FREE Virtual Education Opportunity

by Heather on October 24, 2020

As a resource to the lymphedema community, this year anyone can attend the virtual exhibit hall at the National Lymphedema Network’s online conference!The Lymphedma Advocacy Group is one of dozens of exhibitors, so if you’ve ever want to chat with a member of our board this is a chance to do so.

Other exhibitors include all of the major manufacturers and suppliers of lymphedema compression supplies and related products. Come and see all of the choices available to patients, and what new products are being introduced. The FREE virtual exhibit hall will be open for 45 minutes each of the next five days. To see the times and access the links for each day’s event click here.

Thank you to all you have already donated to our Match 2020 Campaign! Every dollar matters, and thanks to an Angel Donor, every dollar will also be matched up to $10,000! That means your donation has twice the impact and we can reach our $20,000 goal twice as fast. We are more than one-third of the way there, so please consider donating $20, or whatever is right for your budget.

To make a secure online donation, or to get the address to donate by check, please visit our Match 2020 Campaign. Thank you for your support!

Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org


 

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.
 

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