The Little Girl Who Had Eight Limbs

The Little Girl Who Had Eight Limbs
The little girl who had eight limbs and was worshipped as a deity starts school
She was born with a unique body - eight limbs and two torsos fused at the hips.
Now Lakshmi Tatma, the Indian toddler whose plight touched the world, has grown up and started school.
Two years after a ground-breaking operation to separate her from a parasitic twin, Lakshmi is a lively and bubbly four-year-old.
She loves playing cricket with her older brother, has a tendency to boss around her newfound friends and remains firmly a daddy's girl.
When I think of the way she was, never in a million years would Lakshmi have been able to go to school or have the life she does today,' said her mother Poonam, 26.
All the things she's capable of now were impossible two years ago.
I often try to think what she might be like today if she hadn't had the operation - she couldn't even sit up before and now she runs around like other children.'

Born in a dusty farming village in India's poorest state, Lakshmi was revered as a deity and worshipped from birth.
Villagers, who believed she was the reincarnation of the Hindu goddess of wealth and fertility, would seek her blessing daily and leave gifts at her bedside.
But Lakshmi's resemblance to her mythological namesake came at a terrible price. She could not walk, stand, or even sit.
The little girl was joined to a headless parasitic twin that had stopped developing in her mother's womb. Doctors were convinced she could not have survived into adulthood.
Now fully recovered from the 27-hour operation to save her, Lakshmi is almost unrecognisable from her former self.
Beneath the surface, however, lurk a series of medical problems that threaten her future and will require years of surgery.
Six months after the complex operation to remove Lakshmi's parasitic twin, doctors discovered she had developed scoliosis, or a curvature of the spine.
Without a complex operation to correct her spine doctors have warned her back will be forced into increasingly severe deformities as she grows, possibly leaving her disabled.
Separately, Lakshmi requires an operation to 'detether' her spine after it was discovered she was born with abnormal tissue connecting the spinal cord to her nervous system.
In a further operation orthopaedic surgeons must perform a procedure to 'close her hips', which are set too far apart and result in an unusual 'gaited' walk.
Finally, plastic surgeons will need to find a way to create buttocks for Lakshmi, which did not form in the womb because of the unique way she was connected to her parasitic twin. In the same operation surgeons will have to fix related problems with her bladder and intestines.
Lakshmi has come such a long, long way but we're very scared for the future,' said her mother Poonam.
Brave: Lakshmi Tatma, dressed in her school uniform and standing proudly on her own two feet, smiles at her home in Jodhpur earlier this month
Miracle recovery: Lakshmi plays with her younger sister Saraswati as her mum Poonam looks on at their home this month
Daddy's girl: Lakshmi and her dad Shambu at their home this month. Lakshmi's parents are still fearful for her future, despite the success of the operation
Born to impoverished parents in the frequently lawless state of Bihar, in India's volatile northeast, Lakshmi faced an uncertain future until a wealthy doctor heard of her plight and offered to operate on her for free.
Orthopaedic surgeon Dr Sharan Patil, owner of the Sparsh Hospital in Bangalore 2,000 miles south, travelled to Lakshmi's remote village in 2007 to meet the child and offer her parents the chance of a lifetime.
After more than a month planning the separation, Dr Patil's team attempted the first operation of its kind in the world.
Hundreds of journalists camped outside the hospital throughout the 27-hour surgery.
Lakshmi's fame, having spread from her tiny village around the world, prompted Sucheta Kriplani Shiksha Niketan (SKSN), a charitable school looking after disabled children in the desert state of Rajasthan, to offer her parents a place to live and the chance of an education for Lakshmi and her brother Mithilesh.
Dr Bhairoon Singh Bhati, the secretary of SKSN, said: 'Lakshmi is a special case for us. She's a very challenging case because you can never tell from her medical history when she might next fall ill.
Her scoliosis is an example of the problems Lakshmi faces because we had no way of knowing she would develop a curvature of the spine.
Similarly, despite all the problems she still faces we have no way of knowing what may crop up in the future.
The biggest difficulty caring for Lakshmi is that she's a unique case - there's never been a child like her before so we have nothing to refer back to.'
Under Dr Bhati's guidance Lakshmi has started school, joining her elder brother as the only members of their family to ever receive an education.