The following was written by my friend Ernie who had DBS surgery in 2010 at the age of 60. Deep Brain Stimulation is a neurosurgical procedure introduced in 1987, and approved by the FDA for PD in 2002, involving the implantation of a medical device called a neurostimulator (often referred to as a 'brain pacemaker'), which sends electrical impulses, through implanted electrodes, to specific parts of the brain. DBS does not cure PD but it can help manage symptoms and improve quality of life.
Ernie’s DBS Story
Yikes! He’s going to stick two electrodes in my brain! Why did I agree to have DBS—this deep brain stimulation surgery?
Sinemet was wearing off quicker despite dosage increases to over 2000 mgs/day. Further increase is not recommended. Parkinson Disease in the driver seat meant more hours of tremors, rigidity, and off-balance careening. My neurologist suggests DBS. I see a neurosurgeon who is reputedly one of the best.
DBS helps control tremor, dyskinesia, and dystonia. The usual improvement is 40%, but the neurosurgeon says I can expect 70% improvement. 70% improvement! Wow! I was starting to get a good feeling about DBS.
The neurosurgeon asks about concerns. Doc, I’m bald. Friends who had DBS have scars that look like their surgeons had forgotten to replace their divots. The neurosurgeon says that he has gotten really good at filling the insertion sites. He describes at great length his technique. I ask him if he could glaze my windows!
On the day of the surgery I felt confident until I saw the medieval torture device that my head would be locked into for the next six hours. Fortunately I was asleep when they put my head in the cage and drilled the holes in my skull. I was awakened in the operating room. The brain has no pain receptors. Feeling no pain, I was ready!
The OR was filled with people. One neurologist sat near me. She manipulated my arms and legs to trigger neurons to fire. The torture cage limited my field of vision. All I could see was her ear adorned by a loop earring. She explained what was going on. Doctors operated computers that amplified the sounds of my neurons firing and showed a 3-D image of my brain. A neurosurgeon inserted the electrode. The head neurosurgeon was like an orchestra conductor. He watched the 3-D brain image and listened for the burst of sound each neuron made as it was engaged by the electrode. He would call out to the doctor moving my limbs to “bend his left foot more to the right” or “lift his right leg”. He would call out to the neurosurgeon inserting the electrode “down .02 millimeters”, or “up .01 millimeters”. When the cacophony of neurons sounded just right, the doctors would cheer. The electrode was in the right place. Neurons in different regions of the brain have different sounds. The sounds tell where the electrodes are. This procedure was repeated in the other hemisphere of my brain.
For the rest of the operation, I was asleep again. The surgical electrodes were replaced with the DBS electrodes. Wires were run subcutaneously from these electrodes to a box placed below my right collar bone. The box contains batteries, a programmable microchip and an antenna. The antenna is plugged into a device that can turn the power on or off and program the electrodes. The doctors have the master programming device. Patients have a device that can turn the power on or off, change programs and change voltage levels. In two weeks the electrodes will be activated.
Post-op. Awake for most of the operation, I did not have the usual anesthesia hang-over. I was ready to have some fun with unsuspecting family and physicians. I was planning not to recognize my wife when she came in, but she walked right passed me! I had to call her back. Ernie, you’re supposed to be a gorked-out zombie!
One of the surgeons and more family arrived. The surgeon asked me questions. What city are we in? Chicago! Who is the president? Truman! What day is it? I look at him dazed and confused. The doctor looks at me confused. In unison my family says, “Ernie, stop fooling around!” “Okay, Nixon is president.”
Two weeks pass. I anxiously wait for the electrodes to be turned on. Without medication, I can barely stand and walking is nearly impossible. The electrodes are programmed and activated. My mobility is checked again. Still without medication, I get up from my chair and glide up and down the hallway like Fred Astaire. It’s a miracle!
Five years later. DBS still helps to control PD symptoms but DBS is not a cure. Six months after surgery, PD began to reassert itself. Symptoms started coming back. Dosages of Sinemet that had been lowered have gradually increased to pre-surgery levels but I was able to stop taking one med and my physical motor symptoms are not as bad. Do I have regrets about DBS? No!
4 comments:
Excellent description leavened with humor. This may help many with PD who are considering their options.
i have dystonia which is similar to pkinsns.i have dbs.helps a bit
Dystonia is a neurological movement disorder that results in sustained muscle contractions which cause twisting and repetitive movements or postures that can be very painful. Parkies can develop dystonia as a consequence of the disease or as a side effect of the meds. Thank you for your comment and letting us know that DBS may help.
i love your text ernie. im wary of medtrrronix
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