Resources

Below is an evolving list of information sources that may be useful to those who suffer from lymphedema and/or their caregivers. If you would like to recommend an addition to this page please Contact Us with your suggestion.

Lymphedema Events:   

Ongoing ~ LE&RN’s Symposium Series, free and online

April 20-22, 2017 ~ Cancer Metastisis through the Lymphovascular System:
Biology and Treatment
conference, SanFrancisco, CA. Patient Summit on April 22nd.

April 28-30, 2017 ~ Lipedema & Dercums Disease:
Goals for the Future and Tools for Today
conference, Salt Lake City, UT

October 10-15, 2017 (details forthcoming) ~ National Lymphedema Network’s 
13th International Conference, Orlando, FL

(Additional lymphedema-related events can be found on the LANA Calendar.
If you have an event you would like listed here please contact us.)
 
Lymphedema Organizations:
 
 
Lymphedema Online Groups:
 
 
Lipedema Resources:
 
Lymphedema Providers
directories to find lymphedema doctors and/or certified therapists in your area:
 
 
Compression Garment Assistance Programs:
 
Also check with your local American Cancer Society chapter, if cancer related lymphedema, or your local Komen chapter, if breast cancer related – some have garment assistance programs, but they aren’t generally advertised.
 
Scholarship Opportunities:
 
 
Lymphedema Studies, Clinical Trials, etc –
please participate to help researchers find better treatments and maybe even a cure!
 
 
Apps for Lymphedema:
 
LymphTracker (tool to track your measurements)
 
Lymphedema Treatment Products, Manufacturers:
 
 
Lymphedema Treatment Products, Suppliers: