Episode 2

World Braille Day with Emma Thomas

Published on: 8th January, 2025

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

Next Episode All Episodes Previous Episode

The SEND Sofa

Sign up to receive The SEND Sofa updates!

Sign up for 'The SEND Sofa' updates!

We respect your email privacy

Support The SEND Sofa

A huge thank you to our supporters, it means a lot that you support our podcast.

If you like the podcast and want to support it, too, you can leave us a tip using the button below. We really appreciate it and it only takes a moment!
Support The SEND Sofa
J
Joe m £50
You deserve every penny ❤️
Show artwork for The SEND Sofa

About the Podcast

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
Support This Show

About your host

Profile picture for Tahnee Morgan

Tahnee Morgan

Mum of three beautiful children, teacher, presenter, voiceover artist and of course SEND mum.