Christmas is over, and so is Hanukkah. And we may have missed the official date for Festivus, December 23rd, but is there ever really a bad time to air grievances? Of course not. And we have plenty of them. Join us as we share all the things that grind our gears in the special needs world. This is not an episode of solutions, but rather a space to recognize all the things that drive us batty and a place for you to know that we see you from our side of the trench. Happy Festivus!

Origins of Festivus

After a three year hiatus, Angie and Meg are back, and this time, Angie is in the hot seat. After completing her doctorate, Angie is here to share with us how and why she did it, and what it all means. You'll find out about her research which was dedicated to learning about caregivers who started businesses with and for their children with intellectual and developmental disabilities to provide a pathway to meaningful employment. Truly, her work was an extension of idea behind this podcast. Tune in and find out what she learned about caregivers and herself!

If you'd like to learn about the caregivers she interviewed and the insights gained, here's a copy of her published dissertation. For some orientation to the document, Chapter 1 is the "Why", Chapter 2 is the "What", Chapter 3 is the "How", Chapter 4 is what I found, and Chapter 5 answers the final question, which is what does it all mean?

We are still here, and we have both missed you all.

Christina Adams, journalist, writer, disability advocate, and camel milk investigator, shares with us her powerful early intervention story of her son with autism and how she was able to help him through diet and camels. She outlines what she calls her "crazy camel journey" and how her research and travels to Isreal took her to a place of healing. She shares her website with us as a resource that details how camel's milk can help several conditions, from allergies and gut issues to neurodevelopmental issues. Join us as we learn about the amazing qualities of camels and how their milk can be a part of your healing journey!

Join us as we talk to Hannah Lowe, founder of the L-CMD Foundation and mother to Austin, who has LMNA-related congenital muscular dystrophy. Like many rare disease families we've talked to, her son's condition was caused by a random genetic mutation. There is no treatment or cure, and given how rare it is, they are unsure about his prognosis or life expectancy, making the mission even more urgent. The L-CMD Foundation she started inspires hope for a stronger tomorrow by seeking treatments and, ultimately, a cure. We talk about balancing grief with action, and Hannah exemplifies this in her graceful and determined approach to saving her son.

If you've ever worried about what adulthood might look like after high school or you've ever been inspired to create a meaningful space for your child to spend adulthood, tune in to our interview with critically acclaimed author, Cammie McGovern.

Cammie McGovern was awarded a creative writing fellowship at Stanford University, and has received numerous prizes for her short fiction. Her stories have appeared in many magazines including Glamour, Ladies Home Journal, Redbook and Seventeen , and she is the author of another novel, The Art of Seeing. She lives in Amherst, Massachusetts with her husband and three children, the eldest of whom is autistic. She is one of the founders of Whole Children, a resource center that runs after-school classes and programs for children with special needs.

This week we chat with Leylani Cardoso, warrior parent, and mother of Sophia, her daughter with Down Syndrome. Leylani and her family helped Sophia bring her passion for food and entertaining to life by creating the YouTube Channel Cheeky Sassy Me