Hello my name is Sly. I’m 33 years old. Started to show symptoms at age 21, diagnosed at age 25. Fun fact: before I got diagnosed is that I hiked half Dome in Yosemite. It took me and my family about fifteen hours.
When I moved in an apartment with my ex-wife, she started to notice it would take a long time to bring my cup of coffee from the kitchen to the living room. A simple 1 minute task turned into a 30 minute task. I was a 4 year basketball player and 2 years baseball player in high school. I was always called clumsy Sly in college. Then I got diagnosed later that year with SCA2.
When Were You Diagnosed? Which Type (If Known)?
Diagnosed at age 25 I have SCA2
How Has Ataxia Impacted Your Life?
In high school I had a normal childhood. Played basketball all four years and baseball for two years. Went to college and I was always known as Clumsy Sly. I thought that was normal so I didn’t think anything about it. Fast forward to now. I woke up one morning and my balance issues progressed recently. It’s definitely hard day in and day out. I live life day by day. I currently still work as a cashier at a grocery store. I’m trying to be active until I can’t anymore.
What is One Thing You’d Like the People to Know About Ataxia?
One thing I would want people to know about ataxia is that I want everyone to be patient with me. I may slur my words but I’m like any other human being. I have feelings too.
Share Your Advice – How Can Others Support Someone with Ataxia?
Just be patient with me. Be supportive to my condition.
What is Your Ataxia Story?
As an organization dedicated to improving the lives of those affected by Ataxia, we believe that each story has the power to inspire, connect, and empower others. We invite you to share your personal Ataxia journey with us.
Are you here to read the personal stories, but haven’t yet joined as a member? We hope you find comfort in reading about the experiences of others on their Ataxia journey. We invite you to join as a member to receive a new member story each month. It’s free, and you’ll be kept up-to-date on the latest developments in the Ataxia community.
Recent Member Stories

Shannon
Finding Balance: My Journey to a Rare Diagnosis For years, I brushed off the dizziness, fatigue, and the way my feet sometimes seemed to have Read More…

Jorge Alonso
My name is Jorge Alonso, I am 33 years old I was diagnosed with ataxia at 31 or 30, although I really felt the disease Read More…

Abdulrahman
Hello, I’m Abdulrahman – in the beginning I was shocked, but then I digested the news, my lifestyle and way of living really helped me Read More…

Ben Williamson
Living and Dying with Spinocerebellar Ataxia Type 7: A Carer’s Perspective Affiliation: Husband and primary carer of patient with confirmed SCA7 (ATXN7 gene, 10/49 CAG Read More…

Maitreyi Viswanathan
http://youtu.be/sYccDzT25eY?si=f6GkonkY4FvsyFHy The video above is from Maitreyi’s personal YouTube channel, in which she discusses her experiences living with Ataxia. Mature topics are discussed, viewer discretion is Read More…

Ana
When I turned 20, I started to notice something was different about me. I had a brain MRI, which showed that I probably had Ataxia. Read More…