Experiences with PT for EDS/POTS symptoms?

I did therapy a couple of times but we didn't know that I had hypermobility issues when I did it. As a result, my therapists ended up pushing me too far and I had several dislocations. The second time around, they didn't push me as hard (new place a few years later) and listened to me when I said something hurt. The second time gave me some temporary relief, but the pain ended up coming back. I kept up with the exercises, so it wasn't for a lack of trying

I’ve been doing PT consistently for 5 years. Started with 3 times a week and now I’m at once every 3 weeks for maintenance. My advice is have them try multiple different treatments to see what is most effective with your body. For me it’s dry needling/accupuncture, deep tissue massage, and resistance bands/isometric exercises. It’ll leave lots of bruises, especially at first, so don’t be alarmed about that. Ask about strength building exercises to help reduce sprains, subluxations, and dislocations. I have found treatments are much more effective when I’m bluntly honest about what, where, and how much it hurts.

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