TMS & EDS
Hi everyone, I was wondering if anyone here has experience with TMS and also has EDS or hypermobility. I’m nearing the end of my treatment sessions, but these questions recently came up because my provider is considering extending my treatment.
I’m curious if EDS or hypermobility could affect how quickly someone responds to TMS, or if connective tissue/collagen-related issues might mean needing more sessions than the average person before noticing improvement.
I’d really appreciate hearing any personal experiences or insights. Thank you!