A family is seeking help with a rare disease case involving their young son, Zachary de Wet, who was diagnosed with Mucopolysaccharidosis Type 2 (MPS II) or Hunter syndrome, a rare genetic disorder caused by a missing or malfunctioning enzyme, in March 2021. Zach’s parents, Jacques and Michaney de Wet, have been fighting a legal … Continue reading Family seeks help for rare disease case – Can you offer support?