“Thanks so much Guys for interviewing Noah. AAC has been my life for the last 18 years with my daughter who has a rare genetic disorder. The world needs to know that everyone has something to say even if they can’t use their mouths to say it!
My daughter was to shy to say HI at ability fest. She said it was ‘loud, funny, hot’. Maybe next year she will have a chat.
Love your work fellas💜”
Cri Du Chat Syndrome Mum via Apple Podcasts ·