Simon Ibell is an advocate for Human Potential and a Role Model for Persons with Disabilities. Ibell’s condition, known as MPS II (mucopolysacharridosis) or Hunter syndrome, is rare and is the result of an enzyme deficiency, which affects most of his major organs, his joints, and is both painful and debilitating. Living with MPS II has taught Ibell that every moment of life is precious. He continues to learn how people perceive and handle disabilities and he uses this knowledge to lower the barriers and help bring about change.
The iBellieve Foundation is Simon’s official organization that aims to conquer MPS II and related Lysosomal Storage Disorders.
To learn more about Simon, please visit www.simonibell.com