The AE Caregiver Series

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 Caregiver Series: Stories and Perspectives from Caregivers of Autoimmune Encephalitis patients.To learn more about Hashimoto's Encephalopathy, Autoimmune Encephalitis, and HESA visit wwww.hesaonline.info

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 Caregiver Series: Stories and Perspectives from Caregivers of Autoimmune Encephalitis patients.To learn more about Hashimoto's Encephalopathy, Autoimmune Encephalitis, and HESA visit wwww.hesaonline.info

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 AE Caregiver Series: Stories and Perspectives from Caregivers of Autoimmune Encephalitis patients.To learn more about Hashimoto's Encephalopathy, Autoimmune Encephalitis, and HESA visit wwww.hesaonline.info

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 Caregiver Series: Stories and Perspectives from Caregivers of Autoimmune Encephalitis patients.To learn more about Hashimoto's Encephalopathy, Autoimmune Encephalitis, and HESA visit wwww.hesaonline.info

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 Caregiver Series: Stories and Perspectives from Caregivers of Autoimmune Encephalitis patients.To learn more about Hashimoto's Encephalopathy, Autoimmune Encephalitis, and HESA visit wwww.hesaonline.info

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 Encephalitis.This is Episode 2 in The AE Caregiver Series: Stories and Perspectives from Caregivers of Autoimmune Encephalitis patients.To learn more about Hashimoto's Encephalopathy, Autoimmune Encephalitis, and HESA visit wwww.hesaonline.infoTo learn more about Anti-NMDAR Autoimmune Encephalitis visit www.antinmdafoundation.org

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 of Autoimmune Encephalitis patients.To learn more about Hashimoto's Encephalopathy, Autoimmune Encephalitis, and HESA visit wwww.hesaonline.info