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Life in the Void

Hosted by Whitney Dafoe · health · EN-US

46 episodesAudience: 3
Apple PodcastsWebsite

About this Podcast:

Living with ME/CFS and Long Covid and other Chronic Illness or Disability. Follow me while I explore the challenges, the suffering, the darkness and the light while living with a chronic illness or disability. Along the way I will share insights into how I survive, how I struggle, and how I STAY ALIVE. ❤️

Pitch Analysis

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Contact path

Public web form

Booking probability

30%

Guest openness

Selective

80/100
Required Score

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Questions about Life in the Void

What is Life in the Void about?

Living with ME/CFS and Long Covid and other Chronic Illness or Disability. Follow me while I explore the challenges, the suffering, the darkness and the light while living with a chronic illness or disability. Along the way I will share insights into how I survive, how I struggle, and how I STAY ALIVE. ❤️

Who hosts Life in the Void?

Life in the Void is hosted by Whitney Dafoe. The show has published 46 episodes to date.

What has Life in the Void covered recently?

Recent episodes include "From Nothingness" (31 August 2026, 2 minutes), "The Compassion Gap" (8 August 2026, 15 minutes), and "Impossible Decisions" (8 June 2026, 6 minutes).

How often does Life in the Void publish?

Life in the Void publishes roughly monthly, with episodes averaging 7 minutes across 46 episodes.

How hard is it to get booked on Life in the Void?

Booking probability for Life in the Void is 30%, and the host is rated Selective on guests. Life in the Void requires a Pod Score of 80 or higher. Life in the Void's contact route on record: public web form.

Who should pitch Life in the Void?

The strongest fits for Life in the Void are Health & Wellness Services. Life in the Void has a health audience.

About the host

Whitney Dafoe hosts Life in the Void, a health podcast with 46 episodes published.

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Recent episodes

Our AI reads these to draft pitches. Use them as grounding for a pitch that cites a real guest and a specific topic.

  • Aug 31, 20262 minS3

    This is a poem about living with ME/CFS and the void of any kind of feeling that can strike us during sick days/worse periods and how absolutely devastating and dehuhumanizing it can feel. ✏️ My ME/CFS Blog ❓What is...

  • Aug 8, 202615 minS3

    I explore the gap in compassion between ME/CFS deaths and sufering and the suffering and death of other people whom the world rallies around, fights for, and supports. ✏️ My ME/CFS Blog ❓What is ME/CFS? My Story ME/CFS...

  • Jun 8, 20266 minS3

    A video exploration of the impossible decisions ME/CFS patients have to make, constantly having to decide between two options that will both make our health worse. And how much more difficult these decisions get when...

  • May 28, 20268 minS3

    …even when ME/CFS starts taking from your mind, you think there’s some limit - something that’s yours, that is sacred and defines you in some way, or is just you in some core way that nothing, including ME/CFS can...

  • May 7, 20261 minS3

    Imagining but never doing Dreaming but never experiencing Longing but never feeling Seeing but never touching Believing but never receiving Envisioning but never achieving Driven but never accomplishing Loving but...

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  • Episode #2

    In The Hospital

    Apr 9, 202617 minS3

    In January this year I spent 3 weeks in the hosptial for a pretty serious infection and related conditions. My experience there was at once a surprise and a discouraging setback that added to my symptom burden. In this...

  • Episode #1

    2026 Update

    Feb 16, 20266 minS3

    I had a very serious medical incident happen right after posting my last video about talking again and have been through a lot...I'm ok now, I’m recovering and my body is going through "growing pains" or maybe more...

  • Dec 18, 202512 minS2

    I started eating again in 2024. After 11 years not eating a crumb of food or even drinking a drop of water. I got all fluids and nutrition from tubes inserted into my body. For 11 years. In 2025 I have another big...

  • Episode #21

    One Thing ☝️

    Nov 5, 20252 minS2

    …every single researcher at Ron’s recent Working Group Meeting - every researcher there said they don’t care if they are the ones to discover the cure for ME/CFS, they just want a cure to be found to end our suffering...

  • Aug 27, 20257 minS2

    My Jtube broke finally and I have to go to the hospital tomorrow and I’m feeling stressed...It is so hard seeing the real world and really feeling it and then coming back to my room and closing all the doors…The...

  • Aug 7, 20255 minS2

    To all those living in silence and darkness. Today we take a moment in silence and darkness to honor your courage, your bravery, your resilience, your strength, and we acknowledge your profound suffering, agony and...

  • Jul 30, 20255 minS2

    That is ME/CFS. We live with world champion symptoms with no idea what is causing them or what will happen with those symptoms or what our future holds. We hold onto hope but are often crushed by this harsh, unrelenting...

  • Jul 22, 20258 minS2

    I see people protesting the rights of many marginalized groups and important issues. I see people up in arms over injustices faced by people all around the world…BUT WE ARE DYING. Not to mention suffering endlessly from...

  • Episode #16

    Dear America,

    Jul 7, 20259 minS2

    The "Big Beautiful Bill" that Trump signed into law on the 4th of July will take away insurance from an estimated 17 million people, mostly from people on Medicaid. I want to tell you how losing Medicaid would impact me...

  • Jul 4, 20254 minS2

    This 4th of July, if I could fly an American flag, it would be flown upside down…Today should be a disgrace to all Americans…Today President Trump signs into law a bill that will take away healthcare from 17 million...

  • Jun 11, 20255 minS2

    I’ve done most of my "growing up" here in bed. And lately I’ve realized that "growing up" hasn’t been about figuring out the whole universe, but a process of acceptance - accepting that I don’t have it figured out and...

  • Jun 5, 20253 minS2

    I feel like I am in a position where I have to be against the whole world because the whole world is against me…But I don't enjoy that, I didn't choose that. I was put in this position. I love this world. I want to be a...

  • May 28, 20256 minS2

    I'm sick of ME/CFS being compared to a never-ending flu. This ain’t no f*ing flu. I feel like every system in my body is broken and in pieces. I am mentally and physically 1% as alive as I used to be…But even if you...

  • Episode #11

    Unseen Courage

    May 12, 20252 minS2

    Starting a new day with ME/CFS, with full awareness of the suffering that lies ahead and the helplessness of a reality with no effective treatments, no suport from the world around you, and no concrete knowledge of a...

  • Episode #10

    This Is ME/CFS

    May 9, 20259 minS2

    This is ME/CFS. Unrelenting. Unforgiving. Never ending. You fight and fight for crumbs of life that most muggles throw away. Crumbs that are not even good enough for the dogs. And then ME/CFS launches a new assault and...

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