PUBLISHED 11.28.17
The Lymphedema Treatment Act
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This article was written by Heather Ferguson, the Founder and Executive Director of the Lymphedema Advocacy Group. Heather’s relationship with lymphedema began with the birth of her twin boys, Devdan and Dylan, in September of 2006. Dylan was born with primary lymphedema. Her desire to advocate on behalf of lymphedema patients took root when she . . . → Read More: The Lymphedema Treatment Act