It's been slightly more than a year since 17-year-old Michelle Crandall hanged herself in the garage of her mother's Costa Mesa home. Along with the more common upsets of adolescence, Michelle was plagued by the fact that she was a dwarf. She ultimately found it impossible to cope with being different in a society that has tended not to recognize the special needs of short-statured people.
As reported in View last June, Michelle's father, Richard Crandall, quit his job as an electronics salesman three months after the teen-ager's death. Founding the nonprofit Short Stature Foundation and Information Center, Crandall proceeded to devote all his time to lobbying for the rights of little people, and increasing public awareness of what it means to be short-statured.
Since that time, Crandall, also a dwarf, has worked with doctors to compile a list of more than 50 physical abnormalities that may occur in short-statured people. He believes the list will add substance to his campaign to have short stature officially recognized as a disability, a move that would make little people who needed it eligible for financial assistance. Many of the physical disabilities on the list may be corrected or minimized by early detection, Crandall said, so it is important that this and other information be readily available to short-statured people and their parents.