What kind of pain meds are most of you on if you have POTS syndrome...

[Guest guest]

HI to all! I am going to my pain doctor today and have been taking

oxycodone but the amount I am taking I am afraid it is interfering with

the POTS syndrome. I was wondering what those of you who have ACM,

Ehlers Danlos and POTS syndrome take for your pain. I am at my whits

end and hurting. They tried giving me tim released morphine but it did

nothing to releve pain and I was awake for three nights straight taking

it since I have central sleep apnea.

Thanks,

Beth