advertisement
Reply
 
Thread Tools Display Modes
Old 01-16-2008, 03:35 AM #1
Roy Browning Roy Browning is offline
Junior Member
 
Join Date: Nov 2007
Posts: 15
15 yr Member
Roy Browning Roy Browning is offline
Junior Member
 
Join Date: Nov 2007
Posts: 15
15 yr Member
Default Neurontin or Tegretol ? ...

Hello Folks,

Something went wrong after having sinus sugery and I am
now suffering from nocturnal trigeminal neuralgia. When I
try to sleep I get electric shock-like snaps inside my head
and I can't sleep without heavy medication. An MRI of my
brain shows a completely normal ganglion. Apparently, the
secondary trigeminal branch was damaged from CO2 laser
burns to my right inferior turbinate ... too small to be seen
on an MRI. (no facial pain common to typical TN)

The Neurontin stops the nocturnal electric snaps, but it's
destroying my mind, memory and thought process. It's
gotten so bad that I can't even carry on a conversation
without forgetting what I'm saying or unable to understand
what the other person is saying. This has started after about
two years on Neurontin.

Will I have less horrific mental effects with Tegretol?
(I only need the meds at night)

Thanks.

-Roy
Roy Browning is offline   Reply With QuoteReply With Quote

advertisement
Old 01-16-2008, 04:42 PM #2
RLuckyL RLuckyL is offline
Junior Member
 
Join Date: Dec 2007
Posts: 23
15 yr Member
RLuckyL RLuckyL is offline
Junior Member
 
Join Date: Dec 2007
Posts: 23
15 yr Member
Default sugery

It would surely seem the sugery set it off, but I was wondering if you are the first one in your family to suffer from this or is there some history in the family of this problem?
RLuckyL is offline   Reply With QuoteReply With Quote
Old 01-17-2008, 12:32 AM #3
Roy Browning Roy Browning is offline
Junior Member
 
Join Date: Nov 2007
Posts: 15
15 yr Member
Roy Browning Roy Browning is offline
Junior Member
 
Join Date: Nov 2007
Posts: 15
15 yr Member
Frown

Quote:
Originally Posted by RLuckyL View Post
It would surely seem the sugery set it off, but I was wondering if you are the first one in your family to suffer from this or is there some history in the family of this problem?
No record of this in my family. The CO2 laser that the
ENT 'doctor' used appeared to be defective as his assistant
actually had to hit it with a screwdriver to get it working.
He may have burned me with a much higher temperature
than he should have. I required 3 times the normal dose
of injected anesthetic to tolerate than CO2 burning pain.

But anyhow, I was wondering which was harder on the
mind and memory ... Neurontin or Tegretol?

Thanks.

-Roy
Roy Browning is offline   Reply With QuoteReply With Quote
Old 01-18-2008, 10:11 PM #4
Corkybird's Avatar
Corkybird Corkybird is offline
Member
 
Join Date: Jul 2007
Location: Northeast Ohio
Posts: 245
15 yr Member
Corkybird Corkybird is offline
Member
Corkybird's Avatar
 
Join Date: Jul 2007
Location: Northeast Ohio
Posts: 245
15 yr Member
Default

Neurontin and Tegretol work differently. I have the atypical type of TN for 10 yrs. When I first started with it, Tegretol did nothing for my pain, yet I've been able to keep pain under control with Neurontin for over 7 yrs.
__________________

.


We are friends for a reason. Sometimes we don't know why until we've been friends for a long time !!!

Take time to laugh, it's music to the soul.
.

__________________________
Those who dwell among the beauty and mysteries of the earth are never alone or weary of life.
Rachel Carson

.
Corkybird is offline   Reply With QuoteReply With Quote
Old 01-18-2008, 10:22 PM #5
kimmydawn's Avatar
kimmydawn kimmydawn is offline
Senior Member
 
Join Date: Sep 2006
Location: Ohio
Posts: 3,455
15 yr Member
kimmydawn kimmydawn is offline
Senior Member
kimmydawn's Avatar
 
Join Date: Sep 2006
Location: Ohio
Posts: 3,455
15 yr Member
Default

Hi there!

I have TN, and have had on and off (what I call) sleep starts for many years. It sounds exactly like your experience.

I do it on and off and when it's on, it's a maddening experience trying to get into a deep sleep. I've tried to explain this to people and the closest explanation I could find was called "sleep starts". It DOES feel electric and scared me to death when they first started.

We share something else...my TN is due to extensive maxiallary sinus surgeries. The first one was reconstructive and necessary due to a large cyst in the right maxiallary sinus (I believe the TN began then as the pain is the same but lesser and hasn't gone away since that initial cyst that went so long the surgeon said it was the largest he'd ever removed). The second two were more clearing and reconstruction. I'm told I need another, but not happening.

When mine is acting up I usually do alright when I get past the "falling asleep" period. That can take hours though with the electric shocks.

I've used neurontin, tegratol and lyrica. I couldn't tolerate any of them due to the side affects so I stick with a mild narcotic to help the pain. Some tolerate other meds better than one, but I was unlucky there.

I wish you more than well trying it. Please let us know how it goes.

KD
kimmydawn is offline   Reply With QuoteReply With Quote
Old 01-25-2008, 01:54 AM #6
Roy Browning Roy Browning is offline
Junior Member
 
Join Date: Nov 2007
Posts: 15
15 yr Member
Roy Browning Roy Browning is offline
Junior Member
 
Join Date: Nov 2007
Posts: 15
15 yr Member
Default

Quote:
Originally Posted by kimmydawn View Post
Hi there!

I have TN, and have had on and off (what I call) sleep starts for many years. It sounds exactly like your experience.

I do it on and off and when it's on, it's a maddening experience trying to get into a deep sleep. I've tried to explain this to people and the closest explanation I could find was called "sleep starts". It DOES feel electric and scared me to death when they first started.

We share something else...my TN is due to extensive maxiallary sinus surgeries. The first one was reconstructive and necessary due to a large cyst in the right maxiallary sinus (I believe the TN began then as the pain is the same but lesser and hasn't gone away since that initial cyst that went so long the surgeon said it was the largest he'd ever removed). The second two were more clearing and reconstruction. I'm told I need another, but not happening.

When mine is acting up I usually do alright when I get past the "falling asleep" period. That can take hours though with the electric shocks.

I've used neurontin, tegratol and lyrica. I couldn't tolerate any of them due to the side affects so I stick with a mild narcotic to help the pain. Some tolerate other meds better than one, but I was unlucky there.

I wish you more than well trying it. Please let us know how it goes.

KD
Hello kimmydawn,

Mild narcotics don't kill nerve pain, so it does not sound
like you have what I have ... unless I just haven't used
the right ones.

I too had extensive sinus surgery for sinusitis, but the
nocturnal *jolts* inside my head didn't start until after
the CO2 laser turbinate reduction burns.
I've got Vicodin, Vicoprofin, and Norco, but I don't remember
them stopping the nocturnal jolts or nerve pain deep inside
my nose. It's been so long since I've used them I guess I
forget. Maybe I should try them again. I haven't had a decent
nights sleep in over 4 years. It's like a slow, torturous death.

-Roy
Roy Browning is offline   Reply With QuoteReply With Quote
Old 01-27-2008, 02:49 PM #7
EE03 EE03 is offline
Member
 
Join Date: Sep 2006
Posts: 616
15 yr Member
EE03 EE03 is offline
Member
 
Join Date: Sep 2006
Posts: 616
15 yr Member
Default

Roy, there are a lot of meds out there besides tegretol and neurontin. A lot of people have good luck with trileptal, and less of the cognitive problems. I'm no doc, but see yours and discuss the other meds and give them a try. It can't hurt.

Take care, Ellena
EE03 is offline   Reply With QuoteReply With Quote
Old 01-29-2008, 08:23 AM #8
Roy Browning Roy Browning is offline
Junior Member
 
Join Date: Nov 2007
Posts: 15
15 yr Member
Roy Browning Roy Browning is offline
Junior Member
 
Join Date: Nov 2007
Posts: 15
15 yr Member
Angry

Trileptal (150mg-450mg) in the evening is useless. It has no effect
on the nocturnal nerve snaps that are sparking inside my head.

Only getting 'stoned' on Neurontin will suppress the nerve snaps
and allow me to sleep ... and along with it goes my mind and memory.


Trileptal (useless for nocturnal nerve snaps)
Lyrica (useless for nocturnal nerve snaps and I can't urinate properly on it)
Keppra (useless for nocturnal nerve snaps)

My nocturnal nerve snap intensity was made worse after several visits to
a Chinese accupunture doctor, when, after 4 so-called treatments
with the needles. I called him and he just made up excuses and said he
cannot help me. $400.00 down the drain.

-Roy
Roy Browning is offline   Reply With QuoteReply With Quote
Old 02-04-2008, 09:14 PM #9
nick nick is offline
Junior Member
 
Join Date: Jan 2008
Posts: 6
15 yr Member
nick nick is offline
Junior Member
 
Join Date: Jan 2008
Posts: 6
15 yr Member
Default

I am experiencing facial numbness prior to and after sinus surgery. A CAT scan at my request after surgery revealed my sunus' still clogged. Taking gabapentin but it seems I need large doses. Taking more than prescribed along with ibuprofen and tylenol. Not much relief.

nick
nick is offline   Reply With QuoteReply With Quote
Old 03-02-2008, 10:32 AM #10
numbum46 numbum46 is offline
Junior Member
 
Join Date: Mar 2008
Location: Southern Arizona
Posts: 16
15 yr Member
numbum46 numbum46 is offline
Junior Member
 
Join Date: Mar 2008
Location: Southern Arizona
Posts: 16
15 yr Member
Tongue neurontin or tegretol?

Quote:
Originally Posted by kimmydawn View Post
Hi there!

I have TN, and have had on and off (what I call) sleep starts for many years. It sounds exactly like your experience.

I do it on and off and when it's on, it's a maddening experience trying to get into a deep sleep. I've tried to explain this to people and the closest explanation I could find was called "sleep starts". It DOES feel electric and scared me to death when they first started.

We share something else...my TN is due to extensive maxiallary sinus surgeries. The first one was reconstructive and necessary due to a large cyst in the right maxiallary sinus (I believe the TN began then as the pain is the same but lesser and hasn't gone away since that initial cyst that went so long the surgeon said it was the largest he'd ever removed). The second two were more clearing and reconstruction. I'm told I need another, but not happening.

When mine is acting up I usually do alright when I get past the "falling asleep" period. That can take hours though with the electric shocks.

I've used neurontin, tegratol and lyrica. I couldn't tolerate any of them due to the side affects so I stick with a mild narcotic to help the pain. Some tolerate other meds better than one, but I was unlucky there.

I wish you more than well trying it. Please let us know how it goes.

KD
Wow, I have TN from a herpes outbreak on and around my mouth last year. But, I have had those electric jolts when falling asleep for much longer. I think they may have started after having 3 ECT treatments(electro-convulsive therapy) That was a horrible experience. When you get the electric jolts, do you have different parts of your body move too? I get that plus my mouth including my teeth clamp down so I always have sores on my tongue from biting it. I take neurontin and Cymbalta for the pain(Cymbalta also for my depression and neurontin for my seizures too) I also have RLS and take mirapex for that at night. I am on a lot of meds due to these problems plus having FMS/CFIDS etc. I also am on an extended release narcotic as well as a fast acting one for breakthrough pain. I have been wondering how to even explain these "electric jolts". It can be maddening, but I also take trazodone at night for sleeping, which helps a great deal. but, when trying to nap during the day it can be frustrating. I still do wake up many times during the night from these jolts and the subsequent biting of my tongue.
numbum46 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
Tegretol anybody razzle51 Medications & Treatments 4 06-17-2007 06:15 AM
what is neurontin? lostmary Reflex Sympathetic Dystrophy (RSD and CRPS) 8 06-14-2007 01:42 PM
Neurontin? theoneRogue420 Reflex Sympathetic Dystrophy (RSD and CRPS) 13 05-13-2007 05:24 PM
Tegretol anybody razzle51 Epilepsy 8 12-28-2006 12:48 PM
Question on Neurontin lookingup58 Meralgia Paresthetica 2 10-07-2006 01:49 AM


All times are GMT -5. The time now is 10:19 AM.

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.