new and ignerent
 

don't know what I'm doing, maybe this will work???????????

I noticed--
 

--that you also posted over at the New Members Introduction forum about having idiopathic peripheral neuropathy; hope you check back over here and tell us more (as much as you can about your history, testing, symptoms, etc.).

Just come back on and hit Post Reply, and then type as long as you want (and then click Sumbit Reply). We've got a lot of helpful people here who will share their expertise and empathy.

a brief? history
 

time on earth: 58 yrs
# of kids: 5- 4 on earth and 1 in heaven
marital status: m
ethnicity: cauc
sex: (what's that) m
as I mentioned 30+ yrs of having idiopathic peripheral neuropathy. can't even begin to count the number of doctors I've seen, I do have a list of who I've seen and what they did but it reads like a whole volume of encyclopedias.
I grew up on an apple orchard in michigan, originally my grandpa's then my dad's, started out picking apples, peaches, pears etc and finally graduated to driving the tractor as my dad sprayed the trees. because of blood testing that I have had done, have found extremely hi levels of organophosates which we used b4 the dnr and epa were even in existence. my third second opinion at the u of m hosp (teaching) believe that it is possible that it (pn) could be caused or at least contributed to because of this. regardless of how or why I got this disease, I have it now. so we don't choose the hands we are dealt just how we play the hand. and the 2 rules I live by "don't sweat the small stuff and it's all small stuff" drugs that I am currently taking are lyrica 300mg/day (pain)
ultram 300mg/day (pain)
ibuprofen 2400mg/day (pain but mostly for inflamation)
norvasc 5mg/day (I also have raynauds)
pletal 100mg/day (I also have PAD)
cymbalta 75mg/day (pain and depression)
percocet 10/325 as needed (pain)
stadol nasal spray as needed (pain)
and last but not least
metanx 2/day (this is a relatively new prescription but is simply hi doses of b-2, b-6 and b-12 which are all essential for healthy nerves and has a added bonus of making the insides of our veins and arteries slippery so that nothing adheres to them)
if anyone out there has found anything that works for them pleeze pleeze let me know as I am always looking for that magic bullet and have tried just about everything that has crossed my path in 30+ yrs to relieve, alleviate, dispell, rid, cast out, etc this disease
just one more short piece of history (much more to follow)
after trying many drs, drugs, appliances etc I came to the conclusion that we all have to deal with a certain level of pain and I just needed to bite the bullet and deal with it... then about 12 yrs ago the pain level took a giant leap upward to where I couldn't even tolerate a sheet to touch my feet at night (even though I am numb to about mid-calf I still have much pain) so I started seeing drs again and testing again and more drugs again and after about 7 yrs of trying everything they and I could find I am just biting the bullet again....taking drugs, destroying my liver and kidneys, shortening my life but without the drugs I have no quality of life, and trying not to bite the head off from everyone around me :).... life is good and there's a lot to be grateful for and a lot of beauty that surrounds me but still.....

neuropathy does get better
 

Zebhurtz.
Read the above stickies. page #3 #27 reply and others too.

I am 76 have had PN for 10 years. Finally took 240mg morphine a day to get my pain down to surviable level until i cure myself. Am now using Cymbalta and it works. Never give up. Try anything.I also use Lidocaine patches on my feet.

George

for toxin induced PN
 

assuming the mitochondria were damaged, the types of
nutrients used are acetyl carnitine, CoQ-10, biotin, and
alpha lipoic acid (newer version is r-lipoic).

But after so much time has passed, I don't recall seeing that improvements would be possible.

This e-book lists the effects of various chemicals used by farmers. Do you know what you used?

http://books.google.com/books?id=V7_...K7tg#PPA568,M1

I think it would be helpful to see an environmental physican.
http://www.aaemonline.org/

If your diagnosis was done in the past, newer approaches do exist today. It might be worth seeing one now. Some toxins and many heavy metals stay in the body bound to fat. And some can be removed (not all).

idiopatic / toxic PN
 

Since my PN is probably toxic - I would like to know how it started, what were the very firsy symptoms that you had and where in your body you felt it then and today. 30 years is a long time...
For me - yoga and meditation are doing great..

toxic zeb
 

first off let me start by saying that I'm sorry to hear that you also have this dreaded disease and although there isn't a cure (yet) there is help both here and drs
my pn started with just plain old foot pain, saw drs and drs and chiropractors and more drs. had orthotics made, tried tens units and got the most relief from a chiro so I learned (with the help of many books) to align my spine at home by using doorways, chairs etc then as you probably read in my bio I bit the bullet and just took the pain...then it took a giant leap upward and I started looking for answers again, was diagnosed and started down the long dark path of finding the right drug cocktail that would work for me
how did you become toxic?
are you sure you are?
what symptoms are you having?
everyone is different yet there are similarities

toxic PN
 

I used to work with chemicals in a Lab with no proper conditions. one day I started to feel like ants in my toes, a few days later - these ants were all over my body. and a while later - my skin all over my body were numb. then the pains started - muscles pains here and there. All my tests were normal including NVC, QST, MRI. All this is more then 3 years. My neuro think that because it was a rapid onset with a very little progression - it might be toxic.

I really want to know what is the origin - for meanwhile it is idiopatic.

Do you have pain all over your body or just in your legs? (I didn'y get it). Do you still work with these chemicals? if not - how long after the onset did you stop working with the chemicals?

This is a very interesting thread.

We live in Ontario Canada. My husband is a farmer and for yrs. he did custom crop spraying and cattle spraying for lice and warbles.

It never occurred to us that there may be any connection.

The main spray are atrazine, 24D, 24DB, MCPA for the crops.

He can't recall the name of the active ingredient in the cattle spray but the name of the spray was Warbicide.

all those chemicals make
 

make farming hazardous these days.

There are many links to incidence of Parkinson's and use of
pesticides and other organic compounds, for example.

http://persianoad.wordpress.com/2008...cide-exposure/

I'm sorry for your pain
 

I too suffer from this disease. It is so frustrating when the levels of pain are not consistant with what you are attempting to treat them with. The rollercoaster is so demanding. You can be feeling relatively "good", and....without any warning...bam! The pain can bring you to your knees. It would be so nice if PN was like a headache. Take 2 aspirins....pain goes away. But, PN is an insidious disease. It seems to sometimes have a mind of its own. I feel for every person dealing with this malady.