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Ehlers-danlos hypermobility type

Jun 23, 2018 8:14 PM

I'm new to the forums, but just a quick question. Anyone with EDS, have any better ways of pain management other than hydrocodone? I hate being a pill popper as it is, but hydrocodone just really makes me tired. It helps but makes me tired. Any thoughts appreciated!

Jun 26, 2018 5:29 PM

I am in the process of testing right now. Have been arguing with doctors for to many years to remember. Try exploring the herb kratom.

Jun 29, 2018 10:40 AM

I’m seeking a diagnosis and seem to have all the symptoms of hEDS, and the only thing that’s helped my pain is CBD

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