Anna Olson
Walk MS: Marshall Ambassador 2010, diagnosed in 2004
What do you remember from the day you were diagnosed?
My mom had been with me throughout my testing and both parents were there for the official diagnosis. A lot of times you hear about people, especially young people, getting misdiagnosed or going through a lot before they are finally diagnosed. For me, it didn’t take long. There were about two weeks between the time there was something noticeably wrong and my diagnosis. I especially remember my diagnosis because it was Homecoming week at school. My neurologist was very nice, and even though I went through a lot of testing during the day I made it back for the homecoming football game and other activities that night.
Why did you decide to participate in Walk MS: Marshall?
Both of my grandmothers had MS, so I was walking for more than myself. I really wanted to walk for everyone in the community who struggled with the disease both those I knew and those who didn’t tell anybody about it.
What do you enjoy most about Walk MS: Marshall?
I like when I see other people there who are helping in this fight. I know a lot of the people who are walking and it’s great to see them all come together for a common cause.
What is the one thing you wish people could understand about MS?
Just because somebody looks normal doesn’t mean MS hasn’t affected them in some way. I have experienced this as a teenager in high school and again in college. I get tired faster than my friends and it sometimes takes me longer to do things — which is not a visible symptom. Many people with MS don’t use wheelchairs or assistive devices but the disease still affects their lives. Don’t judge someone who may be having a tough day, because tomorrow might be better. Even if it’s not, this is what we’re fighting for.