I’m so lucky to be able to have massage therapy every other week. While I wasn’t diagnosed with Ehlers-Danlos syndrome (EDS) until I was 22 and didn’t start regular massages until several years after that, I’ve since learned that they are critical to my well-being and pain management. However, not everyone with EDS can access massages. They typically aren’t covered by private insurance here in the U.S., and finding a practitioner who is familiar with…

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