And why is it? ....

 that the font keeps changing in my posts?   😀

Session 3 - some relief

We finally got a call back from the London Hospital. The doctor not only confirmed some of my thoughts - specifically that we need to treat each side individually and that the left side needs to follow the right instead of keeping pace, but also prescribed Sinemet CR (controlled release) for use overnight.

It may not be ready at the pharmacy today. Hoping it doesn't take too long to come in.

In the meantime awesome friends are offering some relief from the heat and the stress this evening.

We are blessed.

Why does my life seem to be; I complain, God provides, I wonder if God will, God does. He is always faithful!

Take, take, take

 Sometimes Parkinson's seems like it just takes and takes and takes.....

What it gives back is humility. I can no longer do it all. Why I ever thought I could is a QUESTION FOR ANOTHER DAY.

Session 3 - what 1.5mA on both sides does to me

Hi B,

We are doing well. DBS - is being a bit of a pain. Ok, more than a bit. In concept the surgery is fantastic. It's just harder to dial in the settings than we expected. I was diagnosed with PD in the Spring of 09, but these past few days have been the worst symptoms and/or side effects that I have (that we have - as Judi has had to help me more than ever) ever had. It runs from extreme tremors, lack of strength, inability to move - especially overnight, to vivid dreams where I yell and act out.

We have contacted the hospital but have not heard back yet. I am working on some theories within the constraints of what I am "allowed" to do with DBS settings, and that is a whole 'nother story about my thoughts on health care.

Thank you for all your prayers and support. We have HOPE (in God's plan) and hope (in the DBS technology) and know that we will get "there".

I have some fundamental disagreements with how my settings are being updated and I am seeking answers from other experts. And I really want to explain that, by experts I mean other PD patients who have had DBS.

Church family update

 The second programming session was this past Monday. The stimulation levels have now reached a point where I can really notice a difference. In fact, we bumped up the level from 0.5mA (milliamps) to 1.0mA and I was having a bit of trouble tolerating it. I ended up lowering it to 0.8mA. Tuesday I was in bed most of the day just catching up on sleep.

I am tolerating 1.0mA much better today.

Thank you very much for all your prayers and best wishes. I really appreciate it.

Quick Phone call

Well I thought that it would be a longer phone call, but health care professionals are stretched so thin that they don't have time to be thorough anymore.

Heather called this morning and we bumped up the level from 0.5mA to 1.0mA. I had tested this level earlier for a few minutes and knew there would be an effect. And then, just as quickly as she came, she was gone. The next appointment will be in person.

So - how do I feel?

At 1.0, I have dyskinesea very similar to when my first dose of the day is kicking in. It was a little difficult to deal with, so I dropped it to 0.8, then raised it back to 0.9. I'll try to get it to 1.0 in a while. 

We're making progress!

Programming - Baby Steps

 Judi and I were up bright and early this morning (6:30am) to be at the hospital for programming at 9:30am. Good thing too, as we arrived at the hospital at 9:20.

The programming process consisted of setting the values of each probe independently and checking how I felt and what my PD symptoms were. The settings could completely remove my tremor, etc. and then could turn in to double vision, tingling, hot flashes, etc. when pushed higher.

They then packaged the settings and set the output to 0.5 (mV? - not sure of the units) and stated that we would leave it there for two weeks to get my brain accustomed to being stimulated this way.

The next meeting will be over the phone and we will up the mV setting and re-evaluate. They also reduced my medication frequency from 2.25 hours to 3.5 hours. This see-saw approach of "raise the stimulus and reduce the medication frequency" will continue until we find the right settings for me.

I had forgotten to take my meds along today (the testing and programming took place unmedicated) as I had asked Judi to hide them from me so that I didn't take any without thinking. They got me two sinemet to get me home. Unfortunately there was a delay on the 401 that lasted an hour or more so I went "down" hard and Judi had to finish driving home.

We're home now, and I'm eager to see how the new schedule works. I think that how I feel overnight will be a good indicator of what to expect from these settings.