14-Year-Old John Dilgen, from Staten Island, New York,
was born with a strange and rare skin disease. He had no skin on his legs and
arms when he was born. John’s disease is incurable which due to which his skin
fall of even with the slightest touch. The little boy was diagnosed with a rare
genetic disease, EB – Epidermolysis Bullosa, due to which his skin blister,
burst and leaving raw sores to infections. He spent all his life wrapped in
bandages to prevent his skin from damage and falling.
Early Diagnosis
W hen he was 16 months old he was diagnosed with Recessive
Dystrophic Epidermolysis Bullosa. It is a more grave form of the disease which
causes difficulty eating and swallowing. It has also some other bad affects
including loss in fingernails and toenails, anemia and failure to thrive.
His Disease
EB is a result of missing type VII collagen. It is a type
of protein which helps the top layer to skin to be bind with the other layers
under it. This is because of his skin cannot stay on his body and continuously
fallen eve with soft touch.
Fund Raising
John needs and oxygenated tub making his baths less
painful and his family is lack of sufficient financial resources to buy it.
They have started a campaign for fund raising for him and luckily strangers
came forward and donate for him. Family is successfully has made over $108,361,
of the original target of $40,000.