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Sunday, August 21, 2011

The Paraphernalia

Well, no one told me about all the paraphernalia that goes with DBS.

I mean, I knew I had to recharge, but was stunned to learn that I had to carry all this home from my session with Medtronics....
My implanted device is rechargeable, meaning that surgery to change the battery is every 9 years instead of 3. So I need to recharge my battery every one to 3 weeks. The bulk of the 'booty' is to recharge the recharger!
To recharge ME, I need to sit still for an hour with a disc draped over my device. (a difficult task in itself; I'll watch a movie).
THAT recharger requires a charger that plugs into the wall.
In case you get as confused as me, there are 3 manuals that I can read; in 3 languages.

Then there's the smaller device that looks like a mobile phone.




(right)


That tells me if I am switched on or not, and allows me to program the device in me as much as the neurologist allows.
Guess it will be handy to carry around if I accidentally get switched off while walking into a shop with theft control...

1 comment:

  1. WELL KARYN...WE SHALL CALL YOU MS.ROBOCOP...DONT OVER CHARGE...DON'T WANT YOUR HAIR TO FLY AWAY...LOL...

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