My sense is that Calmare is often worth a try. There are not a lot of clinical trials of it (and none, to my knowledge specifically for CRPS-mostly for cancer related pain). My daughter and another child we know both tried it and got relief to different degrees, but it did not last for either. I have heard anecdotal evidence of others for whom the relief is quite long-lasting. You can find a treatment center here:
http://www.calmarett.com/locations.html
I'd love to hear other people's experiences with it.
Lori
Quote:
Originally Posted by stomper1
Thanks for the post Sarah's Aunt. My daughter has CRPS and we've had limited success with injections but it has recently returned - this time a bit worse than it was before. I have read a lot about this therapy but my doctors are very skeptical. Would it be possible for my daughter to contact you or your niece to talk about the treatment?
thank you!!!!!
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