How did you feel when you when you were diagnosed with Multiple Sclerosis? Take a Read, Comment to show your Support and Share if you can Relate.
When I was diagnosed in 2012 I almost felt like it was the end of the world.
My diagnosis gave me an answer to a lot of questions about my problems. My fatigue, loss of concentration and even vision issues finally had a reason.
But as I went along I started proving that it wasn’t my MS. I began going back to school to first get my associate degree and instead for my bachelor’s degree in business administration with the concentration in healthcare administration.
I have the full support of my family even with the loss of my younger, but the only sister two years after my diagnosis.
The recent loss of my father has given me loads determination with the final finish of my degree in December and the start of the master’s degree in business administration with the concentration in healthcare administration.
I am not defined by MS.