Stuart Wickison The Boy Who Can Never Grow Old

Stuart Wickison The Boy Who Can Never Grow Old

As a child Stuart Wickison developed Duchenne Muscular Dystrophy a rare, genetic, life-limiting disorder. He is not expected to live beyond his twenties.

Duchenne Muscular Dystrophy or DMD is a genetic condition that only affects boys. They’re born able-bodied and only find out the full prognosis in their teens. DMD is caused by mutations of the gene which produces dystrophin, a protein essential for the healthy development of muscles in the body.

Gigantiform Cementoma The Boy with a Tumour for a Face

Gigantiform Cementoma The Boy with a Tumour for a Face

Novemthree Siahaan is a young Indonesian boy developed what has been called a colossal tumour on his face known as Gigantiform Cementoma.

Novemthree’s saviour arrived in the form of Dr. David Lui, a Buddhist missionary from the Tzu Chi Foundation. Dr Lui agreed to send Novemthree to Haulien in Taiwan to see specialist who could attempt the extremely complicated process of removing the tumour.

Identical Quads - The Mathias Girls

Identical Quads – The Mathias Girls

12 weeks after Allison Mathias fell pregnant she was told she was expecting triplets. A routine ultrasound found a fourth baby; she was having quads.

The chance of giving birth to quadruplets, naturally, in 1 in 800,000. The odds of those quads being identical are then one in eleven million. Unlike fraternal multiples who do not necessarily look alike and can even be a mix of sexes, identical quadruplets can only come from the same egg.

Jordan: The Boy with Proteus Syndrome

Jordan: The Boy with Proteus Syndrome

Jordan was born with a rare genetic condition, Proteus Syndrome, which, in it’s extreme form affects less than one hundred people in the world.

Soon, Jordan and Tracy will fly to America to visit the National Institute of Health in Washington D.C. The institute is one of the few places, in the world, that specialises in treating Proteus sufferers. For Jordan, his biggest hope is that they find a way to keep him walking.

Rebecca Medley can’t stop Eating: Prader Willi Syndrome

Rebecca Medley and Katie Williams have a rare genetic disorder called Prader Willi Syndrome where they eat uncontrollably; an incurable condition.

Prader-Willi Syndrome also causes a wide range of learning difficulties, Rebecca gets special needs support at her local primary school. PWS will affect Rebecca’s social development, sexual development, and mental development.

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