NeuroTalk Support Groups

NeuroTalk Support Groups (https://www.neurotalk.org/)

- Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)

- - Morphine Pump (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/11055-morphine-pump.html)

Hello everyone,

I am new to this site, and new to actively participating in any web site,
such as this, so please be patient with me. Also, feel free to give me
advice and correct me if I do something wrong.
Now with that out of the way, I would appreciate your opinions and advice as soon as possible on morphine pumps. I have done research on them,
but have never talked to anyone who has had experience with them.
I have to make a decision on Monday, the 15th, to have one put in or not.
It is my last option. I currently have a stimulator, which does not really
help.
I have had RSD for 10 years. It originated in my knee and for the last
5 years it has spread throughout my entire body, from the top of my head
to the tip of my toes. As I am sure you are aware, the pain is devistating.
I have tried all the pain meds, none of them really help. For my flare ups,
I have to go to the ER for injections of morphine. That just about covers
my history.
Again, I would greatly appreciate any advice anyone could give me on
their experiences with morphine pumps.
Thank you so much!
MelissaB

Melissa,

First welcome to the site, and feel welcome to ask anyting and everything that you want about anything!! I have had RSD in my right foot and ankle and now my whole leg and my lower back for going on 5 years. I have 2 stims implanted and they stopped working about 6 mos after having them put in. I am getting the pain pump on feb 12th and it too is the last option for me. I have talked to people to about the pump and everthing is positive that i have heard . I have a foot deformity due to the RSD and my doc is hoping that with the pump that this will flatten out and be able to wear a normal shoe again! From what ihave heard the surgey is alot like having the stim implanted, except for the trial part, which i hated!

If you have any questions ask away.. have you looked on medtronics web site??? that will tel you alot about the pain pump too! Are you getting the new one??

Talk to you later!

Amber

Hi MelissaB - welcome to the forums!

I did a full forum search on morphine pumps -here is the results link-
http://neurotalk.psychcentral.com/se...searchid=32779