Why I write:

"Somebody is waiting on you to tell your story. To share how you're being rescued. To share how scary it is but how beautiful it is. So take a step. Confess the beautiful and broken. It happens one word at a time." --Anne Jackson

27 March 2012

My ovaries were killing me. Literally.

Just two weeks after the evening I discussed in my last post, we moved out of state for me to go to school. Part of my scholarship was 100% coverage for any services provided by the health clinic, so within a month of our arrival, I made an appointment with the university gynecologist. I wanted answers and figured that starting all over with a new doctor might occasion them.

Words cannot express how grateful I am for the incredible health insurance the university provided me and the amazing doctors who helped me. Dr. A was my first doctor at the university, and he listened patiently to my story. He promised me we’d find an answer. When I’d finished giving him all the pertinent details, he began asking me some questions—how much energy did I have, what were my eating habits, what was my typical menstruation cycle. Answer by answer, we elucidated the constellation of symptoms and their probable cause: polycystic ovarian syndrome (PCOS). It explained so many of my body’s abnormalities. In order to verify the diagnosis, we checked my thyroid, blood sugar, and hormone levels. Just as Dr. A suspected, the culprit was PCOS. He referred me to Dr. C, a specialist at the university in female reproductive disorders.

Dr. C gave me tons of information on PCOS. She explained that the catalyst for my sugar cravings and low energy level was insulin resistance, which often accompanies PCOS. Additionally, my hormones were imbalanced, causing irregular periods and other embarrassing problems. Gone untreated, Dr. C told me that PCOS would likely lead to diabetes and perhaps eventual death from it. Despite the enormity of my frustration with my body and the severity of the issue, I still struggled with the decision to start Metformin. For one, a family member of mine had experienced serious problems as a result of taking it. But also, I didn’t like the thought of being on a medication for the rest of my life, especially at the age of 24. After a few weeks of serious thought and prayer, I filled the prescription.

The first six weeks I was on the drug weren’t my favorite days. Metformin causes nausea, painful cramps, and trapped gas, to name a few. I started on the lowest dosage possible and still felt awful. Every time I had to increase the dosage, the symptoms redoubled. But after I’d paid my dues—about ten weeks in—I started seeing a genuine difference in the way I felt. I dropped 10 pounds almost instantly and found it much easier to lose weight even after that, having regulated my insulin imbalance. I had more energy. My menstruation cycle regulated. I felt better than ever, truly. I felt well, healthy. It seemed, honestly, like everything had improved. Except my sex life.

Oddly, the one thing I’d gone in for answers about went unaided. It wasn’t Dr. A’s fault or Dr. C’s fault. It was simply that hormones and insulin and cysts were apparently not causing my dysfunction. When I mentioned this to Dr. C, she said, “It’s so odd…Normally, women with PCOS have a higher sex drive and lower occurrence of dysfunction, due to elevated testosterone levels. We’ll figure it out, Amie. I promise.”

She meant it.

If you want more information on PCOS, this is a good place to start. You’ll find a list of symptoms, treatments, FAQ, and other good stuff there.

1 comment:

  1. It's amazing to me how many of us have the diagnosis... and how so many medical professionals still don't understand it. I also didn't realize you had posted about this just a few days before me!

    ReplyDelete