Talia Oatway, ex-partner of Geordie Shore star Aaron Chalmers, has shared her terrifying experience as her young son Oakley battles a rare genetic syndrome called Apert Syndrome. Oakley, who will soon undergo his 11th operation, recently faced a life-threatening situation that required intubation and hospitalization. Talia described the moment when panicked nurses rushed in to save him, leaving her in fear. Now in a high dependent unit, Oakley, who hasn’t been awake since Friday, is one of less than 100 children in the UK with Apert Syndrome, which affects the skull, face, hands, and feet. Talia, who also has three other young children, spoke out in an attempt to raise awareness and provide support to other parents of unwell children.
Talia recounts the traumatic experience of seeing Oakley in a critical condition and the uncertainty surrounding his impending surgery. She expressed her hopes for his recovery and the challenges she has faced as a single parent. Despite the difficult situation, Talia remains grateful for the support of the NHS staff and the online community, which has provided invaluable advice and encouragement. She emphasizes the importance of sharing Oakley’s story to shed light on Apert Syndrome and highlight the struggles faced by families with unwell children.
Aaron and Talia welcomed Oakley in 2022 but have since ended their relationship, with Talia describing the past months as the toughest of her life. The couple split in December 2022, and Talia has had to navigate the challenges of single parenthood while dealing with Oakley’s health issues. She remains committed to raising awareness about the condition by sharing updates on social media and connecting with other parents facing similar situations. Talia appreciates the support she has received from the healthcare professionals and the online community, as well as the strength and resilience of her son Oakley.
The emotional toll of seeing her son in a critical condition has taken a toll on Talia’s wellbeing, but she continues to advocate for more openness about children’s health issues. She acknowledges the power of positive thinking and the importance of keeping hope alive for Oakley’s recovery. Talia believes that sharing her son’s journey can help other families dealing with similar challenges feel less alone and more supported. She encourages people to learn about Apert Syndrome and the struggles faced by families with children affected by rare genetic disorders.
While Talia remains hopeful for Oakley’s recovery, she is also realistic about the challenges ahead. She acknowledges the uncertainty surrounding his condition and upcoming surgery but remains determined to stay strong for her son. Talia hopes that by sharing Oakley’s story and raising awareness about Apert Syndrome, she can help other parents facing similar struggles find support and understanding. Despite the hardships and fears she has experienced, Talia is committed to being a voice for families dealing with rare genetic disorders and advocating for better resources and support for those in need. Through her openness and resilience, Talia is making a difference in raising awareness and offering hope to families in similar situations.
