Syndromes without a name
Listen now
Description
Kate and Mandy met with the divine Heather and Sue, they chat all things SWAN - Heather Renton runs Syndromes Without a Name (SWAN) Australia - Sue’s book is called Take The Shot - The PDF version of The Ripple Effect from Melbourne City Mission can be found here - SWAN facilitate different types of events throughout the year with some of events coming up in March including Undiagnosed Children’s Awareness Day (UCAD) Morning Tea, UCAD community family fun day (in Northcote, Victoria), and SWAN siblings group. For locations and dates click here - Kate’s make a difference is Kitty Flanagan’s 488 Rules for Life Live shows are coming up real soon! 8 March 2020 at the Comedy Store in Sydney, tickets available here 21 March 2020 in the York of Lilydale, tickets available here 28 March 2020 at the Yarraville Club, tickets available here Website: www.toopeasinapodcast.com.au Email: [email protected] For information regarding your data privacy, visit acast.com/privacy
More Episodes
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...
Published 04/17/24
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...
Published 04/10/24