Pain pump, I have one, how about one for you?
I have had an implanted pain pump in my abdomen for about 18 months. It is a miracle. I get a total of 4.764 mgs. of Dilaudid, If I administer all of the 10 extra micro does I can have in 24 hours. If I don't use those extra doses I get 2.74 mgs. over 24 hours. The effect is 300 times more effective than if I took the same dose orally. I go to my doctors office every 3 months to have the pump refilled. I'm there for about 15 minutes. The actual process of refilling the pump takes no more than 5 minutes and is painless. No prescriptions to worry about, no one wondering if I'm misusing or selling my pain meds, no one making me feel like a drug addict or a criminal. In our current climate this is even more important than it was two years ago. Many Doctors want nothing to do with pain patients or writing scripts for pain meds. I know many of you have been there. This method is especially good for back issues as the drug is delivered via a catheter which runs up my spin. Yes, I still have pain but it's pain I can live with. If your Doctor doesn't know about this or doesn't want to do it contact a pain clinic. The Doctor who put mine in is a Neurosurgeon. If you have any questions please respond.
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Does anyone know of a way to keep my implanted morphine pain pump from "jiggling around" like a tub of jello. I don't want it too flop around too much. I was thinking of getting a 4" Ace bandage and wrapping it around my belly to help keep the pump in place. Sound crazy?
Appreciate your suggestions.
I can’t do anything. I’m 60 and live with this pain 24/7. I’ve had this for more than 10 years. I’ve been getting Botox the last year. It only helps a little and only for 8 weeks. I’m at the end of my rope almost. Where can I go to see your sons doctor?
I am on suboxone for pain that Def helps but of course I'm now labeled as a drug addict. Something I've fought against since my 30s when I began this horrible pain journey.
I live in maine and not even a bit hopeful for a pump. I'm 55 yrs old.
I have had my medtronics pump since April. After 4 or 5 adjustments of dosage (hydromorphone), I had excellent pain relief for about a week. Then, the pain in my buttocks, lower back, and burning in feet returned. I have had dye test that showed that the pump is working properly. I have had 3 or 4 more adjustments and may be getting slight relief, but nothing like that one week, or the trial.
Have you had your pump readjusted? My pain Doc says I am at a high level of dosage, so, how can I know how much is too much? I was really hoping, like you, that after several years of drugs, spinal fusion, spinal cord stimulator, PT, etc, the pump would help give me a good portion of my life back. Anything relevant from your experiences would be appeciated. Glad that someone has had success with the pump.
Have tried anything natural to help with your pain?
I am trying to get away from pharma meds where my liver and body are just getting hammered every day...
I got my pain pump April 11,2023. It was a three year battle with the insurance. They agreed to pay for the pump after the first year but not the Dilaudid. I had done trials with morphine and Prialt(sea snail venom) and had urinary retention with both. The only two pain meds FDA approved for the pump are those two. Actually BCBS is suing some pain management clinics for return of payment because they used dilaudid which is off label. Sorry for meandering. The pump is a slow process . Right now I go every month to have the dose increased. It is very individualized and takes time to find the right dose. We are getting ready to increase that to every two weeks. I am currently at 0.0110 continuous infusion over 24 hours. I have to laugh when I compare that to the oral equivalent. So far my pain has dropped from a 9 to between 6-7. I look forward to continuing this journey and have nothing negative to say. I have had no side affects and am thrilled with the gradual improvement.
Good Morning - I've been reading your comments on your pain pump. A new PM has suggested I get one as well. I noted in one of your comments that you stated it did not help your Neuropathy. I have a SCS, which does help to somewhat reduce my actual back pain, but the SCS and the highest levels of meds allowed today, do not touch my very severe burning in my feet & legs spreading into my thighs. (Left/Right at different levels and intensity.) I wonder if you have the same type of Neuropathy that I have? Or if it is not caused by your damaged spine, maybe in your arms or other spots? Mine is from damaged nerve roots in lumbar spine. Why doesn't your pain pump reduce that pain also? Can you explain more on this topic please? Thanks!
I have very similar symptoms. No doctor can pinpoint the exact source of my pain. The pump gave me decent relief for about a week. Then it kind of stopped. They are perplexed. I am at a relatively high dosage, but what is too high? We just moved to Delaware so I have to find new docs.
I wish you luck finding a doctor to help you with your pain pump. I have considered getting a pain pump in the past but I’ve heard that some doctors don’t like to service pain pumps that have been implanted by other doctors. I don’t know if it’s true, but I can only imagine that might be the case. But I hope you will find someone and figure it out. If it gave you relief for a week, it seems like a willing and capable pain management doctor could find the problem and fix it.
Who should I contact (eg. Neurology Department) at the University of Rochester Medical Center located in Rochester, New York for a pain pump consideration?