Chronic Victory Podcast #67 - Ehlers Danlos Syndrome w/ Hannah McDowell episode artwork

EPISODE · Mar 20, 2022 · 57 MIN

Chronic Victory Podcast #67 - Ehlers Danlos Syndrome w/ Hannah McDowell

from Chronic Victory Podcast · host David Montez/ Hannah McDowell

In this episode, my friend Hannah McDowell joins us to discuss living with Ehlers Danlos Syndrome (EDS).  She's currently working as a nurse and formed her own local support group.  We both have similar types of EDS, but our symptoms can be way different.  Let's talk!Topics:Hanna's superhero origin story..Ehlers Danlos Syndrome (EDS).Postural Orthostatic Tachycardia Syndrome (POTS)Discrepancies in diagnosis.Frustration with diagnosis. Support group life.Support & people who GET IT.Working as a nurse.Music Credits:Song:  "Dry Socks"Artist:  "Aphelion" (Daryl Danks & Bethan Collier)Soundcloud:  Click HereThe Healthy PlaceSupport the podcast and small business! Go to findyourhealthyplace.com and use code: victory4uWild Theory CBDSupport the podcast..farmers..small business & yourself! Go to wildtheory.com and use code: victory4Disclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.Support the show

In this episode, my friend Hannah McDowell joins us to discuss living with Ehlers Danlos Syndrome (EDS). She's currently working as a nurse and formed her own local support group. We both have similar types of EDS, but our symptoms can be way different. Let's talk! Topics: Hanna's superhero origin story..Ehlers Danlos Syndrome (EDS).Postural Orthostatic Tachycardia Syndrome (POTS)Discrepancies in diagnosis.Frustration with diagnosis. Support group life.Support & pe...

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Chronic Victory Podcast #67 - Ehlers Danlos Syndrome w/ Hannah McDowell

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How long is this episode of Chronic Victory Podcast?

This episode is 57 minutes long.

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This episode was published on March 20, 2022.

What is this episode about?

In this episode, my friend Hannah McDowell joins us to discuss living with Ehlers Danlos Syndrome (EDS).  She's currently working as a nurse and formed her own local support group.  We both have similar types of EDS, but our symptoms can be way...

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