Working with MS...
- Oct 15, 2024
- 2 min read
Updated: Nov 15, 2024
I was diagnosed with MS 10 years ago. I lost feeling in my left foot. I thought it was my shoes. I fell and fractured my foot. I waited until I was healed, but I still couldn't use my left foot. The doctor suggested physical therapy. So I went and one look at my foot and she told me she couldn't help me right now. She told me it had nothing to do with a fracture, that it was something more. I went to my general physician and he agreed. He refered me to a neurologist.
After numerous tests to rule out everything under the sun, a spinal tap finally gave us the information my neurologist dreaded. I have Multiple Sclerosis.
I was single, successful in my childcare career, and refused to let it bring me down. I immediately wanted to know my options and what we could do for me to have a successful life. I never thought it would deter me from working or living. I would go for monthly infusions of medication and would try to "fit them" into my schedule. My bimonthly neurologist visits also had to fit into my work schedule. I was too stubborn to have them interfere with my life.
I was working at a large cooperate childcare center as the Director. I was determined to run the school as I would before my diagnosis. However, it got harder and harder. Between the stress, my appointments, and my exhaustion I had to admit defeat. I couldn't run the school with the vigor that I once had.
I moved to a smaller school, the one that started my career in childcare. The owners wanted to start minimizing their presence there and wanted a director to help them run the school. It was a much smaller school and they were extremely hands on so we ran the school together as a team. I wasn't as tired and even if I was, they helped me pick up the slack. It was perfect.
I have since left that school because after the birth of my second child, I realized my energy level would not allow me to be a full time Director as well as mom of two. I stay at home with my boys which became a blessing because now I write. I write my dreams, my daydreams, and any other fantasies that come up. I am venturing a new path and my curse ended up being my blessing.




Kelly, I read your blogs and found them very interesting.
Your blog about the importance of reading to your boys every night brought me back to when our boys were kids. I didn’t read to them every night but did tell them “hot air balloon” stories which I think brought their imaginations to life just like I’m sure happens for Connor and Declan when you read to them.
The blog about your MS diagnosis and how the affects of MS basically led you down a path to where you are today is very interesting. The fact that in the end you were able turn this whole thing into an opportunity to write a novel is really a great story itself.