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#11 | ||
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Member
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I'm sorry that you are going through this; I very much understand. Sjogren's can be hard to diagnose, and if your SSA-SSB antibodies are negative, they use the Schirmer eye test for dry eye & a positive lip biopsy that shows antibody infiltration. When this began for me 13 yrs ago, they thought it may be Sjogren's, but my bloodwork was negative. I've since found out dry eye/mouth is an autonomic nervous system symptom. Mine are only mildly dry.
I have the same doctors...either arrogant or apathetic. I have lost hope that a clear cause will surface. What I do know...I have crappy genetics as far as my lumbar/cervical spine, my vitamin D & b12 was low (low 200's for both at one time) I am heterozygous for several mthfr mutations, & I have a 7 mm Chairi 1 malformation that all my neurologists to date blow off as nothing. Just keep swimming!
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Idiopathic Sensorimotor Polyneuropathy Atypical Migraine Chiari 1 malformation 7 mm PLIF L5-S1 Sept. 2013 Lumbar MRI March 2013: degenerative changes from L3 to S1. L3 and L4 have tiny annular tears with disc bulge. L5-S1 bilateral pars defects anterolisthesis (spondylosis/spondylithesis?) I have an annular tear here too, along with a conjoined left L5-S1 nerve root. Mild effacement of the thecal sac at the origins of the bilateral S1 nerve roots, left greater than right. Mild bilateral Neural foraminal stenosis. |
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#12 | ||
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Junior Member
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Quote:
Then the trouble began. In less than three months I could not feel my feet and my hands. I do not have a lot of pain, but when I do, It is intense burning, shocks and cramps especially in my hands. My feet hurt when I am on them for more than an hr. 3600 mg of gabapentin and 60 mg of cymbalta. Hard to be proactive when you cannot stand. |
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#13 | |||
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Wisest Elder Ever
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Have you been tested for heavy
Metal poisoning?
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All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
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#14 | |||
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Member
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Wow it sounds similiar to me since my symptoms started after wisdom teeth surgery. Were you given steroids or any after care treatment?
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#15 | ||
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Junior Member
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Thank you for caring mrs D. I have been tested for heavy metals. I was hospitalized for 5 days in Dec. Extensive work-up. Many more blood tests from the neuro-muscular specialist. I am still waiting to see the results personally. The neurologists have been horrible with feedback. I remain hopeful. His nurse sent me an e-mail stating that he could find nothing except evidence of neuropathy and he refused to fill out my long term disability papers for my employment and temporary disabled ID card. I cannot walk very well and certainly cannot drive. What a TOOL!!
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#16 | ||
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Junior Member
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I was given steroids for the first month. I could not really tell if they were helping or not. My pain was constant and progressing. I started with Prednisone and 300 mg of gabapentin. I am now on 2400 to 3600 mg of gabapentin and 60mg of cymbalta!! The cymbalta really helped me. Meds are complex. Works for some and not for others.
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#17 | |||
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Member
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#18 | ||
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Junior Member
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Yes. They did not really help me. When I was hospitalized, the neurologist stated that I should not have been given steroids, but, they did not cause this.
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