Too Peas In A Podcast Mandy Hose and Kate Mulholland

One of our last snap peas ... we love to hear your beautiful speak ("speed") pipes. Thank you for sending them peas. Hosted on Acast. See acast.com/privacy for more information.

Kate and Mandy chat to Trish, pea mum of three children diagnosed with autism and ADHD, with her oldest child also diagnosed with a pathological demand avoidance (PDA) profile. Trish talks about the journey of diagnosis, which began when her eldest peashoot was in high school and just as COVID was beginning. This then sparked her own journey towards an adult diagnoses of ADHD,

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Mandy and Kate talk to Sonja, a self proclaimed Norwegian princess and introduces us to her gorgeous daughter Emmy who lives with Patau Syndrome or Trisomy 13. Emmy was born 7 weeks prematurely, in a dramatic entrance which has paved the way for Emmy's life so far. Sonja shares the story of Emmys birth, her time in SCN and the genetic testing and diagnosis of Patau Syndrome and the

Mandy and Kate chat to mother and daughter dynamic pea duo Vicki and Rachel from Newcastle. Vicki is a mum of five kids and wife to her husband Neil, who has an acquired brain injury due to a stroke. One of her children also has neurofibromatosis, ADHD and learning disabilities. Her daughter Rachel was a young carer for her siblings and her stroke-affected stepdad, and recently bec

Kate and Mandy talk to Bec, a mad Carlton (boo) supporter and Pea partner and mum to a husband and two boys with disabilities. Her husband Luke has a a congenital deformity of his left hand, plus lived with an undiagnosed dislocated elbow for decades. Her eight-year-old boy Henry has autism and ADHD and is also gifted. Her younger son Kieran is profoundly deaf in one ear and h

Hello lovely Peas, pop us in your ears today and hear our announcement. We have loved sharing our lives with you over the last 5 years, but as they say, all pea things must come to an end. So on Mothers Day this year we are hanging up our headphones and turning the mics off, 5 years after we started. We still love each other very much and are so happy to be even better friends than

Mandy and Kate chat to Maya, founder and CEO of Rare Wear - adaptive fashion for kids with disabilities - and Pea mum to six-year-old Lloyd, who has a rare genetic condition called Iqsec2 Associated Disorder and lives with developmental, medical and mobility issues. Maya chats all about Lloyd’s birth when she was just eighteen years old, and the long journey towards diagnosi

Kate and Mandy chat to Alex, a registered music therapea from Devonport, Tasmania. Alex talks all about her journey through the almost magical profession of music therapy.  Growing up in a musical family, Alex was interested in music and singing, but felt a strong sense that there was more to it than just performing or entertaining people. Spotting a music therapy confere

Mandy and Kate chat with Belinda, meditation teacher, shiatsu practitioner and Pea! Belinda is passionate about helping and supporting people on their health journey. She is the founder of Vitaliqi and loves showing people how they can feel better and turn their physical and mental health around naturally.   Belinda’s natural health career was inspired by her exper