The Los Angeles Dysautonomia Network (LADN) is a 501(c)(3) nonprofit organization that provides life-changing support to dysautonomia patients and caregivers in California through mental healthcare, community programs, education, and healthcare access grants.

LADN's monthly support group has been meeting since February 2018 and has grown into a supportive community of over 1,000 dysautonomia patients and caregivers across LA county and the greater California area. LADN registered as a nonprofit organization in February of 2023.

LADN staff include Executive Director Sally Krueger-Wyman, Outreach Director Emily Suñez, and Program Coordinator Judy Craig. We each live with dysautonomia and know firsthand how challenging a dysautonomia diagnosis can be, as well as how helpful and validating it is to be part of a dysautonomia community.

The average patient waits almost 5 years for a dysautonomia diagnosis and, even then, faces more questions than answers. We’re working to change that, and we could use your help. We hope you will join us by learning more, donating, and spreading awareness!

The board members of LADN are: Danielle Hinde (Board Chair); Tobi Harper Petrie (Secretary); Dante Quazzo (Treasurer); Sally Krueger-Wyman, MNLM; Nancee Jaffe, MS, RDN; Brianne Slusarenko, DPT; Emily Suñez, MA, C-SLDI; Lindsey Wyman, JD, MPP; and Lori Wynstock, MD.

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