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Amey/Neurontin

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In a message dated 12/7/2004 6:38:45 PM Eastern Standard Time, RSD-CRPSofAmerica writes:

THERE ARE A FEW SIMPLE THINGS THAT HELP WITH RSD AND THATS IT!! AND "NEUROTTIN IS "NOT" FOR RSD"!!!

Amey,

With all due respect, I totally disagree. Neurontin has helped me so much with the burning pain. Without it I would not be able to function on the level that I do. Maybe it does not work for you but we are all different. You say that Topamax is OK but not Neurontin. They are both from the same class of drugs, miscellaneous anticonvulsants and are very similar. There is nothing wrong with off label use it is legal and is done all of the time. I say YES to Neurontin but hey, that's just me! Take care, Love Jai

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> In a message dated 12/7/2004 6:38:45 PM Eastern Standard Time,

> RSD-CRPSofAmerica writes:

> THERE ARE A FEW SIMPLE THINGS THAT HELP WITH RSD AND THATS IT!!

> AND " NEUROTTIN IS " NOT " FOR RSD " !!!

Amey -

I'm in agreement with many others here in the group on many

levels...first, doctors, hospitals and drug companies are going to

make money anyway, if I happen to stumble on something that works

for me while they're raking in the bucks, who cares? Secondly, I

also agree with others in the group that hardline negativity has no

benefit in this group. Save it for your therapist. People with

this disease need hope and I say let us get it any way we can.

Third point, I was on high doses of Neurontin for a few years and it

was impressive in the way it kept certain elements of my pain in

check. The only reason I discontinued it was I did experience some

of the short-term memory problems that are a side effect of the

drug. Unfortunately, as long as I have to work for a living, I need

that part of my brain to function normally, so I have to take a

different approach to managing my pain.

Please call on whomever you need to speak with so you can feel a bit

more at ease about your situation because your post indicates that

you're pretty uncomfortable.

Peace, love and pain relief!!!

Cliff

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> In a message dated 12/7/2004 6:38:45 PM Eastern Standard Time,

> RSD-CRPSofAmerica writes:

> THERE ARE A FEW SIMPLE THINGS THAT HELP WITH RSD AND THATS IT!!

> AND " NEUROTTIN IS " NOT " FOR RSD " !!!

Amey -

I'm in agreement with many others here in the group on many

levels...first, doctors, hospitals and drug companies are going to

make money anyway, if I happen to stumble on something that works

for me while they're raking in the bucks, who cares? Secondly, I

also agree with others in the group that hardline negativity has no

benefit in this group. Save it for your therapist. People with

this disease need hope and I say let us get it any way we can.

Third point, I was on high doses of Neurontin for a few years and it

was impressive in the way it kept certain elements of my pain in

check. The only reason I discontinued it was I did experience some

of the short-term memory problems that are a side effect of the

drug. Unfortunately, as long as I have to work for a living, I need

that part of my brain to function normally, so I have to take a

different approach to managing my pain.

Please call on whomever you need to speak with so you can feel a bit

more at ease about your situation because your post indicates that

you're pretty uncomfortable.

Peace, love and pain relief!!!

Cliff

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