She is six years old.

She has never taken a single step on her own.

Selin was born at just 26 weeks. She is a twin — her brother is healthy, but Selin’s early arrival changed everything.

She lives with hydrocephalus and cerebral palsy.

She cannot walk.

She cannot sit independently.

She cannot speak.

Her vision is very limited.

But she feels love deeply. She recognises our voices. She responds to touch. She fights every single day in ways most people will never see.

As parents living in the United Kingdom, we have searched for every possible option to help our daughter. Recently, we found a specialised 28-day neurological treatment programme in Mexico that may help stimulate damaged brain tissue and improve her quality of life.

It is not a guaranteed miracle.

But it is hope. A real medical opportunity.

The total cost for the treatment, hospital stay, and required medical tests is approximately $50,000 (around £40,000) — an amount far beyond what we can manage alone.

We are not asking for sympathy.

We are asking for a chance.

A chance for Selin to improve her mobility.

A chance to communicate.

A chance to experience more of the world around her.

If you are able to support Selin — whether through a donation or by sharing her story — you are giving her something priceless: possibility.

Thank you for taking the time to read about our daughter.

Thank you for standing with our family.