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1) TO RELIEVE PERSONS DIAGNOSED WITH OR IN THE PROCESS OF BEING DIAGNOSED WITH LYMPHANGIOLEIOMYOMATOSIS (LAM), THEIR FAMILIES AND CARERS BY THE PROVISION OF SUPPORT AND INFORMATION ON LAM 2) TO EDUCATE HEALTH PROFESSIONALS ABOUT THE CAUSES AND TREATMENT OF LAM 3) TO ADVANCE RESEARCH INTO LAM AND DISSEMINATE THE KNOWLEDGE GAINED AS A RESULT OF THE RESEARCH