I met Jenna Baker in my 2D Design class this semester. We quickly became friends, and I thank God for that. She inspires me whenever I am around her. My struggles do not compare.
Jenna has awful things I cannot pronounce. So maybe it should come from her:
"When I was 11 years old, I was diagnosed with Alopecia Universalis, an auto-immune disorder that causes you to lose all your body hair, from head to toe. I was in 6th grade, and by the time I was ready to enter 7th grade, all of my hair had fallen out. I started middle school completely bald. I chose not to wear a wig and to just enter the world of junior high just the way I was. Turns out, it blessed me in ways I can not describe- it shaped me into the person I am today.
Then, when I was 17, I was diagnosed with Fibromyalgia. Fibromyalgia is a chronic condition characterized by widespread pain in your muscles, ligaments and tendons, as well as fatigue and multiple tender points where slight pressure causes pain. Fibromyalgia occurs in about 2 percent of the population in the United States. The constant pain caused me to miss a substantial amount of my senior year of high school, and has caused trouble since moving out to Provo to attend BYU.. I have had to miss a lot of class and work due to the pain.
Most recently, October 2010, age 20, I was diagnosed with an Oligodendroglioma. It is a rare form of brain tumor that occurs in approximately 9 in 1 million people (usually in middle-aged adults; more likely in men than women). I have had two brain surgeries where the tumor was removed- the first surgery in Utah by Dr. Reichman, and the second in Virginia by Dr. Watson. Starting January 3rd, I will begin Chemotherapy. The treatment will last 6 months and will consist of 5 days on, 3 weeks off for those 6 months.
So, medically, I have a history that would blow your mind. But what makes me special isn't that I am bald, or that I have a brain tumor. What makes me special is that I don't let it get me down. Every day I find something that helps me be happy. I let life happen, and I make the most out of it. I choose to be happy. That's what makes me special."
Jenna's roommate drew faceless portraits of all their roommates, and Jenna's is obviously in the middle. Jenna is not shy about her baldness...it is just a part of her life.

Fibromyalgia is painful. I cannot tell you how painful because I do not know. But I do know that Jenna would take the elevator to our class on the fifth floor of the HFAC because climbing the stairs was too painful on her knees.
Her family was extremely affected by her health problems, but were always supportive and optimistic. Jenna nannies for her niece, Addie. Fortunately, Jenna is able to have children despite her chemotherapy (and multiple other) treatments.
Jenna is blessed to be alive. I think there must have been a time when her family and friends begged for those eyes to open again. Her eyes were also reopened to a new perspective on life.

Jenna knows sign language, and here, she signs "pain." It is a motion you put wherever the pain lies, and though there is pain in many of her muscles and tendons, she chose to put it by her head.
When I asked Jenna why she chose not to wear a wig, she said that she was young at the time, and chose to be herself...she stuck with it, and only wears a wig (sometimes) on the Sabbath, to dress up for church.
The amazing thing about Jenna is that she loves life, family, friends, and God so deeply, and doesn't let her health get her down. I have only known her for a couple months, but she is a wonderful example of survival, strength, humility, gratitude, and love.
Jenna's blogs:
http://virginiaisforloversisforjenna.blogspot.com/p/what-makes-me-special.html
http://livestrongjenna.blogspot.com/

























