Little Sajida is battling a rare metabolic disorder known as phenylketonuria (PKU), which requires a strict diet and specialized medical formula with no alternative. Her mother lives with constant fear, worried she will not be able to afford the expensive formula her daughter depends on, as any interruption could lead to serious and lasting damage to Sajida’s health and development. Sajida urgently needs continued access to her specialized milk and essential treatment to prevent severe complications and protect her future. Her family, already overwhelmed, is struggling to keep up with the ongoing cost of care, hoping for support to ease this heavy burden.