Reply
 
Thread Tools Display Modes
Old 12-19-2008, 10:24 PM #1
Leslie Leslie is offline
Member
 
Join Date: Jul 2008
Location: Atlanta, GA
Posts: 154
15 yr Member
Leslie Leslie is offline
Member
 
Join Date: Jul 2008
Location: Atlanta, GA
Posts: 154
15 yr Member
Default

[QUOTE=Brian;430531]Hi Leslie, regarding those blood sugar levels.... i would be trying my hardest to get those sugars levels back down to normal ranges and keep them there, low carb dieting and exercise can help lower sugar levels a lot and get rid of the real possability of frank diabetes happening, i am not trying to scare you but the warning signs are there now and there is no telling when frank diabetes will show its ugly face, whilst you have a chance now to do something about it, i would really take it seriuosly, even if by any chance the high blood sugars are not the cause of your PN, knowbody needs to deal with diabetes on top of PN.

Unfortunatly there are still a lot of the medical proffessionals out there that don't take prediabetes seriously, i still come accross doctors these days that try to argue the point that only full blown diabetics get nerve damage, i know it certainly can and does happen at Prediabetic levels, i hope one day they will stop their stone age way of thinking.

best of luck anyway,

Thanks Brian! My endo doc had already done a 2 hr glucose tolerance test about 3 months ago and all results came back fine. I am wondering if he will take these results seriously. I certainly am and if he doesn't I'll be looking for a new doc. I have already been researching diabetes and the proper diet, exercise, etc. Our hospital offers a 30 hr class on diabetes and how to live with it. I've enrolled. While I was out finishing Christmas shopping my husbands cleaned out the cabinets of all "sweet stuff" so we are all taking this very seriously. I've joined a walking group so we are definately having a lifestyle change. Just to bad it's at Christmas. I can't count the cakes and cookies I've had to pass up!!!!
Leslie is offline   Reply With QuoteReply With Quote
Old 12-20-2008, 07:24 AM #2
glenntaj glenntaj is offline
Magnate
 
Join Date: Aug 2006
Location: Queens, NY
Posts: 2,857
15 yr Member
glenntaj glenntaj is offline
Magnate
 
Join Date: Aug 2006
Location: Queens, NY
Posts: 2,857
15 yr Member
Default Well--

--monoclonal gammopathy is certainly something that bears watching, but in about 65% or so of cases there is no other associated systemic disorder. In that case it is labeled "monoclonal gammopathy of undetermined signifigance" of MGUS for short.

Unfortunately, even in such cases, the rogue antibodies can interact with nerve and produce neuropathy symptoms.

This is not an easy situation to fix--either from the neuropathic standpoint or from any others. The treatments tend to be immunosuppresant, along the same lines as are used for many blood cancers, and tend to have their own significant side effects . . .unless there is evidence of a systemic disorder, treatment for any neuropathy linked to it tends to focus on symptom reduction, with a policy of "watchful waiting".
glenntaj is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Leslie (12-23-2008)
Old 12-21-2008, 08:53 PM #3
jakatak jakatak is offline
member
 
Join Date: Apr 2007
Posts: 249
15 yr Member
jakatak jakatak is offline
member
 
Join Date: Apr 2007
Posts: 249
15 yr Member
Default

I didn't know I had MGUS, until I was diagnosed with PN. I was told it was about the size of a freckle, and in past three years, it hasn't grown. My doctor told me that there are many people running around that may have this disorder, and just don't know it, because they aren't typically tested for this malady. It is a pre-cancerous condition that can lead to multiple myeloma. So, one does need to be tested on an annual basis. However, it doesn't necessarily lead to MM. It is a minor concern, but mine hasn't changed in size, and that is a relief.
jakatak is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Leslie (12-23-2008)
Reply


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
Question about 6 question cdr form Bobby17 Social Security Disability 18 07-14-2013 11:36 AM
Question: how do you get whispers Multiple Sclerosis 10 08-23-2008 08:08 AM
Question Please? Silverlady Peripheral Neuropathy 7 08-15-2008 10:19 PM
cdr question lady bug Social Security Disability 2 07-24-2008 09:48 AM
Question Sandel Reflex Sympathetic Dystrophy (RSD and CRPS) 10 11-10-2007 03:41 PM


All times are GMT -5. The time now is 08:20 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.