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In this raw and deeply moving episode of Narcolepsy Navigators, we meet Meg—a 36-year-old adoptee, student, and mental health advocate navigating life with narcolepsy type 1, CBID, Behçet’s syndrome, and bipolar disorder. Meg shares the emotional rollercoaster that led to her diagnosis after a devastating car crash, including the haunting vivid dreams, overwhelming fatigue, and misunderstood cataplexy that shaped her early adulthood.

From managing multiple chronic conditions to challenging cultural expectations as a Korean-American adoptee raised in a "tiger mom" household, Meg reflects on identity, resilience, and finding connection through vulnerability. Her candid reflections on depression, dating with chronic illness, and the harsh realities of invisible disabilities will resonate with anyone who’s ever felt like their body betrayed them.

🔹 Chapters:
00:00 – Introduction & Background
04:00 – The Car Crash That Changed Everything
08:00 – Diagnosis: Relief Meets Devastation
12:00 – Comorbidities: Bipolar, CBID, Behçet’s
21:00 – Sleep Struggles, Advocacy & Academic Life
37:00 – Parenting, Future Plans, and Honest Reflections
53:00 – “Would You Press the Red Button?”

This is a powerful reminder that even when life reroutes us, it doesn’t have to end the journey

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***If you find these symptoms relatable, please seek medical advice.***

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🎙️ Ever dropped mid-conversation and had to explain it wasn’t drugs?

In this deeply personal and unexpectedly hilarious episode of Narcolepsy Navigators, we sit down with Cristina, the creator of Gourmet Recovery, to explore how she navigates life with Narcolepsy Type 1, cataplexy, and a solid sense of humor.

Cristina opens up about the frustrating path to diagnosis, being dismissed with chronic fatigue and fibromyalgia, and how her sleep attacks affected school, work, relationships—and even public spaces. From falling asleep in church to hallucinating on public transport, Cristina shares it all: the scary, the silly, and the soul-shifting.

We also talk:

• [05:44] Misdiagnosis and finding the right doctor
• [08:51] The emotional impact of being finally diagnosed
• [11:05] Medication side effects, sleepwalking, and the helmet joke
• [17:44] Her healing journey through intuitive eating & cooking
• [23:00] How humor helps her reclaim control
• [27:44] Why she wears a bracelet in public
• [34:32] The truth about naps and real-life memory struggles
• [45:48] Would she press the button to remove narcolepsy?

Cristina reminds us that there’s no right way to live with narcolepsy—only your way.

📲 Follow her at @GourmetRecovery on IG & FB.

Subscribe for more inspiring episodes, share to raise awareness, and join the conversation by sharing your experiences.

Follow and support Narcolepsy Navigators:

www.napsforlife.com

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Youtube: https://www.youtube.com/@NarcolepsyNavigatorsPodcast

***If you find these symptoms relatable, please seek medical advice.***

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What happens when exhaustion is brushed off as “just stress” or “just pregnancy”?

In this moving episode of Narcolepsy Navigators, Emma Cooksey—host, author, and now Sleep Apnea Program Manager at Project Sleep—shares her long, harrowing journey with undiagnosed obstructive sleep apnea (OSA). After years of misdiagnosis, Emma’s wake-up call came behind the wheel—when she fell asleep while driving pregnant.

Emma dives into her diagnosis story, the daily challenges of adapting to CPAP therapy, and her mission to reshape how sleep apnea is seen and treated—especially for women, younger adults, and people who don’t fit the “classic” profile.

Now leading the Sleep Apnea Squad, Emma is on a mission to raise awareness with Project Sleep’s bold campaign, “Sleep Apnea: Let’s Face It”—a movement designed to highlight real people living with sleep apnea and crush outdated stereotypes.

Highlights:

[08:52] Falling asleep while driving: Emma’s turning point
[16:20] What CPAP therapy doesn’t tell you
[24:50] “Let’s Face It” and sleep apnea stereotypes
[35:47] The deadly risks of going untreated

Bio:

Emma Cooksey is an award-winning patient advocate. She was diagnosed with obstructive sleep apnea at the age of 30, after more than a decade of unexplained health issues. In 2020, Emma launched a weekly podcast, “Sleep Apnea Stories” to break down stereotypes of sleep apnea while also raising awareness of symptoms and treatment options.

In her current role, as Sleep Apnea Program Manager, Emma runs Project Sleep’s Sleep Apnea Education and Awareness Program. Through this program, she develops new awareness and educational initiatives, to empower people with sleep apnea to seek diagnosis, support, and care. Emma was born and raised in Scotland, holds a Law degree from Aberdeen University, and now lives in Florida with her husband Jason and their two girls.

Tune in for a conversation that’s educational, emotional—and necessary.

Subscribe for more inspiring episodes, share to raise awareness, and join the conversation by sh

Subscribe for more inspiring episodes, share to raise awareness, and join the conversation by sharing your experiences.

Follow and support Narcolepsy Navigators:

www.napsforlife.com

Instagram: https://www.instagram.com/narcolepsynavigatorspodcast/
Facebook: https://www.facebook.com/people/Narcolepsy-Navigators/61558638497300/
LinkedIn: https://www.linkedin.com/company/narcolepsy-navigators-podcast
TikTok: https://www.tiktok.com/@narcolepsynavigators
Youtube: https://www.youtube.com/@NarcolepsyNavigatorsPodcast

***If you find these symptoms relatable, please seek medical advice.***