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#1 | |||
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Junior Member
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Hi all,
I'm new here but not new to PN! I've had years of on-again off-again symptoms, most recently a severe onset of pain in predominantly my right foot and now use a Canadian crutch to walk due to the weird sensations, foot drop and paralyzed small toes (the 3 smallest). My neurologist's latest blood tests detected the presence of the neurological antibody GD1b IgM, and I have been referred to another neurologist in May. MRIs all normal, NCS show neurophysiological evidence of predominantly axonal sensory neuropathy & EGM was normal. I'm presuming the new Dr will order a lumbar puncture next as a nerve biopsy is apparently not needed. Does anyone here have any history of this disease & course of treatment? I'm hoping it qualifies me for IVIg? I'm in Australia so it's quite strictly controlled. I would love to get back to the gym & karate after 6 years of back problems then this! Thanks for any & all comments! Mairi ---------------------- History: 1997 - bilateral carpal tunnel decompression after pregnancy 2011 - L4-L5 microdiscectomy 2012 - L4-L5 ALIF 2013 - L5-S1 ALIF Currently taking daily: 6 x 665mg slow release paracetamol 100mg pregabalin 10mg escitalopram |
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#2 | ||
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Grand Magnate
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Kitt -------------------------------------------------------------------------------------------------------- "It is what it is." |
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#3 | |||
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Wisest Elder Ever
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This is a good article explaining:
I have to use this format for the link, because once you go there the address does not show properly to share the link with others. Quote:
People with IgM elevations should stay hydrated, and avoid high fat meals (like Ice cream etc) which thicken the blood. Keeping the blood more fluid with dietary interventions may improve circulation in the periphery. If you have elevated triglycerides, diet and fish oil can help reduce that too...as triglycerides make the blood thicker as well.
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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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#4 | ||
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Member
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sounds like guillan barre antibodies.
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#5 | ||
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New Member
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Hi there, my husband suffers from total body CIPN. He was given IVIG in the hope of some pain relief, but it was not successful for him either time. I hope you have better luck!
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"Thanks for this!" says: | Mairi (04-01-2015) |
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#6 | |||
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Junior Member
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