In a poignant story that has captivated many, Allison and Michael Beacham share the harrowing experiences of their daughter, Mattison, who has battled life-threatening health issues from a very tender age. Diagnosed with biliary atresia, a rare and serious liver condition, Mattison has undergone an astonishing 25 surgeries, including a liver transplant, before even reaching her third birthday. Tragically, she also lost five fingers during her medical journey.
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The Beachams welcomed Mattison in 2020, with Allison, 45, reporting a smooth pregnancy with no apparent complications. However, during a routine check-up at just two months old, they received alarming news from a substitute paediatrician. The doctor pointed out concerning trends in Mattison’s growth, suggesting a visit to the emergency room. “They had obviously known something that my husband and I did not about our little peanut,” Allison reflected.

Upon arrival at the emergency department, the initial comments from specialists about the possibility of biliary atresia sent shockwaves through the family. “We’d never heard of it. But once they explained the prognosis, our shock turned into a demand for answers,” Allison recalls. Biliary atresia is characterised by blocked or damaged bile ducts, leading to serious liver dysfunction if not addressed promptly.
In a lawsuit filed against Orlando Health Winnie Palmer Hospital for Women & Babies, the Beachams claim that the hospital failed to effectively treat Mattison following her birth. Allison accuses them of allowing her condition to deteriorate, leading to a situation where her body was essentially being poisoned. The delay in performing a critical procedure known as the Kasai operation reportedly contributed significantly to Mattison’s precarious health situation.
Describing the extensive toll this ordeal took, Allison asserted, “Mattie passed away nearly seven times during her journey to a new liver.” The negligence claim details how the hospital did not conduct the necessary life-saving surgery in a timely manner—64 days passed instead of the critical 30 days post-diagnosis. This delay resulted in Mattison spending 182 nights in critical care and left her teetering on the brink of total organ failure.
Despite the challenges, the resilience displayed by both Mattison and her family has been notable. “Her soul was that of a warrior,” Allison affirmed. After a painstaking search for a donor, Mattison ultimately received a liver transplant, but not without tragedy—the procedure left her with the loss of her left hand.
This tumultuous experience shifted the perspective of Allison and Michael entirely. They realised that their previous anxieties and lifestyles paled in comparison to the fight for their daughter’s life. “We became a force—a two-pack,” Allison described. “Everything else we used to allow to worry us became irrelevant.” Both parents drastically altered their careers, prioritising Mattison’s welfare over their professional pursuits.
In the wake of their experiences, the Beachams have initiated Mattie’s Law, collaborating with AdventHealth to promote universal newborn screening for biliary atresia. The legislation has already seen success in Florida, where it passed the state Senate unanimously, resulting in funding for a pilot screening programme.
Looking forward, the Beachams are determined to spread their advocacy efforts nationwide, driven by the painful loss of another child with the same condition during their hospital stay. “This is a fixable issue,” Allison asserted. Early detection and timely surgical intervention significantly increase the chances of survival for affected infants.
With the implementation of Mattie’s Law, the Beachams hope to save numerous lives while also reducing healthcare costs associated with delayed treatments. “By implementing this law nationally, we will save 50 to 75 babies’ lives each year and save $250 to $300 million in healthcare costs,” Allison stated resolutely. She is committed to ensuring that no other family should face the uncertainty and heartbreak they endured with their daughter.
As the couple continues their fight alongside their resilient daughter, Mattison—affectionately referred to as “Miracle Mattie”—they aim to raise awareness and prevent the delays in diagnosis that so often lead to tragic outcomes for infants facing biliary atresia.
