|Prep Sketch for oil painting|
After high school Micki worked and put herself through college, it was there where her life changed. In high school she was picked on for having skin that looked different and for having “bumps” all over her arms and legs. But in college she met a group of friends who accepted her and helped her come out of her shell, she learned about true friendship and she is still friends with these people twenty-five years later. It was also when she learned about Neurofibromatosis (NF). When she was twenty-five Micki was sick and went to the emergency room with difficulty breathing, upon having an x-ray the doctors discovered a “spot” on her lung and suggested follow up. The radiologist Dr. Roush happened upon Micki as she was getting dressed and noticed the café au lait marks. He said “oh, you have neurofibromatosis”? With a puzzled look Micki asked, “neuro what”? Micki had never heard this despite having gone to several doctors over the years regarding “the spots”. After this interaction and a referral to his friend, a dermatologist, she received confirmation of NF1. Upon the initial diagnosis Micki was terrified from what she found in medical journals and the difficulty she had trying to find a doctor to treat her. But luckily, she found a doctor who knew a doctor that lead her to a wonderful group of doctors at The University of Cincinnati who help her navigate the ups and downs of NF1. Micki has had a hysterectomy in addition to surgeries to remove tumors from her lung, leg, arms, back and eye. After much consideration and research, she made the decision not to have children due to the risk of passing it on. Micki continues to deal with chronic pain and has had to learn to adjust to life with it.
Despite the diagnosis Micki has gone to college and graduate school where she graduated in the top five percent of her class. She has worked with people with disabilities for over twenty years. Micki has hiked a small portion of the Appalachian Trail even making it up to the top of McAfee Knob in Virginia, while her softball days are few and far between, she has found a new passion for baking, gardening, hiking, biking and golf. She has completed 4 half marathons to raise awareness of people with disabilities and has raised money for NF research with these half marathons. You can find her on nice days doing one of these activities or volunteering for a few different causes.
While receiving the diagnosis and living with NF is not easy for the individual or the family, Micki wants to let the world know that people with disabilities hidden or visible are people too. You too can reach your dreams with determination and support from loved ones. On bad days when Micki is struggling with pain from NF or struggling with feeling down and isolated because it hurts for someone to touch and comfort her. She tries to remember, God gives his toughest battles to his strongest warriors. Micki will continue to fight for her fellow NF Brothers and Sisters.