Thanks for the info everyone! I hope it's not something I have but I'll be seeing a EDS doc next year. If anyone else has any insight or experience with EDS/lyme I would love to hear from you.
But you have had the flexible joints since before LD?
EDS can just be that - hypermobility - don't think it has to
come with pain. I knew someone who had that - and it never bothered or hindered him
The onset of pain is most likely Lyme.