Cape Times

Crowdfundi­ng to help ease sick boy’s medical bill

- Staff Writer

A CROWDFUNDI­NG campaign has been set up to raise funds for the medical treatment of 10-yearold Caden Benjamin who suffers from a rare, fatal and incurable genetic disorder known has Prader-Willi syndrome.

His condition has taken centre stage in his short life – making it difficult for him to make friends and live a healthy, active life.

Caden, from Standerton, Mpumalanga, weighs 85kg. He faces constant hunger that he is never able to satisfy – his brain doesn’t receive the signal that he’s full, forcing him to eat anything he can find.

Not uncommon with his condition is the desire to eat non-edible items to curb his hunger, which introduces a number of complicati­ons to his body.

He also has difficulty breathing due to his obesity, and was fitted with a Tracheosto­my pipe at the age of 3.

His condition has also affected his intellectu­al ability and has caused behavioura­l problems. At 10 years old, he has been unable to attend school and can’t read.

Caden lives with his mom, grandmothe­r and two cousins.

His mother, Zola Benjamin, has given up her job where she was involved with a second-hand clothing business to provide her son with the 24-hour care he needs. His father left before he was born.

Caden’s specialise­d medical requiremen­ts have caused an enormous strain for the family as he has to travel to the Steve Biko Hospital in Pretoria three times a month to meet a specialist.

Due to his physical condition, Caden requires physiother­apy once to twice a week to help him with breathing. The treatment and transport amounts to R650 a session. Caden also requires nappies and has special dietary requiremen­ts.

His family has been confronted with the likelihood that he won’t make it – but every time he defies the odds and keeps on fighting.

“I was lucky enough to meet this charming young man in February. This was shortly after he received a letter from his doctors stating there was nothing more they could do for him in terms of treatment, and that he needed to be made comfortabl­e at home. This is the road that has led me to crowdfundi­ng on BackaBuddy. I hope Caden’s story moves you. Together we can give him a fighting chance,” says campaign creator Gila Sacks.

A crowdfundi­ng campaign was set up for Caden on donations-based crowdfundi­ng platform, BackaBuddy. The project went live on August 24 and so far secured one donation from Gila towards the target of R150 000.

“Both Zola and Gila have requested that all funds be managed directly by BackaBuddy and be paid directly to necessary recipients to ensure complete transparen­cy with donors, which we have agreed to,” said BackaBuddy marketing officer Zane Groenewald.

To support Caden’s campaign visit https://www.backabuddy. co.za/champion/project/for-caden

 ?? Picture: ZOLA BENJAMIN ?? RARE DISEASE: Caden Benjamin (10) from Standerton, Mpumalanga is suffering a rare, fatal and incurable genetic disorder known has Prader Willi syndrome.
Picture: ZOLA BENJAMIN RARE DISEASE: Caden Benjamin (10) from Standerton, Mpumalanga is suffering a rare, fatal and incurable genetic disorder known has Prader Willi syndrome.

Newspapers in English

Newspapers from South Africa