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I was just diagnosed with hypermobile EDS and have been referred to a PT that specializes in connective tissues disorders. I have fought for this diagnosis for a long time and finally received it. I’m wondering what other things help you guys with pain/flares/extreme hypermobility? I’m looking for all the suggestions I can get. Thanks! 😊
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Ehlers-Danlos Syndrome (EDS)
Diffuse connective tissue disease
Generalized pain
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Things that are helpful for me are the CBD muscle freeze from Mary's medicinals, big soft heating pads, and shoulder massagers. All can get on the pricey side but good investments for pain in my experience!
Gentle massage and a good careful chiropractor to help get things back in place when they are really far out of place
Braces, my AFOs have been life changing. I feel more stable and roll my ankles less
☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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