Just4Children wants to fundraise for Yasmin so that like other children her age she will be able to walk, run and play in the parks.

Yasmin was born on time,but very weak and tiny.

At 20weeks of pregnancy after scan doctors discovered a cyst on Yasmin's brain.A mum was told that the cyst will not affect Yasmin's development.

But after giving birth Yasmin's mum noticed something is not right.Yasmin didn't smile or concentrate on toys.Her head was very weak.

When Yasmin was 1year old she had an appointment with a neurologist.After a genetic blood test Yasmin was diagnosed  with ultra rare chromosome disorder called inverted duplication and deletion of chromosome 8p.

That was shocking news for both parents and the rest of the family.

Apparently Yasmin needs lots of support and therapies.

She is 3years old girl now,but she doesn't walk,sit or crawl.Also she has severe global development delay.

Yasmin needs lots of therapies,especially physiotherapy,hydrotherapy,hippotherapy,sensory integration,speech and language therapy,occupational therapy.NHS can only offer limited sessions on some therapies.She could benefit alot from all of them.

Help Yasmin to have what she deserves,happy life,without pain and limits.

Thank you for your support.