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DiscussionAnyone with foot parasthesia? Not exactly neuropathy but similar.
Neuropathy | Last Active: Sep 24 8:46pm | Replies (7)Comment receiving replies
Replies to "OMG!! Your symptoms sound just like mine. I had the spinal block and then developed worse..."
@daisy22
I had surgery on L3-L5 (decompression/fusion) because spinal injections for pain were not working anymore and I could not stand/sit/walk for long without my hips/buttocks/legs/feet feeling numb and weak.
I also had L4 spondylolisthesis vertebrae slipping over L5. I could feel my vertebrae move with certain movements which felt weird. They used hardware to stabilize my spine. See pictures below.
I have noticed a marked improvement of symptoms since surgery. The surgery was extremely painful and a full 3 month recovery time for me but if it helps me recover some quality of life (I am 55), it will be so worth it.
MRI from a spine specialist would be best. EMGs by neurologist only test limb long nerves and isn’t a reliable way to determine spinal cord/nerve root compression symptoms that travel down limbs. For example, my EMGs of legs were “normal” but I had many symptoms from lower back down to feet all stemming from my lumbar spine. I also have small fiber neuropathy (confirmed via skin punch biopsy done by neurologist) so this added to foot numbness.
Good luck getting the right doctors and tests/diagnoses. You can feel like you are getting the runaround but keep advocating for yourself if you are not getting answers or treatment options for your symptoms and root causes.