I just saw a new doctor for a consult. He is the 4th doctor to tell me I need an SCS.

This one worked for many years with Stanton Hicks, and just parted the Clev. Clinic last year. He has implanted "hundreds" of SCS.

I have 3 main questions.

1)He told me that the main reason he recommends the SCS for me is that it will stop my spreading. (if the thing works for me, that is) This is the first I have heard that an SCS will stop spreading.

If you have an SCS that you use - did it stop spreading for you?

2) Also - this was most curious.... I told him that missing any work, past 1 week vacation time, would be a great hardship for me, and that means I need to drive. He said it would be no problem for me to drive within 2-3 days of trial or final implant.

Everything I have read is that people are told no driving for 4-6 weeks.

3) He said it should stop my need for taking medications, etc. by stopping all or nearly all my pain. He said that if the trial works, the implant should work. I said I have read of many people that have had the final one not work. He said that depends on the skill of the doctor... be sure to have one who has done hundreds of them and your outcome will be better.
Anyway, I am curious as to how the pain will be gone? The Medtronics site says it will be replaced with tingling simiar to hitting your funny bone. Well, I don't think hitting my funny bone is very pleasant. I've had times when I had to much neurontin and my hands and feet tingled terribly. I hated that. Is that what I would have? Their site also says it works better for arm and leg pain, but mine is mostly in shoulders, upper back, and now traveling down my entire back. I plan to see my regular pain doctor and my neurologist about this again before doing anything. The whole idea just scares me to death.

However, the RSD was pretty stable for the first year. Now, it is moving at what I think is fairly rapid rate. Showing up in my left big toe, for no reason, and this travel down my back is coming pretty fast. About 6" this week. Stopping the spread would be the main reason I would do it.

My mind is really whirling.

Hi,
I am so sorry to hear that you are having such difficulties. It's very frustrating. What has your treatment plan been for the past year? Have you had series of Blocks, Epidurals etc? Are they just not working now?

Moving to a SCS is a big step. And I can understand why your mind is whirling. As what you want is relief and your doctor paints a pretty good picture that the SCS is going to be the answer to all your problems. If all that these 4 doctors said to you was true we'd all have SCS's. There would be no more suffering from RSD.

I've never heard that SCS stops RSD from spreading.

There are people who have had SCS that have to continue to take meds orally.

With the trial, they tell you to be very careful so that you do not jar the leads. There is a whole list of things that you can't do. If it were me? I would want to run, jump and play and really test that bugga out to see if it really works! But as far as Medtronics is concerned, they want you to sit calmly, with your legs crossed and watch TV for the whole time! No bending, squating, twisting, the list goes on and on.

I hope some of the people w/ SCS's will share their experiences with you.

Please do not be intimidated by Doctors. Remember it's your body. It's the only one you have.

I have had the ANS Genesis (non-rechargeable) and now have the ANS Eon (re-chargeable),

I only had RSD in my right arm - until I had the trial for the SCS - that is when it spread to the left arm.

I had a lead move and was using high settings on the SCS so I had revision surgery. They could not get IV's in my arms so they tried (several attempts) to get IV's in my feet - I ended up with a central line because they could not get IV's in my feet either, but that is when the RSD spread to my feet and legs.

I have pretty much stayed on the same meds before and after the SCS with adjustments (some higher).

I have been told that I have the most severe form of RSD though that very resistant to treatment. So you could be totally different.

I have had a couple stellate blocks, which were good blocks (hand warmed etc) but no pain relief. No epidural or other infusions tried. I am not on "pain" meds per se... but do take topomax, baclofen, calcitonin, and clonadine. With all of those, my pain is mostly reduced to a feeling of very severely strained muscles. Although I am fairly misesrable, it is tolerable. I have not had at any time the burning or severe skin sensitivity. Just recently, I developed a small spot on my good foot, on a toe, that feels like someone holding a burnt out match to the skin, so that might be the start of burning.

I am able to do most things. I work at a computer sit down job, and can drive, although longer than half an hour gets to me. I don't have the strength I used to have, so can't open jars etc... but I have worked hard at therapy to be able to still putter in the flower garden, etc... even though it is a struggle, I fight to be able to keep doing these things and not stop.

So, for me, as I say, the main reason to do the SCS would be to stop spread, and in the back of my mind, it seems to me I have read about people having spread after the SCS. This doctor seemed to want to talk about nothing BUT the SCS. I am just not sure I am bad enough for that.

Say it does spread through out my body in the way it is right now - I could probably continue to live pretty much as I am now. At least I hope so.

jllenrad - your experience is just what type of thing that scares me about this. I am getting by "ok" as is. What if I went for this and things happened like it did for you? I would be much worse off. This guy said he has never had anyone get spread from having an SCS implanted - yet I know I have read it over and over.

However, RSD will soon cover my entire back.. so on the other hand, it won't make much difference, I suppose... but most of my other 3 limbs remain pain free - spots in them here and there are not, but most is ok ... for now.

It just feels like an SCS would be rocking the boat on a fairly calm sea for me. Sure, the idea of no meds and no pain is like dangling a carrot in front of a horse - but......????

Morning,

It just seems to me that this doc seem fishy to me!! my doc has done lots of them too and everything you siad is the total oposite in realilty.

First Question,
Stop it from spreading?? good lord i wish it did!! I had my SCS implanted in Feb of 2003 about 7 mos after the diagnosis of RSD, and the trial seemed to work, but once he did the perm implnat it stopped working after about 5 mos or less, so i had to have 3 revision surgeries. yes it feels like tingling, but not like hitting your funny bone, but it does take some getting used to and like if you arch your back to strech.. i always like like a jolt but you get used to it! and know what will give you that jolt and what wont! Also another q for you or to ask your doc. We all had a trial with the scs, and mine was 2 weeks of having the trial in and hanging out before the perm was put in. And then after the 2 weeks i was able to get the perm put in (in a day surgery) , but also that you have many many restrictions for at leats 6 weeeks after surgey so the leads dont move. no bending twisting , no lifting of a milk jug wt or over, no hands above the head and NO DRIVING for 3 weeks. All to prevent the leads from moving and it to work correctly so you dont need revision surgery! I have not read or heard of anyone being able to go back to everything in a week!! the surg is not that bad but not that good to be up and mobile and ready for work.!!???

3rd question,
I have been 3 years out of my scs and still on ALL my meds that i had before!! And i also have another stim implnated in my RSD leg, its called a perpheral nerve stim, and that one doesnt help at all either and keeps me on my meds and in Jan i will be getting a pain pump! I will truly be bionic for sure!! lol

Im not trying to scare you by any means but i had no one to ask these same questions too and was totaly in the dark about this and dont want anyone else to be and also have it sugar coated either. The stim worked wonders for me in the begining!! it almost relieved about 40-50% of the pain levels and was in heaven. But then it stopped working and had 3 revision surgeries to try and get that coverage back, all to no avail. You have to try at least the trial of the stim to see if it will work!! thats the evil with this disease, no one konws what will and what wont work and when!! and we have to try all the options out there to seee if this one will work!!

Also in regards to the spreading, when i first got the scs, i had it in my foot and toes alone. Now.. after 2 stims and revision surgeries, and still on meds, it had gone all the way up my leg and back and into the thigh of the good leg!! so nope it doesnt stop and if your doc finds that trick let me know!!

K. gotta try and get some breakfast! if yo uhave any questions let me konw!!!


Amber

I've been looking through the archives from Braintalk.

A couple of comments that haven't been mentioned.

I've taken out the "authors names".


I've had the spinal cord stimulator "offered" to me twice in the last year. The first time was last year at the Cleveland Clinic. I saw a well-known pain management doc who spent almost no listening time with me but was quick to talk about the SCS and insisted that I take a video home. I felt like he was marketing the machine. I learned virtually nothing about my condition from him, except that he thought the SCS was my last hope. Two weeks after returning home, I received a call from one of his office people, asking if I planned to get the SCS. I laughed and replied, "Oh, I thought you were calling to see how I was feeling"!!! LOL Then proceeded to tell her I wasn't interested.

The second "offer" was last week, when I saw a pain management doc here. It was his opinion, also, that SCS is my only hope for pain relief. This was AFTER I'd told him the story about the Cleveland Clinic doc who'd sounded like a Medtronic salesperson! You guessed it--a few days later I got a call from his office telling me that I needed an appointment for some sort of test before I could have the SCS implanted! I had to laugh again, as I'd given that doc no indication that I wanted it. BTW, this doctor told me that the cost, including implantation, is $43,000! That would be out of pocket for me, as my insurance doesn't cover this pre-existing condition!!

Have any of you had a similar experience with big-time marketing of the SCS? For those of you who have now, or who have had an SCS implanted, please don't misunderstand my intention. We all have to make choices, and I may have to make that one someday, just not now. I'm cynical about this--can you tell?! I just don't like, or trust, medical personnel who treat chronic pain sufferers like they, we, are stupid!!!
And...another one...

As a matter of fact I have, and know of a lot more who have also been told it was their last option..Either the SCS, or the Medtronic infusion pump..Well the reason being is that I know some Dr.'s gets $25,000.00 from the company for everyone he implants.... That, my friend, is the reason Dr's preach to us about it being our last option..It isn't really that we HAVE to have it, or that it is our LAST option, it is because it puts $25,000.00 in their pocket..So, don't think your DR. is a so concerned, and worried me, type of dr, when it comes to those 2 things,because it is $$$$$$ that they are concerned about...lol .....
I know that this is alarming. But Marketing is a big Issue! And I'm unsure if you are going to Clev. Clinic or not. Not that I personally have any opinion about Clev. Clinic or their doctors on staff. Just that they have been mentioned so many times throughout the years regarding implantation of SCS.

I believe that you should have as much material and opinions available to you. I spent hours going through the archives, knowing that I would find this point of view.

I'm leaving the members names out, because they have not been active for years so I can not ask their permission. In my opinion, legally, if it's in the archive, it's ok for me to copy and paste here. My apology to the writer, if they recognise their post and they have a problem w/ me helping our new member. No harm was intended. Just support.

Dana

http://web.archive.org/web/*/braintalk.org

I hope that this link works. If not try putting in a search for "way back machine" -- and then from there try http://braintalk.org Hopefully one of these will put you through to some of the archives. What I picked up was only some of the threads from 2000-2004. If you go to "old" BT and do a search on "Archives" -- there are some smart members who have different instructions on how to get through to some links. I take no credit. lol.

Ok...back to the discussion at hand.

In my opinion, this doctor pushing you towards an SCS...his tactics SUCK! To put a person in pain in this position of stress like he has, is just awful. Enough said. I'm happy that you are hearing ALL sides to the story of SCS so that you can make an educated decision for what is right for YOU.

I have had many blocks and epidurals. Like maybe 6-9 probably on the average per year. I also had 2 five day continuous epidural which was done as an inpatient hospitalization. The 1st continuous epidural worked wonders on me giving me lasting relief. But the 2nd a couple of years later, I think, didn't work as perfectly. But I'm telling you just to have 5 days of relief and a month or so, is fine w/ me. Sometimes doctors don't understand what "relief" means!

Many members have posted that blocks/epidurals just don't work on them and this is quite normal for RSD'rs. Others like me, even though I've had RSD for almost 7 years SGB's (blocks) and epidurals (which hit both arms) still continue to provide me with wonderful lasting relief. My doctor gives blocks in a series. Meaning I receive them once a week and have at least 3 or 4 until my pain decreases. Having just one just doesn't work! Oh, and he doesn't put anybody to sleep. My procedure from the time my bed starts to roll to the time I'm back in recovery...7 minutes. You will find that how each Doctor administers blocks vary quite differently from patient to patient, state to state.

There are members who have had facet injections here. Hmm. Can't think who they are for the life of me.

If you want to take my opinion, I'd go for an injection as fast as possible. In your list of questions...? I'd make sure that your doctor does have the aid of a florescope! This is the fancy name for an x-ray machine. This way your doctor is not going in blind. Before I was transferred to my current doctor, I had about 6 blocks done w/o a florescope. Urgh. They were very difficult, long, and painful. The numbing medicine is the only pain I ever feel. He takes a picture first and administers the 1st shot of numbing med-hurts a little...then of course, the deeper shot hurts a little more. I use my LaMaze techniques of deep breathing and try not to ignore my lovely doctor talking to me about how I should quit smoking! This is his way of keeping me calm....he thinks he is funny huh?

The steroid is good. When I'm in awful pain, and doctor knows there is alot of inflammation he adds steriod to the injection. The series of blocks/epidurals that I get, he can't add steriod to each of them. But when he does, I sure can tell.

We also had who we called "Our Resident Block Expert" -- Cam. I sure hope that she will find us. She has oddles of info and her mind is a sharp as tack! Not like mine which I forget my own name from time to time. Darn meds!

Anyways....That's it for now.

Dana

I may not be on exactly the right list, but perhaps my experience will be helpful to someone.

I had an ANS stimulator implanted for thoracic back pain (peripheral rather than spinal column) - both surgeries were more invasive than I had expected and I wished I had scheduled more time away from work for more than 1 week after the permanent implant. I think doctor's intentionally don't tell you what the recovery is going to be like??

Like others on this post, I also had trouble with the trial lead being pulled out of place - I went on a business trip flying to Boston - surprised they let me on the plane with wires coming out of my back and a big stimulator unit. The unit worked great on my way to Boston, but with the lead pulled out I was screwed on the way back!

It's true what they say - don't expect a 100% solution. My wife seems to think I'm supposed to be cured now and that I shouldn't need ice packs or still be in pain, what can I say - no magic bullet here!!

Was it worth it - I was just hanging on to be able to make it through a work day and support my family, with serious concerns I would have to become disabled. Now, I'm just managing pain with good days and bad days. If my battery ever dies I get a rude awakening for how bad things were before.

I use my unit full blast all the time and end up charging about 2 hours a day. I've broken about 4 different charging kits now tripping on the wires or bending them wrong - ANS replaces them quickly but I wish they were more hardy.

In case you are using an external TENS or interferential unit - the sensations are similar. They told me that the implant would be more powerful than the external units - it's certainly more convenient and practical than trying to keep the stickies in the right place where I can't reach, but more powerful, no. I would gladly have a second battery and unit installed to blast this pain with more power.

My doctor didn't even mention this option to me, but I know ANS also has an RF option with an external battery - if you struggle to manage the pain with an external TENS or interferential unit, you may want to take a serious look at this.

They tell you not to drive with the SCS turned on - I've been jolted once or twice in the beginning but otherwise I can't imaging driving without the SCS.

Good luck to all!