Patients, care providers, and compression suppliers should all check out the Center for Medicare and Medicaid Services’ new page, Lymphedema Compression Treatment Supplies! It contains guidance that complements the information below, as well as links to important resources, especially for prescribers and suppliers. 

PATIENTS & CARE PROVIDERS

Eventually, you will be able to search for suppliers who sell compression by using the Medicare Equipment and Suppliers online search tool. Typically, Medicare participating providers also take other types of insurance, so even if you are not a Medicare beneficiary, this will be a helpful tool. If you do not have a supplier physically located in your area, do not worry, there will be online options. Because we do not know how long it will take for this directory to be updated, our group is currently working on assembling a list of participating providers and will share that with you as soon as it’s available. 

CURRENT & FUTURE SUPPLIERS


If you have not yet completed the below action item, it’s not too late!

The final rule is a huge victory for patients, but our work is not done yet. Please visit our Take Action page if you have any insurance plan other than traditional Medicare and haven’t contacted your own insurance provider yet. 

Below is a summary of the LTA final rule. You can read the full 65 pages here. We have also inserted notes into our group’s public comment document, which can be read here, to indicate which of our comments were incorporated into the final rule.

Lymphedema Treatment Act Final Rule Coverage Summary

What will be covered:

Frequency allowances:

Coverage requirements:

Codes and reimbursement rates:

Deductibles and copay:

PLEASE NOTE: The final rule also outlines the process for making future changes to and/or additions to coverage if/when needed. This is very important, and ensures we will not be in the position of needing to get another law passed if adjustments to the coverage need to be made, or if new treatment supplies become available and need to be added to coverage.

Together, our advocacy made all of this possible! If you are able to make a donation to support our continued work, we would be so grateful. Thank you! 

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