29 - 22 minutes - 41 MB

Charlotte Clark shares her amazing journey about her beautiful baby Blaze, who was diagnosed with Trisomy 18 during the pregnancy. Charlotte bravely shares the challenges and concerns she faced during this time. If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SOFT UK, please visit our pages: Website: www.soft.org.uk Facebook:  http://www.facebook.com/SOFTUK Instagram: https://www.instagram.com/soft_uk/ ...

In Conversation With Lauren: A Siblings Perspective

July 14, 2022 14:19 - 26 minutes - 49.2 MB

In a conversation that demonstrated many emotional ups and downs over the years, we spoke to Lauren, sister to Christine, who passed away 25 years ago from Trisomy 18. A really interesting account of how a sibling experiences the death of a sibling at a young age and how this can affect someone at every stage of life thereafter. If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SOFT UK, please visit our page...

In Conversation With Becky: Thin Places (Bereavement)

July 11, 2022 06:03 - 24 minutes - 46.3 MB

Becky shared her story of baby Heidi's life including pregnancy, diagnosis and birth. She explains how she managed to overcome the negative outlook from doctors and find some positivity for her experience. If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SOFT UK, please visit our pages: Website: www.soft.org.uk Facebook:  http://www.facebook.com/SOFTUK Instagram: https://www.instagram.com/soft_uk/ Twitt...

In Conversation With Becky: Thin Places

July 11, 2022 06:03 - 24 minutes - 46.3 MB

Becky shared her story of baby Heidi's life including pregnancy, diagnosis and birth. She explains how she managed to overcome the negative outlook from doctors and find some positivity for her experience. If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SOFT UK, please visit our pages: Website: www.soft.org.uk Facebook:  http://www.facebook.com/SOFTUK Instagram: https://www.instagram.com/soft_uk/ Twitt...

In Conversation With Paul: A Dads Perspective (Dads/ TFMR)

July 04, 2022 06:40 - 30 minutes - 56.3 MB

In a very emotional and honest conversation, we heard from Paul McClean, Ben's Dad. This powerful story discusses difficulty falling pregnant,TFMR and seeking help following a loss. It's definitely not to be missed and we hope that it's a story that will help many others facing a similar situation.  If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SOFT UK, please visit our pages: Website: www.soft.org.uk ...

In Conversation With Paul: A Dads Perspective

July 04, 2022 06:40 - 30 minutes - 56.3 MB

In a very emotional and honest conversation, we heard from Paul McClean, Ben's Dad. This powerful story discusses difficulty falling pregnant,TFMR and seeking help following a loss. It's definitely not to be missed and we hope that it's a story that will help many others facing a similar situation.  If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SOFT UK, please visit our pages: Website: www.soft.org.uk ...

In Conversation With Sandeep: A fathers perspective of Trisomy 13

June 16, 2022 09:16 - 42 minutes - 79.3 MB

In honour of Father's day this year, we spoke to Sandeep Sankoli, husband to Sonia, from SOFT UK and father to Dhian, and two other young children. Listen to this unusual story including IVF treatment, and a missed diagnosis of Trisomy 13 during pregnancy. Hear how long it took for the family to get a conclusive diagnosis and all about their journey with their precious son. It is a really great account by a Dad and so enlightening to hear his perspective on things. If you have a story to sh...

In Conversation With Sandeep: A fathers perspective of Trisomy 13 (Bereavement)

June 16, 2022 09:16 - 42 minutes - 79.3 MB

In honour of Father's day this year, we spoke to Sandeep Sankoli, husband to Sonia, from SOFT UK and father to Dhian, and two other young children. Listen to this unusual story including IVF treatment, and a missed diagnosis of Trisomy 13 during pregnancy. Hear how long it took for the family to get a conclusive diagnosis and all about their journey with their precious son. It is a really great account by a Dad and so enlightening to hear his perspective on things. If you have a story to sh...

A siblings perspective of Trisomy

June 03, 2022 08:38 - 11 minutes - 20.5 MB

In a first for SOFT podcasts, we spoke to Faith Jackson - Docherty, a sibling affected by Trisomy 18. She tells us of her memories of her baby sister Charlotte, from when she was 4 years old. The importance of parents speaking openly and honestly is apparent when she tells her story. A useful listen for any expectant parents wondering how to handle a diagnosis of trisomy 13/ 18 with their other children. If you have a story to share, or wish to connect with other families, then please reach...

Fundraising With The Flock: Flockmass

May 26, 2022 07:21 - 9 minutes - 17.8 MB

Listen to this upbeat chat about the first gaming fundraiser done for SOFT, late last year. We discuss the group that took on the challenge; plus all the people involved in making the event a success. A really unique and fun fundraiser that ended up over achieving the set target. To find out more about The Fock head over to: https://www.twitch.tv/team/theflock If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect wi...

Trisomy Awareness Month: Empowering Hope

March 31, 2022 08:56 - 45 minutes - 84.6 MB

We spoke to an amazing couple, Sarita and Kareem Edwards about their incredible 5 year old son, Elijah with full Trisomy 18. It's an inspirational way to end off #TrisomyAwarenessMonth as he is so well for a child with this condition. The podcast includes an endearing guest appearance by Elijah himself. It's also a wonderful opportunity to hear from a Dad when we discussed how this diagnosis affected them as a couple. It's all summed up with their message of hope and love at the end. If you...

Trisomy Awareness Month: Empowering Hope (Living with trisomy)

March 31, 2022 08:56 - 45 minutes - 84.6 MB

We spoke to an amazing couple, Sarita and Kareem Edwards about their incredible 5 year old son, Elijah with full Trisomy 18. It's an inspirational way to end off #TrisomyAwarenessMonth as he is so well for a child with this condition. The podcast includes an endearing guest appearance by Elijah himself. It's also a wonderful opportunity to hear from a Dad when we discussed how this diagnosis affected them as a couple. It's all summed up with their message of hope and love at the end. If you...

Trisomy Awareness Month: Talking with Gareth, a trustee and fathers perspective (Bereavement)

March 23, 2022 09:00 - 23 minutes - 43.9 MB

This conversation with Gareth is an important one, as we hear how Dads can be affected by baby loss. His daughter, Phoebe, lived for 3 days and he found it terribly difficult to deal with at the time. His involvement with SOFT began by running sponsored races to raise funds for SOFT and has evolved to him 'meeting and greeting' people at SOFT conferences and now as a Trustee. We value his involvement and it's interesting to hear how SOFT has changed in the time he has been involved. If you ...

Trisomy Awareness Month: Talking with Gareth, a trustee and fathers perspective

March 23, 2022 09:00 - 23 minutes - 43.9 MB

This conversation with Gareth is an important one, as we hear how Dads can be affected by baby loss. His daughter, Phoebe, lived for 3 days and he found it terribly difficult to deal with at the time. His involvement with SOFT began by running sponsored races to raise funds for SOFT and has evolved to him 'meeting and greeting' people at SOFT conferences and now as a Trustee. We value his involvement and it's interesting to hear how SOFT has changed in the time he has been involved. If you ...

Trisomy Awareness Month: Talking with Juliette, a trustee and volunteer perspective

March 16, 2022 09:00 - 14 minutes - 26.9 MB

We spoke to Juliette about her personal journey with her daughter, Amelia, who had Trisomy 18. It's touching to hear how she has both relied on SOFT for support and now provides it as a support volunteer and trained bereavement counsellor. It's truly a labour of love for the Bradley family, as Juliette's husband, Matt, helps SOFT with their website and IT. If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SO...

Trisomy Awareness Month: Talking with Juliette, a trustee and volunteer perspective (Bereavement)

March 16, 2022 09:00 - 14 minutes - 26.9 MB

We spoke to Juliette about her personal journey with her daughter, Amelia, who had Trisomy 18. It's touching to hear how she has both relied on SOFT for support and now provides it as a support volunteer and trained bereavement counsellor. It's truly a labour of love for the Bradley family, as Juliette's husband, Matt, helps SOFT with their website and IT. If you have a story to share, or wish to connect with other families, then please reach out to:  [email protected] To connect with SO...

Twitter Mentions

@soft_uk 45 Episodes