Held in His Hands: Jhanko’s Prader-Willi Journey

Started 7 months ago

Open end-date

R 85 389
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of R 100 000 goal
R 0
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115
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STORY

About This Campaign

organiser-empty-profile-picture
Mignon Marais
Organiser
1 
BaB campaign
Location
Harties
South Africa
Location
Started 7 months ago
Open end-date

Baby Jhanko was born with Prader-Willi Syndrome, a rare genetic condition that affects growth, muscle tone, and appetite regulation. Children with this syndrome require specialized medical care and close monitoring, especially in their early months.

Since birth, Jhanko has faced many challenges, yet he continues to show incredible strength and bravery every single day. He has spent 2 months in the NICU, during which time he has received a PEG feeding tube to support his nutrition and 3 blood transfusions to help his recovery. Every day, Jhanko fights tirelessly, showing resilience and courage beyond his age.

His medical journey is ongoing, and the costs of his care are very high. In the near future, Jhanko will not be able to attend school and will need specialized care at home to protect him from infections and support his growth and development.

We are asking for your support to help cover thes...

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