I recently found out that my friend, Jesse Lee from high school was diagnosed with MS. I don’t know alot about MS and saw an opportunity to learn about the disease and share it with others. Jesse is a really cool guy (and funny) so when I found out about him and MS, I was really interested to learn more. Below is my interview with Jesse. Please read it. I assure you it will touch your heart and inspire you. You can donate too MS and help Jesse raise money for the cause here or by following the links below. Did you have symptoms, how did you know? The first two symptoms I encountered were numbness in my fingers and face and blurry vision in one eye. It was in the summer of 2007 while playing baseball. I have always been a good athlete and all of a sudden I was missing fly balls because of my blurry vision and the numbness caused my coordination to be off. I contacted my Doctor who originally gave me eye drops. Once the eye drops didn’t work I was sent for an MRI. When did you find out you had MS? After my first MRI came back and showed some lesions on the brain, a neurologist that I was referred to said there was a possibility that I had MS and sent me for more tests and a second MRI. The results of those tests confirmed I did in fact have MS and I was officially diagnosed in March of 2008. This was a very frustrating time because as you can see it took almost a year to diagnose and so much uncertainty was surrounding while other symptoms started to arrive and get worse. These other symptoms included; loss of balance, poor short…