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Old 06-16-2010, 01:02 PM
bobinjeffmo bobinjeffmo is offline
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Join Date: Mar 2009
Location: Lohman, MO
Posts: 120
15 yr Member
bobinjeffmo bobinjeffmo is offline
Member
 
Join Date: Mar 2009
Location: Lohman, MO
Posts: 120
15 yr Member
Default Run, roll, get away as fast as you can!

One more story that scares the living death out of me. Please tell me, it wasn't really this bad - but I'm afraid it was worse. First, steroids only make the body feel better, but as far as doing anything for RSD there's not a chance in you know where that it will help much. Then to hear a person masquerading around as a doctor say that he's not even sure RSD is real, well I'm just blown away. Guess my Mayo's team are all just amateurs who got their degrees in a Cracker Jack box. The last time I heard the kind statement you just told about not believing RSD exists but if it did, you've got it came from someone who's autistic, but not a doctor. How can a person not believe but at the same time say you do have something? With all my heart, I'm so sorry you went through this day of living hell. Bob.

Quote:
Originally Posted by firegirl View Post
My primary doc called the neurology department to see if they had any ideas to help this flare I am in. Neuro doc said for me to take Prednisone & come in 2 weeks later to see him. I didnt take the Prednisone bc I've taken it several times with no results. So, my appointment was today. I wasnt expecting him to suggest anything I havent already tried or at least looked into. The doc's student came in first & said u definately have RSD & kept trying to give me a physical exam, which I am too sensitive for. Then, the neurologist came in. He said that "he's not sure that he believes RSD exists, but if it does, that is what I have". haha!! are you kidding me????? Then he starts saying, maybe you just have shingles (since April '07???). I had NO symptoms of shingles at all besides pain on one side of my body. He recommended I let him do another EMG....yeah right....way too painful. His other suggestion was that I should get a spinal tap done to see if there is inflammation at the rot of the nerves. If so, he would put me on a med for that. Finally, he gave me a PT referral (already had PT, OT, and aquatics). He made the referral bc I told him I didnt want the EMG & spinal tap. I brought up my concerns about the spinal tap leading to spread, but of course he said RSD doesnt spread!!! What a joke & a waste of time.....Not to mention, I am in horrible pain from the 2 physical exams.
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cindi1965 (06-17-2010), loretta (06-16-2010)