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| Episode | Date |
|---|---|
|
S1E22 Conclusion: There’s hope out there. | Anddd that’s a wrap on World Encephalitis Day 2021!
|
Feb 23, 2021 |
|
S1E21 My approach to self-advocacy
|
Feb 22, 2021 |
|
S1E20 2021 World Encephalitis Day Conference Highlights | Get ready for LIGHTS, CAMERA, ACTION on Feb 22!
|
Feb 21, 2021 |
|
S1E19 Be kind to yourself in recovery
|
Feb 19, 2021 |
|
S1E18 Neuropsychological (and sometimes IQ) testing—it’s important!
|
Feb 18, 2021 |
|
S1E17 Meeting another encephalitis survivor, in PERSON?! | Get the deets on the World Encephalitis Day Conference!
|
Feb 18, 2021 |
|
S1E16 What IS encephalitis, anyway? | How it's impacted my life
|
Feb 17, 2021 |
|
S1E15 My doctor stood me up | on medical trauma and anxiety
|
Feb 16, 2021 |
|
S2E14 In appreciation of two neurologists, countless nurses, and… hospital blankets.
|
Feb 15, 2021 |
|
S1E13 My FIVE year diagnostic journey
|
Feb 13, 2021 |
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S1E12 Differentiating being lazy vs. being sick
|
Feb 12, 2021 |
|
S1E11 It's infusion day!
|
Feb 12, 2021 |
|
S1E10 A year in the life of an autoimmune encephalitis survivor
|
Feb 11, 2021 |
|
S1E9 Encephalitis recovery details *juicy*
|
Feb 09, 2021 |
|
S1E8 Caregivers, you the real MVPs
|
Feb 08, 2021 |
|
S1E7 Primary depression? Anxiety? Or an autoimmune illness?
|
Feb 07, 2021 |
|
S1E6 Embarrassing brain fog, and seeking comfort
|
Feb 06, 2021 |
|
S1E5 My glowing review of neurologists (NOT)
|
Feb 05, 2021 |
|
S1E4 Quality of life illnesses: an overlooked issue in medical care
|
Feb 04, 2021 |
|
S1E3 Brain dysfunction, verbal fluency issues, and social situations
|
Feb 04, 2021 |
|
S1E2 You don't need to go through this alone | on integrating into the encephalitis community
|
Feb 02, 2021 |
|
S1E1 Major updates + countdown to World Encephalitis Day February 22, 2021
|
Feb 01, 2021 |
|
S0E0 One year after hospitalization from autoimmune encephalitis
|
Aug 19, 2020 |