Here at the Sabrina Love Foundation some of our precious children need specific equipment to help make their lives better and easier. One of these kids is Mivuyo Tyanase who is diagnosed with arthrogryphosis – a rare congenital disorder that results in very limited movement especially in his elbows, wrists, fingers, hips, knees and feet caused by multiple joint contractures. He is such a bright little boy and has developed his own special way of using his body to move his arms.
Due to the limitations of government provision of specialist equipment, Sabrina Love Foundation recently purchased a custom made standing frame for him to use at home and a special chair for him to be able to participate with the other children at the crèche. In June he will be going for a further assessment which might result in him being provided with a power chair, if the government is not able to then the Sabrina Love Foundation will be doing everything we can to try and provide one for him through our many fundraising events. We would love nothing more than to see this bright, happy, content little boy being able to move around freely in his own environment instead of being carried. We hope this dream will come true.
