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.
Listen to this episode as a podcast: www.buzzsprout.com/1923926
To learn more about Hashimoto's Encephalopathy, Autoimmune Encephalitis, and HESA visit wwww.hesaonline.info
Негізгі бет The AE Caregiver Series - Episode 1: Joli and Her Husband's Journey with Hashimoto's Encephalopathy
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