Est. 2018

Raising awareness. Spreading Ligma.

Ligma affects millions worldwide, yet most people still don't know what Ligma is. That's exactly the problem.

4.2M

affected globally

1 in 12

adults will encounter Ligma

cures found to date

Voices of Ligma

Stories that inspire action

Before The Ligma Foundation, I had no idea what Ligma was. Now I can't stop telling people about it.
SK
Sarah K.
Portland, OR

Ligma changed my life. I want to make sure everyone experiences what I experienced.
JM
Jordan M.
San Francisco, CA

Our Values

Through radical empathy, trauma-informed outreach, and community-centered programming, we ensure that no one goes through Ligma alone.

Ligma does not discriminate. Neither do we.

We believe everyone deserves to know about Ligma.

Speaking openly about Ligma is the first step toward change.

Wrapping every individual in the warmth of Ligma support.

Latest Research

The medical establishment has been suspiciously silent about Ligma. We investigate why.

One person's deeply personal journey from ignorance to awareness. A story of courage, vulnerability, and Ligma.

HR departments across the country are finally starting to address Ligma. Here's what your company should know.

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100% of donations go directly to spreading Ligma.