A family with five members has endured an 18-month journey to diagnose their youngest child’s rare and life-altering medical condition. Skyla Smith, aged 3, started experiencing chronic leg pain before she turned two, causing her significant distress. Despite multiple doctor visits, her condition, later identified as Juvenile Idiopathic Arthritis (JIA), took a year and a half to diagnose.
Skyla’s mother, Elaine-Maree Telfer, expressed her frustration at being repeatedly told that it was just growing pains. The diagnosis in October 2025 revealed that JIA, affecting 1 in 10,000 children in the UK and more common in girls, was the cause. This condition prompts the immune system to attack the body’s joints, potentially leading to irreversible damage if left untreated.
Although relieved to finally have a diagnosis, Elaine-Maree also feels anxious about Skyla’s prognosis. Skyla’s daily routine now includes weekly methotrexate injections, anti-sickness medications, and folic acid to manage side effects. Despite the challenges, Skyla continues to have good and bad days, engaging in activities like ballet and attending nursery.
Elaine-Maree, along with her partner David and older children Leo and Jax, remains committed to providing Skyla with a fulfilling childhood. They receive support from Juvenile Arthritis Research, a charity dedicated to helping those affected by JIA. Elaine-Maree aims to raise awareness about the condition and offer guidance to parents facing similar situations, emphasizing the importance of early detection.
Highlighting the lack of awareness surrounding JIA, Elaine-Maree hopes Skyla’s story will resonate with other parents. She advises keeping a diary and documenting symptoms if a child repeatedly complains of pain, as this can aid in a quicker diagnosis. By sharing their journey, Elaine-Maree aims to empower other families navigating similar challenges.
