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dear kimber,

thanks for the advice. its hard to see the responces to my posts? i

wish elavil worked. i need to find a compasionate dr. i saw one who

said he deals with opiates. ive seen him three times and he is asking

me for too much info. i have some embarrasing things and dont want

him reading everything. he hasnt given me anything but accupuncture

that really hurts my feet. ive been getting bad cramps and cant deal.

i saw my g.i. dr who gave me 20 2mg diludid. it takes alot of pain

meds to get rid of neuropothy pain. i can barely type as my arm has

pain shooting up it.

the pancreatitis is enough but now ive got to deal with my neuropothy

and pancreatitis. my dr. told me i could get a pain pump but i know

nothing about it. anyway sorry to complain. take care,

fred

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Heidi,

Gosh I wish we didn't have to feel this way with doctors all the name of

controlling our pain. I hope all goes well for you when you see him.

I used to have my darvocet where I had 5 refills at a time with no

waiting period for a new refill. It isn't working that way anymore. I

now have to have the RX called in every month and approved. And can I

say that my pain has been fairly well controlled in these last months

without much use of narcotics that I didn't have to call for a rx of

darvocet in about 3 months. I'd say that was good! So go figure these

new rules suddenly. Same goes for all my other narcotic rx as well.

Everything must be approved and called in every month. I can't imagine

what he would do if I asked for (and truly needed... which I don't as of

yet) the patch you are on as he told me the strongest pain medication

out there that can be prescribe is the percocet 5's that I have. Isn't

that a joke!!! He told me that if my pain was worse than the percocet

could handle and I didn't wanna go to the ER, that I needed to just

" suck up the pain " . I truly don't think he knows that I know

differently. Or am I wrong and is it different for a D.O. MD in

prescribing than it is for a just a MD?

Sandy in Ca

hhessgriffeth wrote:

>

>Now that the month's trial is over, I'm afraid that the doc's going to want to

go

>ahead and drop the strength down to 50 mgs., which I now know won't be

>enough! I meet with him on Tuesday, let's hope that I can convince him that I

>need to stay where I was and not drop the meds any further.

>

>With love, hope and prayers,

>Heidi

>

>Heidi H. Griffeth

>South Carolina

>SC & SE Regional Rep.

>PAI

>

>

>

>

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  • 2 weeks later...

Hi Thease doctors are really thinking we are taking so many meds just for the

heck of it excuse me. But they have no idea what PC feels like. we do. we live

the thing every day. Makes me so sick. I would like to be normal, walking

around. dare to think my pain management dr ever had a case of CP. WoW What the

Earth would fall. He would have all the meds he needed. we are damaged people.

we need the drugs becase we are very ill. But it's all about the drugs just how

much they can give or thier liceness is or could be taken. I somtime think it

would be better if they gave us too much then it would be done, and one less

pain to deal with. less money in ther pocket for sure, sorry I guess I was

venting. hope I didn't hurt anyones feelings. I guess we keep trucking from

here. See ya.

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