Sain Mumtaz, 22, has been seriously disfigured by Proteus syndrome which has caused certain parts of his body to continue growing.
Brave: Sain Mumtaz from Lahore has battled with his disfigurement since he was child
He has been accepted by locals in his neighborhood on the outskirts of Lahore, in Pakistan, but the disease has left him with ongoing medical problems and he finds it difficult to get around
Love for life: Despite his appearance and related medical problems Sain is embracing life
Kind: Locals have accepted Sain and call him their 'giant friend'
Love for life: Despite his appearance and related medical problems Sain is embracing life
It is thought that Sain suffered from a unique variation of Proteus syndrome - which also affected 'Elephant Man' Joseph Merrick - because of the symmetrical deformity on his face and skull.
Heartbreakingly Sian once believed his terrible affliction was a curse bestowed on him by a vengeful God, leaving him listless and depressed.
But supportive friends and family have kept his spirits high and he is now determined to embrace life.
Kindly locals refer to him as their 'giant friend' and are determined to discover a cure for Sian who in turn hopes he will meet the woman of his dreams.
Family: Sain is pictured at his Lahore home in Pakistan with his family who have been very supportive throughout
Sain and his family hope for a cure so he can find love. He told how people were once afraid of his appearance bu that he has grown to be accepted
He said: 'I've been this way since I was born. My face, arms and legs all differ in size and people assume I'm not like other normal human beings.
But I'm mentally fit and understand everything, I live like my life like everyone else despite all my family including my mother, father, brothers and sisters all being born without the condition.
People used to run away from me. But now they treat me normally and sit and talk to me when I am out.
They call me their friend. One day I hope to be cured and meet a woman who will love me.'
If Sain is suffering from Proteus syndrome there will be nothing doctors can do for him. But his family cling on to the hope that he is suffering from an undiagnosed and treatable disease
Sain Mumtaz (right) pictured with his father Wazir Ali (left) who is desperate to find a cure for his son
Sain hasn't seen a doctor since he was a boy when he was told it was Proteus Syndrome and nothing could be done to help him.
If Proteus is the correct diagnosis for his condition there may be nothing that can reduce the weight of his massive limbs.
But his family cling on to the hope that Sain is suffering from some other overgrowth disorder and if this is true then there may well be treatments that can help him.
His father, Wazir Ali, said: 'We want to discover what is wrong with him, and whether anything might be done to improve his day-to-day life.
'He has hopes for his future, one day he would like to run a rickshaw business and find a wife.'
| Posted: at | |
Ngeboju
Hollandear
Frankijones
kebella
........yu already no that 
...heheh...if yu wanna smell what kebella is cooking........bring it up!!
ajanni
fuckinjoe2
uwa190
BournIdentity
pamela224
lanudja
chicco77
etibaba
TRENDING GISTS 
How Abusive Nigerian Man, Beat Wife To Death Months After Relocating To The UK
74Yr Old Woman Robs Bank At Gunpoint After Losing Her Life Savings To Online Scammers
VIDEO: “I Don’t Believe In Cohabiting Before Marriage” – BBN Star, Ifu Ennada Spills
THROWBACK: Zenith Bank’s Management Team Pay A Visit To Allegedly Apologies To Fayose - Photos+Video
See Tuition Fee Receipts Yahaya Bello Paid American School From 2025 Session Through 2031
SuperComputer Predicts EPL Title Winners After Victories For Both Arsenal And Man City