Healthcommunities.com
Home Search SiteMap Contact Us Forum Store Physician Board

Living with RSD

This section is a place to share stories about Living with RSD

Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation.

You may also Help others by sharing your story.

To quickly access health information from your website's browser, download
Healthcommunities.com's healthchannels toolbar.

July 2009

  • Reflex sympathetic dystrophy (RSD), also called complex regional pain syndrome (CRPS) - by soaringeagle - (Wed, Jul 01 2009)
    I have Reflex sympathetic dystrophy (RSD), also called complex regional pain syndrome (CRPS), in my right foot.It is going on 7yrs now I had it.Have pain all the time needle feeling , like foot fell asleep and a electric shock feeling.It gets bad at times like you touched an electric fence [more..]
  • new procedure - by maryanne - (Wed, Jul 01 2009)
    Hello, Like all of u , I have rsd I too have try nerve blocks without success but I’m going to try a new procedure. The new procedure is with clodronate [more..]
Archives:
  • 2009 January February March April May June July
  • 2008 January February March April May June July August September October November December
  • 2007 April May June July August September October November December

  • The submissions from our site visitors do not reflect the opinion of Healthcommunities.com, Inc. (HC). The Content of HC's sites is intended for informational and educational purposes only, and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. HC does not provide medical advice. Never disregard professional medical advice or delay seeking it because of something you've read on an HC website. Always seek the advice of your physician or other qualified health care provider regarding any medical question or condition. (See also: Website Disclaimer)



    Home