How I’m doing 3 years after deep brain stimulation for Parkinson’s – Parkinson’s News Today

Note: This column describes the authors own experiences with deep brain stimulation for Parkinsons disease. Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a therapy.

Its been three years since I had deep brain stimulation (DBS) for Parkinsons disease, so I thought it was time to revisit the surgery and assess its impact on my life.

I was diagnosed with Parkinsonsin 2015. When I first heard about DBS, I thought it was a last-resort sort of treatment, so I didnt pay it much attention. But as my symptoms worsened, I learned more about it and eventually concluded that it was the best option for me.

After the surgery, my excellent neurologist warned me that patients often forgot how bad their symptoms were before surgery, so theyd start complaining about minor issues and not focus on the positive impact of DBS.

That day, I went home and wrote a list of all the changes Id noticed. I dug that list out today to see where I stand three years later.

Tremor: Before surgery, I had a high-amplitude, unpredictable tremor, mainly in my arms. It would leave me breathless. Now, I still tremor, but not as often, and the bulk of it is in my feet and legs, which doesnt bother me as much as having it in my arms. The other day, I threaded a needle, which I wouldnt have dreamed of doing three years ago.

Medication: Before surgery, I took carbidopa/levodopa every two hours around the clock. I also used the Neupro (rotigotine transdermal system) patch to deliver medication, but it gave me a rash, was expensive, and had to be changed every 24 hours. Now, I take carbidopa/levodopa four times a day, and its tremendously freeing not to be concerned with such an onerous medication schedule.

Pain: Before surgery, I had neck pain for years. Right away after DBS, my neck pain was gone, and, knock on wood, it remains gone.

Stiffness: Before surgery, I was super-duper stiff in my neck and shoulders; this started even before my diagnosis. Now I have just a bit of stiffness in my neck and shoulders.

Sleep: Before surgery, I couldnt sleep through the night, and Id wake up several times with a tremor. Now I sleep through the night.

Walking: Before surgery, I had problems with my toes curling. Initially, right after surgery, my toes stopped curling, but about two years ago, they started to do so again. Im currently getting Botox injections every three months. The jury is still out on whether this treatment is helping me, but I can still walk quite well.

Slowness: Before surgery, I moved with turtle-like slowness, a condition known as bradykinesia. The slowness improved initially, but now Im definitely slowing down again.

Appetite: Before surgery, I lost my appetite as eating just became too tiring. I lost quite a bit of weight. Now Im hungry again, and though I regained most of my weight in the first two years, it recently started dropping again.

Fatigue: Before surgery, I was exhausted. Today, I still am!

My confidence is something I didnt put on the list but should have. Before I was diagnosed with Parkinsons, I did a fair amount of public speaking, taught cooking classes, and loved participating in conversations. Before DBS, if I did any public speaking, my tremors would go wild, which was awkward and a bit embarrassing for me. My confidence took a nosedive.

After DBS, I started participating in discourse again, and my confidence soared. Im in a weird space these days because its not my tremor that slows or stops me, its my voice. My speaking pace is slower and a bit thicker, which is annoying, so I participate less than I want.

So the big question is am I happy that I had deep brain stimulation surgery for Parkinsons? Yes, I am. Before I had it, Id lost hope. I couldnt imagine a day without tremors. I couldnt imagine a day not being ruled by medication. I took neck pain for granted. I had given up on getting a good nights sleep and enjoying meals. Now, I feel so lucky to look back and know I made the right decision for myself and my family.

Note:Parkinsons News Todayis strictly a news and information website about the disease. It does not provide medical advice,diagnosis, ortreatment. This content is not intended to be a substitute for professional medical advice, diagnosis, ortreatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those ofParkinsons News Today or its parent company, Bionews, and are intended to spark discussion about issues pertaining to Parkinsons disease.

Go here to read the rest:
How I'm doing 3 years after deep brain stimulation for Parkinson's - Parkinson's News Today