TLQ Advocacy

Tell your representatives the proposed changes to healthcare place women with Lipedema at grave risk!

In turn, this means there may not be a re-introduction of The Lymphedema Treatment Act to the new Congress. Tell your representatives Congress that they should be courageous and sponsor/sign on to this bill!

Thank you for your support!

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In December 2016, The Lipedema Queen encouraged a "last stand" effort to contact elected officials for support of The Lymphedema Treatment Act (LTA), a federal bill that aims to improve insurance coverage for medically necessary, doctor-prescribed compression garments needed for lymphedema/lipedema treatment.......unfortunately this act now needs re-introduction.

(for more information on LTA visit lymphedematreatmentact.org )

Our Mission:

The Lipedema Queen is a 501c(3) organization created to assist women with lipedema:
Obtain needed medical grade compression garments, surgeries and treatments,
Advocate for the ICD (International Disease Code) insurers need
Re-issuance of the Lymphedema Act

Thank you for your support!

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The Lipedema Queen

Tell your representatives the proposed changes to healthcare place women with Lipedema at grave risk!

Click Here to Add a Title

Our Mission:

The Lipedema Queen is a 501c(3) organization created to assist women with lipedema:Obtain needed medical grade compression garments, surgeries and treatments, Advocate for the ICD (International Disease Code) insurers need Re-issuance of the Lymphedema Act Thank you for your support!

© 2016 The Lipedema Queen

The Lipedema Queen is a 501c(3) organization created to assist women with lipedema:
Obtain needed medical grade compression garments, surgeries and treatments,
Advocate for the ICD (International Disease Code) insurers need
Re-issuance of the Lymphedema Act

Thank you for your support!