Interviews

Our Trip to DC. by Heather Ferguson

YOUR SUPPORT IS ESSENTIAL!

 The proposed federal legislation “Lymphedema Diagnosis & Treatment Cost Saving Bill of 2010” is important to all of us and the Lymph Notes Team urges all of you to “pitch in” and help.

This is the story, as told by Heather Ferguson, of a trip to Washing by a band of dedicated volunteers and their successful effort to build greater support for this law.

Got a question or comment? Go to the Living With Lymphedema forum. Share your stories in My Stories.