View Single Post
Old 04-17-2008, 12:40 AM
Wing42's Avatar
Wing42 Wing42 is offline
Member
 
Join Date: Aug 2006
Location: San Diego
Posts: 365
15 yr Member
Wing42 Wing42 is offline
Member
Wing42's Avatar
 
Join Date: Aug 2006
Location: San Diego
Posts: 365
15 yr Member
Default Mine improved too

in spite of a negative prognosis from three neurologists. I was in severe pain and burning for years, with loss of balance, foot drop causing frequent stumbles, no ankle reflex in left and 50% in right, and hardly able to walk. The pain ranged from 6-8 on the 0-10 scale with breakthrough pain at 9 or 10 experienced as either electric zaps, or feeling like a carnivorous worm was eating at my toe and metatarsal joints. I also had extremely hypersensitive skin, and other areas where the skin was numb enough to stick a pin in.

Now, I walk or hike an average of 12,000 steps a day on my pedometer, have wonderful balance (not as good as in 1992, but I'm 65 yrs old now). My pain ranges from 0 to 4 with very occasional breakthrough pain in the 6 or 7 range, about 2 now as I type this. Both ankle reflexes were measured at 100%. There are still some mildly numb skin areas, but almost no hypersensitivity. I still show some neuropathy when tested with two points, tickle, and vibration. EMGs and nerve conduction tests have always been normal since my PN was small fiber sensory.

OK, it's not healed, but I can happily go through the rest of my life like this. No longer does the pain wakes me up, stop me from walking or driving, and is never so bad that it's hard to concentrate.

The program I've followed all these years is on page 3 of the stickies. There have been changes to it the past couple of years, but the the essential program hasn't changed. It's a hassle to edit old postings on this forum, but I'll work with a moderator to do so one of these months.

A CHANGE: I meant page 2 of the stickies. The neuropathy must be affecting what remains of my brain.

From mrsD:
Edit to direct new members: These three links are to the 3 part posts of Wing42's suggestions:
http://neurotalk.psychcentral.com/post9580-18.html
http://neurotalk.psychcentral.com/post9583-19.html
http://neurotalk.psychcentral.com/post9586-20.html
Keep in mind that this is what HE found helpful for himself.
There is NO ONE protocol that will work for each individual with
PN.
.. people vary, and have different genetics and chemistries.
__________________
David - Idiopathic polyneuropathy since 1993
"If you trust Google more than your doctor, than maybe it's time to switch doctors" Jadelr and Cristina Cordova, "Chasing Windmills"

Last edited by mrsD; 10-06-2012 at 11:52 AM. Reason: adding Wing42's sticky links:
Wing42 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
aj30 (12-12-2014), chalk14 (07-25-2012), DejaVu (05-27-2010), DonnaG (04-17-2011), Elyse Sherwin (02-07-2010), fb123 (09-14-2008), IH8PN (02-23-2014), JB63 (07-13-2011), khakis (07-20-2012), kiewa (04-17-2008), Leslie (10-29-2008), Marie33 (11-30-2012), MikeB (07-14-2012), mistyangel (12-04-2011), mojovandy (02-22-2013), Nabilejlm (02-02-2012), Stace67 (12-29-2010), thecoon (03-20-2019), Tinaanne56 (02-09-2012), yupings (11-08-2013)