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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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.
Sarah - A Beacon of Hope - Bilateral Meniere's, E46
Meniere's Muse
56 minutes 18 seconds
1 year ago
Sarah - A Beacon of Hope - Bilateral Meniere's, E46
Welcome to Season 3! Todays guest, Sarah is here to share her story of going bilateral in her Meniere’s journey this past year. Sarah has been on the show 2 other times, in Season 1, Episode 2 she shares her vestibular journey and in Episode 27, we flip the tables and she interviews me where I share my emotional journey.
In this episode, Sarah opens about these and many other topics:
~ phantom sounds that replaced her low frequency hearing, tinnitus
~ EMDR Therapy, community connection,
~ noise sensitivity, progressive hearing loss, noise fluctuation
~ community connection, importance of support
Connect with Sarah:
Instagram
YouTube
Dear Meniere's, Letters and Art, A Global Meniere's Project
If you would like to reach me, Heather:
Instagram: https://www.instagram.com/menieresmuse/
YouTube Channel: https://www.youtube.com/channel/UCaR0emfgfCVb0vPqjQcbGwQ
Podcast: https://podcasters.spotify.com/pod/show/menieresmuse
Email: menieresmuse@gmail.com
Leave a VOICE MAIL, that may be used on a future episode at www.speakpipe.com/menieresmuse
If you would like to learn more about Vestibular Disorders Association please go to the vestibular disorder association website at www.vestibular.org.
REGISTER for VeDAs Life Rebalanced LIVE at www.vestibular.org/lrl
Help us MAKE VESTIBULAR VISIBLE!
Remember to love yourself and be gentle with yourself, lean on this beautiful community, and lastly believe healing is possible.
See you soon warriors!
Music: Bensound.com/royalty-free-music
License code: Q25BEF068CTQS5M6
#Nystagmus #hardofhearing #hearingloss #EMDR #therapy #EMDRtherapy #phantomnoises #bilateralmenieres #menieres #menieresdisease #vestibulardisorder #balancedisorder #hyperacusis #migrainetriggers #progressivehearingloss #progressivehealing #earpressure #auralfullness #earpressure
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.
