Spinal cord stimulator

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randy71

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Just when everything seems to be going good something always seems to happen. I think the paddle in my back has moved. Has any one else had this happen? What were the changes you felt. Mine didn't work very well to start with. Now it does nothing to relieve the pain. Now I can only walk 10 to 15 minutes and my back hurts so bad I have to lie down. I also seem to have a "pressure" in my back I didn't have before.
 
2 of my paddles moved, when I had them in as a trial. I was suppose to go back in for a follow up in 5 days, but by 3 days, the pain had not only not gotten better, but had gotten worse and I ended up in the ER. My back began to spasm in the area that the leaRAB entered and where they were placed. I then got in to see the Dr. the very next day, after the ER and they did an X ray of my leaRAB. That is when they said that 2 of them had come loose. I am glad I found that out before having them implanted. I would highly suggest you go back to the Dr. that place them in and have them do an X ray. They were able to do this for me, in the Drs. office. BTW, what type of unit is in you?

Lorie:angel:
 
Thanks and Happy Easter to you too. Actually, the stimulator and the morephine pump are two diffferent things. 1st they will try the stimulator, which is a lead that they attach to my spine and when it is turned on, it gives a vibrating feeling instead of pain. Because of my scar tissue, it may not work, but w/o trying it...then I will be on meRAB. the rest of my life. The Dr. will probably try the pump, at that point, if we can find a medicine that I can take. I am allergic to moraphine, so that one wont work for me.

How are you doing? I have been thinking about you.

Lorie:angel:
 
Hey,
Do you like the SCS? Are you glad you did it? I am actually a SCS candidate and I just keep dragging feet about having it put in!! I'm really scared! How bad is the surgery to have the leaRAB placed? How often do you have to go back to have the battery changed, etc? Any info you can share would be greatly appreciated!

Deb
 
I just saw the specialist who is going to surgically implant my unit. He said that there would be a very small incision and I would be walking out that day. He also showed us how you recharge the battery by holding the charging unit, up to your skin and place it over the battery (which is under your skin). So, they don't have to go back in to change out the battery. He said that I would need to re-charge it every 5 or so years.

My surgeon uses the advanced bionics stimulator.

Good luck,
Lorie:angel:
 
Hi Lorie,
When are you having the unit implanted? Do you have nerve pain in your legs and do they think it will help that? I also have scar tissue...how does that impact the benefits of the SCS? Thnak you so much for your advice. I have had 3 docs recommend the SCS and like I said, I am very nervous about it!

Deb
 
Hi Deb,
I have to 1st set up a physical to be cleared and to get an EKG and a chest X ray and labs. Once I get that done, they said to call and set up the surgery. I have found a place that can do all of the pre-surgical work ups, all in one place. So, I think I should be able to get an appnt. with them within the next 7 days or so. Then I am guessing that I would be able to get into a operating room in another 2 weeks. (My fusion, which was going to be 4 hrs. long and required 2 Dr. to correlate their schedules, took 3 weeks to get on the surgery schedule. This is just a 1 1/2 hr. procedure with just 1 Dr.)

Yes, I have terrible feet and leg pain. Most of the leg pain is under control with Neurontin. It makes it liveable, but the feet are a constant, my Butt is a mess, my SI area in swollen and painful everyday. The SI is permanently out of its socket. Now I have Bursitis on the opposite side from the SI joint. Those aren't even touched with my oxycontin and neurontin. Since I have tried everything else, including radio frequency, the stimulator is my last hope. If it does not work, I will be on meRAB. the rest of my life and will be in this ongoing pain.

As for scar tissue, it makes it a lot more difficult to thread the lead to the spine, if ther is scar tissue in between your back and your spine. I have already gone into the PM office to have the stimulator trial put in. What should have been an hr. procedure was 3 1/2 hrs. He tried everything to push through the tissue, but it was like rock. So, he tried to send the lead up to the lowest part of the spine that he could get to and finally placed the leaRAB at T9, 10, and 11. I never got the vibrations to get high enough to get to my back and hips. W/i 4 days, I was back and in so much pain. The stimulator rep. met me at the PM's office and when they looked with an X ray, and the rep saw where the leaRAB were placed, he said that was why I could not get the results up in my back. The leaRAB needed to be much lower. But they could not get them any lower and so they took the leaRAB out. Now, I am going in to see if a specialist, that works with special spine issues, can surgically open me up and place the leaRAB in the correct place. It is a 50/50 chance that it will work, but it is my last option. So, I am giving it a try.

I would definatly ask your Drs. what their experiences have been with people that have scar tissue. Make sure that you tell them that you know of a person or a couple of people that have had problems getting the leaRAB to the correct place in the spine, due to scar tissue. This way they will realize you know what you are talking about and won't brush the ? off by saying it is not a problem. Also, the other issue with scar tissue is if you already have it, you are more likely to have more scar tissue build up around the lead, on your spine. If something were to go wrong and you needed to take it out and it was stuck to your spine...well you can imagine the difficulty that comes with that situation.

I still think its worth the try, but go in it with all the knowledge that you can get and don't hesitate to let your Dr. know what you have learned.

Good luck and please keep us posted. I will do the same when mine is finished.

Lorie:angel:
 
Happy easter Lorie,
that the surgery you having done a stimulator put in?I hope it helps you,I know few who got really sick had to remove it.its a morphine they use in the pump.maybe work for sure hope so.
 
Thanks so much Lorie! I will anxiously await your input after your SCS is placed. Let me know when you are scheduled so I can keep you in my prayers. Hope you feel better my dear!

Deb
 
Was wondering the same , I've been having horrible spasm's when I bend or lean over. Maybe my paddle moved also ? I started another thread about this , I was wondering if anyone that had the implant experienced spasms and pain in new areas ?

Deb I have a 3" scar where they did the laminectomy to run the paddle down my spine . The surgery wasn't that bad , and with the medtronic unit its rechargable , but may need replaced in 5 years. It works wonders for leg pain.


Shawley
 
Shawley-I too have the severe muscle spasms with any bending or leaning. My Drs. can't give me a reason and I was beginning to wonder if it is just me. I am sorry you have this too, but I am relieved that someone understanRAB. I also am always getting new areas that hurt. I feel like every month when I go in for my meRAB. that I am complaining about a new pain and wonder if they are ever going to start to think I am just making pains up :). Just in the last 2 weeks it is the top of my left foot. It feels like a huge bruise, with the lightest touch to it. Also, the backs of both of my legs, when I am walking.

Anyway, I just wanted to get that off my chest I guess. Sometimes I feel like I don't want to mention anymore new pains. Can you tell me how long you were in the hospital for the implant, or was it an outpatient procedure? Also, what was the recovery like. Thanks a lot.

Lorie:angel:
 
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