Patient self advocacy with Ehlers Danlos

This video is about a large part of patient empowerment ; patient self advocacy when you have a rare disease such as EDS.
Disclaimer: content is for informational purposes only. I am a person formally diagnosed with EDS, making this content for the purpose of informing friends, family, and other humans about EDS. I am not a medical professional, and nothing in these videos should be taken as medical advice.
EDS Playlist link: EDS: • EDS
Thumbnail photo credit : garten-gg on pixbay pixabay.com/photos/background...
Background photo credit : auretjansen on pixbay pixabay.com/photos/zebra-afri...
Relevant sources in no particular order
esoftskills.com/healthcare/em...
ehlersdanlosnews.com/health-i...
/ a_guide_for_self_advoc...