Jeremy Stenberg: Tourette Syndrome Interview

We met him in an earlier post (Celebrities with Tourette Syndrome (TS)) but we decided to post this Jeremy Stenberg interview because it is instructive and inspiring. It paints a portrait of a young man living with TS who embraced his condition and who is very successful at what he does.

This interview is lifted from a newsletter issued by the Tourette Syndrome Association (TSA). TSA is an organization which leads public education and awareness campaigns on TS. It also funds research focused on understanding the disease (particularly what causes it) and the ways by which it can be cured.

Read on, fellow Healthwatchers, and be inspired by this Jeremy Stenberg Tourette Syndrome interview:

TSA: We’ve interviewed people in a wide range of professions, including some impressive professional athletes, but you are our very first FMX pro. Please tell us when and how you got started in your exciting career.

Jeremy: I started with the Metal Mulisha crew at 16. I was in the right place at the right time. They were my first sponsors and I’m still with them. I was trying freestyle at 14 or 15 watching videos of it. It came naturally to me. I started riding when I was two. My parents put me on a little motorbike. We’d go for holidays in the desert and my dad would take me riding every day. It is something I love doing. I’m pretty blessed by getting paid for doing what I love to do.

TSA: After all this time in competition, are you fearless?

Jeremy: No, I still get scared, but that’s the fun of it. You feel much better accomplishing something with that little bit of fear.

TSA: What about injuries?

Jeremy: I’ve been injured. I fell off my bike 25 feet in the air, broke my left leg and my right ankle. I’ve broken each ankle 14 times and my left leg just once. I’ve had broken ribs, a collapsed lung, a lacerated liver … lots of injuries.

jeremy stenberg twitch - tourette syndrome2

TSA: Does TS have an impact on your performance as an athlete?

Jeremy: I don’t think so, not a negative impact. It’s helped me get more fans and given me a nickname “Twitch.” It was a little weird at first and kind of bothered me, but now it’s stuck and I’m fine with it. All my fans know me as “Twitch.” It’s all good.

Because of my tics I got teased in school and got into fights, but I think it made me stronger. I had to prove that I can still do this, that I’m still ‘normal’, that I have tics, make funny faces and shake my head, while still riding.

TSA: What was your life like when you were growing up with TS?

Jeremy: I was making noises and clearing my throat, but I was sent to doctors because they thought my parents were beating me. I had bruises, cuts and black eyes. I was just a boy having fun and being pretty fearless. The injuries sent me to the neurologist and that’s how we found out I actually had TS.

TSA: What was the impact of your TS symptoms at school?

Jeremy: I wasn’t into school. They put me in Special Ed for having TS. That made my day way easier. I could do the work — if I wanted to, but I didn’t. They said I needed to pay attention and that I had ADD. I didn’t focus on schoolwork. I did the least possible. Some kids are into school. I wasn’t.

TSA: There are many FMX fans among the Inside TSA readers, any advice for young riders in the TSA family?