Has anyone experienced RSD after a stress fracture to their foot? What was your outcome? - rsd after stress fracture
In May, I had a stress fracture of the 5th Metatarsal of his right foot, and I still have pain. An orthopedic surgeon diagnosed the pain as RSD-something with my nerves exaggerate with the trauma of separation. Has anyone ever experienced? If yes, what was your score and how is it treated? I am in physical therapy for now, but what has happened, all of you?
Thursday, February 4, 2010
Rsd After Stress Fracture Has Anyone Experienced RSD After A Stress Fracture To Their Foot? What Was Your Outcome?
2 comments:
I also have RSD / CRPS I am simply a knee-surgery two years ago, and I in my right leg from knee to my toes would now. RSD / CRPS is often caused by simple changes, such as a fracture, sprain or other injuries. Currently I am working with my SDSR spite of my pain is completely under control with my pacemaker for the spinal cord (SCS), have had problems, but it was really the only long term solution for my pain (from many other treatments are temporary, but my CBS has more of a long term solution). I have my SCS 60-80% relief of pain, and if it works, I usually have a 100% owned obtain relief of pain.
I also have physiotherapy and desensitization therapy for a few months ago, I went to SDSR worse, but for many people who are doing their best, something that is difficult to RSD / CRPS is that each patient reacts differently to different treatments. 'd Say I worked as a doctor MANEGMENT pain at this time (I get a referral to an orthopedic surgeon), and LSympahtetic Umbar blocks to ease a total of 5 for a period of several months (after my pain but only lasted one weeks), so my doctors have begun to move to another treatment. I've had too many drugs for pain and never lorotab (or OxyContin pain drug Lyrica or Neurontin for the nerve, I have) three different times during a period of several months, which contribute not much to do with my pain, but some patients are given medication to relieve the nerve. Finally I tried a test on the spinal cord Stimualtor for 5 days, my pain is at 100% for 5 days was inside, so I applied, I have had 2 operations to fix and replace the battery on various issues. Currently, I'm pretty good. I live my life in less pain than before my MCS, and I'm pretty happy. Some days are worse than others, depending on whether my pain is rupture or not, but I'm generally pretty good. Good luck! If you have any questions, please contact me, and here are some useful sites for RSD / CRPS are
www.rsds. org
http://www.neurologychannel.com/rsd/
www.rsdhope.org
http://www.rsdfoundation.org/en/index.ht ...
I also have RSD / CRPS I am simply a knee-surgery two years ago, and I in my right leg from knee to my toes would now. RSD / CRPS is often caused by simple changes, such as a fracture, sprain or other injuries. Currently I am working with my SDSR spite of my pain is completely under control with my pacemaker for the spinal cord (SCS), have had problems, but it was really the only long term solution for my pain (from many other treatments are temporary, but my CBS has more of a long term solution). I have my SCS 60-80% relief of pain, and if it works, I usually have a 100% owned obtain relief of pain.
I also have physiotherapy and desensitization therapy for a few months ago, I went to SDSR worse, but for many people who are doing their best, something that is difficult to RSD / CRPS is that each patient reacts differently to different treatments. 'd Say I worked as a doctor MANEGMENT pain at this time (I get a referral to an orthopedic surgeon), and LSympahtetic Umbar blocks to ease a total of 5 for a period of several months (after my pain but only lasted one weeks), so my doctors have begun to move to another treatment. I've had too many drugs for pain and never lorotab (or OxyContin pain drug Lyrica or Neurontin for the nerve, I have) three different times during a period of several months, which contribute not much to do with my pain, but some patients are given medication to relieve the nerve. Finally I tried a test on the spinal cord Stimualtor for 5 days, my pain is at 100% for 5 days was inside, so I applied, I have had 2 operations to fix and replace the battery on various issues. Currently, I'm pretty good. I live my life in less pain than before my MCS, and I'm pretty happy. Some days are worse than others, depending on whether my pain is rupture or not, but I'm generally pretty good. Good luck! If you have any questions, please contact me, and here are some useful sites for RSD / CRPS are
www.rsds. org
http://www.neurologychannel.com/rsd/
www.rsdhope.org
http://www.rsdfoundation.org/en/index.ht ...
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