Hospital was like a second home to 19 year old Lilli Sim as she was painstakingly undergoing reconstructive surgery for a completely deformed face.
Diagnosed with a rarest of rare diseases, Lilli Sim was one of those, one in 120,000 babies born with Craniofrontonasal Dysplasia (CFND) disfiguring her entire facial symmetry. And due to that she has breathing problems, social stigma, bullying and constant medical intervention. But now she is almost on recovering phase.
At birth she was given just three months to live
Lilli Sim from Australia spent a lot of time in hospital, undergoing treatment for her rare facial abnormality named Craniofrontonasal Dysplasia. After several reconstructive surgeries, doctors stated she is now going to be normal which is a miracle.
Lilli was also diagnosed with Cohen syndrome from birth and had just 3 months to live. Today she is twenty years old.