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Old 03-21-2015, 09:31 PM
jenng jenng is offline
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Join Date: May 2013
Posts: 135
10 yr Member
jenng jenng is offline
Member
 
Join Date: May 2013
Posts: 135
10 yr Member
Default Coriny...

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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