Well, surgery went well on Monday. I was amused because the anesthesiologist had to come in and place my IV because the nurses were too scared to poke me. The nurses said they didn't see anything so they didn't want to poke me 8 times. I agreed with them and thanked them for not doing so because I've had some horrible nurses who have stuck me up to 18 times, no exaggeration.
The IV went into my right wrist, so it was in an odd place. The anesthesiologist gave me the medicine to put me to sleep while the doctor was injecting numbing medicine into my back. I yelled ow a few times and he injected more. The anesthesiologist asked me if I felt the medicine yet and I shook my head no. She gave me two small syringes of something plus versed. Then, pushed the Propofol, twice. The doctor realized that my IV wasn't working and went over to my wrist and pressed down on it at a funny angle...and then ALL of the medicine hit. I don't remember anything after that, not even being woken up to see if the spinal cord stimulator (SCS) was working properly in the right area. I woke up and the anesthesiologist moved quickly to unhook my IV because the Propofol was still in there heading to my vein, trying to make me sleepy again. I was amused. The staff at this place are great. I would recommend them to anyone who needs pain management. Their bedside manner is fantastic and it's hard to find a doctor who will actually listen to you first.
After they taped me up, I went into recovery where they fine tuned the SCS with a computer. They gave me a remote where I could control the amount of stimulation myself or turn it off while driving.
I laid down when I got home from surgery and laughed so hard because the stimulation was turned all of the way up. I had to wait for my husband to bring the remote inside.
Last night, I slept without tossing or turning, which is something I haven't done in a long time because I couldn't feel pain in my left knee. I was able to walk around more. It was nice not to have that constant sharp pain along with aches. It was all gone.
Then, I went to sleep the wrong way with my back brace on and moved the leads. Now, they will only work if I'm sitting a certain way or if I lay down. So, I called the doctor and asked them to pull the leads out and that I would like to have the permanent implant done. The Rep for Boston Scientific (who represents this machine I'm using for the SCS) will call the doctor and put me on the schedule to have the leads pulled out tomorrow, which is good because I'm allergic to this tape. It itches like crazy!
So, I will be put on the schedule to have this one permanently and I'm excited about it. If I can get this under control, maybe I won't vomit as much because vomiting is my pain response too.
Then, I can just focus on my stomach. I need to get that taken care of. I have an appointment with the GI doctor on Monday and an appointment with the Nutritionist to go over a diet plan later next week. I'm still severely nauseated, but not as bad as I have been. That could be wishful thinking on part of the temporary implant but we'll see.
I'm just excited to finally have my knee taken care of and to have finally found someone who will help me. Then, I can focus on my stomach.
Pictures of my back are below:
The idea was suggested to me (by my MD) that a blog/diary might help me feel better by venting my frustrations and struggles with Gastroparesis. Also, I hope I can help others who may have the same thing through my own experiences. For more information, please email: emilysstomach[at]gmail.com or follow on Twitter: http://twitter.com/emilysstomach or like us on Facebook: http://www.facebook.com/emilysstomach or Instagram: http://www.instagram.com/emilysstomach
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Showing posts with label boston scientific. Show all posts
Showing posts with label boston scientific. Show all posts
Wednesday, September 26, 2012
Monday, July 9, 2012
Boston Scientific - Electrical Stimulator
I went to the pain management doctor for my knee. They would like to install a device, permanently, near my spine, attached to a ligament.
The link is here: http://www.bostonscientific.com/procedure/ProcedureLanding.bsci/,,/navRelId/1000.1002/method/Procedure/id/10001261/seo.serve
This also tells more about it: http://en.wikipedia.org/wiki/Spinal_cord_stimulator
This is a really HUGE decision for me. I'm not sure what to do. If the doctor does decide to put the electrical stimulator in my stomach for gastroparesis then the two would interfere. To be honest, my stomach pain and vomiting is eclipsing the knee pain. My husband thinks that if I get the implant and stop the pain in my knee, that I won't vomit so much. My pain response is to vomit. Also, gastroparesis causes me to vomit too.
I think I'm going to do the trial and see if it provides so relief. I can't tell you how badly I'd like to get out of the house, eat at a nice restaurant, and maybe catch a movie. But most of all, I want to be able to hike again. I miss hiking. It was the one thing I loved to do. Now with the gastroparesis, I can't do much but sit at home near a bathroom.
I did manage to make it to Columbia and Augusta this past weekend with the bucket in the car. I doped myself up on all of the antinausea meds I was given and hoped for the best. The traveling took a lot out of me and I slept for the rest of the weekend. I woke up sick on several occasions. I want to be able to drive my stick shift again. I hate automatics. There's so many things I've taken for granted that I wish I hadn't.
So far, I've had:
Gastroparesis
Ovarian Cysts
Endometrosis
Osteoporosis
A Septic Knee
Meniscal Tear
Lateral Release
Broken Right Arm (which started all of this mess)
Hypoglycemia
When I see all of my friends having kids, I sometimes feel like I want kids... but I wouldn't want to pass my awful genes to anyone...that wouldn't be fair. I'm like a walking case for Doctor House, even though he might kill me five times to help me. How do people manage to have kids with gastroparesis? I can't imagine how intense the morning sickness would be. I throw up six times a day, at least. Plus, it burns my throat and mouth because I have nothing left in my stomach. Half of my taste buds have been burnt off so that I can't taste anything. I'm not hungry in the slightest. The doctor also put me on lyrica, which is a nerve pain pill. I haven't noticed much of a difference yet.
Back to the big decision...I have to get a psychological evaluation before they can even try the trial because my insurance mandates it. I have that on the 23rd. I'm also meeting with the motility specialist on the 11th. I just hope that no one puts me back in the hospital. I've been so weak and tired lately. I have been trying to drink as much as I can but like clockwork, every 2 hours after I eat or drink something, it comes right back up. I'm really tired of bleaching my toilet.
The link is here: http://www.bostonscientific.com/procedure/ProcedureLanding.bsci/,,/navRelId/1000.1002/method/Procedure/id/10001261/seo.serve
This also tells more about it: http://en.wikipedia.org/wiki/Spinal_cord_stimulator
This is a really HUGE decision for me. I'm not sure what to do. If the doctor does decide to put the electrical stimulator in my stomach for gastroparesis then the two would interfere. To be honest, my stomach pain and vomiting is eclipsing the knee pain. My husband thinks that if I get the implant and stop the pain in my knee, that I won't vomit so much. My pain response is to vomit. Also, gastroparesis causes me to vomit too.
I think I'm going to do the trial and see if it provides so relief. I can't tell you how badly I'd like to get out of the house, eat at a nice restaurant, and maybe catch a movie. But most of all, I want to be able to hike again. I miss hiking. It was the one thing I loved to do. Now with the gastroparesis, I can't do much but sit at home near a bathroom.
I did manage to make it to Columbia and Augusta this past weekend with the bucket in the car. I doped myself up on all of the antinausea meds I was given and hoped for the best. The traveling took a lot out of me and I slept for the rest of the weekend. I woke up sick on several occasions. I want to be able to drive my stick shift again. I hate automatics. There's so many things I've taken for granted that I wish I hadn't.
So far, I've had:
Gastroparesis
Ovarian Cysts
Endometrosis
Osteoporosis
A Septic Knee
Meniscal Tear
Lateral Release
Broken Right Arm (which started all of this mess)
Hypoglycemia
When I see all of my friends having kids, I sometimes feel like I want kids... but I wouldn't want to pass my awful genes to anyone...that wouldn't be fair. I'm like a walking case for Doctor House, even though he might kill me five times to help me. How do people manage to have kids with gastroparesis? I can't imagine how intense the morning sickness would be. I throw up six times a day, at least. Plus, it burns my throat and mouth because I have nothing left in my stomach. Half of my taste buds have been burnt off so that I can't taste anything. I'm not hungry in the slightest. The doctor also put me on lyrica, which is a nerve pain pill. I haven't noticed much of a difference yet.
Back to the big decision...I have to get a psychological evaluation before they can even try the trial because my insurance mandates it. I have that on the 23rd. I'm also meeting with the motility specialist on the 11th. I just hope that no one puts me back in the hospital. I've been so weak and tired lately. I have been trying to drink as much as I can but like clockwork, every 2 hours after I eat or drink something, it comes right back up. I'm really tired of bleaching my toilet.
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