Like many sufferers of RSD (Reflex Sympathetic Dystrophy Syndrome) or Chronic Regional Pain Syndrome (RSDS/CRPS) I found a lack of information on the topic and treatment alternatives. I put together this site to bring it all together. I hope it helps you. If you feel I can add something to the site about chronic pain or RSD, tell me. I do not feel that we need to suffer with RSD alone. Sometimes comparing notes helps, and a medical degree does not provide a monopoly on insight into RSD or CRPS.
I will update it as often as I can and to eventually add on discussion boards, and the likes. As all of you know, some days are good, others are bad, so please bear with me. I will be consicentious.
I have been diagnosed with RSD for about 3 years now, am a Registered Nurse, and have been for over 20 years, and find comfort in expanding what I know about this horrible disease.
For those of us who live with RSD, also known as Reflex Symathetic Dystrophy Syndrome or Chronic Regional Pain Syndrome (CRPS), know it can be very tough to try to overcome the RSD pain. Living with chronic pain daily is very tough, not curable, but can be manageable, through the judicious use of medication, therapy and lots of trial and error. I know it from first hand experience as a sufferer and a health care professional. I hope you enjoy my site About RSD and CRPS.