The SEND Sofa

著者： Tahnee Morgan
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  • 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 thesendsofa
    Copyright 2025 Tahnee Morgan
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あらすじ・解説

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 thesendsofa
Copyright 2025 Tahnee Morgan
代替医療・補完医療 衛生・健康的な生活
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    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.


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    53 分
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