Hi everyone,
I am just finding my way around this excellent site. Mrs D and Glenntaj have already been in touch as I posted on the wrong site to start with, I am introducing myself my name is Marie from Loch Lomond in Scotland,I am looking to hear from people that have the same or similar symptoms or anyone that wants a chat. I
understand Peripheral Neuropathy comes under a lot of umbrellas.
I feel so alone at times as friends and family do not understand what problems you have. My problem is Small Fibre Sensory Neuronopathy not to be confused with neuropathy (to do with dorsal root ganglia), at the moment I feel really ill with flu like feeelings and hands and feet are getting worse( not neuropathic pain) finding it harder to use extremities, my other symptoms are throbbing burning pain in extremities, tingling iin face and perineum. my worst fears now are I feel my memory and hearing is being affected, I also have to use intermitant catheters . Please would love to hear from anyone with similar problams