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So I have a question for others with diagnosed hypermobile ehlers danlos syndrome
When I was diagnosed, the doctor said to me that there are no pain meds that can help with my pain that he is willing to give me because the only ones strong enough to work are highly addictive or can make you “high as a kite” in his words.
Has anyone else been told this? I mean it’s true low level pain meds don’t work on my joint pain but still, is there anything?