Saturday, December 13, 2014

The Ascent- An essay I wrote my first year in college

I wrote this essay during my first year of college about my battle with Endometriosis and thought I would share it with you all! :) Too bad so many things have changed and the ending of this is no longer true. :(


The Ascent
Since I was a child, I have dreamed about climbing to the top of Mount Everest. I watched a show on The Discovery Channel where they showed an episode about a woman who spent several days climbing to the top of Mount Everest and it inspired me to want to accomplish that as well. Thinking about the journey, the steps I would take, and the experiences I would go through, excites me. As I sit here, thinking about how amazing it would be to climb to the beautiful peak of that mountain top, I realize there will be triumphs and struggles along the way and I may never reach my destination. It takes me back to one of the roughest times in my life when I was diagnosed with Endometriosis, when I did not know if I could climb to the top of my life’s expedition.
 In February of 2010, I was a senior in high school. While everyone was deciding on what college to go to, along with what they wanted to do after they graduated, I was at home trying to decide what doctor I should see next and that he/she may be able to figure out what was going on in my body. The intense burning in the pit of my stomach was unbearable and I did not think that anyone could solve my medical mystery. I felt as though I would live in agony for the rest of my life. Every night, I woke up frightened, thinking I was going to die, or that I had some form of abysmal cancer.  They ran test after test with no answer. My life was flipping upside down and I felt as if I was tumbling to the bottom of a colossal mountain.            
After I graduated, I still had no answers. My family started to think I was imagining the pain; the pain that I was enduring for so long. I was told countless times by multiple doctors and the people I thought cared for me, that it was all in my head. I finally decided to I take it upon myself to find answers. I frantically searched the internet for information that could lead to my diagnosis. I viewed several articles on “causes of abdominal pain in young women,” and I finally found something that caught my attention. Web MD had information about a disease called Endometriosis. “The name endometriosis comes from the word ‘endometrium,’ which is the tissue that lines the inside of the uterus. Endometriosis occurs when tissue that looks and acts like endometrial tissue is found outside the uterus, usually inside the abdominal cavity” (Web MD). The article stated the different symptoms the disease could cause, and matched my symptoms perfectly such as severe abdominal pain and lower back pain. As I read more about this, I made an appointment to see my doctor and she confirmed that it was a good possibility that this is what I had. In October, I had my first surgery that led to the diagnosis of Endometriosis.
My fiancé was with me when I had the surgery as well as when I had my post-operative appointment. We learned together that I will be struggling with Endometriosis for the rest of my life. She explained that it may be hard for us when we are ready to conceive. She said that it wasn’t impossible, but we would have a lower chance than woman with no reproductive diseases. Every little girl dreams of becoming a mother one day and when I heard the news, I was heartbroken beyond belief. I know there are many different options such as adopting or having a surrogate mother, but I had always pictured the day I would give birth to my healthy baby boy or girl. I was imagining his or her sparkling, blue eyes looking up at me while I pondered how I could create such a beautiful little being.  A hundred questions came rushing into my mind, such as, “will I ever get to feel that feeling?” “will my fiancé leave me if I can’t get pregnant?” “am I going to end up paying thousands of dollars in fertility treatments?” and  “Why is this happening to me?”
I later discovered more physical problems that were caused by my disease. I moved to Oklahoma from Texas to live closer to my fiancé’s family and quickly realized that working as a waitress, eight hours on my feet, was not practical. The pain was so excruciating and radiated throughout my entire body making it almost impossible to stand. I had to quit my job after three short months of working. Surprisingly, my fiancé’s mother offered me a position working for her at home where I would not have to be on my feet all day. I was very grateful for such a generous opportunity. However, after a few months I felt very isolated. I did not know anyone in Oklahoma and working at my mother in law’s house made it almost impossible to make friends. I became depressed so I decided to try working for a daycare and I loved it. I got to work with children and made a lot of great friends. It made me ecstatic to be doing something that I loved, and being out of an office chair. Sadly, after a few months my manager at the daycare was starting to get very annoyed with me because I had to keep missing work for doctor’s appointments, or because the pain was so bad that day that I could not even get out of bed. I was starting to get embarrassed by the amount of times I called in, so I ended up putting in my two weeks’ notice. After this I became to believe there was no hope for me to get a real job outside my mother in law’s house. It was extremely upsetting to think that I was going to have to sit inside of a tiny office for the rest of my life. I dreamed of being a teacher at an elementary school one day but I did not know how I could accomplish that if I cannot stay on my feet for longer than thirty minutes.

After going through all these struggles, I never thought I would overcome this disease and get passed all the difficulties it has caused me. I am now happily married to my biggest supporter who has stood by my side for three surgeries and beyond. My doctor thinks that our chances of getting pregnant are pretty high since my Endometriosis has been improving so we have begun trying for our first child. I am currently working with my mother in law again where I have received a promotion and I can work at home or at the company’s warehouse. I can now interact with people every day and it’s really exciting to be sociable again. This is my first year of college and I am majoring in Early Childhood Education, where I hope one day I can become a first grade teacher. Staring at the bottom, not knowing how I was going to deal with this disease, I slowly climbed my way up through the struggles and complications that I did not think I could survive. I have not quite reached the top of where I want to be, but I know now that if I do not give up and keep on climbing, I will one day accomplish my life’s purpose.  


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