I was wondering if anyone in the group who is on Neurontin as an anti
depressant has experienced pain reduction as well??? or if any rheumy is
experimenting with it's application with fibro.
From what I gather, most of the info on ancillary uses comes from
anecdotal reports not clinical trials.
Wishing you peace~Mag
I'll let you know what the neurontin does to me.
--
Jean
ICQ# 19761807
xjeah...@mindspring.com remove the x to reply
Breathe life into this feeble heart
Lift this mortal veil of fear
Take these crumbled hopes, etched with tears
We'll rise above these earthly cares
Cast your eyes on the ocean
Cast your soul on the sea
When the darK night seems endless
Please remember me
-- Loreena McKennitt
margaret zimmermann wrote in message
<13683-36...@newsd-124.bryant.webtv.net>...
14 months ago I woke up with what I can best describe as having a bolt of
excruciating electrical pain in my face. I had one more later that day. My
face and teeth are in pain with something diagnosed as atypical trigeminal
neuralgia. (With regular trigeminal neuralgia the pain shoots on and on.)
Anyway, because I was also having a lot of heat, tingling, and numbish feelings
in my hands and feet, the neurologist put me on neurontin - 300 3X a day. He
says it is just a part of my fibromyalgia and listed it under fibromyalgia.
Sadly, to say, 3 of my fibro friends have this also. When my Dad had a bout of
bad back pain last year, the doctor put him on neurontin too. It deadens the
nerve pain - therefore can be used for both our diagnosis. Without a nerve
problem, I have no information about it being useful for other pain. Take
care.
Marie
Let's hope that as they learn more about the gaba system, even more
positive stuff can be developed for pain.
Wishing you peace~Mag
Janice
I have been taking Neurontin for the past three months and find that it does
help both with sleep and with pain. I'm not sure if it gets the pain, under
control because I always Hurt but, I do think that it helps me keep a better
attitude towards my recovery. I know that I will never have full range of
motion like I did a few years back but, I find I don't set around and suffer
as much as I did only a few short months ago.
I Think it works for me but I have heard of different results from others who
are being treated by the same Dr. I must say that I didn't think it was working
at first but after not taking it for about a week as a trial period , I do not
want to be with out it again. I have been warned by my Dr. that it does loose
it's effectiveness after a prolong period of time .
I also take several other medications each day and have tryed several others
on a trial basis and got poor or less than positive results.
The combination of meds I take now have given me the best functional
capabilities thus far. I take Neurontin 1 tab three times a day, Entex La
for my allergies1 tab twice a day, Prilosec for gastric reflex one tab every
AM, Flexeril for muscle cramps and to help relax my muscles prior to bed time.
I sometimes take up to 4 tabs if I have had a real bad day. I find I have
Less Bad Days since I started on the Neurontin than Before. I still stay
active I go to Physical Therapy twice a week and walk several miles a day. I
find it very difficult to use staires and must depend on a cain to get around.
My Knees are very pain ful and I have very bad back pain But, I will NOT quit.
I didn't Do much except set around (FEAR OF MAKING THINGS WORSE) when I first
was diagnosed with FM and the setting around was the worse thing I could have
done for myself.
I think that of all the things I have learned ; A positive Can Do Attitude is a
big part of my active recovery as any of my medications. Diet is also a very
Important Part along with vitamins and nutricianal suppliments.
Best Of Luck And GOD BLESS
If You Need to Talk Just Write Back
I enjoy writing it helps keep my fingers working. RJ.
Krystie Rose
http://www.geocities.com/HotSprings/6028/
Joan @ home
My doctor put me on Neurontin some time ago. It was strictly for pain
relieve because I was taking other medicines for depression. They
started me out at 300 mg then it went to 600 mg, 900 mg, 1200 mg and
1800 mg. I found no pain relieve whatsoever. I was on it for several
months. I finally requested to be taken off of it because it was doing
nothing for me. Of course then I had to be weaned off of it so I was on
it for a little bit longer.
Hope this helps.
Cindy in St. Louis
*************************************
Donna and Cindy Brewer
(Remember, God allows U-turns
on the "freeway of life".)
I
> care.I have just been diagnosed with trigeminal neuaralgia. I am being treated
with nneurontin, 4 pills 3x a day. I started out with the excruciating pain
in my teeteeth and ear, mainly on the right side. I also have neck and
shoulder pain pain. I have found doing stretches are helping some. I have
numbness in my jsauwjjaw and bhind my ear. I would appreciate any input or
support. Feeling lowiiilow. I am 46, and have degenerative arthritus and have
had a total knee replacreplacement a few years ago, which is doing great.
Diane
paojn
>
> Marie
>
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take what I need to stay dressed and functioning.......
Linda
>>
Take Care and thank you kindly! from "Queen of the House."/ Heaven's just a
sneeze away./I'd rather be acting/singing./ Sometimes you're the windshield,
and sometimes you're the bug (splat).