It's been quite a "journey" for most of us, but the beauty of this forum is instead of reading a paper or an article on CRPS, it's "real life" from us CRPSers living in the trenches. For good, bad or ugly.

The information within these threads can be extremely valuable. I can't count the number of times I said to myself after reading a post......that's exactly what happened to me!! Or, that's how I felt. It's just nice to know that although CRPS is rare, we're not alone. Not by a long shot.

Keep in mind that while many of us have similarities with our symptoms, etc., most of us have fairly unique stories to tell. And also know that this condition is widely misunderstood, even among professionals. I completely lost count of how many doctors and therapists I saw until I found the right ones.

CRPS is best treated by a multi-disciplinary approach. A team approach. Meaning oftentimes a primary doctor who coordinates the efforts, then complementary professionals like chiropractors, pain management doctors, neurologists, physical therapists, massage therapists, acupuncturists, mental health professionals.....you get the picture. This isn't like any other condition or problem your husband has ever had. Gets lots of opinions as opinions as to how to treat vary WIDELY.

Good luck, encourage your husband to post here, and keep us updated!