Susan Foley, HESA Executive Director, and Steve Nelson, AE Caregiver, sit down to talk about the challenges that surround caring for someone with Hashimoto's Encephalopathy, a form of Autoimmune Encephalitis.This is Episode 7 in The AE ...

Susan Foley, HESA Executive Director, and Randy Smith, AE Caregiver, sit down to talk about the challenges that surround caring for someone with Hashimoto's Encephalopathy, a form of Autoimmune Encephalitis.This is Episode 6 in The AE C...

Susan Foley, HESA Executive Director, and Janelle Eggins, AE Caregiver, sit down to talk about the challenges that surround caring for someone with Hashimoto's Encephalopathy, a form of Autoimmune Encephalitis.This is Episode 5 in The A...

Susan Foley, HESA Executive Director, and Kacia Hudson, AE Caregiver, sit down to talk about the challenges that surround caring for someone with Hashimoto's Encephalopathy, a form of Autoimmune Encephalitis.This is Episode 4 in The AE ...

Susan Foley, HESA Executive Director, and Heidi Boehme, AE Caregiver, sit down to talk about the challenges that surround caring for someone with Hashimoto's Encephalopathy, a form of Autoimmune Encephalitis.This is Episode 3 in The AE ...

Susan Foley, HESA Executive Director, and Linda Nourse, AE Caregiver and volunteer with The Anti-NMDA Receptor Encephalitis Foundation, sit down to talk about the challenges that surround caring for someone with Anti-NMDAR Autoimmune Encephalit...

Susan Foley, HESA Executive Director, and Joli Lewis, HE Caregiver, sit down to talk about the challenges that surround caring for someone with HE/AE.This is Episode 1 in The AE Caregiver Series: Stories and Perspectives from Caregivers...