SCS & Pain Pumps For spinal cord stimulator (SCS) and pain pump discussions.


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Old 09-01-2010, 09:09 AM #11
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Default Hi

Quote:
Originally Posted by bobinjeffmo View Post

For anyone considering a morphine pump as an option for pain management, here's my two cents worth:

1: If you're looking to be pain free, then you're going to be disappointed. I've found in my situation that the pump helps moderate pain levels better throughout the day, but that it wasn't one solution that took away all my pain. In my situation we also have me on two different kinds of oral opioid.
2: These are not really small devices, so be prepared for the hockey-puck that's going to stick out from under your belly. The thinner you are, the worse it will appear.
3: When I had my second morphine pump installed (first one lasted 5 1/2 years before the battery finally conked out), the pocket they installed my first pump in slid down, hence making my second pump directly under the belt line. Bending over has become much harder. Make sure the install location is high enough so you won't have quite as much problems when reaching down to pick up an item.
4: Anyone that goes to a brand new doctor and announces that they think they need a morphine pump is going to probably not going to get a positive response as they were hoping for since we're talking about a major commitment from both the doctor and patient, not to mention sizable investment and upkeep costs. The only way you can build up this kind of trust with each other is over time. It's my opinion that only those with more lengthy doctor relationships will have this option opened up for them.
5: Since my damage is from the waist down, I'd say that I have had very good coverage as far as how well the pump works.

After living for 5 1/2 years with my first pump, I had come to the conclusion that the thing really didn't make much of a difference since I'd grown so accustomed to it. Then the battery died. For a little over 3 months (I had another surgery scheduled that prevented it from being replaced ASAP), I found my pain levels were simply unbelievable once again. When they got my second pump reinstalled, I was blown away once again about how wonderful this amazing piece of technology can really work. I know it's given me back a much better quality of life, but it's no easy ride.

Anyone who "thinks" this might be an option worth consideration should bring it up with their doctor and then have themselves checked into the hospital overnight so they can be tested. It's not a result you'll have to wait for. You'll know right then on the spot of having morphine going directly into the spinal fluid in the spine is going to help manage your pain levels better.

Always be 100% honest! The worse story I ever read was about a person who lied about getting positive results during the test when he/she hadn't, and so of course the device was installed. That person then complained that the pump had failed, when that couldn't have been further from the truth. It was the patient who failed when he/she said that the test was successful. An open and completely honest relationship is vital with anything regarding pain management.

I just wish everyone could be as blessed with their pain management as I have been. There's no doubt that this goofy puck under my tummy has made all the difference.
Hi Bobinjeffmo

Thanks for sharing your situation with us about your pain pump and so glad to hear that you have benefited from it too.

Pain management is very important to all of us who suffer from chronic pain.

I have a SCS implant and have if for only 4 weeks now, so still quite new to it plus this site. Im getting good results with it too which is terrific. And Im in total agreement with you when you say that you MUST be honest both with yourself and the professionals when trying out these implants. They are there to help not hinder. Thankfully.

I wish you the best of luck and continued relief with your pain pump

Jackie
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Old 09-01-2010, 10:00 AM #12
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Smile Thank you Bob

Hello my Friend-

Good to see you post again, and to re-read thoughts you present about pain management through pump, the manner, method, and process about presenting for evaluation, AND you multiple iterations of the device. You are well experienced beyond many of the rest of us, and you are living the dream of leaps forward in technology. May yours continue to bless you as it currently provides!

Mark56 PJ
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Old 09-01-2010, 08:55 PM #13
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Thumbs up Yes Thank you Bob!

I was sure hoping you'd chime in on this thread!
There seems to be very little discussion on the pain pump.......so you are the first 'Go To' man we've got!
The other's who've received the pumps have drifted off somewhere beyond the great divide....... I think of them often and hope they are doing well!

THANK YOU so much for your commitment to stick around to answer questions and give straightforward feedback!
The pump could very well be the answer many are looking for, but like you say, it's a matter of hooking up and communicating with the right Dr to make this commitment!
You are a true blessing to this forum!

Rae
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Old 09-01-2010, 09:02 PM #14
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Smile Yep- What she said


Mark56

Quote:
Originally Posted by Rrae View Post
I was sure hoping you'd chime in on this thread!
There seems to be very little discussion on the pain pump.......so you are the first 'Go To' man we've got!
The other's who've received the pumps have drifted off somewhere beyond the great divide....... I think of them often and hope they are doing well!

THANK YOU so much for your commitment to stick around to answer questions and give straightforward feedback!
The pump could very well be the answer many are looking for, but like you say, it's a matter of hooking up and communicating with the right Dr to make this commitment!
You are a true blessing to this forum!

Rae
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Old 09-03-2010, 01:31 PM #15
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Default Great thread!

I'd say I get 100% coverage, and 80% pain reduction. Only difference is if I'm in a flare of RSD, the burning on the surface of the skin gets no relief at all from the stims
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Old 09-03-2010, 08:55 PM #16
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Thumbs up Yep

That is the devil of the distinction that I have not received any remark by way of diagnosis from Doc, whether this BURNING feeling of my right foot is something other than remnant radicular neuropathic pain or this other devil of a thing. I would imagine RSD is not touched by stim. Thanks Vanna, you give me something about which to think,
Mark56

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I'd say I get 100% coverage, and 80% pain reduction. Only difference is if I'm in a flare of RSD, the burning on the surface of the skin gets no relief at all from the stims
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