The SEND Sofa

Tahnee Morgan
  • 5.0 (17)
  • KIDS & FAMILY
  • UPDATED WEEKLY
The SEND Sofa

One day last year after another overwhelming morning trying to get my distressed SEND son into school, I came home, slumped on the sofa and sobbed. I was at my wits’ end. I didn’t think I could do it a second longer. It made me think of all the other struggling SEND parents out there, possibly on their sofas, crying too. If I felt overwhelmed, so did they. If I was struggling, perhaps I wasn’t alone. The responsibility and pressure of raising a SEND child can sometimes be too much. How could I bring us all together? I wiped my tears, got out my notepad and pen and wrote the first words that came into my head: ‘The SEND Sofa.’ Holy Shiz. It appeared I was about to start a podcast! And here it is! My name is Tahnee Morgan and my world was rocked when my son, Max, was diagnosed with Kabuki Syndrome in 2017, a rare genetic disorder that affects just 1 in 32,000 births worldwide. In this podcast, I delve into the good, the bad and the ugly of SEND life. Everything and everyone is welcome here. The vibe is genuine, heartfelt and relaxed as I provide a much-needed safe and comfortable space for SEND families to be open and honest about their journey. I will be chatting with parents, medical professionals, therapists and practitioners to gain a better understanding of all things SEND, while having a giggle (or a good cry) along the way. So, grab a cuppa (or a glass of wine!) and join me on the Send Sofa. Instagram @thesendsofa Facebook The SEND Sofa

Episodes

  1. 5 DAYS AGO

    Understanding Dyslexia with Carly Steel

    In this episode, Tahnee is joined by Carly Steel, an Educational Consultant, who works closely with parents of neurodivergent children to enhance their child’s wellbeing, reduce anxiety, and promote family harmony. She is also the author of Consulting Autistic Young People on Their Personal Happiness, published in the Good Autism Practice journal. In honor of Neurodiversity Celebration Week, today we explore the world of dyslexia—a prevalent learning difference that influences how individuals read, write, and process language. Dyslexia is much more than simply reversing letters; It brings unique challenges that can affect everything from academic achievement to self-esteem, but it is also a condition filled with strengths, creativity, and untapped potential. We’ll explore what dyslexia is, how it manifests, and why understanding it is key to supporting those who live with it. Join us as we unpack the myths and truths about dyslexia and highlight the importance of awareness and tailored support. https://www.nessy.com/en-gb Free educational resources https://www.neurodiversityweek.com/powerpoint-presentations Powerpoint presentations to look at with your children. https://www.ipsea.org.uk/ - A leading charity to help you navigate the SEND system. https://www.bdadyslexia.org.uk/ British Dyslexia Association https://www.carly-steel.com/ Email info@carly-steel.com to recieve your FREE 60 Reasonable Adjustments for Neurodivergent Children in School!

    48 min

  2. 5 MAR

    Mind Over Matter with Kelly Kearley

    Life can be incredibly demanding, particularly for parents of children with Special Educational Needs and Disabilities (SEND), who must balance numerous appointments and therapies. It often feels like we’re managing a variety of responsibilities at once, but it’s important to remember that it’s okay to let some things go in order to focus on becoming the best version of ourselves. In this episode, Tahnee speaks with Kelly Kearley, a SEND mother who transitioned from a career in event management in London to becoming a psychotherapeutic counsellor. Kelly founded Mind Over Matter Therapy to offer support, give back, and help others heal from similar experiences. Having walked in the shoes of others truly enhances her ability to offer meaningful guidance. My website: www.mindovermattertherapy.co.uk PTEN UK and Ireland Patient group: www.ptenuki.org Positively Rare book: https://amzn.eu/d/hf9Irx4

    1 hr

  3. 26 FEB

    Rare Disease Awareness Month - Gabby's Story

    In this episode today, Tahnee talks with Gabby Zeppieri, the only adult in the US to be diagnosed with Neutral Lipid Storage Disease Myopathy NLSD-M, a rare genetic condition, where fats (lipids) are stored abnormally in organs and tissues throughout the body. The accumulation of fats in muscle tissue leads to muscle weakness (myopathy). One of the reasons why such a small number of patients have been identified is un-awareness or less information of the disease. https://www.gabbyswonderfulworld.org/

    43 min

  4. 19 FEB · BONUS

    Half Term Reset!

    With the half term holidays in full swing, Tahnee takes some time off to become full time chef, taxi driver, bottom wiper, kids entertainer, cleaner and story teller. In this episode, we meet Isaac (9) and Reeva (4), who both wanted to be a part of the show. What's it like to have a sibling with a disability? and how well do they know him? Let's compare answers!

    29 min

  5. 12 FEB

    Rare Disease Awareness Month - Landree's Story

    Landree Gail, a 7 year old girl from Oklahoma, was diagnosed at the age of 4 with a rare mutation form of Angelman Syndrome. Seizures, disruptive sleep patterns and short attention span are just a few signs and symptoms of this condition. Landree’s mother, April, shares her story with us today. https://cureangelman.org.uk/ https://www.angelman.org/what-is-as/ https://www.instagram.com/colinfarrellfoundation/ https://www.instagram.com/aprilmchesser/

    1h 2m

  6. 5 FEB

    Rare Disease Awareness Month - Leo's Story

    In 2021, Kim and Keith Firmin’s world was turned upside down after they were told during pregnancy that their unborn son had a complex heart - double inlet left ventricle (only 3 out of 4 heart chambers work) and pulmonary stenosis (heart valve disease). At just 9 days old, medical professionals noticed that Leo also had a type 3 laryngeal (Airway) cleft – which had to be surgically repaired 3 times. At 3 weeks old he had tracheostomy surgery. Today, his mother Kim, shares her story with Tahnee. List of CharitiesREACT: for children under palliative care and very high needs. They give large amounts-Family Fund (large amounts every 2 years)-Maia Mouse (£250 minimum given)-Little Teds - Free caravan in Wales: Not wheelchair friendly-Make a wish foundation (3+). -Rainbow trust: Provides a family support worker-Newlife the Charity - Changing the lives of disabled children (newlifecharity.co.uk)- Big grants for large items-Home | JUMP Children's Charity (jumpchildrenscharity.co.uk) - Free photoshoots for families.

    53 min

  7. 29 JAN

    Hope and Possibility with Glenn Wilson

    In this week's episode, Glenn Wilson, a pastor and creator of the Advocate of Hope on TikTok, which is dedicated to supporting parents, especially parents of children with special educational needs and disabilities (SEND) joins Tahnee on the sofa. As a parent of an autistic child, Glenn understands the unique challenges and joys this journey brings. His mission is to encourage and uplift parents, helping them find strength, community, and hope in the midst of the struggles they face on a daily basis. TikTok: @advocateofhope Insta: glennadvocateofhope https://www.kids.org.uk/sendiass-home/ https://www.autism.org.uk/ https://www.uniqueways.org.uk/

    52 min

  8. 22 JAN

    Who is Max?

    One question Tahnee has been asked since starting this podcast is, "Who is Max? Tell us more!" Today we get to find out more about Max, as Tahnee shares her story with us. https://www.kabukiuk.org.uk/ https://www.allthingskabuki.org/ https://www.kabukisyndromefoundation.org/

    31 min

  9. 15 JAN

    Sensory Processing Disorder with Armi Grace Petersen

    Armi Grace Petersen, a maternal health and infant occupational therapist from Illinois, talks to Tahnee on ‘The SEND Sofa’ about Sensory Processing Disorder, also known as SPD. Today, we learn to identify the possible signs of SPD and how it can impact on daily life. The information contained in this podcast is for general educational and informational purposes only and should not be construed as medical advice.   Recommended book: "The Out-of-Sync Child": https://amzn.to/3ZwRxZ5

    29 min

  10. 8 JAN

    World Braille Day with Emma Thomas

    In this week’s episode, we celebrate World Braille Day! A worldwide celebration that takes place on 4th January each year. Tahnee Morgan is joined by Emma Thomas, the mum of 7 year old Archie, a young boy who is keen to show the world that having a vision impairment does not have to hold you back! Braille has become a huge part of Archie's life. Today we find out why. Archie has faced many other challenges in his short life, a kidney transplant being one of them. However, no matter what this family have had thrown at them, they have worked tirelessly together to create a loving world full of possibilities for their son. Sit back and prepare to be inspired by Archie’s story. https://www.rnib.org.uk/living-with-sight-loss/supporting-others/parenting-a-child-with-a-vision-impairment/how-to-make-celebrations-accessible-for-all-the-family/world-braille-day/ Instagram: @thesendsofa Facebook: The SEND Sofa

    36 min

  11. EPISODE 1

    Trailer

    Welcome to 'The SEND Sofa' hosted by Tahnee Morgan

    2 min

Trailer

5
out of 5
17 Ratings

About

One day last year after another overwhelming morning trying to get my distressed SEND son into school, I came home, slumped on the sofa and sobbed. I was at my wits’ end. I didn’t think I could do it a second longer. It made me think of all the other struggling SEND parents out there, possibly on their sofas, crying too. If I felt overwhelmed, so did they. If I was struggling, perhaps I wasn’t alone. The responsibility and pressure of raising a SEND child can sometimes be too much. How could I bring us all together? I wiped my tears, got out my notepad and pen and wrote the first words that came into my head: ‘The SEND Sofa.’ Holy Shiz. It appeared I was about to start a podcast! And here it is! My name is Tahnee Morgan and my world was rocked when my son, Max, was diagnosed with Kabuki Syndrome in 2017, a rare genetic disorder that affects just 1 in 32,000 births worldwide. In this podcast, I delve into the good, the bad and the ugly of SEND life. Everything and everyone is welcome here. The vibe is genuine, heartfelt and relaxed as I provide a much-needed safe and comfortable space for SEND families to be open and honest about their journey. I will be chatting with parents, medical professionals, therapists and practitioners to gain a better understanding of all things SEND, while having a giggle (or a good cry) along the way. So, grab a cuppa (or a glass of wine!) and join me on the Send Sofa. Instagram @thesendsofa Facebook The SEND Sofa

Information

  • Creator
    Tahnee Morgan
  • Years Active
    2024 - 2025
  • Episodes
    11
  • Rating
    Explicit
  • Copyright
    © Copyright 2025 Tahnee Morgan
  • Show Website
    The SEND Sofa

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