I’ve had mine for about 2 years and I love it. It has made such a huge difference in controlling my pancreatitis pain. I would have them put the pump in the backside not in abdomen. This is my personal choice. I didn’t want to catch it on the cupboard as I bent over. I will say it’s a great way to keep the pain away. I still have a little pain but not like I used to. Good luck and if you have any questions let me know!!! ❤️🙏

I "climbed" the WHO pain ladder as recommended by my neurologist for my chemo induced peripheral neuropathy and found that only Percocet worked for me...45mg/day. Not pain free but at least I can sleep better. We pain patients are being persecuted due to a hysteria created by PROP and one Dr. Kolodny...go ahead...look it up for yourself. It's unconscionable!

I have the exact same conditions you do so I added you to my team. I do my morphine orally. I am way to skinny for a pump. I also like to be able to control my morphine intake myself. I just got the doctor to take all the MS Contin out of my dose and I'm on all MSIR. 240 mg. 30 mg 8 X a day. I can't control that pump like that.