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I know, it is probably just one of the many things I need to learn to live with. My condition may actually include POTS. I also get the blood pooling in my feet and legs - sometimes worse than others. I have been diagnosed with SFN and do have some sensory problems. Bit, most of my problems are autonomic - just don't know specifically what it is (e.g., POTS). My neurologist was set to run autonomic tests but I could not go off of my meds because of my arthritis. He feels that the meds I take can hinder the results. He thought we can do the tests when I have a "really bad flare". Well, I hope I never get a "really bad flare" again, although I am sure it will happen again as some point. I do have autonomic problems - pretty much daily; gastroparesis and such. The itching is probably just part of it as it occurs when I have the tingling, etc. Thanks for your help.
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. Last edited by Mere; 10-15-2010 at 10:41 AM. |
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