Where Are My Pillows cover art

Where Are My Pillows

By: Encephalitis Survivor
  • Summary

  • Kicking the sh*t out of brain inflammation (autoimmune encephalitis).
    Encephalitis Survivor
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Episodes
  • S1E22 Conclusion: There’s hope out there. | Anddd that’s a wrap on World Encephalitis Day 2021!
    Feb 23 2021
    It’s been a slice. Thank you to everyone who’s tuned in! For those of you in the midst of a challenging journey right now: know that you’re not alone. Keep going, don’t give up, and don’t lose hope ❤️ ----- This segment concludes the World Encephalitis Day series, which culminates on February 22, 2021! You can find more insight into my story on my blog, http://wherearemypillows.com/ Social links: Facebook: https://www.facebook.com/wherearemypillows  Instagram: https://www.instagram.com/wherearemyp... Twitter: https://twitter.com/wampillows Youtube: https://www.youtube.com/channel/UCkM266dcY9ay4YVpMALAwdg/ Blog: http://wherearemypillows.com/
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    6 mins
  • S1E21 My approach to self-advocacy
    Feb 22 2021

    For some encephalitis patients, finding good medical care is half the battle (or more) towards getting on the road to healing. Many doctors simply lack adequate knowledge or expertise to effectively diagnose and manage this condition. In today’s episode, we cover some of my thoughts on learning how to advocate for yourself in a medical setting.

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    This segment is part of the World Encephalitis Day countdown series, which culminates on February 22, 2021!

    You can find more insight into my story on my blog, http://wherearemypillows.com/

    Social links:

    Facebook: https://www.facebook.com/wherearemypillows 

    Instagram: https://www.instagram.com/wherearemyp...

    Twitter: https://twitter.com/wampillows

    Youtube: https://www.youtube.com/channel/UCkM266dcY9ay4YVpMALAwdg/

    Blog: http://wherearemypillows.com/


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    7 mins
  • S1E20 2021 World Encephalitis Day Conference Highlights | Get ready for LIGHTS, CAMERA, ACTION on Feb 22!
    Feb 21 2021

    From cutting-edge research shared by encephalitis experts, to inspiring stories from patients and caregivers, #WEDConf2021 was a day to remember! Shoutout to the Encephalitis Society, the AE Alliance, the Anti-NMDA Receptor Encephalitis Foundation, Encephalitis 411, and the Hashimoto’s Encephalopathy/SREAT Alliance for orchestrating a superb day of programming (not to mention their work year-round to improve the lives of patients and caregivers!).

    -----

    This segment is part of the World Encephalitis Day countdown series, which culminates on February 22, 2021!

    You can find more insight into my story on my blog, http://wherearemypillows.com/

    Social links:

    Facebook: https://www.facebook.com/wherearemypillows 

    Instagram: https://www.instagram.com/wherearemyp...

    Twitter: https://twitter.com/wampillows

    Youtube: https://www.youtube.com/channel/UCkM266dcY9ay4YVpMALAwdg/

    Blog: http://wherearemypillows.com/

    Show More Show Less
    7 mins

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