Hi all! Long time no see. I had my St. Jude SCS permanently implanted in late August 2013. At first I thought it was great, but within a month, half of my neck and face turned bright red - like a horrible sunburn - and was extremely itchy. I didn't think anything about it though. Exactly 1 year ago, I developed and awful rash on both of my forearms. I went to MedExpress, and the doc there told me I had scabies, I tried the medicine they prescribed for me, and it made it 10 times worse. They cultured some of the rash, and it was positive for MRSA. I wasn't surprised, since I've tested positive for MRSA numerous times in the past from boils.
I scratched and scratched at it (I tried not to scratch, but found myself doing it in my sleep), and within a month or so, I literally had holes in my skin. Liz can tell you about it, as I took pictures of everything all year and have an album posted on Facebook. If anyone wants to see it, find me on fb as Karen Pletcher Campion, friend me, then you can look at the album.
Finally a few months ago, I saw an infectious disease dr. She is highly regarded as one of the best in the country. Well, you had to pick my jaw up from the floor when she said that the spread of MRSA was caused by my SCS, and that it had to be removed.
So I'm scheduled for an explant on Tuesday the 13th. I can't wait, but am also a bit nervous. I'm guessing, and will ask on Monday when they call me with the time for my surgery, that they'll have to remove not only the battery, but also the percutanious leads. I hope they take the leads out, even if recovery is more difficult, otherwise the MRSA won't go away. I haven't used my SCS now for several months, and my skin is finally starting to clear up.
My PM doc is angry at me for having it removed. I guess there go some of his kickbacks!
So has anyone ever developed MSRA, or had their MRSA get worse, because of an SCS?
Oh, and hi Liz!
I hope this works because next up on my list of medical issues to deal with is getting my gallbladder out!