My name is Denise and I was led to this community through an internet search. I have a 16 year old daughter who was diagnosed with RSD @ 3 years ago. (Her doctor now chooses to call this AMPS - Amplified Musculoskeletal Pain Syndrome). It's been a brutal 3 years for my daughter and those who love her, but I'm happy to report that, with treatment, she is currently sooo much better than before. We're hoping that she'll be released by the doctor this coming April. I'm here to gather as much information - and to offer as much support and hope - as possible.

Blessings to all!