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Fund Raising Concert with Elvis Blue

Barnyard – 5 August – R3000 per table

Hanno was diagnosed with a rare genetic disease called Spinal Muscular Atrophy (SMA). This disease affects the nerve cells in the brainstem and spinal cord that communicates with all voluntary muscles in the body. The loss of these nerve cells leads to progressive muscle weakness.

Hanno is unable to sit or walk and therefore has a specialized wheel chair. He requires a ventilator to support his breathing and he feeds through a special stomach tube. Despite his physical limitations Hanno is an intelligent, friendly and loving boy who lives a full and joyful life with his caring family. 

Come celebrate his inspirational life with us and support his family to continue providing the best possible care for him at home.