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Old 04-21-2013, 06:13 AM
amike amike is offline
Junior Member
 
Join Date: Apr 2013
Location: Honolulu, HI
Posts: 30
10 yr Member
amike amike is offline
Junior Member
 
Join Date: Apr 2013
Location: Honolulu, HI
Posts: 30
10 yr Member
Chat Great name by the way!

Hello SFNgirl.

I'm sorry to hear about all the pain and crap you are experiencing. The face incident sounds really sore. As I understand it, anything close to a diagnosis of "trigeminal neuralgia" is about as bad as it gets.

The typical portrayal of symptoms in cases of SFN begins with a "glove or stocking" pattern, meaning the symptoms typically begin in the hands or the feet (or both). The progression over time includes further symptoms going from these peripheral areas up the arms or legs towards the "trunk" of the body. In other words there is a natural progression which follows a systematic "length dependent" pattern.

The "non-length dependent" SFN diagnosis does not follow the typical progression noted above. One way of figuring out if you have non-length dependent version is to systematically review the presentation of your symptoms--did they start in other places on your body before they started in your hands and/or feet? Did they jump to your torso/face before they worked up your arms and/or legs?

There is a good possibility that the nerve biopsy you had done during earlier testing will confirm your diagnoses of NLD SFN/G. You should ask your doctors. The word "idiopathic" in your diagnosis likely refers to either: a) an unknown etiology of your SFN, b) aytpical progression of your SFN without confirmatory evidence of NLD SFN/G; or c) NLD SFN/G as confirmed by the biopsy.

Most physicians don't have an understanding of NLD SFN/G because this is a rare diagnosis. I can't remember the specifics but I seem to recall that it affects only about 5% of the population of those referred to specialized neurology clinics. Most regular MDs just never run into it, even those who specialize in diabetes where SFN is unfortunately fairly common. Where did you have your testing done? I know that UC has the Center for Peripheral Neuropathy which might be good for a second opinion, etc. I'm sure there are other great clinics in your area but I was just reading about this one.

Anyway, hang in there. Which reminds me that the primary treatment for NLD SFN/G is pain management and trying to live a healthy lifestyle. For pain management people often end up having to go with time-release tramadol or time-release morphine (Avinza) or time-release Oxycodone (OxyContin). Hopefully you don't have to go there, but if you do, I hope it helps.

I'd be happy to talk more if you need a friendly sounding board,

Mike
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