Zachary Berger tells his story of lymphatic malformation

Zachary Berger tells his story of lymphatic malformation

pictured above: Zachary Berger (right) with his dad Marc Berger at the 2015 Texas Walk to Fight Lymphedema & Lymphatic Diseases in Plano, TX.

My Story, by Zachary Berger

There is no way I would be who I am today without my tongue. I guess that is the case for most people, but for me, I was

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A beloved mother is lost to lymphedema

A beloved mother is lost to lymphedema

by Jennifer Vitale

My mother, Linda Vitale, was a primary lymphedema patient. For years she struggled with this disease and didn’t even know she had a disease. Her doctors always said she was just extremely heavy. When her legs started leaking fluid, she was told it was a calcium build up

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