The family of a young girl named Melan is continuing their search for medical solutions after she was diagnosed with a rare facial condition linked to abnormal tissue growth. The condition, which gradually alters facial structure, was first noticed when Melan was just over one year old, as a small area of swelling began to change her appearance.

Since then, her parents have made repeated visits to SPMC, consulting specialists and closely monitoring the progression of the condition. According to her family, doctors explained that surgical treatment is often advised when a child reaches around five years of age, due to safety considerations and facial development. Until then, Melan must wait while the condition continues to influence her daily comfort and interactions.

Melan’s parents say the waiting period has been emotionally difficult. While they understand the medical reasoning behind delayed surgery, they worry about the physical and social challenges their daughter faces as the swelling continues to grow. “As parents, it’s hard to watch and feel like time is passing without answers,” her mother shared.

Determined to explore every possible option, the family has decided to seek a second medical opinion from specialists outside their local area. They are currently preparing to travel to Manila, where larger hospitals and advanced facilities may provide alternative approaches or earlier treatment plans. Her father explained, “We respect the doctors who have guided us so far, but we also want to make sure we’ve explored every safe option for our child.”

With the support of generous sponsors, the family is taking steps to make the trip possible. However, the cost of consultations, imaging, and potential surgery remains a major concern. They are now hoping for assistance from a medical center foundation that could help cover the expenses and open the door to treatment.

Melan’s story highlights the challenges faced by families dealing with rare medical conditions, particularly when specialized care is limited or delayed. Her parents hope that sharing their situation will raise awareness and encourage support for children who require complex medical care at an early age.

As they prepare for the next stage of their journey, the family remains focused on one goal: finding a safe and effective treatment plan that will allow Melan to grow, learn, and live with greater comfort in the years ahead.