I have some unfortunate news, but it comes with a silver lining. The August 1st lymphedema learning session for primary care providers that we told you about last week, hosted by the Keck School of Medicine at USC, will only be open to their internal faculty.
We know that there is a great need for more education among healthcare providers, however, and are working with the organizer to plan another session that will be open to healthcare providers outside their organization. We apologize for any disappointment, but that this will ultimately lead to greater opportunities for education.
In the meantime, we hope you are finding our informational handouts for Patients, Providers, and Suppliers helpful. They are displayed below, and these and other materials can be found on our Increasing Awareness page.
All three handouts provide information specific to each group and address the most commonly asked questions. The links above are perfect for viewing or sharing these handouts online, or can be downloaded for professional printing. If you would like to print these items at home, use these versions, which have margins added – Patient, Provider, and Supplier.
Your support makes free resources like these possible. Please consider donating$50, or whatever is right for your budget. Thank you so much!
Heather Ferguson
Founder & Executive Director
Lymphedema Advocacy Group
LymphedemaTreatmentAct.org
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