Intrathecal Pain Pump
I’ve have an intrathecal pain pump for many years, just trying to connect with others that have this device to chat with people about effectiveness and drug therapies.
Interested in more discussions like this? Go to the Chronic Pain Support Group.
I to have a pump with Morphine being the doctors choice. I had been on oral morphine for at least 10 years and being older wanted relief without worrying about addiction and stomach problems. I too have had many adjustments, but remain lower than the tabs I had taken. I think I really started doing much better when I realized that my back pain was being addressed, which is why I originally wanted this pump. I expected all body pains to being addressed, but that is not the case. It was installed so that the spinal cord is sprayed with the measured amount of morphine, and because the back pain is controlled through the spinal cord, and the pain center, it really helps. Other pain, not back, I handle with 600 mg Tylenol. I hope I didn't sound like I was trying to sound like an expert on these pumps, just trying to say, mine works beautifully.
It's great that the pump does such a good job in handling your pain. I'm not expecting 100% pain relief. ^0% would be great. Especially my feet. They have hydromorphone in my pump. My first trial by injection used morphine but did not help. How did they do your trial for the pump?
Keep on keeping on. Have a blessed day.
I have had an intrathcal pain pump since July of 2024. In 2020 a physician preforming a discectomy cut into the arachnoid layer of my spine L5, S1.
For the last 5 years I’ve had electric shocks in my right foot and thigh, continuous pain level 5-9. My pump contains morphine,fentanyl, and baclofin. I have tried every form of P.T.,Water therapy,red light therapy. I can go on and on. Do you have any suggestions for pain relief
Laura
Mine works great. Best thing I ever did. Get a new one next Thursday. The big one ! 2 months between refills ! I use 800 Motrin for all other pain.
Hi, all you pain pump users. I'm back with another problem. Two weeks ago I had my pump's output increased by fifteen percent. I also had four boluses per day. The day after my appointment, I took my usual meds after lunch and gave myself a bolus. About thirty minutes later when I got up and started walking, I noticed that all the pain in my feet and all the pain in the back of my legs HAD DISAPPEARED! Not gotten better, totally gone. I was ecstatic to say the least. Then, the next morning, all the pain had returned. Man, was I disappointed! I went back to my pain doc yesterday, telling him what happened. He didn't seem to have any explanation. Just upped the output of the pump again and added two additional boluses. I went home, pretty depressed, and gave myself all six boluses during the course of the day. Still no relief today. I am wondering if anyone out ther in painpump land has experienced this. To have such great pain relief was amazing. In fact that was the very first time I had gotten any relief from this thing in almost two and a half years. Like I said, I am a bit disappointed and depressed. Looking forward to hearing from some of you. Thanks for listening.
Looking for some insight. I’m struggling and don’t know what to do. I have had two failed disc replacement surgeries in my neck. Both anterior. C5-7. The pain has been horrific for
Nearly 4yrs now. I had the first surgery in May and the pain continued. My surgeon said the disc below needed replaced so 6mos later I had the second. After that, the pain got worse. He dismissed me to a pain clinic. He was done and didn’t have any further suggestions at that point. Fast forward
- I got a second opinion. After many tests, etc- this surgeon showed me scans of the disc replacements. He stated the surgeon put in discs that were double the size of my actual discs. He stated that he consulted with his other surgeons and none could understand what his thinking was behind this action. So my discs are 3mm, 8.5mm, 8mm and then back
To 3mm when you look at the scan.
I had a posterior cervical fusion in December in hopes of stabilizing my neck and ending the pain. Unfortunately, it has only worsened. I live in agony each day. Laying down for bed, driving for work, sitting on the bleachers - everything exacerbates the pain. I don’t know what to do.
I’ve had Botox in my neck and muscles, trigger point injections, you name it. It’s getting worse as the months go on.
What do I do from here? 😭
Please help……thank you
This is so terrible! I don't quite understand how this could have happened...but, there it is. What is your current pain level on the standard 1-10 scale? Have you looked into devices like spinal cord stimulators and pain pumps? Both offer potential help for severe, chronic pain and both have a trial that will give you some sense of whether it will help you. I have had both and the scs worked well for about two and a half years. But, I have read many stories here on Mayo Connect about patients who had very bad experiences. After mine failed, I finally had a pain pump implanted. I am still having it adjusted and looking for any pain relief. All I can say is if you are like me and the pain is so bad that anything offering even a glimmer of help seems wonderful, then check both options out very carefully. There are no guarantees. I wish you well.
I had an intrathecal baclofen and morphine pump for 6 years. Now I have lumbar arachnoiditis because of it. So all my original complaints plus new ones. Arachnoiditis is not common but is becoming more frequent as more procedures on the spine are being done. Best to be as informed as possible as we make these important decisions.