Emily Wallace, a mother from Colorado Springs, has recently faced significant criticism after sharing a TikTok video documenting her family’s preparations for a 10-hour road trip. In the video, which has since garnered over 28 million views, Emily and her husband, William, were seen installing a barrier in the backseat of their car. This divider was intended to help manage the unique challenges posed by their son, Griffin, who has Angelman syndrome.
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Angelman syndrome is a rare genetic disorder characterised by developmental delays, speech and balance issues, and intellectual disabilities, as noted by the Mayo Clinic. For Emily, the installation of the barrier was a practical safety measure aimed at ensuring the comfort of both her son and his siblings during the long journey. “It was about keeping both my kids, myself, and my son safe in the car on a 10-hour car drive,” she stated in an interview.

Griffin, who is eight years old, is described by Emily as a loving child who craves human connection but struggles with personal space. Because of this, the barrier became necessary. “He wouldn’t hurt somebody, but he will grab, hold, squeeze — he wants that deep pressure,” she explained. On a lengthy car trip, such behaviours could be overwhelming for others in the vehicle, making the divider an essential part of their travel plans.
Despite the backlash, which included a flood of mixed responses from viewers, Emily chose to keep the comments section active on her post. She noted that it was important for people to see the varied reactions, as they reflect a broader misunderstanding about the lives of families with children who have disabilities. “People just see them as almost not real, and they are,” she remarked, highlighting the challenges faced by parents in similar situations.
The decision to share this experience was driven by Emily’s desire to increase awareness and understanding of severe disabilities. “I want to make people with severe disabilities not scary,” she stated, reflecting on her own previous hesitations before having Griffin. By offering a glimpse into her family’s reality, she aims to de-stigmatise disabilities and promote empathy.
Commenters on Emily’s video expressed a range of opinions, from support to criticism. Emily acknowledged the negative reactions but remained optimistic, “People do not like me right now… but it’s important that those with empathy can see what people write.” Following the backlash, she created a follow-up video where she addressed some concerns raised by viewers, furthering the discussion around her original post.
She is keen to share her insights and experiences with other parents managing similar circumstances. Despite initial negative feedback, Emily has received numerous messages from fellow parents expressing gratitude for her candidness and saying they would consider similar adaptations for their own family trips. “I want to give people tips and tricks so they can do more things with their kids with severe disabilities,” she added.
Upon returning from the road trip, Emily shared that the divider exceeded her expectations, working remarkably well during the journey. “I wanted to show that these disabilities are not going to define our family,” she asserted. Her dedication is evident in her commitment to ensuring that her children, regardless of their disabilities, enjoy a fulfilling quality of life and create cherished family memories.
Emily’s experience and the response to her video highlight a significant gap in public understanding regarding the daily lives of families with disabled children. By sharing her story and advocating for practical solutions, she strives to foster greater empathy and awareness within society, ultimately aiming to improve access and experiences for all families navigating similar paths.
