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Meniere's Muse
Heather Davies
56 episodes
5 days ago
I’ve spent the last several years trying to figure out how to live my best life with Meniere’s disease and vestibular migraine. I have learned just how important connection is with other vestibular warriors. Through support, stories, conversation and tears, we have shared through social media, we’ve found a community of amazing people that lean on and support each other. I want this podcast to reach other vestibular warriors regardless of their diagnosis or where they are on their journey, to let them know they aren’t alone and living a beautiful life, despite these symptoms, is possible.
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All content for Meniere's Muse is the property of Heather Davies and is served directly from their servers with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
I’ve spent the last several years trying to figure out how to live my best life with Meniere’s disease and vestibular migraine. I have learned just how important connection is with other vestibular warriors. Through support, stories, conversation and tears, we have shared through social media, we’ve found a community of amazing people that lean on and support each other. I want this podcast to reach other vestibular warriors regardless of their diagnosis or where they are on their journey, to let them know they aren’t alone and living a beautiful life, despite these symptoms, is possible.
Show more...
Relationships
Society & Culture
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In Sickness and Strength - Vestibular Minutes S3E54
Meniere's Muse
17 minutes 3 seconds
6 months ago
In Sickness and Strength - Vestibular Minutes S3E54

What does support really look like when you have a chronic illness?  In this deeply personal episode, I share an essay I wrote during the early days of my dizzy journey, a time marked by misdiagnosis, fear and overwhelming change.


This episode is more than a reflection.  It's a conversation about how support shows up, through partners, children, faith communities and sometimes even in the quiet spaces we least expect.  In this episode, I share what it's like to be held with compassion and how we can find or build meaningful support when it doesn't come easily.


Whether you have a strong support system or you’re still searching for one, this episode is for you.  You are seen, you are believed, and you are not alone.


VeDA Support Groups Online Support Groups - Vestibular Disorders Association


Lara’s private FB Support Group (2) Mummy Seeing Double Support Group | Facebook


“8 Minute, One Connection”  S3E52 The podcast episode Heather shares about when you need support from a trusted friend https://open.spotify.com/episode/0XWstWOI5u1LU6F1el00cj?si=drl2SefMTDe6f9k58tdWuA


If you would like more information on vestibular disorders www.vestibular.org


If you would like to reach out to me, Heather, please email me at Menieresmuse@gmail.com or find me on Instagram


Thank you for being here! Don't forget to link, share and subscribe!


#support #supportgroups #menieres #SCCD #vestibularmigraine #medicallyretired #familysupport #vestibular #onlinesupportgroups

Meniere's Muse
I’ve spent the last several years trying to figure out how to live my best life with Meniere’s disease and vestibular migraine. I have learned just how important connection is with other vestibular warriors. Through support, stories, conversation and tears, we have shared through social media, we’ve found a community of amazing people that lean on and support each other. I want this podcast to reach other vestibular warriors regardless of their diagnosis or where they are on their journey, to let them know they aren’t alone and living a beautiful life, despite these symptoms, is possible.