https://www.newyorker.com/culture/p...y-life-brain-aneurysm-surgery-game-of-thrones
This article is crazy. Reading these details and how close she came to dying both times is terrifying. Some excerpts:
The article also goes into detail about her childhood, her fear of not being able to remember her lines if she suffered brain damage, why she feels lucky and grateful, and how she is helping a charity for people who have suffered from brain injuries.
This article is crazy. Reading these details and how close she came to dying both times is terrifying. Some excerpts:
The diagnosis was quick and ominous: a subarachnoid hemorrhage (SAH), a life-threatening type of stroke, caused by bleeding into the space surrounding the brain. I'd had an aneurysm, an arterial rupture. As I later learned, about a third of SAH patients die immediately or soon thereafter. For the patients who do survive, urgent treatment is required to seal off the aneurysm, as there is a very high risk of a second, often fatal bleed. If I was to live and avoid terrible deficits, I would have to have urgent surgery. And, even then, there were no guarantees.
That first surgery was what is known as "minimally invasive," meaning that they did not open up my skull. Rather, using a technique called endovascular coiling, the surgeon introduced a wire into one of the femoral arteries, in the groin; the wire made its way north, around the heart, and to the brain, where they sealed off the aneurysm.
The operation lasted three hours. When I woke, the pain was unbearable. I had no idea where I was. My field of vision was constricted. There was a tube down my throat and I was parched and nauseated. They moved me out of the I.C.U. after four days and told me that the great hurdle was to make it to the two-week mark. If I made it that long with minimal complications, my chances of a good recovery were high.
One night, after I'd passed that crucial mark, a nurse woke me and, as part of a series of cognitive exercises, she said, "What's your name?" My full name is Emilia Isobel Euphemia Rose Clarke. But now I couldn't remember it. Instead, nonsense words tumbled out of my mouth and I went into a blind panic. I'd never experienced fear like that—a sense of doom closing in. I could see my life ahead, and it wasn't worth living. I am an actor; I need to remember my lines. Now I couldn't recall my name.
I was suffering from a condition called aphasia, a consequence of the trauma my brain had suffered. Even as I was muttering nonsense, my mum did me the great kindness of ignoring it and trying to convince me that I was perfectly lucid. But I knew I was faltering. In my worst moments, I wanted to pull the plug. I asked the medical staff to let me die. My job—my entire dream of what my life would be—centered on language, on communication. Without that, I was lost.
While I was still in New York for the play, with five days left on my SAG insurance, I went in for a brain scan—something I now had to do regularly. The growth on the other side of my brain had doubled in size, and the doctor said we should "take care of it." I was promised a relatively simple operation, easier than last time. Not long after, I found myself in a fancy-pants private room at a Manhattan hospital. My parents were there. "See you in two hours," my mum said, and off I went for surgery, another trip up the femoral artery to my brain. No problem.
Except there was. When they woke me, I was screaming in pain. The procedure had failed. I had a massive bleed and the doctors made it plain that my chances of surviving were precarious if they didn't operate again. This time they needed to access my brain in the old-fashioned way—through my skull. And the operation had to happen immediately.
The recovery was even more painful than it had been after the first surgery. I looked as though I had been through a war more gruesome than any that Daenerys experienced. I emerged from the operation with a drain coming out of my head. Bits of my skull had been replaced by titanium. These days, you can't see the scar that curves from my scalp to my ear, but I didn't know at first that it wouldn't be visible. And there was, above all, the constant worry about cognitive or sensory losses. Would it be concentration? Memory? Peripheral vision? Now I tell people that what it robbed me of is good taste in men. But, of course, none of this seemed remotely funny at the time.
I spent a month in the hospital again and, at certain points, I lost all hope. I couldn't look anyone in the eye. There was terrible anxiety, panic attacks. I was raised never to say, "It's not fair"; I was taught to remember that there is always someone who is worse off than you. But, going through this experience for the second time, all hope receded. I felt like a shell of myself. So much so that I now have a hard time remembering those dark days in much detail. My mind has blocked them out. But I do remember being convinced that I wasn't going to live.
The article also goes into detail about her childhood, her fear of not being able to remember her lines if she suffered brain damage, why she feels lucky and grateful, and how she is helping a charity for people who have suffered from brain injuries.
