The Latina Endometriosis League of America (LELA) works to increase awareness and understanding of endometriosis within Latina communities. Through culturally responsive education, advocacy, and community engagement, LELA helps address disparities in endometriosis information and supports people navigating the disease.
LELA — Latina Endometriosis League of America
Endometriosis advocacy and education organization centering Latina communities and improving awareness, support, and access to information about the disease.
- Founded/Led by: Mariela Guzman
- Resource Access: National, Online / Virtual
- Community Focus: BIPOC-Led / BIPOC-Centered, Culturally Responsive
About This Resource
Connect With This Resource
- Visit Website
- TikTok
- YouTube
- info@LELAFoundation.org