The Lipedema Queen

 Where Curves Meet Courage

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Our Board

Dedicated to women with Lipedema

Katia Page

President/Founder

 As a woman with lipedema, I have overcome many struggles, not unlike many of my sisters who also have this disease. One of the largest obstacles for women with lipedema is the financial burden associated with getting the medical help that is needed.  I started the The Lipedema Queen as a way to try to assist women with lipedema get the treatments, surgeries, supplements, and compression garments needed in order to improve and prolong their lives.   For more on my story, click here

email: [email protected]


Nastasiia Lespinasse

Secretary

I choose to support all people who are afflicted with this disease bc I KNOW how worthy and important this cause is. I am a paralegal and a surgical technologist and it is my joy to be a part of this organization and help anyone who has been affected by this disease. I give my full support to this cause and implore all to do the same. This is an organization that is close to my heart and am honored to be a part of it and all the good things it's bringing to the community. Please support this cause.

Nas

Audrey Zuckerman

Treasurer

 I have worked in the banking and financial field for over 25 years. My career has grown from management of branches to VP of the bank to  investments. I decided to be apart of this The Lipedema Queen Organization because I witnessed how badly this disease can tear down women's bodies and how hard it is for them to pay for the little things to preserve a descent quantity of life. I want to be part of the solution in helping others live a better life.

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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