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

(Additional lymphedema-related events can be found on
the LANA Calendar and LymphActivist’s 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:
Miscellaneous Lymphedema-Related Information & Products: