VICTORY CELEBRATION FOR PASSAGE OF LTA & CONGRESSIONAL AWARDS CEREMONY

Washington DC

On May 22-23, 2023, over 100 lymphedema advocates with the Lymphedema Advocacy Group gathered in Washington DC to celebrate the passage of the Lymphedema Treatment Act (LTA).  Among the advocates who attended this event were LLN members Debbie & Clint Labarthe, and their grandson, Carson Sollenberger, a primary congenital lymphedema patient, seen here with Heather Ferguson, Founder/Director of Lymphedema Advocacy Group.

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The Lighthouse Lymphedema Network is a 501 (C) (3) organization of individuals who are lymphedema patients, or who have an interest in lymphedema.

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