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The SEND Sofa

Podcast The SEND Sofa
Tahnee Morgan
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 ...

Available Episodes

2 of 2
  • World Braille Day
    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: @thesendsofaFacebook: The SEND Sofa
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  • Trailer
    Welcome to 'The SEND Sofa' hosted by Tahnee Morgan
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    1:45

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About 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 thesendsofa
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