Los Angeles Dysautonomia Network (LADN) began as a monthly support group in February 2018 and has grown into a supportive community of people with dysautonomia across LA county and the greater California area. LADN registered as a nonprofit organization in February of 2023! We are so grateful for everyone who has had a part in growing and supporting our organization!

LADN is run by volunteer co-presidents Emily Suñez and Sally Krueger-Wyman, who live with dysautonomia. We 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. LADN’s goal is to improve the lives of people with POTS and other forms of dysautonomia in California. We welcome those living with all forms of dysautonomia, as well as their care team, to join the Los Angeles Dysautonomia Network.

Donations to LADN help cover our operating expenses involved with running support groups, holding education and wellness workshops, and hosting social events to build community among California’s dysautonomia patient population. Donations also aid our efforts to launch a grant program in late 2023 to assist with medical expenses for people living with dysautonomia.

In addition to Sally and Emily, the founding board members are Barbie Faze; Nancee Jaffe, MS, RDN; Michael Osborn; Lindsey Wyman, JD, MPP; and Lori Wynstock, MD. Frank Suñez is secretary and treasurer.

Thanks to our electrolyte sponsors, we look forward to giving away free samples of Normalyte and LMNT at our event!

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