Promotion and deepening of knowledge on the subject of lymphedema and lipedema among professionals and patients. Providing available information to patients and professionals regarding all types of treatments. Distribution of professional materials. Establishing a support group for patients throughout the country. Organization of lectures, study days and an annual conference for organization members. Support for research dealing with this field. Promotion of the rights of patients with lymphedema and lipedema in state institutions in the fields of health, medicine and nursing (health maintenance organizations, hospitals, national insurance and the Ministry of Health). Maintaining contact with similar organizations in the country and abroad to promote common goals. Encouraging the training of physiotherapists to specialize in treatment. Establishing support groups for lymphedema and lipedema patients to increase accessibility to patients throughout the country. Encouraging the establishment of exercise groups for people suffering from lymphedema and lipedema and providing tools for self-treatment. Encouraging professionals to work in the field of lymphedema and lipedema research, in all matters related to treating the patient population in the country, testing the proposed treatments and building new programs for self-treatment
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Health or life-saving