Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 07-20-2010, 01:07 PM #10
smae's Avatar
smae smae is offline
Member
 
Join Date: Jul 2010
Posts: 458
10 yr Member
smae smae is offline
Member
smae's Avatar
 
Join Date: Jul 2010
Posts: 458
10 yr Member
Default

Not all people with PN have pain in both hands and feet--I've read a lot of stories of people who have just one or the other.

I have already had a second opinion... I was diagnosed at Mayo Clinic... and the diagnosis was confirmed by my neurologist.

I've never heard of Methadone before today... but I'm still waiting to hear back from my doctor on possible medicines... if any...

Quote:
Originally Posted by mrsD View Post
I have some history on methadone:

1) It used to be a brand name, Dolophine. And at one time when there were few opiates available, it was used for severe pain.
Like Cancer. At one time it was a legit pain management option.
It is not just for detoxing heroin addicts.

2) methadone is the generic name and is a useful alternative because it does not cause the euphoric highs that other opiates do (esp heroin), so it can be used to detox heroin without the "pleasure" which is the addictive part. It is very cheap and works for some PNers in very low doses.

I do think doctors are going to be resistant in giving a young person opiates.

That history of back pain you have, Sarah, and your lack of PN in the hands, bothers me. A nutritional cause would be affecting your hands too. I think getting another opinion in your case might be helpful. If your pain in your toes and legs is due to compressed nerves in the spine, a solution for that may present itself. But that would be your decision. Most PNers go thru many diagnostic opinions. Codeine is not a good drug for chronic pain...it has to be activated in the liver before becoming useful.
http://www.medscape.com/viewarticle/420696
__________________

.


♥ "Hope is more than a word; it's a state of being. It's a firm belief God will come through. Life brings rain... hope turns every drop into the power to bloom like never before." -Holley Gerth ♥

My name is Sarah and I am 25 years old. I have a lot of chronic health problems. Peripheral neuropathy and POTS (postural orthostatic tachycardia syndrome) keep me bedridden the majority of the time. I also struggle with degenerative disc disease, disc desiccation, spondylolisthesis, arthritis, polycystic ovarian syndrome (PCOS) with insulin resistance, allergies, sound sensitivities, and other health problems.
smae is offline   Reply With QuoteReply With Quote
 


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
New kind of rebuilder???? MelodyL Peripheral Neuropathy 35 07-17-2023 04:52 PM
Article about the rebuilder... aloneouthere Peripheral Neuropathy 42 01-21-2014 01:11 AM
PN and ReBuilder-effective ??? tinglytoes Peripheral Neuropathy 18 01-02-2011 03:34 PM
WOW! Rebuilder System! Mindyk2 Peripheral Neuropathy 0 05-07-2010 12:23 PM


All times are GMT -5. The time now is 12:02 PM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.