Multiple Sclerosis Reflection

In the winter of 2010, my mother was diagnosed with Aggressive Progressive Multiple Sclerosis (MS) by her neurologist through a number of tests. This was the end result after months of going from doctor to doctor without an answer to what the issue was. In my case, having been with my mother during the process of determining what condition was plaguing her, I was given a chance to reflect on the importance of little things in life and develop my zeal to put forth my best effort in situations that life threw out. This unforeseen calamity developed my drive to help others in any little way possible and contribute in greater ways to society.
With the diagnosis for my mother, I had to help out at home a lot more, which proved to be an experience that led me to try volunteering. I helped my mother in various aspects like getting groceries, administering shots for medicinal treatment over one year, helping out with chores at home, and setting up her physical therapy unit. In spite of all that was going on, my mother continued her job at both home and
I began this process by forming a team called MS Brigade, which has participated in two walks so far. This team was created by myself, with the help of a few family friends, including some who had MS also. Through this team, I developed my leadership skills and contributed to a good cause by gathering donations for the National MS Society. However, it was during the time that I was gearing up for my team's second walk that I had a sudden health challenge. This caused me to be hospitalized and diagnosed with Autoimmune Encephalitis and Muscular Dystrophy. However, this did not stop me from taking part in the walk. Though I started homeschooling during the course of my long recovery phase, I continued to volunteer at Mount Sinai Hospital, worked at 82nd Street Academics this past summer, and currently volunteer regularly at my local