This holiday season, you can make a difference for those living with dysautonomia. Your gift to the Los Angeles Dysautonomia Network helps provide vital resources, education, financial assistance, and community support to individuals navigating this complex condition. Together, we can empower patients, raise awareness, and build a stronger, more connected community. Donate today and give the gift of hope and support to patients and families in need. We are so grateful for your support!

Take a look at our awareness video to learn more about dysautonomia!

In 2024, your support has made it possible for us to:

Expand our programs to include a monthly gentle yoga class and a professionally-facilitated caregiver support group—resources that are having a huge impact on our patient community.
Increase our grant program funding by over 66%, allowing us to provide healthcare access and direct financial support to low-income patients in need.
Serve a rapidly growing community, with membership increasing by an astounding 95% this year alone.

We’re not stopping there! In 2025, we plan to launch a youth dysautonomia support group to ensure that young individuals with dysautonomia have the support they need.

Donate Now to support LADN's mission!

Double Your Impact: Many employers match charitable donations—check if yours does!

Take a look at LADN's mission in the video below!

Our History:

The Los Angeles Dysautonomia Network (LADN) is a patient-run 501(c)(3) nonprofit organization. Co-founders Sally Krueger-Wyman and Emily Suñez have first-hand experience living with dysautonomia. They know 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 monthly support group has been meeting since 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.

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.

LADN's board members are: Barbie Faze; Tobi Harper Petrie, Danielle Hinde, Nancee Jaffe, MS, RDN; Sally Krueger-Wyman; Michael Osborn; Dante Quazzo; Brianne Slusarenko, DPT; Emily Suñez, Lindsey Wyman, JD, MPP; and Lori Wynstock, MD. Frank Suñez is secretary and treasurer.

LADN 2024 End-Of-Year Giving Campaign

Give to Support Dysautonomia Patients this Holiday Season