June 2025 is Lipedema Awareness Month

Lipedema Awareness Month – June 2025

You’re not alone. You’re not broken. It’s not your fault.

Every June, we come together to raise awareness, build community, and create a powerful movement of support and education for those affected by lipedema.

This year, something extraordinary is happening…

More women in our community are discovering something life-changing...
It’s not their fault. Their bodies aren’t broken. And they are not alone.

And that’s exactly what we’re doing this June — together.


Heart-to-Heart TRIBE Circles

Meet in-person for connection, support, and shared experience.
Learn more here

Heart-to-Heart TRIBE Circles

Special Webinars

Join these free educational sessions designed to empower and inform:

  • Compression Confusion? Let’s Clear It Up for Lipedema
    June 17 | 6:00–7:30 PM EST
    Register here

  • Finding the Right Place for Surgery in a Holistic Lipedema Journey
    June 27 | 1:00–2:30 PM EST
    (Registration link coming soon)


Meet the Experts – Live Conversations

Real talk with experts who care and understand:

  • Catherine SeoJune 2 | 4:00 PM EST

  • Siobhan HugginsJune 9 | 3:30 PM EST

  • Dr. CarmodyJune 16 | 5:00 PM EST

  • Dr. FaerberJune 20 | 12:00 PM EST

Visit our Events Calendar to grab the links to these live interviews. Go to Events Calendar


Coming Soon – Book Launch!

Preorder now:
Lipedema: Principles and Practice of Diagnosis and Treatment
Preorder on Amazon


Save the Date – September 26–28, 2025

Lipedema Congress

Principles and Practice of Diagnosis and Treatment
A 3-Day Heart to Heart Virtual Event Conference

Join us for a powerful 3-day virtual event focused on the latest in lipedema research, diagnosis, and treatment. The Lipedema Congress brings together leading experts, practitioners, and patient advocates for an educational and heart-centered experience. Don’t miss this transformative event designed to inform, inspire, and empower.
Reserve your spot

Lipedema Congress: Principles and Practice of Diagnosis and Treatment – Heart to Heart 3-Day Virtual Event Conference

Plus… Tons of Resources

All of this is everything we’ve dreamed of for our community.

After years of feeling alone and misunderstood, we are finally building the support system we all needed back then.

You’re not alone anymore.
This is your space. Your people. Your path forward.

The Lipedema Project has evolved from the early work of Lipedema Simplifed and has more extensive information about lipedema. Please visit http://lipedemaproject.org/ to learn more.