Overview

Zac's Attack for a Cure is a chapter of the Lymphatic Education & Research Network. My name is Zac Berger, and with my family, we are here to ATTACK THE CURE for Lymphatic Malformation, a lymphatic disease from which I and many other children and adults suffer. Lymphatic malformations are rare, non-malignant masses consisting of fluid-filled channels or spaces thought to be caused by the abnormal development of the lymphatic system. These malformations are usually apparent at birth or by two years of age. When evident at birth (congenital), lymphatic malformations tend to be soft, spongy, non-tender masses. The specific symptoms and severity of lymphatic malformations varies based upon the size and specific location of the malformation. Some lymphatic malformations can be massive. Lymphatic malformations, regardless of size, can potentially cause functional impairment of nearby structures or organs and disfigurement of affected areas. It is important to note that affected individuals may not have all of the symptoms discussed below and that one child’s experience can vary dramatically from another child’s experience. Parents of affected children should talk to their physician and medical team about their child’s specific case, associated symptoms and overall prognosis. The specific symptoms that develop depend upon the size and exact location of a lymphatic malformation. We are working with the Lymphatic Education & Research Network (lymphaticnetwork.org) to shine a light on LM (lymphatic malformation) and raise money for research with the goals of a cure, treatment and prevention. Please join us in our fight by donating and becoming a supporting recurring member: https://lymphaticnetwork.kindful.com/?campaign=1090282