I Thought It Was Just Healing
After I was implanted, I was told the pressure, dizziness, and burning were “normal healing.” I trusted that for too long. Looking back, the symptoms were my body yelling that something wasn’t right.
Caution: If symptoms keep getting worse instead of slowly better, don’t shrug them off. Ask again. Push harder.
That’s Just Your Other Condition
More than once, my symptoms were blamed on other things – migraines, my acoustic neuroma, stress, anything but the cochlear implant. It delayed real answers and left me doubting myself.
Caution: When everything is blamed on something else, ask directly: “Could this be related to the device or surgery?” and ask for that question to be noted in your chart.
We Don’t Treat Symptoms
At one point I was told, “I don’t treat symptoms.” I left that visit feeling small, scared, and completely on my own.
Caution: You deserve providers who take your symptoms seriously. If you feel brushed off, it’s okay to ask for a second opinion or a different provider. Although other otolaryngologist will tell you to see your implanting surgeon. Very hard to get second opinions.
Even When You Don’t Feel Like Keeping Records – Do It
I started tracking things right away because I was having memory issues and knew I might forget details. By February 2022, I told my surgeon I thought something was wrong. I even pulled out my notebook and went through my symptoms. He told me things were okay. I was told that they were all normal - until my explant
I did my part. I kept notes. The problem wasn’t that I didn’t speak up – it’s that what I said wasn’t taken seriously or documented.
Check your records not once, but twice. Go with your gut.
Caution: Even simple notes on your phone – dates, symptoms, and names – can make a huge difference if you ever need answers later.
This page isn’t here to scare you.
It’s here to slow you down for a minute and help you ask better questions.
I went into my cochlear implant surgery trusting “it will all work out.” I was never told that the electrodes could never make it into the cochlear I wish I had known more, asked more, and pushed harder when my body started telling me something was wrong.
Once I felt something wasn't right is after I did one year of vision therapy and Vestibular Physical Therapy and continued to see Dr. Smith.
Although I was being told everything was fine and that I was doing great. I felt like I was going to die. This was, by far, the worst pain I have ever experienced.
Theee years later (almost to the date) Dr. Driscoll finally agreed to remove my implant. Although I was feeling much better, I needed time to let my cranial nerves to heal. My cochlear implant has been out for a little over a year, and as of 12/16/2025, my cranial nerves are not completely healed, especially my memory and eye nerves. My life consisted of doctor appointments and working around the house and Hawk Heaven Tevern. (Vestibular therapy)
The attorney I should have retained prior to surgery and requested Mayo Clinic and Cochleat Americas to receive all copies of my records
More to come in my book.
"Use caution when selecting an implant and an Otolaryngologist aka ENT Specialist"
TK