Lucy.... if you go back to the first page of PN forum... you will see that the first 4 posts at the top of the page, have the word "sticky" in the beginning.

This thread of responses, is the first sticky on that 4 item list.

Stickies do not move with time...they are stuck at the top so they can be referenced quickly and easily.

Hi.
I am new here, just found you on Google.
My wife has had diabetes for about 7-8 years now. Over the last 2 1/2 years, I have been working and being her caregiver.
In Oct 09, they shut my plant down and layed all of us off.
This gave me alot of time to research all about her issues regarding diabetes.
I found this on the web while researching my wifes neuropathy symptoms.
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I live in the foothills of the Sierra Mtns. in Calif.
These people have an office in Jackson, Ca which is only 20 minutes from me I am going to call them tomorrow (they are open Mon-Wed-Fri only...)
They say it is FDA, Medicare, and Insurance approved for treating this horrid disorder.
At this point, I will try whatever it takes to at least minimize her pain and discomfort.
Once my wife goes in to see them and they do whatever it is they do, I will post the results,**

what are the stickies

Welcome to Neurotalk JoJo....

Two posts above yours explain the stickies. You posted in one of them, right here.

Stickies remain at the top of the page, and do not move. So you know where to find them each time.

This forum has been here since Sept 06. So there are many many posts to read and learn from. It takes time but it is well worth it. At the top of the index of each page, is a "search" function. Type in your keyword.... like "chemo" and search for posts that show up in answer. You can search many terms this way. Shoes, drug names, etc. Searching can save you time and also the time of other members who have answered many questions over and over. So do practice using "search".

I have idiopathic small fiber peripheral neuropathy. All I've been offered was neurontin. I'm taking 1800 mg. a day and have been getting acupuncture which helps. The pain is really problematic and I'm having trouble with my balance and get very light headed. The neurontin gives me trouble with my short term memory so I'm looking for ways to minimize the need for drugs. I am wondering if anyone has tried high power laser therapy.

hi
I have copied your post onto the main part of the forum as it is more likely to get replies there than on this thread which is specifically for discussing improvement of PN

here is the link to your post so you can check for replies
http://neurotalk.psychcentral.com/thread121123.html
welcome

I do not see stickies.. Please help

Hi Parinda
mrsD has explained well how to see the stickies

this thread IS one of the sticky ones too

Hello Parinda, and Welcome to NeuroTalk.

We have a new subforum listing here at this link with much of the information that has been on the stickies and elsewhere on this forum for the past 4 yrs.

This is the link.
http://neurotalk.psychcentral.com/forum119.html
Some of the subjects there are still evolving and being worked on, but do look there too for information.

Our members here have been posting for about 4 yrs now, so expect to settle in with some coffee/tea and start reading.

My father had a failed back surgery. Now he suffers from severe peripheral neuropathy. I got him to start taking brewer's yeast. But, there is no b12 in it. Please let me know.