Where Are My Pillows

Where Are My Pillows

By Encephalitis SurvivorHealth & Fitness
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Where Are My Pillows episodes

  • S1E22 Conclusion: There’s hope out there. | Anddd that’s a wrap on World Encephalitis Day 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 ❤️
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    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/
    7 min
  • S1E21 My approach to self-advocacy

    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/


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

    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!).

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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/

    8 min
  • S1E19 Be kind to yourself in recovery

    Most likely, recovery will NOT be linear, pretty, or fast. From one encephalitis survivor to another: don't disregard your mental health, and allow yourself time and patience to recover physically AND psychologically from surviving encephalitis.

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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/

    6 min
  • S1E17 Meeting another encephalitis survivor, in PERSON?! | Get the deets on the World Encephalitis Day Conference!

    World Encephalitis Day: what’s it about? In today’s episode we reminisce about last year’s conference and discuss what’s going down this year for 2021.

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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/

    5 min
  • S1E16 What IS encephalitis, anyway? | How it's impacted my life

    Schooling, career trajectory, social life, family ties—encephalitis can radically throw all of these things upside down. Despite the disruptive impact it's had on my life, I'm also incredibly thankful to have overcome the worst of it and to have a renewed sense of optimism for what's to come!

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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/

    8 min
  • S1E15 My doctor stood me up | on medical trauma and anxiety

    What does medical trauma and medical system-induced anxiety feel like? Let me tell you a story…

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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/

    8 min
  • S2E14 In appreciation of two neurologists, countless nurses, and… hospital blankets.

    Striking gold… with neurologists?!! Yup! In today's holiday podcast edition, we explore some of the wonderful healthcare providers I've encountered during my encephalitis journey.

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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/

    7 min
  • S1E13 My FIVE year diagnostic journey

    The unfortunate reality is that the majority of doctors have inadequate skill and expertise in diagnosing autoimmune encephalitis. Making things worse, few providers will readily admit to this.  If there’s one thing to take away from this episode, advocate for proper testing and imaging investigations early on.

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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/

    8 min

About Where Are My Pillows

From the publisher's feed

Kicking the sh*t out of brain inflammation (autoimmune encephalitis).