Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 08-31-2008, 10:09 AM #27
mrsD's Avatar
mrsD mrsD is offline
Wisest Elder Ever
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
mrsD mrsD is offline
Wisest Elder Ever
mrsD's Avatar
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
Lightbulb thanks..

please check those two results... B12 actual number, and
the bicarb test (you may not have had it)

Vancomycin is absorbed orally....not much but enough over time and also in some circumstances such as GI inflammation may increase blood levels.
http://books.google.com/books?id=F0n...sult#PPA329,M1

Vancomycin is a known PN causer.

Xifaxan is less absorbed...3% or less.

When a young person gets PN one really has to consider toxins, and drugs first. Also hereditary PNs like CMT--Charcot Marie Tooth can be tested for.

The elevated fasting insulin suggests the beginning of insulin resistance and may in females point to PCOS as well, or elevated adrenal functioning (but you said you were tested for this already--Cushings?)

I was 30 when my hypothyroid problems started in my feet.

I think diabetic PN is not likely for you yet. It takes TIME to develop and you are young still.

Most sarcoid patients have it in the lungs. But it can occur anywhere. There is a forum with information on this and a novel treatment. Google The Marshall Protocol ( we cannot link to other health forums here) and check sarcoid out. Even if you do not get that treatment, there is info there that may help you understand this better.
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei

************************************

.
Weezie looking at petunias 8.25.2017


****************************
These forums are for mutual support and information sharing only. The forums are 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.
mrsD is offline   Reply With QuoteReply With Quote
 

Tags
optic neuritis, peripheral neuropathy


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
RLS and peripheral neuropathy jarrett622 Peripheral Neuropathy 20 04-29-2012 06:29 PM
peripheral neuropathy mommab New Member Introductions 5 09-05-2010 03:17 PM
peripheral neuropathy lizmindurbiz New Member Introductions 9 07-14-2008 02:15 PM
Hello, I have peripheral neuropathy Tammy72 New Member Introductions 5 05-01-2007 08:14 PM
Peripheral Neuropathy trish New Member Introductions 1 02-24-2007 08:08 AM


All times are GMT -5. The time now is 10:42 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.