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Re: Re: Neuro visit, not really worth it debbie

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Hi Debbie:

That's " in my opinion " . It's one of the few computer

word speaks thingys I know! lol.

Kathe in CA

--- deebs87 <dlohf@...> wrote:

> Hi Kathe,

>

> Right now I don't ake Cymbalta, just Elavil. It's

> not covered by my

> insurance and either is Lyrica. My nerve pain is

> mostly in my gluts

> and and my upper hanstring on the right. Two Ultram

> seem to help

> strangely enough. I read that on one of the sites

> when I research

> the piriformis syndrome. Since I don't see my rheum

> till Nov I will

> call next week to be seen sooner. Yes I do have

> fibrromyalgia which

> I have had since 1992. Only recently symptoms

> started getting worse.

> This board has been very helpful as my new one.

> What is IMO?

>

> warm hugs,

>

> Debbie L

>

>

>

> >

> >

> > Hi Debbie:

> >

> > Sorry that you have been given yet another

> diagnosis,

> > but at least you now have a name for your pain. I

> am

> > sorry the neuro did not help you more. It could

> be

> > some of the meds I take for nerve pain might have

> > helped you - I take Cymbalta (which is an

> > anti-depressant but is also used for Fibro pain)

> and

> > Lyrica (which is also used for diabetic peripheral

> > neuropathy pain). Both of these meds help with my

> leg

> > pain, and might help you - ask your doctor about

> it.

> > Seems awful that all they can do is keep injecting

> > you.

> > Have you been dx with fibromyalgia? If not,

> something

> > to look into, IMO. Take care -

> >

> > Kathe in CA

> >

> >> >

> > >

> >

> >

> > __________________________________________________

> >

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