Mandy and Kate are here with you on this very last episode of Too Peas In A Podcast! They listen to many of your beautiful speakpipes - thank you so much for sharing what this podcast and community has meant to you in your Pea journey. Mandy and Kate also thank the many people who have been involved from the start, from Kelly who designed the cute logo, to Adam who wrote the beautiful theme song, to the Sound Engineer who listened to every single moment over 5 years and edited every single...

Kate and Mandy chat to Phoebe, Education Officer at Werribee Open Range Zoo and Zoos Victoria! Phoebe is a triple Pea - a qualified peacher, a Pea mum of two boys both diagnosed with autism and ADHD, and herself recently diagnosed with autism and ADHD.  Phoebe is passionate about her job at the Zoo where she’s been working for the past 16 years. School children from all across Victoria of all ages come to Zoo on excursions to learn about conservation, and Phoebe says that the environment can...

Kate and Mandy chat with Amanda, Pea mum of two daughters, a carer for her dad, a teacher of one day and a wonderful carer. Amanda introduces us to her family and youngest daughter Bella who has autism and an intellectual disability. Bella is also our own Molly's BFF. Amanda shares with us about the early years with Bella, her mainstream beginning in school and her move to specialist schooling after the school encouraged the move. Bella has thrived in these schools and is in a core friendship...

Mandy and Kate chat to Alex, Pea mum of 3 sons and a very interesting person. Alex shares with us about the birth of her son Harry who was diagnosed with Down Syndrome on the same day he became very unwell and was transferred to intensive care at another hospital. During this time in hospital, Harry was also diagnosed with Hischsprungs Disease, which is a condition of the large intestine. Once Harry was stable he came home and Alex began learning about his conditions. Harry had early...

Kate and Mandy chat to power pea mum and daughter duo Sue and Mia.  Mia has Okur-Chung neurodevelopmental syndrome (OCNDS) and is a Special Olympics athlete and admin assistant. Pea mum Sue is also a peafessional Maternal and Child Health Nurse.  Sue and Mia talk about Mia’s early years, including her diagnosis, early intervention and school. Mia also talks about swimming for Special Olympics, doing triathlons with Inclusive Sports Training and the opportunities she’s had to travel overseas....

It's International Pea Week, Day 2 and Mandy and Kate chat to Kelly, ( in their nighties gifted from Kelly ) a mum of 4 and the owner and founder of Comfort on the Spectrum. Kelly introduces us to her family and her son Max who has a diagnosis of Norrie Disease which means Max has been blind from birth. He was also diagnosed autistic at 8 years old. Max spent lots of his younger years learning skills including braille and was in mainstream primary school. This meant a lot of advocacy for...

For Day 1 of International Pea Week, Mandy and Kate chat with Chloe - the self-described all-rounder and big heavy metal fan!  Chloe is the proud sister of a brother with autism, she’s also a disability support worker and a volunteer with the Melbourne West Special Olympics team.  Chloe’s life mission is to pay it forward and make the world a better place! Mandy met Chloe while she was volunteering as Team Support at the 2022 Special Olympic National Games and became a fan of her big heart,...

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, and the game-changing experience of taking medication for the first time. Trish also chats about parenting her...

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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 mosaic nature of the results. This time was gut wrenching whilst Emmy was in hospital and they couldn't be...

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 became a mum to 2-year-old Amelia, who is a gorgeous little SWAN girl.  Rachel talks about Amelia’s birth and early...

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 has developmental coordination disorder, formerly known as dyspraxia.  Bec talks about the diagnosis journey for her...

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 we were 5 years ago, and now we have so many new friends too. You can stay connected with us...

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 diagnosis when he was 2 and a half years old. Lloyd is a full-time wheelchair user and is peg-fed, and is a chill and happy...

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 conference happening in her hometown of Brisbane, she decided to head along to explore it. Little did she know that she was about...

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 experiences of being a Pea mum to a daughter with type 1 diabetes. She found that meditation and shiatsu have helped her better manage...

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This week, Mandy (Kate is sick!) chats to Louise, Pea mum to 3-year-old Isabelle who lives with Severe Combined Immunodeficiency (SCID) or the ‘bubble baby condition’  - a life-threatening genetic condition in which affected babies are unable to fight bacterial, viral or fungal infections. Louise shares her story of Isabelle’s diagnosis thanks to the quick and insightful actions of two supportive paediatricians, and her months-long hospital stay in a positive pressure room, all while the...

Mandy and Kate recap their recent trip to Parliament House to celebrate all things neighbours and belonging and connection with the excellent people from Neighbours Every Day - Relationships Australia’s social connection campaign.  Neighbours Every Day aims to help create and share belonging across Australia, and build the inclusive communities you want to live in, one relationship at a time.  Kate and Mandy are Neighbours Every Day Ambassadors and flew up to Canberra to celebrate the launch...

Mandy and Kate chat to Rachael, pea mum to a beautiful 5-year-old Robbie, and the Tasmanian representative for Angelman Syndrome Association Australia. Rachael shares the story of her pregnancy, moving to Hobart in preparation for Robbie’s birth, time in the NICU, Robbie’s surgery at only 9 days of age, and his diagnosis of the rare genetic disorder Angelman Syndrome. Rachael talks about adjusting to Robbie’s medical complexities, feeling like the whole world had changed around her,...

Snap Pea 91! Mandy and Kate chat about concerts, and listen to your speak pipes xxx Hosted on Acast. See acast.com/privacy for more information.

Kate and Mandy chat to Lewis from northwest Tasmania, a lovely young guy who studies media and communications and runs YouTube channel Lewlyfe.  Lewis is part of the pea community as he was born with a bilateral cleft lip and palate. Lewis talks about growing up managing all the challenges of multiple surgeries, speech therapy and regular check ups with a whole range of doctors and specialists. Primary school was not much fun as he went to a sporty school when he wasn’t into sports, but he...

Part two of "The Peas are back for 2024" Hosted on Acast. See acast.com/privacy for more information.