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About the Nonprofit

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Los Angeles Dysautonomia Network (LADN) is a 501(c)3 nonprofit organization that supports individuals impacted by dysautonomia through community, education, and financial support. 

LADN was founded six years ago by a group of chronically ill women in Pasadena hoping to help their community. We became a nonprofit in February of 2023 and have grown to serve over 210 dysautonomia patients and caregivers in the following ways: 

• We provide community to an isolated patient population through support groups, social events, a book group, and a peer networking program. 
• We help educate patients and the wider community about dysautonomia through wellness workshops, guest speakers, educational resources, and community engagement events. 
• In 2023, we were able to begin offering financial grants to support patients in need with dysautonomia-related healthcare costs.