New wheels: Lee (right) hands over a wheelchair worth RM2,200 to Aiman (third from right) as he is unable to walk due to the delay in getting treatment for LSD. Also present is Chin (left).
THE Malaysian Lysosomal Diseases Association (MLDA) hopes to raise RM1mil to set up a foundation to be able to better help patients afflicted by the rare genetic disorder.
Its president Lee Yee Seng said this was necessary as many parents did not know where to turn to for help upon discovering that their child was suffering from the disease.
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