Update - We're coming up on 3 weeks since the end of treatment, and my daughter is still in remission - there is no RSD/CRPS pain at all. She still has pain from plantar fasciitis, and muscle and tendon pain, and a lot of fatigue, but no RSD/CRPS pain.

I'm a little worried about the fatigue - the doctor said that the patients are really fatigued after the treatment, especially the first week, but my daughter seems to be still really fatigued. I think I might get some bloodwork done on her if she isn't better by next week. What I'm really afraid about is that she might be getting CFS, which is what I've had for 30 some years now, and is really horrible, too. I'm hoping that she's just on the slow end of recuperating, though.

Anyway, that's an update for anyone that's interested - I think it's good to have lots of info on all different kinds of treatments. I'm hoping that some other people with experience with Calmare will chime in soon!