Scleroderma means hardening of the skin, due to a malfunction of the vascular and immune system resulting in the overproduction of collagen (a protein substance found in the bodys connective tissue). In this second edition of The Scleroderma Book, Dr Maureen Mayes - the leading authority in the field - draws on her extensive experience treating scleroderma to provide up-to-date, practical information that will help patients manage their symptoms and improve their quality of life. Scleroderma can be localized (small patches of hardened skin, which tend to clear up over time), but may become systemic with excess collagen building up in various organs such as the oesophagus, kidneys, lungs, gastrointestinal tract, heart skin, and peripheral nervous system. The disorder most commonly occurs in women between the ages of 20 and 40. However, men and children can be affected as well. The disease is not contagious and is not thought to be inherited and currently, there is noknown cure. Writing specifically for patients and their families, Dr. Mayes offers sympathetic and reassuring advice on matters that often concern those living with scleroderma, such as the best course of action for those who want children, what to do if the disease affects your sex life, and what you can do to help your doctor treat your illness more effectively. The book concludes with a good humoured, frank discussion about how to cope, day in and day out, with an uncertain future-how to be a personliving with scleroderma, not a victim suffering from it. Touching on virtually every aspect of this disorder, The Scleroderma Book provides a reliable source of information and reassurance for patients of any age, no matter how severe their form of the disease.
Part 1: Introduction to terms and types of scleroderma; What is scleroderma?; Localized scleroderma: Limited, localized, diffuse, generalized, systemic and not-so-systemic: Whats in a name?; Systemic scleroderma - diffuse; Systemic scleroderma - limited; Part 2: Epidemiology: Who gets scleroderma and why?; Genetic features of scleroderma: Did you get it from your parents? Can you give it to your kids?; Epidemiology of scleroderma: Number of patients, occupational links and environmental connections; Part 3: How scleroderma affects the body; Raynauds phenomenon, skin involvement and finger sores; Scleroderma and the kidneys; Scleroderma and the gastrointestinal tract; Scleroderma and the lungs; Scleroderma and the heart; Scleroderma and joints, tendons, muscles and nerves; Systemic scleroderma and pregnancy; Scleroderma and sexuality; Overlap syndromes and sclerodermalike conditions; Part 4: Coping with scleroderma; You and your doctor; Living an unpredictable life, facing an uncertain future; Appendix 1: Criteria for the classification of systemic scleroderma; Appendix 2: Scleroderma support groups and resource materials;
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