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Re: Neurontin

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thanks for the neurontin info. at night is the worst time for me, that's when

the swelling happens in my legs and the nerves really fire up. it gets more

noticeable around 11 or 12 at night, very different than during the day.

would you say that the nerves stop firing during the day also from this med?

emily

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> thanks for the neurontin info. at night is the worst time for me,

that's when

> the swelling happens in my legs and the nerves really fire up. it

gets more

> noticeable around 11 or 12 at night, very different than during the

day.

> would you say that the nerves stop firing during the day also from

this med?

> emily

,

Get off of the neurontin. I was on it for 6 months. It just made me

sicker. Buy a hot tub (your doctor can prescribe one and you can

write it off on your taxes as long as it does not improve the sale of

your home. Do it! I bought one at Lowe's for $4,000 and could have

bought the same thing from Hot Springs for $10,000) get your doctor

to prescribe a spa at the hospital, slow aerobic exercises in the

pool, and walk at least 30 minutes a day (having a dog will make you

do it! They are a pain in the beginning but so much love if you are

home during the day!) I went on Serzone an anti-

depressant 100 mg twice daily. This helps immensely. I am not as

tired and upset with what is all going on in the world.

Another thing helps is some protein supplements. I take Whey Protein

twice a day mixed with milk. It really adds energy and you are not as

fatigued or fogged. I also take Magnesium Mallate 825 mg., B6 100

Mg., 2 daily atheletic vitamins, as well as 1000 mg. calcium, vitamin

C, and E. Please check with your doctor's nurse to make sure all of

these things will agree with you with any other medications you are

currently on.

I wish the best of luck to you and if you ever want to chat give me a

holler. I will be publishing a secret remedy from a friend of mine

that helped her get over FMS on Friday so keep watching. I want to

know this secret so badly as she is perfectly normal again! And she

never lost her job over it like I did. I'm on full term disability

but do you think anyone wants to hire us on again? Probably not.

Will see what she says on Friday!

Good luck and keep hanging in there!

TJ

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TJ,

I have to wonder what kind of " friend " would withhold info from you if

she can hear about your suffering for so long but wouldn't share her big

secret until Friday. I sure hope this is true but it's like they say " if it

seems to good to be true...it probably is. " I don't mean to be a wet blanket

but I would hate to see you roped into some scam and spend money because you

believe what she has told you. Are you absolutly positive she even had

Fibro? I mean I know she told you she did and told you her symptoms then she

is suddenly, miraculously cured....bam! just like that!....now she is going

to " share " this info with you.

My gut says she is selling something and it is though a multi-level

marketing thing. I know from where I speak. I almost lost everything in a

multi-level thing a few years back...and the products were actually good but

the rest was just a nightmare. Please be careful. She has you hooked and

now through you she may be trying to hook us all.

Again, I want to say...this may be true but please think hard and be

very careful. There are a lot of people out there that actually believe in

what they are doing and they prey on chronically sick people because we are

so desparate to get well...we will believe and buy anything.

Arizona

> I wish the best of luck to you and if you ever want to chat give me a

> holler. I will be publishing a secret remedy from a friend of mine

> that helped her get over FMS on Friday so keep watching. I want to

> know this secret so badly as she is perfectly normal again! And she

> never lost her job over it like I did. I'm on full term disability

> but do you think anyone wants to hire us on again? Probably not.

> Will see what she says on Friday!

>

> Good luck and keep hanging in there!

>

>

Arizona

-----------------------------------------

Please stop by and visit my Website listed below

http://members.aol.com/artistdesigner/Arizona_/Page_1x.html

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  • 5 months later...
Guest guest

Prescription

--- Wood wrote:

>

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>

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  • 5 years later...

Hi Stephany I have only started taking it in November 2007. I take 100 mg EVERY EIGHT HOURS. I understand from another friend, who is on is for surgery/knee replacement pain, that his doctor emphasized how important the every eight hours is to success with this drug. Not three times a day, as with meals. Every eight hours. So far, I have no noticable side effects, other than the wonderful relief from severe pain. But as always with my PG, it is almost impossible to establish cause and effect definitively. I am also having the first healing over of the three active lesion areas which started up mid summer (following pneumonia and work/moving/gardening frenzy and overexertion). I could pass over the benefits of the Neurontin in favor of the lesion healing theory, except that I forgot a dose on Christmas night in all the excitement. When my pain was all of a sudden returning and visions of the wheelchair started dancing in my head, I remembered

that I was three or four hours late with the Neurontin. So that tipped the mental balance in favor of the Neurontin. Who knows? I may be noticing a tiny, tiny bit of dizziness. But compared to the severe dizziness and nausia i had with oxycodone (and no noticable pain relief) I really can't even detect it at all. Is your EN noticable right now, so that you can notice a pain difference? Tinastephanyiniowa wrote: Tina, how much neurontin are you taking? I'm taking

it for a chronic cough, and I would like to compare dosages and effects!Stephany in Iowa (EN for 20+ years)

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