Tuesday, June 17, 2014

DBS; Before and After

The DBS implant is working great!  Here is a little movie clip I did about it:


By the way, we didn't have a tornado.  Our house always looks like this :-)

Saturday, March 29, 2014

Helpless in the grip of dyskinesia yesterday.  They adjusted my DBS implant and one side was way too high. The posturing and strange movements were alarming and sometimes painful but... kind of hilarious too.  I called it "Supreme Dyskinesia" because I kept sticking my arm out in front of me in a "Stop in the Name of Love" gesture.  Seriously, though, it gave me a new appreciation for the struggles of people who live with dyskinesia; I wouldn't want to fight that battle.  I, at least, can just turn my implant down.

I am retired now.  Well, at least my layoff took effect and I'm not working; I'm still a little too young to actually retire.  Time to start that disability adventure!

Saturday, February 1, 2014


It's been a while.  To all those who left such lovely comments which haven't gotten answered yet, I'm so sorry, but I just haven't had the heart.  Now the DBS implant is working incredibly well, but I've had a host of digestive system issues to deal with, along with depression.  I'm losing my job; come Monday I'll have 60 days to find a new one, but I think I'm going to hang up my hat.  There are things I should be doing to take care of my PD that I haven't had time for, and things that I want to do while I still feel good.

It's a whole new chapter...

Saturday, October 12, 2013

What does Parkinson's Feel Like...Now

I thought that since my PD has advanced and my weapons against it have been upgraded, I should revisit the "What Does Parkinson's Feel Like" article.

Because of the DBS implant, i don't often have really bad symptoms, but sometimes...you remember that old Mickey Mouse cartoon where Mickey and Donald and Goofy end up in a giant's castle and Goofy falls into the Jello on the dinner table?  It was so funny to watch him struggle to get out of the gelatin, moving so slowly and getting very frustrated.  Well, that's what Parkinson's feels like to me sometimes.  Not so funny.  I try to walk faster and I simply can't.  I try to unscrew a cap from a bottle or jar and I move so slowly!  And then there's my face.  Mom always used to say "don't make faces; what if your face froze that way?" What if, indeed... I feel myself sitting there with an idiotic look on my face, usually an entirely inappropriate look, and it's very hard to change expressions.  I'm sure people must think I'm either a sour old lady, or a harmless, grinning idiot.  My voice is getting softer, my speech slurs like I've had one too many martinis.  I have too much saliva in my mouth, so when someone asks me a question, sometimes all that comes out is a bubble.  The fatigue is overwhelming, even if the other symptoms are under control.  Our house is deteriorating around us, i can't do more than about half an hour of housework at time, and since I'm still working full time, I'm usually not up for even that when we get home.

I know that I'm very lucky; the DBS is working like magic for me, and I shouldn't complain.  I'm just getting a little tired of the whole thing.  I need a cure.

If this is Parkinson's Disease, he can have it back...

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About Me

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I'm a lucky lady. I have a wonderful husband of 27 years, a fantastic 25 year old son (I'm so proud of him!) a loving and supportive family, the best friends in the world, a job that I love, and... Parkinson's Disease. I was diagnosed in September 2006. That was a jolt, but I'm learning to deal with it.