“This is Tabitha,” the message said. “I’m calling about the results of your MRI. Please call me back.”
I did.
“How are you?” she asked.
“Fine, I hope,” I said. “You tell me.”
This started back on New Year’s Day. Actually, you could probably trace the migraines back to age six or even earlier, but this part starts with New Year’s Day. I woke with a headache, and while I had perhaps had a bit too much champagne the night before, this was worse than a hangover and it escalated as the day progressed. A workout did not help. A shower did not help. A nap did not help. The pain grew worse. Sometimes, throwing up takes the edge off of the pain.
Vomiting made the pain worse. An unrelenting pain, as if pincers squeezed the top of my brain. I threw up the whole way to urgent care. The doctors there took care of the pain and recommended that I see my doctor, just to be sure. The revolving door of “my doctor’s” practice is a story for another time, but the nurse practitioner referred me to a neurology practice, just to be sure, where the aforementioned Tabitha, a physician’s assistant referred me for an MRI, just to be sure. This, after all, was probably one of the top three worst migraines that I’ve had in my life.
I’ve never had an MRI. I had a CT scan about maybe six or seven years ago when another migraine had me in the emergency room. Nothing showed up on that, so I joked to my husband and FB friends, “don’t worry, it’s not a brain tumor. It’s never a brain tumor. It only feels like a brain tumor.” That was the Monday before last. Tabitha called me yesterday.
“There is a 4 millimeter mass on your pituitary gland,” she informed me.
I almost laughed.
Then, I was curious. What exactly is a pituitary gland? What does it do? Where is it located? (Not at the base of you skull, as I thought, by the way, but right behind your nose.)
Also, I was relieved. Is there an actual cause for this pain I’ve suffered ever since I can remember? Probably not. Probably this was like the tumor they discovered on my brother’s thymus gland when they x-rayed him for a debilitating muscle spasm. Still.
In two weeks, I must go back for another MRI, this time “with contrast.” The worst part of that will be the IV. I’m not fond of IVs. I could only stand the one in the urgent care because it was less painful that my head. Also, based on this and a prior experience there, they are really good with a needle there.
I’m not worried. No, really! Most of what I’ve read on Dr. Google suggests that pituitary tumors give little cause for concern and the treatment is not at all as dreadful as you might think. But I’m walking around in this odd, half-daze of uncertainty. My response mechanisms feel in a state of suspended animation. “How are you?” “Oh, I possibly have a brain tumor. Yourself?” My husband is distressed, and I feel for him. To tell anyone who cares about me would just traumatize them unnecessarily at this point. So, I’m holding it in because my honest-to-god gut response is entirely inappropriate. My reaction would, in fact, hurt other people, especially if this turns out not to be anything at all but a shadow on an image.
You see, I still want to laugh.
I want to say, “well, of course I have a brain tumor! Good things have been happening in my life so why wouldn’t I have a brain tumor?” I want to say, “want to hear something stupid? I might have a brain tumor!” A brain tumor, not a dangerous one, not a big one, just a small pituitary one that will probably be treated through medication or outpatient surgery is just so fittingly, ridiculously something that would happen to me and I want to laugh out loud about it.