LADN is a 501(c)(3) nonprofit organization supporting individuals impacted by dysautonomia in the Los Angeles and greater California area through community, education, and financial support.
Community
LADN members build community through monthly support group meetings and social events. Our “LADN Links” program pairs like-minded dysautonomia patients together to encourage friendships and community-building outside our monthly support groups.
Education
LADN builds awareness and education about dysautonomia through our social media pages, as well as our education events and local awareness campaigns.
Financial Support
LADN has a Grant Program to help cover dysautonomia-related healthcare expenses for dysautonomia patients in California who demonstrate financial need.
Upcoming Events
Kind Words from Our Members
“LADN is my sanctuary and only safe space where I can share my frustrations, fears and all the inner dialogue that no one else in my life can even begin to understand. Having a chronic illness isolates you in a way that is unbearable some days and LADN brings some levity and light to an otherwise untenable situation.”
— Danielle H.
“LADN is an encouraging space, where I'm able to freely ask questions and share honest frustrations. The collective wisdom of this group is tremendous! I'm grateful for consistency in connection as WE navigate the rollercoaster life of chronic illness.”
-Katrina B.
“I call [LADN] my Tribe – my people who I can just talk to without having to worry what are they going to think or will they think I’m exaggerating.”
-Liz B.
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