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Neurostimulation stimulater implant

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aliveso4
Regular Member
Joined : Aug 2009
Posts : 22
Posted 10/17/2009 4:03 PM (GMT -7)
Compensation is the only thing on my mind right now uniquelyme........The unit I had inputted I now find out was  not yet okayed by the FDA and the second battery that was put in less than 60 days ago is already heating up when I recharge it that it sacares me to the point that I think it is going to explode.  I work around and know aboput electricity.  Not good when it goes afowiceburgol  .  The point of all of this is is the fact that I was lied too on 3 different occassions now.  When I was having problems, after I had the battery switched  out and now after the fact when I am still being told that they have no idea what could be amiss...........DAUGH,  can you spell lie and understand where my brain is at??It is one thing to stretch the truth, but an out right lie is a lie...And I have been lied to now for the past 17 plus months. Would you feel; that  this should be worth compensation if it was in yhour back??  Not a very good thing me thinks........I have only witnessed at least 200 people who have  under gone the same procedure I had in the last 12 or so months here.  The lie keeps growing and gaining speed.  Think about it.  I am mad and hurt both in body, mind and spirit as well as money wise.  Each time I had to take off my wife had to take off from her employment to take me.  Cannot drive yourself home under drugs.......More money and lost itime.  I believe that is the meaning of lost time and fair compensation for unprofessional conductt by a dr. and or drs. med. group........Hopefullly this forum will not be deludged by my fellow causulties from here in ///san antonio, tx.  I am just the tip of this iceburg in this area.  dlt
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uniquelyme
Veteran Member
Joined : Nov 2008
Posts : 1037
Posted 10/17/2009 4:32 PM (GMT -7)

 

 

Well, that falls under the *** category if you ask me....What were they thinking?  Is the all mighty dollar really worth having a patient spontaneoulsy combust?  Not for me.... I think you are on the right track... There are always commercials for Lawyers that do this kind of thing...they love it....especially something as blatant as this.

 

How can you walk around knowing that this thing could burn up at any moment?  I would be freaking out!!!  Oh Boy!!!  It never gets any better for us does it?  What else can we expect?  I mean, all we want is to live our lives with as little pain as we can, not have to worry about catching on fire smhair , and having Dr.'s that actually want to help us...Is that too freakin much to ask for?  I say NO...it's not.

 

I thought I had problems...at least I don't have one of those to worry about.... Now I'll be watching my TENS unit like a hawk...I mean, it could go up in flames while I'm using it....or it could start smoking...or anything... shocked

 

Oh My Goodness!!! I am thinking of you and I will send good thoughts, thoughts about anything but batteries burning up...ok?

 

Sorry, I just thought some humor would help..

 

Me.

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aliveso4
Regular Member
Joined : Aug 2009
Posts : 22
Posted 10/17/2009 6:00 PM (GMT -7)
Hello all again, just  finished doing a little experiment with my laser temperature shooter.  My back unit when in operational mode runs at 87.7 degrees while my opposite side with no implant is 87.1 degrees.  Appr. 8;inches between the two points.  While my charger is reunning the temp. rose to 88.4 degrees and is again turning itsself off before it finishes recharging itself.  Happy days are here again.  Another question is who or ;where are the other forms of these units sold,,,,,,meaning the medtronic and the others I have heard mentioned??  I do not think my eon has a very good track record compared with names I have heard from the group.......I have a meet with these nuts ?Friday,  see if ;they will tell me before I tell them what I know.  Should be very interesting, to say the least......Will let all know the outcome.  May help someone else out there..Later on,.. dlt---------still---- aliveso4
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BionicWoman
Regular Member
Joined : Jul 2008
Posts : 243
Posted 10/17/2009 7:53 PM (GMT -7)
I'm confused. What unit do you have that wasn't approved by the FDA when it was implanted in March of 2009?
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uniquelyme
Veteran Member
Joined : Nov 2008
Posts : 1037
Posted 10/18/2009 3:09 PM (GMT -7)

Yes, I am confused too...Why would a Dr. install a unit that isn't approved?  Isn't that asking for a lawsuit?  I mean, unless he got his medical lisence in the tropical rainforest of Uganda or Ziymbabwa isn't that illegal?

I know if I were about to have this unapproved unit put inside my back I would run run run...far away, and never return to that Dr.  Maybe I'm being too harsh, but it seems kinda hinky to me...

Me.

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aliveso4
Regular Member
Joined : Aug 2009
Posts : 22
Posted 11/5/2009 8:04 PM (GMT -7)
I am glad to see so many people on this site are aware what is happening to people out there in the real world.  There are things you can be doing, such as to aid others who are looking for help with there recall problems.  I wrote on this forum looking for aid, I received some good advise and help.  What I saw in responce was people who could not believe a dr. would do anything so vial as to do something that would harm someone , there patient.  They do it everyday..... Everyday.  Yes I am going to sue the ---- out of 4 people, the 4 who were involved in harming me then and now ever going, and refusing to relate to me that they did anything to me that has harmed me.   darn is that rick or what.  What is called harm,?  Having to have another 2 hour surgery again with in 6 months or the pain of fricking battery acid inside  of your gut??   Explain it to me...  But it is my gut, right.  I dont think that there are many people on this forum who have anything else better to do but pop pills and read about other peoples problems and relate their problems and suck down another perscribed pill.  I tried a medical procedure to get the hell off of medications of any sort.  I am pretty much tired of drugs, for others it is different they get used to the enjoyment of a cheap high , thanks to there ins....Do all of yourselfs a favor and get yourselves a new dr. and get the hell off drugs if you can.  When you give advise and can not remember giving it to someone in a forum and come back wondering how I came up with the web site where I found the imformation on the fda suit, it is time to stop helping others.  and so on...  My suit is going forward and I hope to find others who have problems with the EON stimulator.  Anyone else out there who is having problems, please let me hear from you, there is strength in numbers.  One can start it , but it takes more than one complaint to get someone to take notice and to get something done.   anone interested can reach me through this forum.  I will check back from time to time.  Thanks to all.  dlt
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BionicWoman
Regular Member
Joined : Jul 2008
Posts : 243
Posted 11/5/2009 8:23 PM (GMT -7)
I'm still confused as to what unit was implanted in you that wasn't approved by the FDA in March of 2009...? The information in the FDA link above wasn't about a lawsuit and it wasn't about a unit that didn't have full FDA approval for use. If that's the information you based your statement on, I think you seriously understood the meaning of the letter in that link.
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hotrod256
New Member
Joined : Jan 2010
Posts : 1
Posted 1/16/2010 6:44 PM (GMT -7)
Failed back surgery syndrome i guess. Had a micro discectomy 5 years ago pain constantly horrible...this week has been nitemare going to yet another pain clinic soon. Lortab vicoden etc my best friend but really screws up my system. I was told be a RN when i had my last epidural that the hospital that he worked for discontinued allowing the nuerostimulators from being implanted there due to liabilities but that every patient that had it done that he knew personally did amazingly better after the implant. I am seriously considering it. Will talk to my new pain clinic asap. The pain meds are so rough on my whole system plus they just are not doing the job anymore...It appears that the skill and knowledge of the Dr is crucial in the success of this or I guess anyother procedure. Anyone have a suggestion as to where the absolute best place to go to get this done? thank you so much.....
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melliflious
Regular Member
Joined : Dec 2009
Posts : 79
Posted 1/17/2010 11:03 PM (GMT -7)
Hmm I'm glad this popped up, as this was something the Mayo guys and I talked about last week. The last time I went up there they were really pushing this, the guy I saw last week said we'd put it on the back burner, pull it out as a last resort. I was talking with my physical therapist about it, and she was shocked that they would consider putting it into someone my age (23), especially as a woman. She is pregnant herself, and told me about how much the spine changes during pregnancy. Hopefully this isn't ever something I'll have to deal with, but now I'm curious. Have any other young women had this implant? Were there concerns if/when you decide to have children? Like I said, hopefully this doesn't become an issue for me, but now I'm really wondering if this is something that doctors are keeping in mind. Hope everyone had a relaxing, pain-free weekend!

Jenna
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catahoula
Regular Member
Joined : Dec 2009
Posts : 184
Posted 1/18/2010 11:54 AM (GMT -7)
I also have a nerve stim but its in my head. I agree with most posts , that either the leads are in the wrong place or it may be turned up too high.  Make sure you have the tech adjust it to your comfort level and be sure YOU are happy with any result before you decide if you want to make it permanant. I have never heard of a 3 hour trial period and would never trust one. I just think the longer the better and under the most different situations to see if it helps.

good luck, I hope it helps you

cat

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Tirzah
Veteran Member
Joined : Jul 2008
Posts : 2323
Posted 1/18/2010 5:50 PM (GMT -7)
Jenna,
I had mine implanted at 28. Yes, it could be impacted if I become pregnant. I have mine implanted in my buttock. I had a choice to implant the battery pack just below my collar bone or somewhere lower. I wanted it not to show if I wore low-rise pants (I know, totally vain) so that's why I picked where I did. I'm very happy with my choice. Honestly, I was literally bedridden 100% of the time more days than not. I couldn't even get up to use the washroom. So the reality is that pregnancy would have been high-risk even without the stimulator implanted. I made peace several years back when I first found out I have Chiari that I would adopt children rather than try to have my own. But it is a bit of a risk. Sometimes you can take every precaution short of abstinence and still end up pregnant. So I have a fantastic ob-gyn who is experienced in managing high-risk pregnancies, including experience with 5 women who successfully delivered with neurostimulators/spinal cord stimulators implanted prior to conception. You can still have ultrasounds just like normal. There is a chance, though, that the leads can move (especially if you get pregnant within the first 18 months after the implant) and that could affect how much relief you get. There is a chance that the weight gain could cause problems at the battery pack site. I have experienced that even with as little as 10 pounds of extra weight. This is especially true if you are underweight or at the bottom of your weight range. In those cases, the battery is implanted much closer to the skin's surface. There have been some reports with people putting on weight post-op and ending up with the battery pack pulling the skin taught & a few cases that were not properly managed where people even developed a small hole in their skin where the battery pack showed through. They were all treatable, but obviously any of those situations are less than ideal.

I would strongly recommend that if you are considering the stimulator implant (and please, do not do it unless your pain is totally unmanageable & is not able to be treated by any non-surgical options), that you sit down with both your PM & your OB-GYN and discuss how pregnancy could affect the stimulator. I haven't followed the most recent research, but originally there were some questions as to whether it was safe for the baby to turn the stimulator on while you're pregnant. Perhaps that has been resolved. But truly, the stimulator implants, while not as serious as fusion surgery or discectomies, are surgery and should be considered as such. I don't understand people who refer to them as "permanent TENS units". It is surgery & a serious decision. If you're like me & you're life and ability to function & ability to have children is totally destroyed anyways, then I really would encourage you that adoption is a beautiful process. I know so many people who have adopted & were so happy. I can't wait until my turn to adopt comes. It's just not worth it to trade a healthy, productive life for a dangerous pregnancy and the possibility of having your own children. I am able to do so much more because of my SCS. I can get up & go to work & clean my home & visit with friends. It has literally been life changing.

but it is in the back of my mind always that God forbid I ever get pregnant it will be a rough ride ... no pain meds, no stimulator, extra back pain from the baby, plus all the complications of having an SCS. Not a pleasant prospect, but still, I would do the surgery again in a heartbeat.

wishing you well,
frances
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skeye
Veteran Member
Joined : Mar 2008
Posts : 3089
Posted 1/19/2010 11:05 AM (GMT -7)
Jenna,

I'm 21 & I'm fighting to get one at this very moment, except mine will be a peripheral nerve stimulator (ie. it will effect cranial nerves instead of spinal nerves, but it is the same device). We're on our second insurance appeal. Cross your fingers!

Skeye

Post Edited (skeye) : 1/19/2010 11:09:29 AM (GMT-7)

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melliflious
Regular Member
Joined : Dec 2009
Posts : 79
Posted 1/19/2010 10:16 PM (GMT -7)
Frances, thanks for the info. I know adoption can be a time-consuming but very rewarding process, my cousin adopted half-siblings that she originally fostered. I wish you the best of luck with that!!

Skye, I will definitely cross my fingers for you. I hope the insurance people get their act together!

Jenna
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tysmyboo
Veteran Member
Joined : Dec 2004
Posts : 921
Posted 1/25/2010 3:45 AM (GMT -7)

 

 

melliflious said...
Hmm I'm glad this popped up, as this was something the Mayo guys and I talked about last week. The last time I went up there they were really pushing this, the guy I saw last week said we'd put it on the back burner, pull it out as a last resort. I was talking with my physical therapist about it, and she was shocked that they would consider putting it into someone my age (23), especially as a woman. She is pregnant herself, and told me about how much the spine changes during pregnancy. Hopefully this isn't ever something I'll have to deal with, but now I'm curious. Have any other young women had this implant? Were there concerns if/when you decide to have children? Like I said, hopefully this doesn't become an issue for me, but now I'm really wondering if this is something that doctors are keeping in mind. Hope everyone had a relaxing, pain-free weekend!

Jenna

 

Jenna,

I had a Boston Scientific SCS implanted a little more than a month ago and I have been told REPEATEDLY that having this stimulator will not affect pregnancy and that I don't even have to turn my stim off when/if I get pregnant again.

I'm not sure where other people are getting their information, if they are using a different company or what, but my information is from my Boston Scientific Rep as well as my OB.

I wish you the best!

Sara

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melliflious
Regular Member
Joined : Dec 2009
Posts : 79
Posted 1/25/2010 10:50 AM (GMT -7)
Thanks Sarah! I know that for me it was my of who was concerned that with the changes our spins go through during pregnancy, the leads would be displaced. I'm glad to hear Boston Scientific has figured out how to compensate for that! I hope your implant has been succesdul!

Jenna
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IsThereAnEnd?
Regular Member
Joined : Feb 2010
Posts : 66
Posted 2/24/2010 2:54 PM (GMT -7)
I wanted to thank everyone who has replied to this post......I am finding this site to be SO useful and helpful! I am going for my trial implant in two weeks and am praying for some relief!
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wendysp
New Member
Joined : Mar 2010
Posts : 1
Posted 3/27/2010 7:45 PM (GMT -7)
Hi,

I had a trial using a medtronic neurostimulator. I cancelled the surgery because I couldn't get a appointment with the doctor before the surgery and there were too many unanswered questions. The pain relief was 100% during the implanting of the leads into the epidural space (surgeon working with medtronics rep). Once I was off the table, it took hours of programming and the reps never got the right spot. The trial was not very successful although I did get some pain relief by driving up the current to an unbearable high and then turning it off. The distribution of current was in both legs rather than in one which was OK with me. I can understand the benefits if it gets to the right area and in general liked the all day massage.

My questions are around the readouts from the trial. The reps were using a computer that seemed quite sophisticated. I would think from the printouts and from the nurses notes, there would be information that would be useful to the doctor. I wasn't getting that feeling when I went to the presurgery visit and the nurse wasn't going to answer any questions. I learned when the leads were pulled that only one contact had been available which meant that when I stood up, the lead had slipped so there was a lot of room for better programming but what else is there to learn from printouts and where would the nurse have gotten that information? Should I be asking this of my doctor?

BTW, the trial was not very painful - sore. Read a few posts about that. Wondering about the docs hands if the trial was so painful I would look for another doc to do the implant.

Wendy
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rusty3770
New Member
Joined : Apr 2010
Posts : 2
Posted 4/7/2010 3:11 PM (GMT -7)
Hello everyone. I am new to to healing well forums and have read most of the post concerning neurostimulators. My pm doc is recommending I do a trial for a Medtronics unit. I have read all the concerns about the goods and bads of the unit and it seems as though each person is different. Anyways here is my story.

I am 53 and had my first L4-L5 fusion in 1990 when I was 34. In 1991 I had to have the same surgery redone because it didn't fuse but the fusion did take the second time. I went back to college and got a degree in Elementary education and after graduation worked as a school teacher until June of 2007.

In 2004 I had to have a C5-C6 fusion on my neck and it did not take so they tried again in 2005 and the fusion took but I got infection and the cable holding my neck was loose and caused severe nerve damage so another operation in 2006 to remove infection and cable.

Well now here I am on disability since 2007, cause i can't even teach, and the pm docs are recommending an implant which will have to cover both my neck and back. I am currently haveing an epideral in by back, with some success, and nerve blocks, just below my skull, which takes away most of the migraines caused from my neck. I have spinal stenosis and degerative disc with arthritis also causing concerns.

I wonder if the stimulator will let me return to work if successful. Has anyone returned to work after having one put in?

Well there is my story and thanks for having this outlet for chronic pain sufferers.
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LLPLUV
Veteran Member
Joined : Mar 2009
Posts : 1158
Posted 4/8/2010 6:41 AM (GMT -7)
Rusty I have a thread going on right now that is Named My Pending Surgery...

https://www.healingwell.com/community/default.aspx?f=16&m=1765646

I posted about being approached on getting the implant and I had a few questions.  So there and jump in and maybe we both can get some issues cleared up.

And welcome to our forums...

Laurie

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BobbyJ Atlanta
New Member
Joined : May 2010
Posts : 1
Posted 5/12/2010 6:10 PM (GMT -7)
Shirley,

I hope that you get what you need out of the trial. I am currently underway (day 2) of my trial. However, I am not doing the same trial that you are doing. The same item but just in a different location. I am having it in the back of the head and not on the spinal cord.
So far the trial is going great for me. I just wish the best for you.

Good luck.

Bobby J Atlanta GA
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peleegal
New Member
Joined : Jul 2010
Posts : 8
Posted 7/15/2010 5:25 PM (GMT -7)
I have an implant. I received it on April 12,2010. I have had 8 previous neck and back surgeries, with pain radiating down both arms and legs. Everything hurts. The last year has been complete hell. I can't do anything. I tried the 7 day trial in January. It was great, yes, I had pain at the incision sight and it was sore, but my overall experience with the trial was great, I couldn't wait to get the permanent one put in. They put in 2 leads into my spine, all the way up to C-3 and all the way down to the end of my spinal cord with the lead and battery ending above my right buttock. Out of all the surgeries I've had this has been the hardest to recover from. I am still completely exhausted. At this point I'm not sure if having the implant was worth it or not? It seems the leads seem to focus more on my arms and legs than my neck and back pain. I see my doctor in a week and have had the reps from the company try and reprogram the device a couple of times, but nothing is really helping completely. Has anyone had this experience and if so when and if did you start to feel better.
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skeye
Veteran Member
Joined : Mar 2008
Posts : 3089
Posted 7/15/2010 7:10 PM (GMT -7)
Hi Peleegal,

I just had my stimulator implanted 6 days ago. I've pretty much recovered from the surgery. I'm still a little sore, but it's not bad at all. However, you must understand that I'm only 22 yrs old (so I probably recover faster than most people who get the implant), and my pain is in my face, not my back, so my stimulator, which was implanted in my chest, is not a painful area for me to begin with.

Three months does sound like an awful long time to still be in that much pain from the surgery. Have you seen your doctor lately? Maybe something is wrong, such as your leads have slipped. I hope you can get some answers!

hugs,
Skeye
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peleegal
New Member
Joined : Jul 2010
Posts : 8
Posted 7/20/2010 1:47 PM (GMT -7)
Thanks Skeye,
I appreciate the hugs. I've been trying to get a hold of my doctor since Friday. I think my battery has flipped. I haven't seen my doctor since my surgery. He has a PA and I saw him once and then I also saw the reps a couple of weeks ago. I've been calling reps and the doctor since Friday, I'm getting madder and madder as each day passes. I just don't understand why they won't call me back. I've only called one other time since my surgery. It's soooo frustrating. I know it's the battery because I'm charging it right now and when I placed the charger over the battery today it was in a completely different position. I even called again today and told them that and still no phone call. I just seem to be in as much pain as I was before the surgery, except now there are more pains, because of the surgical sites as well. Good Luck with your recovery.
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skeye
Veteran Member
Joined : Mar 2008
Posts : 3089
Posted 7/20/2010 6:55 PM (GMT -7)
Yikes! That sounds really scary! I hope you hear back from your doctor & your rep soon!

hugs,
Skeye
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BionicWoman
Regular Member
Joined : Jul 2008
Posts : 243
Posted 7/23/2010 8:28 AM (GMT -7)
If you're able to charge, then the battery hasn't flipped. When the battery flips, the remote and the charger can no longer communicate with the implant, so you can't charge and all you'll get on the remote is a failed connection icon.
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