The AE Caregiver Series Hashimoto's Encephalopathy/SREAT & Seronegative Autoimmune Encephalitis Alliance
-
- Health & Fitness
Stories and Perspectives From Caregivers of Autoimmune Encephalitis Patients
-
Episode 7: Steve and His Wife's Journey with Hashimoto's Encephalopathy
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 -
Episode 6: Randy and His Wife's Journey With Hashimoto's Encephalopathy
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 -
Episode 5: Janelle and Her Daughter's Journey With Hashimoto's Encephalopathy
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 -
Episode 4: Kacia and Her Daughter's Journey With Hashimoto's Encephalopathy
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 -
Episode 3: Heidi and Her Daughter's Journey With Hashimoto's Encephalopathy
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 -
Episode 2: Linda and Her Son's Journey with Anti-NMDAR 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 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.info
To learn more about Anti-NMDAR Autoimmune Encephalitis visit www.antinmdafoundation.org