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Old 02-23-2011, 02:17 PM #1
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Sheltiemom,

Good to hear you're feeling better. I've been thinking of my own progress since last summer. My symptoms are reduced, and I have almost none of the horrible foot cramping that was so painful. Fatigue is still a big issue, though.

Like you, I have the Forum and especially mrsD to thank.
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"Thanks for this!" says:
mrsD (02-23-2011), Sheltiemom18 (02-23-2011)
Old 02-22-2012, 09:55 PM #2
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Quote:
Originally Posted by Sheltiemom18 View Post
Back in July of 2010 when still dealing with pretty much constant overall burning non-length dependent small fiber neuropathy that began in January 2010, I saw the title of this thread and said, "Yeah, right."

Now it's February of 2011. And there's been no more burning since sometime in the fall, just some residual skin sensitivity which means still not being able to wear certain clothing (fabrics).

The neuropathy is still there but to a much lesser degree. I've been told the cause of mine is Sjogren's Syndrome.

So glad I found this forum and decided to go for the recommended supplements (thanks to MrsD's posts) for these reasons:

1. Bad reactions to neurontin and Lyrica; and

2. MrsD knows what she's talking about.

As Sjogren's is incurable, the neuropathy will probably always be there to some extent. There's dizziness, a little loss of balance, etc. and a lot of photosensitivity (from Sjogren's), but overall doing so very much better. Just keeping my fingers crossed and continuing the supplements.

Sheltiemom18
I am relatively new in this forum. I would really appreciate if you can direct me to the post where Mrs. D listed the kind of foods/diets/supplements/vitamins for Peripheral Neuropathy.

I was diagnosed with idiopathic Peripheral Neuropathy, after having been tested with all sorts of tests. I am willing to try everything just to get relief from this terrible and horrible pain. Like you, even the softest clothing give me pain. I have stabbing, prickly, jabbing, lacinating pain in both my legs and arms. My feet are also painful that it hard to stand and walk.

Do you also feel that intermittent sensation of coldness that creates "goose pimples" in your skin?

Would appreciate your reply.
Thanks.
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Old 12-10-2011, 04:58 PM #3
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How do I find the stickies? Looking for page 2. Sorry I'm new.
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Old 12-10-2011, 05:16 PM #4
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Hello, and welcome
you are on one of the "sticky" threads...if you go back to the index page for this forum, Peripheral Neuropathy, you will see all of the Stckies at the top of the page, with green arrows next to them
http://neurotalk.psychcentral.com/forum20.html

you can also click back from the linked trail just under the NeuroTalk Logo

HTH
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Old 12-31-2011, 03:20 PM #5
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Default Vitamin B

I'm new here to and when I was first suspected I had Neuropathy I did a lot of on line research. The lack of B Vitamins was one thing that kept coming up so I started taking B 6 and 12 supplements. When I finally did see a doc, and blood tests were done on me, the results showed an excess of Vitamin B and the doc told me not to take any supplements. although my Vitamin D was very low and pharmacy amounts were prescribed. Has anyone else had a proble with having too much Vit. B?
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Old 01-01-2012, 07:49 PM #6
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Smirk Time...

When did ur PN start?? how long did it take to improve??

Quote:
Originally Posted by Wing42 View Post
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.
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Old 05-16-2012, 06:42 PM #7
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Quote:
Originally Posted by Wing42 View Post
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.
Spilling through the many layers of info in this wonderful web site... Many years later, thank you for the hope!
Heb1212
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Old 05-25-2012, 12:31 PM #8
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Hi,
I'm new to the forum. Where would I find the stickies?

Thank you,




Quote:
Originally Posted by Wing42 View Post
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.
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Old 05-25-2012, 12:42 PM #9
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Since the poster you are requesting has made his contribution here, YEARS ago, there have been many others and newer information available here.

Here are his two stickied posts:

http://neurotalk.psychcentral.com/post9580-18.html

http://neurotalk.psychcentral.com/post9583-19.html

But you are welcome to read our subforum which has grown quite a bit since 2007.
Go to the main Peripheral Neuropathy page and the link to the subforum is at the very top.
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Old 08-30-2012, 11:38 AM #10
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Quote:
Originally Posted by Wing42 View Post
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.
Where is page 2 of the "stickies?"
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