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#55
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10-02-2011, 03:29 AM
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Re: My Spinal Cord Stimulator
Damn, I didn't know that there was a many of use going around with Medtronic hardware in them. I just had to have my new large pump replaced when it failed after 16 months. My first one worked for just under 6yrs, it was the 18ml version, then I got the "big" 40ml one and it crapped out wayyyy tooooo soon. I had to have an emergency pump replacement in March. i am glad to know that many people are actually getting good results with their units. Take care...
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#57
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10-02-2011, 06:47 PM
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Re: My Spinal Cord Stimulator
Sharon, I know from reading your post that your bleed was due to a malformation and not a clot, right? But I'm curious. I had a bleed also, in 2009 and had a inferior vena cava filter placed while I was in coma. This is because of the high-risk I have of blood clots, and apparently these filters will protect against pulmonary embolism. I was wondering if you also had one and if you have ever had any problems or pain because of it? Isn't walking divine? I have to say, it's probably one of the things I just took for granted, and now when it's a beautiful day out, a walk down the block is just lovely! · |
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#59
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10-03-2011, 05:11 PM
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Re: My Spinal Cord Stimulator
Walking is awesome. After my first major MS bout I was functionally paralyzed on my right side. Defining 'functionally' as in "All the pieces are there and they work, but the remote controls are stuck on pause." I felt pretty sorry for myself at first, but after I retrained the brain signals I was so happy that it was something I had the power to (kinda) reverse (I fall on my ass and/or head a lot) through sheer bitchiness, stubborness and goofy pysical therapy
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#60
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10-03-2011, 07:46 PM
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Re: My Spinal Cord Stimulator
Sharon, I take Neurontin for nerve pain, which from what I read is pretty close to the Pregabalin that you take. I'm up to 1,800 mg a day! I've got an appointment at a pain clinic within the V.A. in a few weeks--there's got to be something else, maybe something natural? There really aren't any side effects, but I still don't like to feel so dependent on the pills. I'd love to go for a walk with you, too! I bet we'd get some looks! We could have some fun with it. And I know what you mean--I couldn't shower on my own for quite a while--there's another thing I used to do every day and not give it a thought. Now I absolutely relish it. That sounds so silly, but I don't care. The one thing that's taking the longest to get better is my attention span. I used to love reading. Devouring a book every couple days was the norm. But that's why it took me a while to get back, everything I do takes serious planning. Thank you so much for sharing your situation! And I see there are others of us here with similar medical things going on. I'm so glad we're all here, still breathing. |