Craig Richardson: A Life Worth Living, with Disabilities

Born in 1981, Craig Richardson was soon diagnosed with a chromosomal deletion, and its grim prognosis. Within a year, he had stopped breathing, and began having devastating seizures. In this account, his mother, a registered nurse who had worked in neonatal intensive care units, relates how their family coped with the exhausting challenges during Craigs twenty-five year life span, with medical insight and the quirky humor that helped them survive emotionally through the years. In 1983, she began networking families with Craigs rare syndrome, Wolf-Hirschhorn or 4P-; the beginning of the 4P- Support Group which has connected over 500 families as a national organization. The book promotes the authors belief that every couple needs to pro-actively work to strengthen their marriage, especially those with difficult situations. In their marriage, they have coped with four cross-country moves as an FBI family, numerous prolonged hospitalizations, the balancing of the needs of three uniquely different sons with their launch into adulthood, and Retirement: The Final Frontier . The book details Craigs birth and his death processes, and addresses the contemporary social issues of abortion, quality of life, National Health Insurance, euthanasia, and the potential for Death Panels to evaluate, and possibly eliminate, those whose lives are adjudicated as not worth living.