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November 20, 2014 at 4:50 am in reply to: Anyone with Pudendal Neuralgia? In bed for days if you take Calcium? #5115KatClemParticipant
Thank you Barbara. I completely understand not having the energy to respond. PNE is another one of those Rare things that doesnt seem to be so rare. I was just curious.
I can see why they could be missed. All these things have their own diagnosis, it’s not until you step way back and look at the whole picture that things start to add up. I see my GI tomorrow to see how he wants to procede with this colonoscopy. Any precautions we should be taking just in case I do have EDS? The last thing I need is a bowel perferation!
I saw how Dr. D’s was triggered by a virus. The only thing I have been doing different is some trigger point injections using B12 and Traumeel. I doubt that would do it? Why so unstable so suddenly? Have I always been this unstable but are just now noticing? I have been paying acute attention for the past few days and I can see where I have been naturally bracing myself. All these times I have to reposition due to pain, it is almost always where I am hyperextended or flexed. The pains I feel when I walk, I can see where my ankles roll a bit and my feet are flat when I stand. My hips sort of roll out to the sides, not a sexy sway more like my leg bones LOL not sure how to describe that…anyway, I can totally see where much of my slow deliberate “guarded” movements are all around bracing myself from hyperextention. Also been noticing how many times a day I am putting something back into place. Is this all new or had I just adjusted over the years? Crazy!
November 19, 2014 at 12:58 pm in reply to: Anyone with Pudendal Neuralgia? In bed for days if you take Calcium? #5112KatClemParticipantGuess not…I must be an albino zebra! LOL
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