Transcript
Andrea Dunlop (0:04)
True Story Media before we begin, a quick warning that in this show we discuss child abuse and this content may be difficult for some listeners. If you or anyone you know is a victim or survivor of medical child abuse, Please go to munchausensupport.com to connect with professionals who can help. There is a family in Renton that I want to introduce you two. Mom Sophie went on an inspiring trip to Zambia in her college years. She's since adopted two girls. One of them has an incredibly rare disorder. Doctors say it's a one in a million chance. The audio you just heard is from a news story that aired on King 5 television back in May of 2019. This story wasn't on my radar, but I had a lot going on back then. I had just had a baby and had a new book coming out. And this was around the time that Munchausen by Proxy was really entering my work life. The month that this story aired, I'd done my very first interview about my own family story for Vanity Fair, and this was followed by an appearance on a local station about my third novel. We came here to forget this was all taking place amid the second investigation into my sister for Munchausen by Proxy abuse of her children. By the middle of that summer, the courts would return my sister's children to her, and a few months after that, the prosecuting attorney would make the decision not to file charges against my sister, Megan Carter, despite the horrifying and voluminous evidence against her. But back to Sophie. In general, seeing stories about sick kids in the news is upsetting for a bunch of reasons. So family friends are banding together. They're trying to raise money, and this is something that is, you know, no little ask. We're talking about like $60,000 for a vehicle for them. So we just wanted to put their positive energy out there. Of course, there are the particular fears and questions that I bring to it, given my experience with my sister. Is this mom telling the truth? What if this child isn't a victim of a rare disease, but a victim of the person purporting to care for them? Even when there are no red flags for abuse, which is mostly the case, these stories are pretty dystopian because they illuminate a tragic failing of our country's healthcare system. The horrible reality that families, many of whom I'm sure would prefer to keep their children's health private, are forced into a situation where they have to perform their trauma publicly in the hopes that kind strangers might step in to relieve the skyrocketing medical bills that could otherwise bankrupt their family. So while I usually avoid these types of stories in my day to day life, once I did see this news report, right away I noticed that Sophie was positioning herself as the only, only one who saw what was happening with her child. I started noticing just kind of weird things or times where her body would just feel really different. Like it would either be super, super tight or like really limp. Doctors visits filled the first few years of life, and right away they found pretty significant brain damage. And so she was diagnosed with CP at the end of 2015. This is like a sandwich. But Sophie quickly realized was experiencing something much more concerning. Complaining to the neurologist, saying, like, she's having seizures. So they would bring her in for an EEG and it was nothing. They're like, no, we don't see anything. Maybe she is. Here's the walls. Sophie admits she started to question her own instincts. There'd be times where she was like, literally totally paralyzed. And I go to her doctors and be like, I know she's walking right now, but like, she was literally paralyzed all day yesterday. And they'd be like, no, that's not possible. And like, but like, she couldn't move, like I'm telling you. And they're like, okay, but she can now. And I'm like, right, I know. But after seeking a second opinion and running through genetic testing, she also has one on the ATP1A3 gene, which is associated with a disorder called alternating hemiplegia of child childhood, which is a extremely rare one in a million genetic disorder. And she's right. It affects one in one million children. It is progressive and has no cure. Wow. Lord, you took me up to the fullest extent on what I told you I was willing to do. This piece on the evening news ended up being the first chapter in what would become a major national news story. This is rare for Munchausen by proxy cases, which usually garner little national coverage outside of the truly sensationalized stories like Gypsy Rose Blanchard and Maya Kowalski. But there were many elements of this story that caught people's attention. For one, there were the optics. Sophie, who is young, white, blonde and conventionally pretty, had adopted two children, sisters from a faraway nation. I went to Zambia after my freshman year of college on a month long mission trip. And when I was there, I just encountered the plight of an orphan. Which one is in the hand? Adoption wasn't on my radar at all. In the televised segment, there are images from Sophie's life with her two adorable girls interspersed with footage from the interview and B roll of Sophie's younger daughter, who we're referring to as Cee, who is smiley and cheerfully dressed in the family's kitchen. At one point, as the two play a game together, Sophie sitting beside her daughter's wheelchair, the little girl says this at all, oh, I don't want to get a poke. I'm so scared. It would be easy to miss this blip in the audio, but the little girl is saying, I don't want to get a poke. I'm so scared. This moment is odd because they're not in a medical setting and there's no medical equipment nearby. To most, this might be a throwaway moment, but for me, it's a harbinger of how this seemingly inspiring story of a mother who'd moved heaven and earth to help two Orph became this so this is Detective Werwerk with the Renton Police Department. Today's date is March 17, 2021. It is approximately 8:03 hours.
