Day of and 2 days after surgery

So surgery was Tuesday, January 8, 2008, check-in time at 3:00 pm. I received a call at 1:00 pm asking if I wanted to come in early, I did and could. So same date, check-in time now at 1:30 pm.

I was checked in, informed of my pending sleepover, called everyone to know about my pending sleepover, and taken back by 2:30-3:00 pm. After a couple of hours I was in the recovery/post-op area. After feeling became the norm and grogginess wore off, the new information being provided to me was that the hospital was full and that I would not be receiving a bed upstairs. Nope, instead I would be staying right where I was and enduring an uncertain night in an uncomfortable bed. (I think that is one reason I was granted up to 8 pillows by the time all was said and done.)

The uncertain night became clearer as time wore on. The bed might have been uncomfortable but my back hurt so badly that my tears and cries for strong medications and requests for those strong medications to come sooner than the 4 hour wait time overshadowed the bed issue.

At one point I asked my nurse for dulaited in between doses of Norco x2. She obliged. It is understandable but still quite astonishing that my back hurts SO much. However, they cut directly over previous, already sensitive, incisions and pulled, threaded and tied into place a new lead.

I must say though that this time seems to have hit the magic spot. In their short programming adjustment I have my right knee covered and when I turn my stimulator up my right leg gets buzzed and then moves over to my left leg. Unlike before where it was my hip, abdomen, back, and left leg long before my right leg, and specifically my right knee. Then after pulling my lead it was 10x worse and the lead was poking into my left hip muscle.

As for my bedridden days. I have gotten out of my bed long enough to walk to the kitchen to see what I want and immediately, but slowly, walk right back to bed. I don't bend. I don't twist. I don't put my hands up high. I don't even lift my own computer if it is too far from me. In two days, I already hear my son going uggg, coming. It's cute, because when I say sorry, he still says it's no problem.

I found out today that I can get an Access Pass for disabled people to the National Parks. Currently you have to pay the park usage fee and place a placard in your window showing you paid, otherwise you receive a ticket. Well, National Parks, Fish and Wildlife, and other State or Government Agencies offer disabled people access to these wonderful natural locations without having to worry about tickets or tags. I am going to look into getting one for my car. Soon to be Patricks car cause he only has 5 more DUI classes from a DUI back in 2000. His teacher gave him tonight off to take care of me. Very nice of her.

On a more personal note: I have a slight rash on my face. Kirsty says it's all stress. All I can think is great. At least I don't go out and do anything important, ya know?? I have also started trying MiraLax. Hopefully it is everything they claim it to be

Since my stay in the hospital, my son acquired a Ball Python baby snake. We have a pretty huge tank for it already. We thank his Uncle Martin for both

All right so I am done. This week I have met my resolution goal. Post more blogs. However, how many is too much? How many is not enough? Please comment and let me know your opinion on how many blogs are enough to keep you properly updated, or to keep my New Year's Resolution Goal of More Blogging.

Pain Free Air Hugs (cause my back hurts too much to receive real ones right now) to All,
-Christine



Previously posted @ MySpace:

Alive and good Went in yesterday @ 1:30, came home today @ 4:30. I had a very nice stay. If you start off treating the hospital staff with MOUNDS of respect, you will get MOUNDS of respect. By the time I left I had a total of 8, yes 8, pillows. I think the most you can have is 2 or 3. But everytime I said I need one for my knee or my back, instead of just rearranging the ones I had, they went and got me another one.

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Comments

  • 1/30/2008 11:05 PM jeisea wrote:
    Hi Christine
    Sounds like you've had a pretty rough time of it. Hope this new procedure brings you some relief.
    Do you know about the brain's involvement in chronic pain. With MRI's they have proven the brain changes with chronic pain. A way to help reduce the pain is to retrain the brain with a message that all is "ok". Lots of things help to retrain the brain, controlled breathing, moving normally and physical therapy, moving with different things going on at the same time like aromatherapy, eating, being happy or sad. Each time you move normally with different things going on reinforces the "ok" message. Acupuncture, hypnotherapy/self hypnosis all help. Take care of you and try and stay positive.
    jeisea
    http://www.crps-rsd-a-better-life.blogspot.com
    Reply to this
    1. 3/7/2008 12:46 PM Christine wrote:
      I am happy that I experienced child birth before this. In Lamaze they teach you how to breath through the pain. I didn't even come close to using the techniques they taught me then (over 10 years ago), however, when my pain flares up now I definitely do the breathing exercises I was taught.

      Thank you for stopping bye - Sorry it took so long to respond.

      Always pain free hugs,
      Christine

      Reply to this
  • 3/20/2008 8:15 AM keli wrote:
    I hope you are feeling better, What type of procedure did you have? I am trying to find your post regarding your procedure but cannot. I will look more and hope you have pain free days!
    Reply to this
    1. 3/20/2008 12:31 PM Christine wrote:
      I have my ups and downs, as you know.

      As for the type of surgery, I had a spinal cord stimulator implanted. It offers some relief from the pain that is RSD. However, it is not for everybody.

      Here is the original date of surgery: http://blog.christineleiendecker.com/2007/08/23/08232007.aspx I then had a lead revision done, and that is what this post was about. If you check the past posts around July and August of 2007, you will find out more about the implant of the SCS.

      Hugs
      -Christine

      Reply to this
  • 10/15/2008 6:48 PM Tasha wrote:
    Hi =)

    I just stopped by to hopefully get some insight on the procedure im about to endure. I too am having a spinal cord stimulator implanted. I gotta say im kinda nervous about it but also relieved to find out i maybe getting some much needed relief from my pain. I already had a ganglion nerve block done but no relief was had after...so my pain doc said this along with the pain meds should hopefully help. I have CRPS II in my rt arm. Was it worth it for u?
    Reply to this
    1. 10/16/2008 7:35 AM Christine wrote:
      Hi. I sent you a personal email last night and I hope to talk with you more in the future.

      I have many posts from July 2007 on that talk about my stimulator progress. Please go through and read them all (if you want of course). I can answer ANY questions, if I know the answer that is. I will be truthful and honest about my experiences, because you will not be able to fight and fight hard if you don't know what's around the next bend.

      I am happy to have my stimulator. I cannot emphasize that enough. It provides me with just enough pain relief.

      In August 2007, before permanent scs, I remember being in "almost" fetal position, crying because everything hurt so badly and nothing, no pills, no warm compresses, nothing was helping, hubby wasn't able help and tried all he could and I just kept snapping at him and snapping at my boy. This happened a lot before my scs, but I only wanted to show one example.

      Since the SCS (both of them) I have had instances of extreme pain. I am still snappy and cranky (my poor family). However, the SCS has helped teach me not to be afraid of the minor jolts and shocks of pain. Don't get me wrong they hurt.

      My SCS has done a lot for me. I pray it does a lot for you.

      Lots of hugs. Please keep me informed.

      Christine

      Reply to this
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