Embracing Holland
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!
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Join us as we explore all of the things giving us life and the things that could make great gifts for the people in your orbit, or yourself! Emphasis on yourself. We cover everything from tools and audiobooks to amazing water bottles, skincare for aging and acne-prone skin, items for dads, items only an autism parent would understand, and some of the people on the internet who do content we love! Meg’s Sanity Helpers: Roku Remotes Portion Cups Multicharging Cables Spot Carpet Cleaner Snag Tool Clothesline Tiles Angie’s Auditory Love: Ragey Spotify Playlist Life Changing...
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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...
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We are still here, and we have both missed you all.
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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...
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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...
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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,...
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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
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For this episode, we share with you another Maryland parent and fellow autism mom, Lia McCabe, who started AutismWish.org which seeks to fulfill the wish lists of families across the country without all of the red tape of government programs. She and her husband also host a podcast called Embracing Autism, which is child focus and helps parents to understand and embrace their neurodiverse children. Give it a listen, follow, and subscribe to support their mission of helping families in the face of fear and the unknown. We talk about: Neurodivergent parenting Empathizing with...
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This episode is all about taking care of the caregiver. Rory Lawrence, mother of a child with complex medical needs and staff member with David’s Refuge, talks with us about the organization she works for that pours into parents turned caregivers, and how she and her husband have found meaningful respite. We also talk about practical ways to weave in self-care that don’t require a sitter but can actually make a difference. Links Rory’s Email -
info_outlineFecal smearing and ingesting are taboo topics that often elicit a considerable amount of shame for families. We felt like it was time to give this topic some attention to those who are struggling in the dark and aren't comfortable reaching out for suggestions in the online support groups. In response to very little information openly available to families struggling with smearing and consuming feces (scatolia and coprophagia), Genevieve Engleman, The Remote OT, shares with us the background behind the behavior, information to reduce the stigma, and ways we can try to prevent and address this issue.
We talk about:
- Why mammals may consume their own feces
- History and incidence of these behaviors
- Reducing the stigma and shame associated
- What the behavior may be communicating
- How to address any potential medical problems that could lead to these behaviors
- What do do if and when it happens
- Ways to use OT, and sensory play to meet the needs currently served by poop play
Genevieve’s Website