Mary talks with her friend Katie De Nardi Grant, a travel agent that specializes in creating vacations for families that have a child with special needs. Katie travels a lot with her daughter Sloan, who has Down syndrome and some other medical issue...
Today is another mini episode and Mary talks about the Run Up For Down Syndrome and her cookie fundraising for the event. She also talks about the Adaptive Dance that Ainsley has been going to since September and some of the ongoing challenges with ...
Mary chats with Melissa Hart about her recently released book “Daisy Woodworm Changes the World”, and about growing up with a younger brother who has Down syndrome. Melissa is a strong advocate for highlighting people with Down syndrome in various m...
This is a mini-episode of Mary sharing what's been on her mind. She talks about Challenger baseball, Mother's Day, some behaviour issues Ainsley is having at school, and trying to have some success gardening (Dennis is unsure of her success!).
Mary talks with Brady Murray of ROD's Heroes-an organization that is dedicated to helping children in orphanages that have Down syndrome and other disabilities, find their forever homes. Hear what happens when Brady decides to do an Ironman and allo...
Mary chats with Darcy Day on how she learned that her 18 year old son Brady, who has Down syndrome, was able to communicate through spelling! It is a fascinating and heart warming conversation about always assuming competence on our kids. Darcy is on...
Mary chats with Cristin Condon who is a life coach, meditation teacher and a Marie Kondo professional organizer. Cristin is a single mom with three kids including her son with Down syndrome and understands how important self-care is for parents of c...
Mary talks with Rose Reif, a Licensed Clincical Mental Health Counsellor, about a topic we don’t hear about too often-grief. Rose provides insight and tips on how to handle and manage the grief of our child’s diagnosis. Rose talks about several thing...
Mary has an eye-opening conversation with author Meeka Caldwell about her "My Friend Anian" book series. When Meeka couldn't find any books about Down syndrome and a black family, she decided to write her own. It's an open conversation about race, D...
Mary talks about what's ahead in Series 5.
In this last episode of Season 4, Mary and Ron have a chat about what Christmas will look like this year. Sleigh Bells SFX Courtesy: License: Attribution 4.0 International (CC BY 4.0) Music Attribution Jingle Bells CC Commons LicenceJingle Bells b...
Mary talks with filmmakers Olivier & Hilda Bernier. The Bernier's have created a film documenting their son Emilio, who has Down syndrome, and his struggle with inclusion in the school system.
Mary tells tales from the 2022 "Rockin Moms Retreat" in Washington DC. Make sure you have snacks and beverages, it's a long episode!
Mary talks with Dr Jonathon Santoro, Medical Director, Neuroimmunology and Demyelinating Disorders ProgramAttending Physician, Division of Neurology at Children's Hospital of Los Angeles about regression.
Mary talks with Sara Peralta, a Behaviour Analyst at the Down syndrome Resource Foundation. Down Syndrome Resource Foundation
Mary talks with Dawn Barclay, author of "Traveling Different: Vacation Strategies for Parents of the Anxious, the Inflexible, and the Neurodiverse". Dawn Barclay's Blog Amazon Link to Traveling Different: Vacation Strategies for Parents of the Anxiou...
Mary has a fascinating discussion with Dr. Vaish Sarathy about functional nutrition. Functional Nutrition Website Dr. Sarathy's Functional Nutrition Podcast
Mary has a fascinating conversation with Dr. Liz Head, Professor, Vice Chair for Research in the Department of Pathology & Laboratory Medicine at the University of California - Irvine, about research into people with Down syndrome and Alzheimers. ...
Mary and Ron catch up on how busy they have been over the first part of the summer. Apologies for Ron's mic
Mary talks with Liv Meriano, a Speech & Language Pathologist at the Down Syndrome Resource Foundation. Down Syndrome Resource Foundation
Mary talks with Ebonie Shaniece and Corinne Turrini about diagnosis and treatments for Infantile Spasms.
Mary talks with New York Times best selling author and podcast host Heather Avis of The Lucky Few. HeatherAvis.comThe Lucky Few FoundationThe Lucky Few Podcast
Rockin' Mom Amanda Brunning shares her adoption story with Mary.
Mary talks with Daria Kolmiiets about leaving Ukraine for Canada back in 2019 and her experiences in Ukraine as the mother of a special needs child, and more. Donation Link for "The Red Cross For Ukraine" Campaign Donation Link to "Ainsley's Army" fo...