Could you or someone you know use a little LTA 101? We have a brief presentation available as a document or Power Point slides that includes all of the basic, essential information.
If you have primary lymphedema you are invited to participate in Rare Across America with the Rare Disease Legislative Advocates group. This is an opporunity to meet with your members of Congress and/or their staff at their local district offices. The deadline to register is July 3rd and information to print and bring is here.
And if you’re attending the International Lymphoedema Framework Conference in Chicago this week please be sure to stop by our booth in the exhibit hall. Myself and several other members of our board will be in attendance and we would love to connect with you!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
