Hello-

I thought this might be a good spot to post something that happened to us tonight. I was taking my daughter for her PT appointment and there was a student PT in the clinic that wanted to meet my daughter and see her foot. (We think we should charge for the show! as her color changes every other minute) It seems that in her University class last night, they spent most of their time learning about CRPS/RSD. She was asking a ton of questions and wants to go back to let her class know. I might go and talk to them. I post this here because I think this 'mystery disease' is starting to get some attention as a true and serious ailment, atleast I got a bit of encouragement tonight--and I needed it too.

It is good to have you back--