 The Lymphedema Advocacy Group is proud to be a finalist for a 2020 RareVoice Award. We are thrilled and honored that our work to improve insurance coverage for lymphedema compression supplies is being showcased! The winner will be announced live at the RareVoice Awards taking place virtually on December 10th, 2020 at 7:00pm EST. For more information and to register (the event is free) click here. I am so grateful for all the lymphedema advocates who use their voice, but would like to give a special thank you to our Board and Committee members (pictured below) whose passion, resilience and dedication to this cause is second to none!
Heather Ferguson  Contributions or gifts to the Lymphedema Advocacy Group are not tax deductible.
As a 501(c)(4) nonprofit organization, the Lymphedema Advocacy Group engages in lobbying activity, in keeping with its mission, for passage of the Lymphedema Treatment Act. |
We are a Finalist for a RareVoice Award!
by Heather on October 28, 2020
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