Replying to:
http://neurotalk.psychcentral.com/sh...28&postcount=6
Hi Eric,
and .....welcome to the forum!

You popped up in the middle of Desi's thread - hard to spot you hidden in the undergrowth, lol!

Hope you don't object to being moved to a fresh thread, but you should hopefully get a much wider response this way and we can concentrate on your several topics without edging in on the other thread. BTW, if you need quick answers, search the forum - advanced search, select only the RSD forum and click for "posts". Some of these topics have come up before, I remember.

You sound a bit like me, btw, arthritic and sensitive to neurontin, I'm low-dose too, but I've no experience of Lyrica. Many others here take it though.

I'm on about 600mg of neurontin per day which I take in a totally unorthodox fashion (OK'd by the doc) - I open the capsule and mix it with water (it's water-soluble) then take it in half doses twice as often, so 150mg x 3 or 4 per day, depending on how I'm reacting to it. Some days I can tolerate it more than others, but in general it suits me, so long as I take it like that. Oh, I'm not advocating this method of dosage in any way, it's just what works for me. Doesn't remove the pain, but pushes it to the background.

I've been taking it now for 3 years, still haven't got used to it...I get the exact same side-effects as you, including memory fog, exasperating, isn't it?! Any higher dose and I feel I'm tripping out, but without the feel-good bits . Bummer.

I also have osteo, plus cervical spondylosis and spinal stenosis (C4-C6) and rheumatoid rather badly in my hands. And I have diffuse RSI too. I'm having more tests done right now for the rheumatoid arthritis which I fear is starting to make itself felt in my hips.

Gawd! It never stops, does it!...

So, pain management; well I get it all prescribed by the docs, but I could opt for PM. For me it's a question of location, I live on an island quite far from anywhere useful, lol!

I think, though, as more doctors are getting locked up in clink for dispensing too many meds, the trend is more towards the PM set-up.

[start rant]----> My view of that is, I'm sick of governments treating us all like babies, but I know it's worse than that; most of these meds are made from natural substances, many growing wild and free I somehow think medicine should be owned by us all. And the hypocrisy of it. Booze (still so freely available, thank goodness) cigs (almost illegal) meds (virtually all illegal unless bought through legal drug runners like the world's government medical systems) and meanwhile, the illegal abuse of hard drugs worldwide is epidemic - this whole government drug cartel thing is really peeing me off - artist shouts at governments in general: "It's not working, guys!" Well, it is working for the government coffers and to hell with the people...BUT.. enough already.. ----> [/end rant] Now see what you started, lol!

Anyway, PMs? Each to his own, is what I say. Every one's situation is different, some have better docs than others, some docs are clueless but local PMs are quite well up on the RSD info - many here, like you and me, have RSD alongside other conditions. Or location problems, like me... So, there's no way to generalize, or have "rules" about any of this, surely, it's just whatever suits you...no?

Anyway, I've gone on long enough, but I'm so glad you found us.
Is your pain technically from RSD itself, or from diabetic peripheral neuropathy which, as far as I can see, are identical? Just being nosey, lol!

I really hope we can be some help to you,
all the best