Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 09-25-2011, 12:40 PM #11
kate525 kate525 is offline
Junior Member
 
Join Date: Jan 2011
Posts: 28
10 yr Member
kate525 kate525 is offline
Junior Member
 
Join Date: Jan 2011
Posts: 28
10 yr Member
Default

Quote:
Originally Posted by mrsD View Post
If you want to...PM me your medication list. Some antibiotics deplete nutrients and some CAUSE PN.

Your dad might benefit from Acetyl carnitine...which may help the chemo PN. It works better, taken while on the chemo, but it is worth a try. Start at 500mg a day and increase slowly if needed to 2 grams or so, in divided doses for him.

You really should get a Vit D test, and B12 test to see where you are with these.

Burning pain can also be from food intolerances. Some foods also release histamine which makes for burning. I get burning from potatoes of all things!

If you were on oral antibiotics for a long time, I'd try some Kefir.
I just was very sick with a GI thing, and a friend suggested this to me...and I'm amazed at how it corrected me! I feel better ALL over too! It has 12 organisms in it to re-establish normal flora in the GI tract. I've just finished my first quart, Lifeway brand, and really recommend it now for anyone recuperating from illness. It is a fermented yogurt drink. And at first when I was so nauseated it was tough, so I diluted it a bit.

I intend to have at least 3 oz a day now FOREVER! That is how good it has been for me! ( I use the unflavored one as the others have more sugar which I try to avoid).

http://www.lifeway.net/

We found this in our local Kroger's!
Yes, Kefir is a staple in my home in addition to 3 other type of probiotics. I have never seen a correlation to any food either. I did just go back on antibiotics(I take small week breaks at times) so my doc thinks it could be a lyme "flare." I just don't know what to think. I start and stop all the time and have never exploded with all over pain. I feel it's getting worse.

Have you any knowledge of the skin biopsy testing? Can it be wrong??

Last I was tested, my B12 (it's beena while though) was around 450 and VD was fine. I still take 50,00 of VD a week regardless.

From your experience, does this sound like it could be hereditary? My dad is fine, he just shruggs it off and moves along. He is stubborn and refuses to take any of the supplements I tell him about. He's not in pain so he just doesn't want to give it any attention(Grrr!). I mentioned him to you from a hereditary standpoint..wondering if you knew anything about it..

I will PM you my list, but I caution you..it's LONG!

Thanks,
Kate
kate525 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
Neuropathy does improve LizaJane Peripheral Neuropathy 364 12-04-2019 03:54 AM
Clinical trials sticky thread Twinkletoes Multiple Sclerosis 4 03-15-2008 09:45 PM
how can we get a thread made sticky? annie Community & Forum Feedback 2 08-28-2006 03:46 PM


All times are GMT -5. The time now is 03:54 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.