I am posting this question on behalf of a family in east London. I recently met a man in his 20's who has cerebral palsy and has also been diagnosed with sensory defensiveness. His mum has done alot of research about this condition, which mostly comes from America. She would like to talk to any one who has been diagnosed with this condition or is a parent of someone with the condition. If you have any information or experience of Sensory defensiveness the family would appreciate having contact with you.