New Member Introductions Welcome to our community! Come in and introduce yourself to other members!!


advertisement
Reply
 
Thread Tools Display Modes
Old 07-03-2011, 04:58 PM #1
Flemibess Flemibess is offline
New Member
 
Join Date: Jul 2011
Posts: 1
10 yr Member
Flemibess Flemibess is offline
New Member
 
Join Date: Jul 2011
Posts: 1
10 yr Member
Confused New member with Neuropathic Pain

I have had chronic rt sided pain( sinus, nose, cheek, teeth, ear,eye and scalp ) pain for 4 yes. It started with a viral infection during chemo therapy( I also have chronic lymphocytic leukemia ). I have been through 5 neurologist , infectious disease specialist, 2 neurosurgeons, and 2 net's. I have tried all the usual meds for trigeminal neuralgia, multiple antidepressants , and narcotics . Almost nothing has been effective. I have constant pain,pressure, burning. I currently use gabapentin and lidocaine patches. The gabapentin dulls the pain most days a bit, not so good today. I have trouble talking for any length of time most days, and it can be a torture to socialize .

All my doctors just seem to want to sweep this under the rug and not deal with it. My leukemia is darting to relapse again and the pain is increasing. I find I don't want to get out bed anymore... I just can't deal.

Has anybody found anything that can reduce the symptoms???? I just want to be able to function..to enjoy my family.
Flemibess is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
tamiloo (07-03-2011)

advertisement
Old 07-03-2011, 06:41 PM #2
tamiloo's Avatar
tamiloo tamiloo is offline
Grand Magnate
 
Join Date: Oct 2006
Location: Northern Utah
Posts: 3,465
15 yr Member
tamiloo tamiloo is offline
Grand Magnate
tamiloo's Avatar
 
Join Date: Oct 2006
Location: Northern Utah
Posts: 3,465
15 yr Member
Default

Welcome to Neuro Talk Flemibess
The pain your in must be horrendous...I have a little tooth pain and it drives me nuts.

We have a great forum for Trigminial Neuralgia below is the link...hope this helps! Take care!!

http://neurotalk.psychcentral.com/forum20.html

__________________
My best friends live in my computer....
.
Suffered with back problems since birth...7 back surgeries to date, the last one being on 5/13/2015. Fibromyalgia, PTSD, Chronic Pain

“Being my sweethearts full-time care partner, I have to remind myself, when some well-meaning friend or relative questions my methods or motives, that I know more than they do because I Live this life 24/7, and they only come for short visits.” Tamiloo


.
Gotta love my Olhipie! Dx'd RRMS 1986, SPMS 2004

.
Watch my Olhipie Skiing....

.
tamiloo is offline   Reply With QuoteReply With Quote
Old 07-03-2011, 07:25 PM #3
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

There are some studies showing using acetyl carnitine with chemo lessens the likelihood of mitochondrondial damage to your nerve cells.

http://neurotalk.psychcentral.com/post653568-5.html
__________________
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
Old 07-03-2011, 11:53 PM #4
Darlene's Avatar
Darlene Darlene is offline
Legendary
 
Join Date: Sep 2006
Location: Once a Texan, always a Texan.
Posts: 11,976
15 yr Member
Darlene Darlene is offline
Legendary
Darlene's Avatar
 
Join Date: Sep 2006
Location: Once a Texan, always a Texan.
Posts: 11,976
15 yr Member
Wink Hello and Welcome to NeuroTalk!!


Happy having you come to be with the whole family. Just let us know if we can be of any help. There are great and caring friends here to assist you. Our shoulders are here for support in many ways. Seems you have been through some ruff times. Please keep us up to date.

Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

Darlene
__________________

.

"Life without God is like an unsharpened pencil -- it has no point.
Darlene is offline   Reply With QuoteReply With Quote
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
Shingles pain vs Neuropathic Pain malawigirl08 Peripheral Neuropathy 5 06-27-2011 01:41 PM
Ms & neuropathic pain PegMeerkatz Chronic Pain 3 10-21-2010 07:40 PM
Neuropathic Pain Hermes New Member Introductions 5 10-19-2010 09:39 AM
Neuropathic Pain Hermes Peripheral Neuropathy 27 09-14-2010 09:34 AM
Neuropathic Pain josephine2007 New Member Introductions 5 02-02-2008 11:06 AM


All times are GMT -5. The time now is 07:35 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 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.